ASGT: studies and clinical evidence

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I'm going to be analyzing the ingredients in ASGT, and posting studies to support their use. This'll be a work in progress, as it's tedious, but I enjoy it. :)

First off, the stim complex, specifically caffeine:

MENTAL PERFORMANCE

In the same 1992 review (1) it was concluded that “When caffeine is consumed in the range of doses found in many foods, it improves the ability of individuals to perform tasks requiring sustained attention, including automobile driving. In addition, when administered in the same dose range, caffeine increases self-reported alertness and decreases sleepiness”. “Adverse behavioural effects occur when caffeine is consumed in excessive doses or by individuals who are overly sensitive to the substance”.

More recent work has confirmed these conclusions. Thus caffeine increases the processing of new stimuli (2), enhances target detection and response preparation (3) and increases the amount of information processed (4). Such improvements in mental performance are likely to have important implications for the performance of every day tasks. Thus caffeine improved both performance on a driving simulator and during laboratory tests of attention (5). Mental performance declines with age. A cross-sectional study of 890 women and 638 men, mean age 73 years, looked for associations between cognitive function as measured by 12 standardised tests and lifetime or current coffee consumption (6). A higher lifetime coffee consumption in women was significantly associated with better mental performance in six tests. Recently published studies have demonstrated that coffee drinking reduces cognitive decline in both men and women. Van Gelder et al (7), examined whether coffee consumption was associated with 10-year cognitive decline in elderly men. The study participants were 676 healthy men born between 1900 - 1920 from Finland, Italy and the Netherlands. The authors concluded that 'Findings suggest that consuming coffee reduces cognitive decline in elderly men. An inverse and J-shaped association may exist between number of cups of coffee consumed and cognitive decline, with the least cognitive decline for men consuming 3 cups of coffee per day'. Similar findings were reported for women in a study that examined the association between caffeine intake, cognitive decline and dementia in a community based sample of subjects aged 65 years and over(8). The participants were 4,197 women and 2,820 men from a population cohort recruited from three French cities. Cognitive performance, clinical diagnosis of dementia, and caffeine consumption were evaluated at baselineand at 2 and 4 year follow-up. The authors found that the psychostimulant properties of caffeine appeared to reduce cognitive decline in women without dementia, especially at higher ages. Interestingly, unlike Van Gelder, these researchers found no relation between caffeine intake and cognitive decline in the male participants of thier study.

References:

1. Liebermann, H.R. Caffeine. In: Smith, A.P. and Jones, D.M. (Eds.), Handbook of Human Performance, vol. 2. Academic Press, London, pp. 49-72, 1992.

2. Smith, A.P. et al. Physiology and Behavior, 67, 9-17, 1999.

3. Lorist, M.M. and Snel, J. Electroencephalography and Clinical Neurophysiology, 102, 401-413, 1997.

4. Ruijter, J. et al. Journal of Psychophysiology, 13, 37-48, 1999.

5. Brice, C. and Smith, A.P. Human Psychopharmacology, 16, 523-531, 2001.

6. Johnson-Kozlow, M. et al. American Journal of Epidemiology, 156, 842-850, 2002.

7. Van Gelder,B.M. et al, European Journal of Clinical Nutrition, 61, 226-232, 2007.

8. Ritchie, K, et al. Neurology, 69, 2007.
There is evidence that caffeine can improve physical performance. In a study on recreational athletes, the consumption of 6mg/kg body weight of caffeine – roughly 490 mg caffeine for a 180 lb. male, or about five cups of coffee - significantly increased muscle endurance during brief, intense exercise. Prior to a maximum effort run, caffeine consumption of 5 mg/kg body weight – roughly 295 mg caffeine for a 130 lb. female, or about three cups of coffee - resulted in significantly greater anaerobic metabolism and improved athletic performance among recreational runners.5
In addition, a study conducted on cyclists found that consuming 6 mg caffeine per kg body weight (about 355 mg for a 130 lb person, or three to four cups of coffee)improved performance times during a cycling trial, regardless of whether caffeine was ingested one hour before exercise or in a series of doses throughout the trial.6
Researchers made another interesting observation in this study – they found that caffeinated soft drinks could act as a replacement for sports drinks during the last part of an event with no loss of performance. They also found that soft drink consumption produced “enhanced performance” when consumed at the end of tasks. The benefits observed were determined to be largely due to the ingestion of a small amount of caffeine - just 1.5 mg/kg body weight (roughly 90 mg caffeine for a 130 lb person, or about one cup of coffee).7 Other research has also suggested that all types of caffeinated beverages, including soft drinks and sports drinks, are of equal value to cyclists in terms of improved performance during a prolonged task.
Consumption of caffeine has also been shown to improve endurance during physical exercise when consumed before the task.8 One explanation for this is that caffeine may lower the threshold for exercise-induced β-endorphin and cortisol release. These hormones produce the so-called “runner’s high,” which may contribute to the reported caffeine exercise benefits. However, further research must be done to investigate this theory.

Effects of caffeine, sleep loss, and stress on cognitive performance and mood during U.S. Navy SEAL training. Sea-Air-Land.
Lieberman HR, Tharion WJ, Shukitt-Hale B, Speckman KL, Tulley R.

Military Nutrition Division, U.S. Army Research Institute of Environmental Medicine, Natick, MA 01760-5007, USA. [email protected]
Abstract
RATIONALE: When humans are acutely exposed to multiple stressors, cognitive performance is substantially degraded. Few practical strategies are available to sustain performance under such conditions.

OBJECTIVE: This study examined whether moderate doses of caffeine would reduce adverse effects of sleep deprivation and exposure to severe environmental and operational stress on cognitive performance.

METHODS: Volunteers were 68 U.S. Navy Sea-Air-Land (SEAL) trainees, randomly assigned to receive either 100, 200, or 300 mg caffeine or placebo in capsule form after 72 h of sleep deprivation and continuous exposure to other stressors. Cognitive tests administered included scanning visual vigilance, four-choice visual reaction time, a matching-to-sample working memory task and a repeated acquisition test of motor learning and memory. Mood state, marksmanship, and saliva caffeine were also assessed. Testing was conducted 1 and 8 h after treatment.

RESULTS: Sleep deprivation and environmental stress adversely affected performance and mood. Caffeine, in a dose-dependent manner, mitigated many adverse effects of exposure to multiple stressors. Caffeine (200 and 300 mg) significantly improved visual vigilance, choice reaction time, repeated acquisition, self-reported fatigue and sleepiness with the greatest effects on tests of vigilance, reaction time, and alertness. Marksmanship, a task that requires fine motor coordination and steadiness, was not affected by caffeine. The greatest effects of caffeine were present 1 h post-administration, but significant effects persisted for 8 h.
Effects of caffeine on human behavior.
Smith A.

Center for Occupational and Health Psychology, School of Psychology, Cardiff University, UK. [email protected]
Abstract
The literature suggests that the following effects on behavior of adult humans may occur when individuals consume moderate amounts of caffeine. (1) Caffeine increases alertness and reduces fatigue. This may be especially important in low arousal situations (e.g. working at night). (2) Caffeine improves performance on vigilance tasks and simple tasks that require sustained response. Again, these effects are often clearest when alertness is reduced, although there is evidence that benefits may still occur when the person is unimpaired. (3) Effects on more complex tasks are difficult to assess and probably involve interactions between the caffeine and other variables which increase alertness (e.g. personality and time of day). (4) In contrast to the effects of caffeine consumption, withdrawal of caffeine has few effects on performance. There is often an increase in negative mood following withdrawal of caffeine, but such effects may largely reflect the expectancies of the volunteers and the failure to conduct "blind" studies. (5) Regular caffeine usage appears to be beneficial, with higher users having better mental functioning. (6) Most people are very good at controlling their caffeine consumption to maximise the above positive effects. For example, the pattern of consumption over the day shows that caffeine is often consumed to increase alertness. Indeed, many people do not consume much caffeine later in the day since it is important not to be alert when one goes to sleep. In contrast to effects found from normal caffeine intake, there are reports that have demonstrated negative effects when very large amounts are given or sensitive groups (e.g. patients with anxiety disorders) were studied. In this context caffeine has been shown to increase anxiety and impair sleep. There is also some evidence that fine motor control may be impaired as a function of the increase in anxiety. Overall, the global picture that emerges depends on whether one focuses on effects that are likely to be present when caffeine is consumed in moderation by the majority of the population or on the effects found in extreme conditions. The evidence clearly shows that levels of caffeine consumed by most people have largely positive effects on behavior. Excessive consumption can lead to problems, especially in sensitive individuals.
A member of the team, Jason Tallis, tested the effect of caffeine on both the power output and endurance of soleus muscles (lower leg muscle) in mice, under both maximal and sub-maximal activities.
He found that a caffeine dosage of 70 µM enhanced power output by ~6% during both types of activity. This effect in humans is likely to be very similar, according to the researchers.
"70 μM caffeine concentration is the absolute maximum that can normally achieved in the blood plasma of a human, however concentrations of 20-50 μM are not unusual in people with high caffeine intakes," explains Dr James.
Resultant caffeine in blood plasma (70μM maximum) may act at receptors on skeletal muscle causing enhanced force production. Scientists already know that ingestion of caffeine can increase athletic performance by stimulating the central nervous system.
Additionally, 70μM caffeine treatment increased endurance during sub-maximal activity, but significantly reduced endurance during maximal activity.

Effect of caffeine on quadriceps muscle pain during acute cycling exercise in low versus high
caffeine consumers.

Gliottoni RC, Meyers JR, Arngrimsson SA, Broglio SP, Motl RW.

Department of Kinesiology and Community Health, University of Illinois, Urbana-Champaign, IL, USA.

This experiment examined the effect of a moderate dose of caffeine on quadriceps muscle pain during a bout of high-intensity cycling in low- versus high-caffeine-consuming males. College-age men who were low (< or =100 mg/day; n = 12) or high (> or =400 mg/day; n = 13) habitual caffeine consumers ingested caffeine (5 mg/kg body weight) or a placebo in a counterbalanced order and 1 hr later completed 30 min of cycle ergometry at 75-77% of peak oxygen consumption. Perceptions of quadriceps muscle pain, as well as oxygen consumption, heart rate, and work rate, were recorded during both bouts of exercise. Caffeine ingestion resulted in a statistically significant and moderate reduction in quadriceps muscle-pain-intensity ratings during the 30-min bout of high-intensity cycle ergometry compared with placebo ingestion in both low (d = -0.42) and high (d = -0.55) caffeine consumers. The results suggest that caffeine ingestion is associated with a moderate hypoalgesic effect during high-intensity cycling in college-age men who are low or high habitual caffeine consumers, but future work should consider better defining and differentiating pain and effort when examining the effects of caffeine during acute exercise.

PMID: 19478340 [PubMed - indexed for MEDLINE]
It goes on, and on, and on. Caffeine also has beneficial effects on age-related mental decline, Parkinsons, and Alheimers, among other interesting things, but those don't relate specifically to ASGT. Suffice it to say, there's a reason caffeine is so widely used.
 

BrYmAsTeR17

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There are just too many factors for caffeine consumption and athletic performance enhancement to be clinically proven. You have to account for age, reaction to caffeine varying, how many mg's each uses and how that amount effects Jon or Sam, level of fitness of the individuals(endurance), food intake before workout, sleep the day before, and intensity that each worked out at. This is too much especially for a timely study.

I can understand the cognitive studies but when I have a cup(or two) of coffee before a workout, that workout can still be crappy compared to the ones without caffeine consumption. In fact, I've had many days where no caffeine was far superior to having caffeine without any other drugs involved(natural).

I just don't think I can believe in this type of study
 
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Uh, derr, obviously a well-rested workout can/will be far superior to a sleep-deprived, caffeine-supplemented workout. But a sleep-deprived caffeine-supplemented workout will beat a sleep-deprived workout sans caffeine nearly every time.The point is not to prove that a given ingredient works in every individual every time under all circumstance. ;) That's impossible. The fact is caffeine is great for performance, and when you add in its anti-alzheimers, anti-parkinsons, anti age-related mental decline effects, as well as its overall safety, it's a good addition to any pre-workout.
 
brad1224

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Uh, derr, obviously a well-rested workout can/will be far superior to a sleep-deprived, caffeine-supplemented workout. But a sleep-deprived caffeine-supplemented workout will beat a sleep-deprived workout sans caffeine nearly every time.The point is not to prove that a given ingredient works in every individual every time under all circumstance. ;) That's impossible. The fact is caffeine is great for performance, and when you add in its anti-alzheimers, anti-parkinsons, anti age-related mental decline effects, as well as its overall safety, it's a good addition to any pre-workout.
yes sir!

nothin but the truth here
 
Craigmatthew

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Good thread man and I will be enjoying the reading. Appreciate the time and effrot it takes to bring these studies together man :)
 
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Quercetin -

http://www.ncbi.nlm.nih.gov/pubmed/19927026

Quercetin's Influence on Exercise Performance and Muscle Mitochondrial Biogenesis
Med Sci Sports Exerc. 2009 Nov 13. [Epub ahead of print]. Nieman DC, Williams AS, et al. Departments of Health, Leisure, and Exercise Science Biology; Appalachian State University, Boone, NC.


A randomized, crossover clinical study examined the effects of 14-days of supplementation with quercetin (1000 mg per day) on 26 untrained adult males. Results showed a statistically significant increase in quercetin blood plasma levels, and a 2.9% improvement in treadmill time trial performance and a non-significant directional increase of 4.1% in muscle mitochondria DNA compared to the control.
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http://www.ajcn.org/cgi/content/abstract/88/4/1018

Quercetin improves endothelial function, blood vessel health
Pure dietary flavonoids quercetin and (-)-epicatechin augment nitric oxide products and reduce endothelin-1 acutely in healthy men.
Am J Clin Nutr. 2008 Oct;88(4):1018-25. Loke WM, Hodgson JM, Proudfoot JM, McKinley AJ, Puddey IB, Croft KD. School of Medicine and Pharmacology and the School of Biomedical, Biomolecular and Chemical Sciences, University of Western Australia, Perth, Western Australia.
Dietary flavonoids may improve endothelial function and ultimately lead to beneficial cardiovascular effects. The objective was to assess whether pure dietary flavonoids can modulate nitric oxide and endothelin-1 production and thereby improve endothelial function.A randomized, placebo-controlled, crossover trial in 12 healthy men was conducted to compare the acute effects of the oral administration of 200 mg quercetin, (-)-epicatechin, or epigallocatechin gallate on nitric oxide, endothelin-1, and oxidative stress. Relative to water (control), quercetin and (-)-epicatechin resulted in a significant increase in plasma S-nitrosothiols, plasma nitrite, and urinary nitrate concentrations, but not in plasma nitrate or urinary nitrite. Epigallocatechin gallate did not alter any of the measures of nitric oxide production. Quercetin and (-)-epicatechin resulted in a significant reduction in plasma endothelin-1 concentration, but only quercetin significantly decreased the urinary endothelin-1 concentration. Dietary flavonoids, such as quercetin and (-)-epicatechin, can augment nitric oxide status and reduce endothelin-1 concentrations and may thereby improve endothelial function.
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http://www.ncbi.nlm.nih.gov/pubmed/17805089


Quercetin reduces illness but not immune perturbations after intensive exercise.
Med Sci Sports Exerc. 2007 September. Nieman DC, Henson DA, Gross SJ, Jenkins DP, Davis JM, Murphy EA, Carmichael MD, Dumke CL, Utter AC, McAnulty SR, McAnulty LS, Mayer EP. Department of Health, Leisure, and Exercise Science, Appalachian State University, Boone, NC
To investigate the effects of quercetin supplementation on incidence of upper respiratory tract infections and exercise-induced changes in immune function. Trained male cyclists were randomized to quercetin or placebo groups and, under double-blind procedures, received 3 weeks quercetin (1000 mg a day) or placebo before, during, and for 2 weeks after a 3-d period in which subjects cycled for 3 hours a day at approximately 57% Wmax. Blood and saliva samples were collected before and after each of the three exercise sessions and assayed for natural killer cell activity (NKCA), PHA-stimulated lymphocyte proliferation (PHA-LP), polymorphonuclear oxidative-burst activity (POBA), and salivary IgA output (sIgA). Pre- to postexercise changes in NKCA, POBA, and sIgA did not differ significantly between quercetin and placebo groups. Upper respiratory tract infection incidence during the 2-wk postexercise period differed significantly between groups. Quercetin versus placebo ingestion did not alter exercise-induced changes in several measures of immune function, but it significantly reduced upper respiratory tract infection incidence in cyclists during the 2-wk period after intensified exercise.


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http://www.ncbi.nlm.nih.gov/pubmed/20190352


The Dietary Flavonoid Quercetin Increases VO2max and Endurance Capacity
International Journal of Sports Nutrition and Exercise Metabolism. Davis, Carlstedt, Chen, Carmichael, and Murphy, University of South Carolina
An independent, randomized, double-blind, placebo-controlled, cross-over study showed that when 12 healthy, active (but not highly trained) men and women consumed 500 mg of quercetin (QU995™) in an enriched drink mix twice daily for 7 days, they experienced a 13.2 percent increase in ride time to fatigue (based on bicycle endurance capacity) and a 3.9 percent increase in VO2max (maximum oxygen consumption).
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http://www.ncbi.nlm.nih.gov/pubmed/19211721

Quercetin Increases Brain and Muscle Mitochondrial Biogenesis and Exercise Tolerance in an Animal Study
Am J Physiol Regul Integr Comp Physiol.2009. Davis et al., University of South Carolina
A scientific study on mice examined the effects of 7 days of quercetin supplementation on markers of mitochondrial biogenesis. Results indicate that quercetin supplementation enhanced mitochondrial biogenesis - the production of cellular mitochondria - in the muscle and brain of mice. This increase in mitochondria was associated with an increase in both maximal endurance running capacity (VO2max) and active involvement in physical activity with the mice being more willing to exercise.
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http://www.ncbi.nlm.nih.gov/pubmed/17136942

Dietary Antioxidant Supplementation Combined with Quercetin Improves Cycling Time Trial Performance
International Journal of Sports Nutrition and Exercise Metabolism, 2006, 16, 405-419. MacRae and Mefferd, Pepperdine University
An independent, double-blind, placebo-controlled crossover study on the effects of FRS on performance in eleven elite cyclists showed a 3.1% improvement in time to complete a simulated 30km mountainous time trial when subjects consumed FRS for a 3-week period.
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http://www.ncbi.nlm.nih.gov/pubmed/20860660

CONCLUSION AND IMPLICATIONS Quercetin potentiated glucose and glibenclamide-induced insulin secretion and protected β-cells against oxidative damage. Our study suggested that ERK1/2 played a major role in those effects. The potential of quercetin in preventing β-cell dysfunction associated with diabetes deserves further investigation.
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Currently being conducted

http://clinicaltrials.gov/ct2/show/NCT00065676

Investigating the Use of Quercetin on Glucose Absorption in Obesity, and Obesity With Type 2 Diabetes

Quercetin has numerous other benefits not pertaining to athletic performance, including liver support, strengthening blood vessels, reducing bruising, slowing peptic ulcers, prostate support, anti-tumor activity, etc.
 
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Schizandra

Shizandra has a number of active components, including a variety of lignans, schizandrin a, gomisin a, and gomisin N, among others. It is widely used in Chinese medicine, as demonstrated below; it's main benefit to athletes is its adaptogenic capabilities. It's also a liver tonic, and I've quote some studies on individual components of schizandra.

Schisandra is a significant herbal remedy that acts as a stimulant all over the body. It helps in rejuvenating as well as conditioning different organs, especially the liver and the reproductive system. Schisandra is perhaps the most popular sex stimulant or tonic that is beneficial both for men and women. The herb has a reputation to enhance discharge of sexual fluids and is also used as a remedy to increase sexual vigor amongst men. Schisandra and/ or its extracts are widely used to heal hepatitis as well as improve the functioning of the liver.

Even though schisandra is considered and used as a stimulant, the Chinese use the herb to smoothen anxiety as well as quiet heart palpitations. Schisandra is also used for healing insomnia as well sleeping complaints. In fact, the herb is an ideal example of how adaptogenic thymes are used paradoxically to heal different body disorders and also to normalize the body activities. Although, most researches on schisandra are said to be vague and still in preliminary stage, Chinese herbal practitioners have been conventionally using the herb’s berries to heal mental disorders like neuroses. Apart from treating patients suffering from lack of memory and bad temper, they use schisandra to improve concentration as well as mental harmonization. It may be noted that these treatments are carried following researches on the substance by their scientists.

Among other uses, schisandra is also used to heal the respiratory disorders like unceasing coughs, gasps and succinctness of breath. It is also useful for treating disorders like night panics, dehydration and urinary occurrence by tuning up the body system and kidney activities. Since the last few years, Chinese herbal practitioners have even begun to use schisandra to cure urticaria or hives and many dermal disorders like eczema. In such cases, the herb or its derivatives are administered to the patients in the form of remedial wine. In addition, schisandra is also used to cure numerous other physical problems like diarrhea, dysentery and even help to restore and improve deteriorating vision and sound perception.
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http://www.ncbi.nlm.nih.gov/pubmed/18515024

Pharmacology of Schisandra chinensis Bail.: an overview of Russian research and uses in medicine.
Panossian A, Wikman G.

Swedish Herbal Institute Research & Development, Spårvägen 2, SE-432 96 Askloster, Sweden. [email protected]
Abstract
Schisandra chinensis (Turcz.) Bail. is often referred to as an example of a medicinal plant with use in modern Chinese medicine. However, Schisandra chinensis first gained recognition as an adaptogen in the official medicine of the USSR in the early 1960s, principally as a result of the large number of pharmacological and clinical studies carried out by Russian scientists in the preceding two decades. Schizandra has now secured an established position within the medicine of Russia/USSR as evidenced by the inclusion of the drug in recent editions of the National Pharmacopoeia of the USSR and in the State Register of Drugs. Pharmacological studies on animals have shown that Schizandra increases physical working capacity and affords a stress-protective effect against a broad spectrum of harmful factors including heat shock, skin burn, cooling, frostbite, immobilisation, swimming under load in an atmosphere with decreased air pressure, aseptic inflammation, irradiation, and heavy metal intoxication. The phytoadaptogen exerts an effect on the central nervous, sympathetic, endocrine, immune, respiratory, cardiovascular, gastrointestinal systems, on the development of experimental atherosclerosis, on blood sugar and acid-base balance, and on uterus myotonic activity. Studies on isolated organs, tissues, cells and enzymes have revealed that Schizandra preparations exhibit strong antioxidant activities and affect smooth muscles, arachidonic acid release, biosynthesis of leukotriene B(4) in leukocytes, platelet activating factor activity, carbohydrate-phosphorus metabolism, the formation of heat shock protein and polyamines, tissue respiration and oxygen consumption, and the tolerance of an organism to oxygen intoxication. In healthy subjects, Schizandra increases endurance and accuracy of movement, mental performance and working capacity, and generates alterations in the basal levels of nitric oxide and cortisol in blood and saliva with subsequent effects on the blood cells, vessels and CNS. Numerous clinical trials have demonstrated the efficiency of Schizandra in asthenia, neuralgic and psychiatric (neurosis, psychogenic depression, astheno-depressive states, schizophrenia and alcoholism) disorders, in impaired visual function, hypotension and cardiotonic disorders, in epidemic waves of influenza, in chronic sinusitis, otitis, neuritis and otosclerosis, in pneumonia, radioprotection of the fetoplacental system of pregnant women, allergic dermatitis, acute gastrointestinal diseases, gastric hyper- and hypo-secretion, chronic gastritis, stomach and duodenal ulcers, wound healing and trophic ulcers. This review describes the considerable diversity of pharmacological effects of Schisandra chinensis reported in numerous studies carried out in the former USSR and which have been confirmed over more than 40 years of use of the plant as an official medicinal remedy. Such knowledge can be applied in the expansion of the use of Schizandra in the pharmacotherapy of European and other countries as well as for the further discovery of new drugs based on the lignans that constitute the main secondary metabolites of this plant.]
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http://www.ncbi.nlm.nih.gov/pubmed/19500070

Evidence-based efficacy of adaptogens in fatigue, and molecular mechanisms related to their stress-protective activity.
Panossian A, Wikman G.

Swedish Herbal Institute Research and Development, Spårvägen 2, SE-43296 Askloster, Sweden. [email protected]
Abstract
The aim of this review article is to assess the level of scientific evidence presented by clinical trials of adaptogens in fatigue, and to provide a rationale at the molecular level for verified effects. Strong scientific evidence is available for Rhodiola rosea SHR-5 extract, which improved attention, cognitive function and mental performance in fatigue and in chronic fatigue syndrome. Good scientific evidence has been documented in trails in which Schisandra chinensis and Eleutherococcus senticosus increased endurance and mental performance in patients with mild fatigue and weakness. Based on their efficacy in clinical studies, adaptogens can be defined as a pharmacological group of herbal preparations that increase tolerance to mental exhaustion and enhance attention and mental endurance in situations of decreased performance. The beneficial stress-protective effect of adaptogens is related to regulation of homeostasis via several mechanisms of action associated with the hypothalamic-pituitary-adrenal axis and the control of key mediators of stress response such as molecular chaperons (e.g. Hsp70), stress-activated c-Jun N-terminal protein kinase (JNK1), Forkhead Box O transcription factor DAF-16, cortisol and nitric oxide (NO). The key point of action of phytoadaptogens appears to be their up-regulating and stress-mimetic effects on the "stress-sensor" protein Hsp70, which plays an important role in cell survival and apoptosis. Hsp70 inhibits the expression of NO synthase II gene and interacts with glucocorticoid receptors directly and via the JNK pathway, thus affecting the levels of circulating cortisol and NO. Prevention of stress-induced increase in NO, and the associated decrease in ATP production, results in increased performance and endurance. Adaptogen-induced up-regulation of Hsp70 triggers stress-induced JNK-1 and DAF-16-mediated pathways regulating the resistance to stress and resulting in enhanced mental and physical performance and, possibly, increased longevity.

PMID: 19500070 [PubMed - indexed for MEDLINE]
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http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1J-4K6645X-7&_user=10&_coverDate=08/07/2006&_rdoc=1&_fmt=high&_orig=search&_origin=search&_sort=d&_docanchor=&view=c&_searchStrId=1473784554&_rerunOrigin=google&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=48ff71068f38512395d3ea57a75e6d98&searchtype=a

Gomisin A improves scopolamine-induced memory impairment in mice ,
aDepartment of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University, #1 Hoeki-dong, Dongdeamoon-ku, Seoul 130-701, South Korea
bCollege of Pharmacy, Chungnam National University, Taejon 305-764, South Korea
cDepartment of Herbal Medicinal Resource, College of Health and Welfare, Daegu Haany University, Gyeongsan 712-715, South Korea
dDepartment of Pharmacy, Sahmyook University, Nowon-goo, Seoul 139-742, South Korea
eDepartment of Pharmacology, College of Pharmacy, Seoul National University, San 56-1, Shillim-Dong, Kwanak-Gu, Seoul 151-742, South Korea
Received 22 March 2006; revised 6 June 2006; accepted 12 June 2006. Available online 15 June 2006.
Abstract
Gomisin A is a component of the fruits of Schizandra chinesis which are widely used as a tonic in traditional Chinese medicine. In the present study, we assessed the effect of gomisin A on the learning and memory impairments induced by scopolamine. The cognition-enhancing effect of gomisin A was investigated using a passive avoidance test, the Y-maze test, and the Morris water maze test in mice. Drug-induced amnesia was induced by treating animals with scopolamine (1 mg/kg, i.p.). Gomisin A (5 mg/kg, p.o.) administration significantly reversed scopolamine-induced cognitive impairments in mice by the passive avoidance test and the Y-maze test (P < 0.05), and also improved escape latency in the Morris water maze test at 5 mg/kg (P < 0.05). Moreover, in an in vitro study, gomisin A was found to inhibit acetylcholinesterase activity in a dose-dependent manner (IC50 value; 15.5 μM). These results suggest that gomisin A may be a useful cognitive impairment treatment, and its beneficial effects are mediated, in part, via enhancing the cholinergic nervous system.
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http://www.spandidos-publications.com/mmr/2/5/725

Gomisin N isolated from Schisandra chinensis significantly induces anti-proliferative and pro-apoptotic effects in hepatic carcinoma

Authors: Su Youn Yim, You Jin Lee, Yoen Kyung Lee, Seung Eun Jung, Ji Ha Kim, Hak Jin Kim, Beung Gu Son, Young Hoon Park, Young Guen Lee, Young Whan Choi, Dae Youn Hwang

Affiliations: Department of Laboratory Animal Resources, National Institute of Toxicological Research, Korean FDA, Seoul 122-704, Korea

Doi: 10.3892/mmr_00000163

Pages: 725-732

Abstract:
Lignans isolated from Schisandria chinensis have been prescribed as anti-cancer and anti-hepatitis treatments in Chinese medicine. To investigate the applications of lignans isolated from Schisandria chinensis in hepatic carcinoma therapy, their apoptotic ability was screened using a cell proliferation assay. Compared to the other lignans, gomisin N induced high apoptotic levels in hepatic carcinoma. Cell morphology and flow cytometric analysis demonstrated that this lignan induced cell death at high concentrations, but did not induce any changes at low concentrations. In addition, the expression levels of Bcl-2 and Bax proteins, which are involved in the apoptotic pathway, were markedly increased in only the 320 µM-treated group compared to the vehicle and other concentration groups, while the expression level of p53 protein remained unchanged in this group. These results suggest that gomisin N is an anti-cancer drug candidate capable of inhibiting the proliferation and inducing the apoptosis of human hepatic carcinomas.
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Effectiveness of the analogue of natural Schisandrin C (HpPro) in treatment of liver diseases: an experience in Indonesian patients.
Akbar N, Tahir RA, Santoso WD, Soemarno, Sumaryono, Noer HM, Liu G.

Department of Internal Medicine, School of Medicine, University of Indonesia, Jakarta.
Abstract
OBJECTIVE: To determine the effect of dimethyl-4,4'-dimethoxy-5,6, 5',6-dimethylene dioxybiphenyl-2,2'-dicarboxylate (HpPro) on patients with acute and chronic liver diseases.

METHODS: An open trial and a prospective randomized and controlled study were performed. The open trial consisted of 56 cases (16 cases of acute hepatitis, 20 cases of chronic hepatitis, 14 cases of liver cirrhosis and 6 cases of fatty liver). Controlled study consisted of 20 cases of Child A chronic hepatitis which were randomly treated with either HpPro or a mixture of known drugs which used as a liver protective agent in Indonesia as control for one week. The patients were then crossed over those two drugs in the next week.

RESULTS: In the open trial, after 4 weeks' treatment with HpPro 7.5 mg orally three times daily, acute hepatitis, chronic hepatitis and fatty liver cases showed rapid decrease of SGOT and SGPT. In the liver cirrhosis cases, SGOT and SGPT were decreased slowly. In the controlled trial, nine patients received HpPro 7.5 mg three times daily orally and eleven were treated with a mixture of known drugs as the controls. After one week treatment, HpPro group clinically showed significant decrease of SGPT and SGOT levels compared to control group (P = 0.035). At the second week, HpPro group showed significant decrease of SGOT compared to control group (P = 0.038) but the decrease of SGPT was not significant (P = 0.096).

CONCLUSION: Treatment with HpPro is effective to reduce liver impairment in acute and chronic liver diseases on Indonesian patients. No side effect of HpPro was observed.
PMID: 10374427 [PubMed - indexed for MEDLINE]

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Info on schizandrin b:

http://en.wikipedia.org/wiki/Schisandrin_B
 
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Cinnamon

http://www.ncbi.nlm.nih.gov/pubmed/20513336

Cinnamon: potential role in the prevention of insulin resistance, metabolic syndrome, and type 2 diabetes.
Qin B, Panickar KS, Anderson RA.

Diet, Genomics, and Immunology Laboratory, Beltsville Human Nutrition Research Center, United States Department of Agriculture, Agricultural Research Service, Beltsville, Maryland 20705-2350 , USA.
Abstract
Metabolic syndrome is associated with insulin resistance, elevated glucose and lipids, inflammation, decreased antioxidant activity, increased weight gain, and increased glycation of proteins. Cinnamon has been shown to improve all of these variables in in vitro, animal, and/or human studies. In addition, cinnamon has been shown to alleviate factors associated with Alzheimer's disease by blocking and reversing tau formation in vitro and in ischemic stroke by blocking cell swelling. In vitro studies also show that components of cinnamon control angiogenesis associated with the proliferation of cancer cells. Human studies involving control subjects and subjects with metabolic syndrome, type 2 diabetes mellitus, and polycystic ovary syndrome all show beneficial effects of whole cinnamon and/or aqueous extracts of cinnamon on glucose, insulin, insulin sensitivity, lipids, antioxidant status, blood pressure, lean body mass, and gastric emptying. However, not all studies have shown positive effects of cinnamon, and type and amount of cinnamon, as well as the type of subjects and drugs subjects are taking, are likely to affect the response to cinnamon. In summary, components of cinnamon may be important in the alleviation and prevention of the signs and symptoms of metabolic syndrome, type 2 diabetes, and cardiovascular and related diseases.

PMID: 20513336 [PubMed - in process]PMCID: PMC2901047 [Available on 2011/5/1]

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Chromium and polyphenols from cinnamon improve insulin sensitivity.
Proc Nutr Soc. 2008 Feb;67(1):48-53. Anderson RA. Beltsville Human Nutrition Research Center, USDA, Beltsville, MD 20705, USA.
Naturally-occurring compounds that have been shown to improve insulin sensitivity include Chromium and polyphenols found in cinnamon (Cinnamomon cassia). These compounds also have similar effects on insulin signalling and glucose control. In a double-blind placebo-controlled study it has been demonstrated that glucose, insulin, cholesterol and HbA1c are all improved in patients with type 2 diabetes following Chromium supplementation. It has also been shown that cinnamon polyphenols improve insulin sensitivity in in vitro, animal and human studies. Cinnamon reduces mean fasting serum glucose (18-29%), TAG (23-30%), total cholesterol (12-26%) and LDL-cholesterol (7-27%) in subjects with type 2 diabetes after 40 d of daily consumption of 1-6 g cinnamon. Subjects with the metabolic syndrome who consume an aqueous extract of cinnamon have been shown to have improved fasting blood glucose, systolic blood pressure, percentage body fat and increased lean body mass compared with the placebo group. Studies utilizing an aqueous extract of cinnamon, high in type A polyphenols, have also demonstrated improvements in fasting glucose, glucose tolerance and insulin sensitivity in women with insulin resistance associated with the polycystic ovary syndrome. For both supplemental Cr and cinnamon not all studies have reported beneficial effects and the responses are related to the duration of the study, form of Cr or cinnamon used and the extent of obesity and glucose intolerance of the subjects.
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http://www.ncbi.nlm.nih.gov/pubmed/17924872

Effects of short-term cinnamon ingestion on in vivo glucose tolerance.
Diabetes Obes Metab. 2007 November. Solomon TP, Blannin AK. School of Sport and Exercise Sciences, University of Birmingham, Birmingham, UK.
Seven lean young healthy male volunteers underwent three oral glucose tolerance tests (OGTT) supplemented with either a 5 g placebo (OGTT (control)), 5 g of cinnamon (OGTT (cin)), or 5 g of cinnamon taken 12 h before (OGTT (cin12hpre)) in a randomized-crossover design. Cinnamon ingestion reduced total plasma glucose responses as well as improving insulin sensitivity. These data illustrate that cinnamon spice supplementation may be important to in vivo glycemic control and insulin sensitivity in humans, and not only are its effects immediate, they also appear to be sustained for 12 h.
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http://www.ncbi.nlm.nih.gov/pubmed/19621136

Hepatoprotective effect of cinnamon extracts against carbon tetrachloride induced oxidative stress and liver injury in rats.
Moselhy SS, Ali HK.

Department of Biochemistry, Ain Shams University, Cairo, Egypt. [email protected]
Abstract
Cinnamon is used to flavor most foods in Arabian countries. The aim of this study was to evaluate the medicinal importance, reflecting an important trend in research. The hepatoprotective activity of aqueous and ethanolic extracts of cinnamon was investigated against carbon tetrachloride (CC1(4)) induced lipid peroxidation and hepatic injury in rats. The elevated serum AST and ALT enzymatic activities induced by CC1(4) were significantly restored to near normal by oral administration of 200 mg/kg of either extracts once daily for 7 days, as compared to untreated rats. There was a significant elevation in the level of liver malondialdhyde (MDA), while the activities of antioxidant enzymes superoxide dismutase and catalase (SOD and CAT) were significantly decreased in CC1(4) intoxicated rats. The results obtained indicated that ethanolic extract has more potent hepatoprotective action than water extract against CC1(4) by lowering the MDA level and elevating antioxidants enzymes activities (SOD and CAT). The possible mechanism of this activity may be free radical-scavenging polyphenol compounds. The hepatoprotective properties were documented by the histopathological data obtained. Consequently, this extract can be used as a therapeutic regime in treatment of some hepatic disorders without any side effects. Further study will be done for separation and identification of active components and for testing antitumor activity.
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http://www.ncbi.nlm.nih.gov/pubmed/15002064

Cinnamon extract prevents the insulin resistance induced by a high-fructose diet.
Qin B, Nagasaki M, Ren M, Bajotto G, Oshida Y, Sato Y.

Department of Sports Medicine, Graduate School of Medicine, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Abstract
The aim of this study was to determine whether cinnamon extract (CE) would improve the glucose utilization in normal male Wistar rats fed a high-fructose diet (HFD) for three weeks with or without CE added to the drinking water (300 mg/kg/day). In vivo glucose utilization was measured by the euglycemic clamp technique. Further analyses on the possible changes in insulin signaling occurring in skeletal muscle were performed afterwards by Western blotting. At 3 mU/kg/min insulin infusions, the decreased glucose infusion rate (GIR) in HFD-fed rats (60 % of controls, p < 0.01) was improved by CE administration to the same level of controls (normal chow diet) and the improving effect of CE on the GIR of HFD-fed rats was blocked by approximately 50 % by N-monometyl-L-arginine. The same tendency was found during the 30 mU/kg/min insulin infusions. There were no differences in skeletal muscle insulin receptor (IR)-beta, IR substrate (IRS)-1, or phosphatidylinositol (PI) 3-kinase protein content in any groups. However, the muscular insulin-stimulated IR-beta and IRS-1 tyrosine phosphorylation levels and IRS-1 associated with PI 3-kinase in HFD-fed rats were only 70 +/- 9 %, 76 +/- 5 %, and 72 +/- 6 % of controls (p < 0.05), respectively, and these decreases were significantly improved by CE treatment. These results suggest that early CE administration to HFD-fed rats would prevent the development of insulin resistance at least in part by enhancing insulin signaling and possibly via the NO pathway in skeletal muscle.
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Mulberrry

http://www.associatedcontent.com/article/917319/health_benefits_of_mulberry.html?cat=5

One benefit of Mulberry is that it contains anthocyanins. Anthocyanins are believed to contribute to the antioxidant properties of berries, and they are the reasons berries have their dark colors. At a 2007 symposium about the possible health benefits of berries, researchers presented theories that because berries contain anthocyanins they were able to: fight cancer, fight aging and neurological diseases, fight or control diabetes and fight against bacterial infections.

Cyanidin, like other anthocyanidins, has putative antioxidant and radical-scavenging effects which may protect cells from oxidative damage and reduce risk of cardiovascular diseases and cancer.

Mulberry juice is believed to be a good source of treating anemia and poor blood circulation. In Chinese medicine, people regularly mix Mulberry juice as a tonic and drink it to alleviate anemic symptoms and to improve their blood circulation. Mulberry also has the health benefit of soothing the nerves. When combined with Chinese schizandra and ligustrum, Mulberry is effective at soothing the nerves after a stressful day.

Mulberry is also a good source of nutrients that lower high blood pressure. The American Journal of Clinical Nutrition reports that eating just five ounces of mix berries a day can lower blood pressure, reducing the risk of blood clots and strokes.

Modern research done in France and Italy conclude that blood clotting and the degradation of collagen in the body leads to inflammation. Mulberry like most berries contains free radical scavengers that protect the body
from degeneration. Specifically, Mulberry contains cyanidin 3-glucoside, which Epidemiological studies confirm reduces the risk of many degenerative diseases such as chronic arthritis and atherosclerosis. Thus, Mulberry fights against inflammation.

Cyanidin 3-glucoside according to the Journal of Medicinal Food also protects the body against cardiovascular disease and diabetes. Mulberry along with improving blood circulation, protecting the body against cardiovascular disease, also cures people who suffer from heart palpitations.
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Mulberry fruit protects dopaminergic neurons in toxin-induced Parkinson's disease models.
Kim HG, Ju MS, Shim JS, Kim MC, Lee SH, Huh Y, Kim SY, Oh MS.

Department of Oriental Pharmaceutical Science and Kyung Hee East-West Pharmaceutical Research Institute, College of Pharmacy, Kyung Hee University, Dongdaemun-gu, Seoul 130-701, South Korea.
Abstract
Parkinson's disease (PD), one of the most common neurodegenerative disorders, is characterised by the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc) to the striatum (ST), and involves oxidative stress. Mulberry fruit from Morus alba L. (Moraceae) is commonly eaten, and has long been used in traditional oriental medicine. It contains well-known antioxidant agents such as anthocyanins. The present study examined the protective effects of 70 % ethanol extract of mulberry fruit (ME) against neurotoxicity in in vitro and in vivo PD models. In SH-SY5Y cells stressed with 6-hydroxydopamine (6-OHDA), ME significantly protected the cells from neurotoxicity in a dose-dependent manner. Other assays demonstrated that the protective effect of ME was mediated by its antioxidant and anti-apoptotic effects, regulating reactive oxygen species and NO generation, Bcl-2 and Bax proteins, mitochondrial membrane depolarisation and caspase-3 activation. In mesencephalic primary cells stressed with 6-OHDA or 1-methyl-4-phenylpyridinium (MPP+), pre-treatment with ME also protected dopamine neurons, showing a wide range of effective concentrations in MPP+-induced toxicity. In the sub-acute mouse PD model induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), ME showed a preventative effect against PD-like symptoms (bradykinesia) in the behavioural test and prevented MPTP-induced dopaminergic neuronal damage in an immunocytochemical analysis of the SNpc and ST. These results indicate that ME has neuroprotective effects in in vitro and in vivo PD models, and that it may be useful in preventing or treating PD.

PMID: 20187987 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/17869225

Cyanidin 3-glucoside ameliorates hyperglycemia and insulin sensitivity due to downregulation of retinol binding protein 4 expression in diabetic mice.
Sasaki R, Nishimura N, Hoshino H, Isa Y, Kadowaki M, Ichi T, Tanaka A, Nishiumi S, Fukuda I, Ashida H, Horio F, Tsuda T.

College of Bioscience and Biotechnology, Chubu University, Matsumoto-cho, Kasugai, Aichi 487-8501, Japan.
Abstract
Adipocyte dysfunction is strongly associated with the development of obesity and insulin resistance. It is accepted that the regulation of adipocytokine expression is one of the most important targets for the prevention of obesity and improvement of insulin sensitivity. In this study, we have demonstrated that anthocyanin (cyanidin 3-glucoside; C3G) which is a pigment widespread in the plant kingdom, ameliorates hyperglycemia and insulin sensitivity due to the reduction of retinol binding protein 4 (RBP4) expression in type 2 diabetic mice. KK-A(y) mice were fed control or control +0.2% of a C3G diet for 5 weeks. Dietary C3G significantly reduced blood glucose concentration and enhanced insulin sensitivity. The adiponectin and its receptors expression were not responsible for this amelioration. C3G significantly upregulated the glucose transporter 4 (Glut4) and downregulated RBP4 in the white adipose tissue, which is accompanied by downregulation of the inflammatory adipocytokines (monocyte chemoattractant protein-1 and tumor necrosis factor-alpha) in the white adipose tissue of the C3G group. These findings indicate that C3G has significant potency in an anti-diabetic effect through the regulation of Glut4-RBP4 system and the related inflammatory adipocytokines.

PMID: 17869225 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/15975709

Mulberry anthocyanins, cyanidin 3-rutinoside and cyanidin 3-glucoside, exhibited an inhibitory effect on the migration and invasion of a human lung cancer cell line.
Chen PN, Chu SC, Chiou HL, Kuo WH, Chiang CL, Hsieh YS.

Institute of Biochemistry, Chung Shan Medical University, No 110, Section 1, Chien Kuo N. Road, Taichung 402, Taiwan, ROC.
Abstract
Anthocyanins, present in various fruits and vegetables as natural colorant, have been well characterized to be involved in various bioactive properties and are wildly used for their antioxidant properties. Furthermore, recent studies have revealed pleiotropic anticancer and antiproliferative capabilities of anthocyanin. Berry extract contains high amounts of anthocyanins and is commonly used in diet or in some therapeutic applications. In this study, we first observed that cyanidin 3-rutinoside and cyanidin 3-glucoside (extracted from Morus alba L.) exerted a dose-dependent inhibitory effect on the migration and invasion, of highly metastatic A549 human lung carcinoma cells in absence of cytotoxicity. The results showed that cyanidin 3-glucoside and cyanidin 3-rutinoside treatments could decrease the expressions of matrix matalloprotinase-2 (MMP-2) and urokinase-plasminogen activator (u-PA) in a dose-dependent manner and enhance the expression of tissue inhibitor of matrix matalloprotinase-2 (TIMP-2) and plasminogen activator inhibitor (PAI). Further analysis with semi-quantitative RT-PCR showed that these alterations were all on the transcriptional level. Further, a treatment of cyanidin 3-rutinoside and cyanidin 3-glucoside also resulted in an inhibition on the activation of c-Jun and NF-kappaB. Together, these result suggested that anthocyanins could decrease the in vitro invasiveness of cancer cells and therefore, may be of great value in developing a potential cancer therapy.

PMID: 15975709 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/17004912

J Med Food. 2006 Fall;9(3):431-5.
Mulberry extract supplements ameliorate the inflammation-related hematological parameters in carrageenan-induced arthritic rats.
Kim AJ, Park S.

Department of Food and Nutrition, Hyejoen College, Heongsung Gun, Chungnam, Republic of Korea.
Abstract
Mulberry fruit (Morus Lhou Koidz.), a rich source of the major anthocyanin, cyanidin 3-glucoside (C3G), has traditionally been used for the treatment of inflammatory conditions including rheumatic arthritis. In this study, we evaluated the efficacy of orally administrated methanolic mulberry fruit extract (ME) in carrageenan-induced arthritic rats, based on previously observed in vitro antioxidant and anti-inflammatory activities. A significant attenuation of hind paw inflammation characterized by fluid accumulation, uric acid production, and rheumatoid factors induced by carrageenan was observed following the intake of both ME (50 mg/kg of body weight) and C3G (10 mg/kg of body weight). Moreover, alterations in hematological parameters such as serum triglyceride, high-density lipoprotein-cholesterol, and atherogenic index following carrageenan administration were partially reversed by the administration of ME. It is concluded that dietary mulberry fruit extracts elicited protection against carrageenan-induced inflammation.

PMID: 17004912 [PubMed - indexed for MEDLINE]
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I can't find the abstract for this:

http://www.ncbi.nlm.nih.gov/pubmed/2779283

The therapeutic effect of mulberry in the treatment of constipation and insomnia in the elderly.
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More about cyanidin (I'll try to find the studies referenced here):

http://www.phytochemicals.info/phytochemicals/cyanidin.php

Antioxidant

Cyanidin and its glycosides are very strong antioxidants and are active at pharmacological concentrations. The antioxidant activity is stronger than that of vitamin E, vitamin C and resveratrol and similar to other commercial antioxidants. Cyanidin quickly neutralizes reactive oxygen species such as hydrogen peroxide, reactive oxygen and hydroxyl radical.
Diabetes

A study in Japan by Takanori Tsua et al indicated that cyanidin may have benefits for the prevention of obesity and diabetes. Cyanidin rich extracts significantly reduced the boy weight gain of mice fed with a high fat diet. Cyanidin reduces blood glucose level and improves insulin sensitivity due to the reduction of retinol binding protein 4 expression in type 2 diabetic mice.
Anti-toxic

Many studies have demonstrated the anti-toxic effect of cyanidin, mainly against mycotoxins. Cyandin reduces DNA fragmentation and oxidative damage by aflatoxin B1 and ochratoxin A.
Anti-inflammatory

The consumption of anti-inflammatory foods, mainly plants rich in anthocyanins, may help to control inflammation. Cyanidin from cherries alleviates arthritis in an animal model and reduces the serum level of malonaldehyde, which is a biomarker to measure the level of oxidative stress. Cyanidin suppress the inflammatory effect of zymosan in rats.) It can have important implications for the prevention of nitric oxide mediated inflammatory diseases.
Anti-cancer

There are numerous studies demonstrating the anti-cancer activities of cyandin. The anti-cancer and anti-mutagenic properties of this anthocyanin is directly linked to its antioxidant properties. In-vivo and in-vitro studies are linking cyanidin to a reduced risk of leukemia, lung cancer, colon cancer, skin cancer and prostate cancer. Cyanidin induces cancer cell apoptosis, reduces oxidative damage to DNA, inhibits cell growth and decrease cancer cell proliferation.
Heart health

Endothelial dysfunction causes the development of atherosclerosis, which can result in heart health problems, including stroke and heart attacks. Cyanidin increases the levels of endothelial nitric oxide synthase and heme oxygenase in a dose-dependent manner and inhibits the formation of reactive oxygen species induced by platelet-derived growth factor, a protein which has been linked to the development of atherosclerosis.
Skin protection

Studies suggest that cyanidin might successfully be employed for skin protection. Ultraviolet radiation of the skin tissue causes production of reactive oxygen species, resulting in oxidative stress, cell damage and eventual cell death or skin cancer. Cyanidin neutralizes free radicals and decreases the number of tumors induced by ultraviolet B radiation in rats. Treatment of cultured skin cells with cyanidin attenuated unfavorable biological changes caused by the radiation.
Ischemia-reperfusion protection

The strong antioxidant capacity of cyanidin can be beneficial in conditions of increased oxidative stress, such as during a myocardial ischemia, cerebral ischemia or liver ischemia. Myocardial ischemia is a disease characterized by reduced blood supply to the heart muscle, usually due to atherosclerosis of the coronary arteries. Its risk increases with age, smoking, high cholesterol levels, diabetes and high blood pressure. When blood supply restores after a period of ischemia reperfusion injury to tissue can occur. Cyanidin reduces oxidative damage to organ cells during reperfusion.
And, um, useless bidbit #231:

The white mulberry is scientifically notable for the rapid plant movement involved in pollen release from its catkins. The stamens act as catapults, releasing stored elastic energy in just 25 µs. The resulting movement is approximately 350 miles per hour (560 km/h), over half the speed of sound, making it the fastest known movement in the plant kingdom[3].
Who the **** wouldn't want to eat THAT? It's almost as good as eating the still beating heart of a lion you just killed with your bare hands, under Chuck Norris' tutelage!


Cyanidin's powerful antioxdant effects:

http://www.ncbi.nlm.nih.gov/pubmed/11811546

Activity and mechanism of the antioxidant properties of cyanidin-3-O-beta-glucopyranoside.
Amorini AM, Fazzina G, Lazzarino G, Tavazzi B, Di Pierro D, Santucci R, Sinibaldi F, Galvano F, Galvano G.

Department of Chemical Sciences, University of Catania, Italy.
Abstract
In the present study, the antioxidant activity, the interaction with reactive oxygen species and the redox potential of cyanidin-3-O-beta-glucopyranoside (C-3-G), the main anthocyanin present in juice of pigmented oranges, were evaluated in detail. C-3-G effects on low density lipoproteins (LDL) oxidation induced by 40 microM Cu at a pH of 7.4 were compared with those of resveratrol and ascorbic acid, two other natural antioxidants. All cyanidin-3-O-beta-glucopyranoside concentrations used (1, 2, 5, 10, 20, 50, 100 and 200 microM) inhibited malondialdehyde (MDA) generation (an index of lipid peroxidation), the inhibition being significantly higher than that obtained with equal concentrations of resveratrol and ascorbic acid (IC50 = 6.5 microM for C-3-G, 34 microM for resveratrol and 212 microM for ascorbic acid). Experiments of LDL oxidation performed at a pH of 5.0 or 6.0 showed that C-3-G antioxidant activity is not influenced by pH variations between 5.0 and 7.4. This suggests that metal chelation, exerted by C-3-G through the eventual dissociation of its phenolic groups, plays a minor role in its protective mechanism. The presence of C-3-G produced significantly higher protective effects of pigmented orange juice (obtained from Moro cultivar) with respect to blond orange juice, when tested on copper-induced LDL oxidation. The evaluation of the direct interaction with reactive oxygen species (H2O2, -O2, OH*), demonstrated that C-3-G is quickly oxidized by these compounds and it is, therefore, a highly efficient oxygen free radical scavenger. The powerful C-3-G antioxidant activity is in excellent agreement with the very negative redox potential (-405 mV), determined through direct current cyclic voltammetry measurements. On the basis of these results, C-3-G should be considered as one of the most effective antioxidants that can be assumed with dietary plants; therefore, pigmented oranges represent a very relevant C-3-G source because of the high content of this anthocyanin in their juice.
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http://www.ncbi.nlm.nih.gov/pubmed/12747740

Cyanidin-3-O-beta-glucopyranoside protects myocardium and erythrocytes from oxygen radical-mediated damages.
Amorini AM, Lazzarino G, Galvano F, Fazzina G, Tavazzi B, Galvano G.

Department of Chemical Sciences, Laboratory of Biochemistry, University of Catania, Viale A. Doria 6, Catania, Italy.
Abstract
The cyanidin-3-O-beta-glucopyranoside (C-3-G) antioxidant capacity towards reactive oxygen species (ROS)-mediated damages was assessed in tissue and cells submitted to increased oxidative stress. In the isolated ischemic and reperfused rat heart, 10 or 30 degreesM C-3-G protected from both lipid peroxidation (66.7 and 94% inhibition of malondialdehyde (MDA) generation in 10 and 30 microM C-3-G-reperfused hearts, respectively, in comparison with control reperfused hearts) and energy metabolism impairment (higher ATP concentration in 10 and 30 microM C-3-G-reperfused hearts than in control reperfused hearts). These effects were associated to C-3-G permeation within myocardial cells, as indicated by results obtained in the isolated rat heart perfused for 30 min in the recirculating Langendorff mode under normoxia with 10 and 30 microM C-3-G. Protective effects were exerted, in a dose-dependent manner, by C-3-G also in 2 mM hydrogen peroxide-treated human erythrocytes. With respect to MDA formation, an apparent IC50 of 5.12 microM was calculated for C-3-G (the polyphenol resveratrol used for comparison showed an apparent IC50 of 38.43 microM). The general indications are that C-3-G (largely diffused in dietary plants and fruits, such as pigmented oranges very common in the Mediterranean diet) represents a powerful natural antioxidant with beneficial effects in case of increased oxidative stress, and at pharmacological concentrations it is able to decrease tissue damages occurring in myocardial ischemia and reperfusion.
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More Mulberry :D

http://pubs.acs.org/doi/abs/10.1021/jf073113b

Regulation of Adipocyte Function by Anthocyanins; Possibility of Preventing the Metabolic Syndrome

AbstractFull Text HTMLHi-Res PDF[532 KB]PDF w/ Links[204 KB]Citing Articles
Takanori Tsuda#
College of Bioscience and Biotechnology, Chubu University, 1200 Matsumoto-cho, Kasugai, Aichi 487-8501, Japan
J. Agric. Food Chem., 2008, 56 (3), pp 642–646
DOI: 10.1021/jf073113b
Abstract
Obesity is defined as the accumulation of excess adipose tissue resulting from various metabolic disorders. Adipocyte dysfunction is strongly associated with the development of obesity and insulin resistance. Metabolic syndrome is characterized by a group of metabolic risk factors in one person. Abdominal obesity and adipocyte dysfunction play an important role in the development of this syndrome. Anthocyanins are used as a food coloring, and they are widely distributed in human diets including berries, suggesting that large amounts of anthocyanins are ingested from plant-based foods. This study shows that anthocyanins have a significant potency of antiobesity and ameliorate adipocyte function in in vitro and in vivo systems and also that they have important implications for preventing metabolic syndrome.
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http://www.ncbi.nlm.nih.gov/pubmed/15226277

Upregulation of endothelial nitric oxide synthase by cyanidin-3-glucoside, a typical anthocyanin pigment.
Xu JW, Ikeda K, Yamori Y.

Frontier Health Science, School of Human Environmental Science, MUKOGAWA Women's University, Nishinomiya, Hyogo, 663-8179, Japan. [email protected]
Abstract
Endothelial nitric oxide synthase (eNOS) plays an important role in maintaining blood pressure homeostasis and vascular integrity. Natural dietary flavoniods are thought to protect against cardiovascular diseases by acting as antioxidants and vasodilatants. This study examined the effect of cyanidin-3-glucoside (Cy3G), a typical anthocyanin pigment, on eNOS expression. Treatment of bovine artery endothelial cells (BAECs) with Cy3G for 8 hours of enhanced eNOS protein expression in a dose- and time-dependent manner was determined by Western blot analysis. Longer incubation (12, 16, and 24 hours) of BAECs with 0.1 micromol/L of Cy3G caused a further increase in eNOS expression, and subsequently Cy3G also significantly increased nitric oxide output 2-fold (24 hours). Furthermore, Cy3G stimulated the phosphorylation of Src and extracellular signal-regulated kinase 1/2 (ERK1/2) in a time-dependent manner. An Src kinase inhibitor, pp2, and MEK inhibitor, PD98059, blocked the ERK1/2 phosphorylation and eNOS expression. Transfection with dominant-negative Src cDNA also inhibited the eNOS expression stimulated by Cy3G. In addition, stimulation with Cy3G for 30 minutes resulted in a phosphorylation of Sp1 that was blocked by PD98059. Cy3G enhanced the binding activity of the transcription factor Sp1 to the GC box in the proximal eNOS promoter of BAECs, as revealed by chromatin immunoprecipitation assay. The present study demonstrated that Cy3G induced eNOS expression and escalated NO production via an Src-ERK1/2-Sp1 signaling pathway in vascular endothelial cells. Increased eNOS expression may help to ameliorate endothelial dysfunction, harmonize blood pressure, and prevent atherosclerosis as long-term beneficial effects of flavoniods.
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http://www.ncbi.nlm.nih.gov/pubmed/15358561

FEBS Lett. 2004 Sep 10;574(1-3):176-80.
Cyanidin-3-glucoside regulates phosphorylation of endothelial nitric oxide synthase.
Xu JW, Ikeda K, Yamori Y.

Frontier Health Science, School of Human Environmental Science, MUKOGAWA Women's University, Nishinomiya 663-8179, Japan. [email protected]
Abstract
Dietary anthocyanins are widely distributed in fruits, vegetables and red wines, and there are several reports mentioning their beneficial effects. Previously we reported that cyanidin-3-glucoside (Cy3G) induced endothelial nitric oxide synthase (eNOS) expression and nitric oxide (NO) production in bovine vascular endothelial cells. In the present study, we show that Cy3G regulates phosphorylation of eNOS and Akt, affects the interaction between eNOS and soluble guanylyl cyclase, and increases cyclic guanosine monophosphate (cGMP) production. Our results suggest that Cy3G enhances vascular eNOS activity, and may help to improve vascular endothelial function.
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Who knew the lowly, shunned mulberry packed such a punch?! :D
 
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ASGT is ok but 200mg caffeine, 1g ALCAR,1g taurine and 2g creatine do me well also and costs next to nothing .

the ASGT tastes alot better then the old version. but still a bit ruff at times.
 
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Ellagic Acid

http://www.ncbi.nlm.nih.gov/pubmed/16190622

Evaluation of estrogenic/antiestrogenic activity of ellagic acid via the estrogen receptor subtypes ERalpha and ERbeta.
Papoutsi Z, Kassi E, Tsiapara A, Fokialakis N, Chrousos GP, Moutsatsou P.

Department of Biological Chemistry, Medical School, University of Athens Mikras Asias Str 75, Goudi, Athens 11527, Greece.
Abstract
Ellagic acid is a plant-derived polyphenol, possessing antioxidant, antiproliferative, and antiatherogenic properties. Whether this compound has estrogenic/antiestrogenic activity, however, remains largely unknown. To answer this question, we first investigated the ability of ellagic acid to influence the activity of the estrogen receptor subtypes ERalpha and ERbeta in HeLa cells. Cells co-transfected with an estrogen response element (ERE)-driven luciferase (Luc) reporter gene and an ERalpha- or ERbeta-expression vector were exposed to graded concentrations of ellagic acid. At low concentrations (10(-7) to 10(-9) M), this compound displayed a small but significant estrogenic activity via ERalpha, whereas it was a complete estrogen antagonist via ERbeta. Further evaluation revealed that ellagic acid was a potent antiestrogen in MCF-7 breast cancer-derived cells, increasing, like the pure estrogen antagonist ICI182780, IGFBP-3 levels. Moreover, ellagic acid induced nodule mineralization in an osteoblastic cell line (KS483), an effect that was abolished by the estrogen antagonist. Endometrium-derived epithelial cells (Ishikawa) showed no response to the natural compound by using a cell viability assay (MTT). These findings suggest that ellagic acid may be a natural selective estrogen receptor modulator (SERM).
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http://www.ncbi.nlm.nih.gov/pubmed/18444155

Dietary berries and ellagic acid diminish estrogen-mediated mammary tumorigenesis in ACI rats.
Aiyer HS, Srinivasan C, Gupta RC.

Brown Cancer Center, University of Louisville, Louisville, Kentucky 40202, USA.
Abstract
Estrogen acts as a complete mammary carcinogen in ACI rats. Prevention studies in this model allowed us to identify agents that are effective against estrogen-induced mammary carcinogenesis. In this study, we investigated efficacy of dietary berries and ellagic acid to reduce estrogen-mediated mammary tumorigenesis. Female ACI rats (8-9 wk) were fed either AIN-93M diet (n = 25) or diet supplemented with either powdered blueberry (n = 19) and black raspberry (n = 19) at 2.5% wt/wt each or ellagic acid (n = 22) at 400 ppm. Animals received implants of 17beta-estradiol 2 wk later, were palpated periodically for mammary tumors, and were euthanized after 24 wk. No differences were found in tumor incidence at 24 wk; however, tumor volume and multiplicity were reduced significantly after intervention. Compared with the control group (average tumor volume = 685 +/- 240 mm3 and tumor multiplicity = 8.0 +/- 1.3), ellagic acid reduced the tumor volume by 75% (P < 0.005) and tumor multiplicity by 44% (P < 0.05). Black raspberry followed closely, with tumor volume diminished by > 69% (P < 0.005) and tumor multiplicity by 37% (P = 0.07). Blueberry showed a reduction (40%) only in tumor volume. This is the first report showing the significant efficacy of both ellagic acid and berries in the prevention of solely estrogen-induced mammary tumors.

PMID: 18444155 [PubMed - indexed for MEDLINE]
-----

http://www.ncbi.nlm.nih.gov/pubmed/11911267

Strong antioxidant activity of ellagic acid in mammalian cells in vitro revealed by the comet assay.
Festa F, Aglitti T, Duranti G, Ricordy R, Perticone P, Cozzi R.

Dipartimento di Biologia, Università degli Studi Roma TRE, Italy.
Abstract
Oxidative stress due to oxygen and various radical species is associated with the induction of DNA single- and double-strand breaks and is considered to be a first step in several human degenerative diseases, cancer and ageing. Naturally occurring antioxidants are being extensively analysed for their ability to protect DNA against such injury. We studied three naturally occuring compounds, Ascorbic Acid, Melatonin and Ellagic acid, for their ability to modulate DNA damage produced by two strong radical oxygen inducers (H2O2 and Bleomycin) in cultured CHO cells. The alkaline Comet assay was used to measure DNA damage and a cytofluorimetric analysis was performed to reveal the intracellular oxidative species. The data showed a marked reduction of H2O2- and Bleomycin-induced DNA damage exerted by Ellagic Acid. On the contrary Ascorbic acid and Melatonin appeared to induce a slight increase in DNA damage per se. In combined treatments, they caused a slight reduction of H2O2-induced damage, but they did not efficiently modulate the Bleomycin-induced one. The Dichlorofluorescein diacetate (DCFH-DA) cytofluorimetric test confirmed the strong scavenging action exerted by Ellagic Acid.

PMID: 11911267 [PubMed - indexed for MEDLINE]
-----

http://www.sciencedaily.com/releases/2009/04/090421154318.htm

Antioxidant Found In Berries, Other Foods Prevents UV Skin Damage That Leads To Wrinkles
ScienceDaily (Apr. 23, 2009) — Using a topical application of the antioxidant ellagic acid, researchers at Hallym University in the Republic of Korea markedly prevented collagen destruction and inflammatory response – major causes of wrinkles -- in both human skin cells and the sensitive skin of hairless mice following continuing exposure to UV-B, the sun's skin-damaging ultraviolet radioactive rays.
See Also:
Health & Medicine
Skin Care
Cosmetic Surgery
Psoriasis
Plants & Animals
Mice
Genetics
Genetically Modified
Reference
Sunburn
Scar
Polyphenol antioxidant
Sunscreen
Ji-Young Bae, a graduate student in the laboratory of Dr. Young-Hee Kang, presented results of the two-part study on Tuesday, April 21, at the Experimental Biology 2009 meeting in New Orleans. The presentation was part of the scientific program of the American Society for Nutrition.
Ellagic acid is an antioxidant found in numerous fruits, vegetables and nuts, especially raspberries, strawberries, cranberries and pomegranates. Earlier studies have suggested it has a photoprotective effect.
But how? The Kang laboratory found that, in human skin cells, ellagic acid worked to protect against UV damage by blocking production of MMP (matrix metalloproteinase enzymes that break down collagen in damaged skin cells) and by reducing the expression of ICAM (a molecule involved in inflammation).
The scientists then turned to young (four weeks), male, hairless mice - genetically bred types of mice often used in dermatology studies because of the physiological similarities of their skin to that of humans. For eight weeks, the 12 mice were exposed to increasing ultraviolet radiation, such as that found in sunlight, three times a week, beginning at a level sufficient to cause redness or sunburn and increasing to a level that would have definitely caused minor skin damage to human skin.
During these eight weeks, half of the exposed mice were given daily 10 microM topical applications of ellagic acid on their skin surface, even on the days in which they did not receive UV exposure. The other mice, also exposed to UV light, did not receive ellagic acid. (Another six mice served as controls, with neither UV exposure nor ellagic acid.)
What happened? First, as expected, the mice exposed to UV radiation without the ellagic acid treatment developed wrinkles and thickening of the skin.
Second, as hypothesized, the exposed mice that received topical application of ellagic acid showed reduced wrinkle formation.
Third, as suggested in the study of human cells, the ellagic acid reduced inflammatory response and MMP secretion due to protection from the degradation of collagen. The ellagic acid also helped prevent an increase of epidermal thickness
To be continued...
 
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Trans-Resveratrol

http://jn.nutrition.org/cgi/content/full/135/4/757

trans-Resveratrol was reported to have health benefits including anticarcinogenic effects and protection against cardiovascular disease. One of the mechanisms by which it exerts its action is through modulating the estrogen response systems. Because estrogen is involved in male reproductive biology, we investigated the effect of trans-resveratrol on testis and spermatogenesis. Adult male rats were divided into 2 groups. The treated group was administered by gavage 20 mg/(kg · d) of trans-resveratrol suspended in 10 g/L of carboxymethylcellulose for 90 d, whereas the control group received only carboxymethylcellulose during the same period. The relative weight of testes did not differ between the groups. However, the diameter of the seminiferous tubules was significantly reduced from 437.5 ± 0.1 µm in the controls to 310.9 ± 0.1 µm in the resveratrol–treated rats. This decrease was accompanied by a significant increase in tubular density, from 3.20 ± 0.18 in controls to 6.58 ± 0.18 tubules/mm2 in the treated group. Moreover, sperm counts were significantly greater in the resveratrol-treated rats (24.8 ± 3.30 x 107) than in the control group (14.1 ± 0.80 x 107), but sperm quality did not differ. Serum concentrations of gonadotrophins and testosterone were significantly higher in the resveratrol-treated group. We identified a novel activity of trans-resveratrol. The daily oral administration of this phytochemical to adult male rats enhanced sperm production by stimulating the hypothalamic-pituitary-gonadal axis, without inducing adverse effects.
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http://endo.endojournals.org/cgi/content/abstract/140/1/50

Is Resveratrol an Estrogen Agonist in Growing Rats?1
Russell T. Turner, Glenda L. Evans, Minzhi Zhang, Avudaiappan Maran and Jean D. Sibonga

Departments of Orthopedics, Biochemistry, and Molecular Biology, Mayo Graduate School of Medicine, Rochester, Minnesota 55905

Address all correspondence and requests for reprints to: Russell T. Turner, Ph.D., Orthopedic Research, Room 3â??69 Medical Science Building, Mayo Clinic, 200 First Street SW, Rochester, Minnesota 55905.

Trans-3,4,5-trihydroxystilbene (resveratrol), a polyphenolic compound found in juice and wine from dark-skinned grape cultivars, was recently shown to bind to estrogen receptors in vitro, where it activated transcription of estrogen-responsive reporter genes. The purpose of this 6-day study in weanling rats was to determine the dose response (1, 4, 10, 40, and 100 �µg/day) effects of orally administered resveratrol on estrogen target tissues. The solvent (10% ethanol) had no significant effect on any measurement or derived value. 17�?-Estradiol treatment (100 �µg/day) decreased the growth rate, final body weight, serum cholesterol, and radial bone growth (periosteal bone formation and mineral apposition rates) at the tibia-fibula synostosis. In the uterus, 17�?-estradiol treatment increased wet weight, epithelial cell height, and steady state messenger RNA levels for insulin-like growth factor I. In contrast, resveratrol treatment had no significant effect on body weight, serum cholesterol, radial bone growth, epithelial cell height, or messenger RNA levels for insulin-like growth factor I. Resveratrol treatment resulted in slight increases in uterine wet weight, but significance was achieved at the 10-�µg dose only. A second experiment was performed to determine whether a high dose of resveratrol (1000 �µg/day) antagonizes the ability of estrogen to lower serum cholesterol. As was shown for the lower doses, resveratrol had no effect on body weight, uterine wet weight, uterine epithelial cell height, cortical bone histomorphometry, or serum cholesterol. 17�?-Estradiol significantly lowered serum cholesterol, and this response was antagonized by cotreatment with resveratrol. These in vivo results suggest, in contrast to prior in vitro studies, that resveratrol has little or no estrogen agonism on reproductive and nonreproductive estrogen target tissues and may be an estrogen antagonist.
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http://www.ajcn.org/cgi/content/short/ajcn.2009.28641v1

Effects of resveratrol on cerebral blood flow variables and cognitive performance in humans: a double-blind, placebo-controlled, crossover investigation1,2,3
David O Kennedy, Emma L Wightman, Jonathon L Reay, Georg Lietz, Edward J Okello, Anthea Wilde and Crystal F Haskell
1 From the Brain PerformanceNutrition Research Centre Northumbria University Newcastle upon Tyne United Kingdom (DOK ELW JLR AWCFH)the School of Agriculture FoodRural Development Newcastle University Newcastle upon Tyne United Kingdom (GLEJO).

2 The research described herein was internally funded, and all materials were purchased on the open market.

3 Address reprint requests and correspondence to DO Kennedy, Brain, Performance and Nutrition Research Centre, Northumbria University, Newcastle, United Kingdom NE1 8ST. E-mail: [email protected].

ABSTRACT

Background: The many putative beneficial effects of the polyphenol resveratrol include an ability to bolster endogenous antioxidant defenses, modulate nitric oxide synthesis, and promote vasodilation, which thereby improves blood flow. Resveratrol may therefore modulate aspects of brain function in humans.

Objective: The current study assessed the effects of oral resveratrol on cognitive performance and localized cerebral blood flow variables in healthy human adults.

Design: In this randomized, double-blind, placebo-controlled, crossover study, 22 healthy adults received placebo and 2 doses (250 and 500 mg) of trans-resveratrol in counterbalanced order on separate days. After a 45-min resting absorption period, the participants performed a selection of cognitive tasks that activate the frontal cortex for an additional 36 min. Cerebral blood flow and hemodynamics, as indexed by concentration changes in oxygenated and deoxygenated hemoglobin, were assessed in the frontal cortex throughout the posttreatment period with the use of near-infrared spectroscopy. The presence of resveratrol and its conjugates in plasma was confirmed by HPLC after the same doses in a separate cohort (n = 9).

Results: Resveratrol administration resulted in dose-dependent increases in cerebral blood flow during task performance, as indexed by total concentrations of hemoglobin. There was also an increase in deoxyhemoglobin after both doses of resveratrol, which suggested enhanced oxygen extraction, that became apparent toward the end of the 45-min absorption phase and was sustained throughout task performance. Cognitive function was not affected. Resveratrol metabolites were present in plasma throughout the cognitive task period.

Conclusion: These results showed that single doses of orally administered resveratrol can modulate cerebral blood flow variables.
More specifically:

Resveratrol Improves Memory and Cogniton
Two recent studies, one human and one animal, were recently published in peer reviewed journals focusing on resveratrol’s effect of memory and logical thinking, or cognition.

The human study, conducted at the University of Northumbria, UK, found that the 24 students who were given either 250mg or 500mg of Bioforte Resveratrol, experienced an increase in cerebral blood flow by 100% after taking one Biotivia Bioforte 250mg resveratrol capsule and over 200% about 45 minutes after taking 2 Bioforte resveratrol capsules.

After administration of the resveratrol the subjects were given a series of mathmatical tests, and the brain blood flow were measured. The result of both one and two Bioforte capsules of resveratrol was a dramatic increase in brain blood flow.
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http://www.ajcn.org/cgi/content/abstract/92/1/5

Am J Clin Nutr 92: 5-15, 2010. First published May 12, 2010; doi:10.3945/ajcn.2009.28435
American Journal of Clinical Nutrition, doi:10.3945/ajcn.2009.28435
Vol. 92, No. 1, 5-15, July 2010
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© 2010 American Society for Clinical Nutrition
ORIGINAL RESEARCH COMMUNICATION
Resveratrol regulates human adipocyte number and function in a Sirt1-dependent manner1,2,3
Pamela Fischer-Posovszky, Vera Kukulus, Daniel Tews, Thomas Unterkircher, Klaus-Michael Debatin, Simone Fulda and Martin Wabitsch
1 From the Division of Pediatric Endocrinology and Diabetes (PF-P, VK, DT, and MW) and the Department of Pediatrics and Adolescent Medicine (TU, K-MD, and SF), University of Ulm, Ulm, Germany.

2 Supported in part by the German Research Association (Deutsche Forschungsgemeinschaft; WA 1096/3-2). PF-P is funded by a Margarete von Wrangell scholarship financed by the Ministry of Science, Research and Arts Baden-Wuerttemberg and the European Social Fund.

3 Address correspondence to M Wabitsch, Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University of Ulm Eythstrasse 24, 89075 Ulm, Germany. E-mail: [email protected].

Background: Caloric restriction leads to retardation of the aging processes and to longer life in many organisms. This effect of caloric restriction can be mimicked by resveratrol, a natural plant product present in grapes and red wine, which is known as a potent activator of sirtuin 1 [silent mating type information regulation 2 homolog 1 (Sirt1)].

Objectives: One main effect of caloric restriction in mammals is a reduction of body fat from white adipose tissue. We sought to identify the effects of resveratrol on fat cell biology and to elucidate whether Sirt1 is involved in resveratrol-mediated changes.

Design: Human Simpson-Golabi-Behmel syndrome preadipocytes and adipocytes were used to study proliferation, adipogenic differentiation, glucose uptake, de novo lipogenesis, and adipokine secretion. Sirt1-deficient human preadipocytes were generated by using a lentiviral small hairpin RNA system to study the role of Sirt1 in resveratrol-mediated changes.

Results: Resveratrol inhibited preadipocyte proliferation and adipogenic differentiation in a Sirt1-dependent manner. In human adipocytes, resveratrol stimulated basal and insulin-stimulated glucose uptake. De novo lipogenesis was inhibited in parallel with a down-regulation of lipogenic gene expression. Furthermore, resveratrol down-regulated the expression and secretion of interleukin-6 and interleukin-8. Sirt1 was only partially responsible for the regulation of resveratrol-mediated changes in adipokine secretion.

Conclusions: Taken together, our data suggest that resveratrol influences adipose tissue mass and function in a way that may positively interfere with the development of obesity-related comorbidities. Thus, our findings open up the new perspective that resveratrol-induced intracellular pathways could be a target for prevention or treatment of obesity-associated endocrine and metabolic adverse effects.
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http://www.diabetesincontrol.com/articles/diabetes-news/9530-ada-red-wine-ingredient-benefits-prediabetes

ADA: Red Wine Ingredient Benefits Prediabetes
Resveratrol, the compound in red wine potentially responsible for its beneficial cardiovascular effects, may also benefit patients with prediabetes, researchers say....

Advertisement
In a small and preliminary study, older patients with impaired fasting glucose taking a resveratrol supplement had improvements in postprandial glucose and insulin resistance, according to Jill P. Crandall, MD, of Albert Einstein College of Medicine in Bronx, N.Y., and colleagues.

"There have been a lot of reports of its benefits in a number of disease states," which is why researchers decided to investigate resveratrol in prediabetes, Crandall stated. But she cautioned that, "This is just the beginning. The findings need to be confirmed in bigger studies."

Previously, resveratrol has shown beneficial effects on insulin secretion, insulin sensitivity, and glucose tolerance, but only in animal models. Its antioxidant and cardioprotective effects in humans are more well known.
However, trials of resveratrol by companies such as Pfizer and GlaxoSmithKline, which have focused on the supplement's anti-aging abilities, have not had promising results.

"It is a small study and needs to be confirmed, as other studies with this drug have been negative," Vivian Fonseca, MD, of Tulane University, mentioned.

For their study, the researchers recruited 10 patients ages 60 to 80 who had impaired glucose tolerance.

Over four weeks, patients took one of three doses of resveratrol (1g, 1.5g, or 2g) with a standard meal that included 110 grams of carbohydrates, 20 grams of protein, and 20 grams of fat.

Main outcomes included glucose and insulin area under the curve, as well as calculated measures of insulin sensitivity and secretion. These parameters were assessed at mealtime and 30, 60, 120, and 180 minutes later. Endothelial function was also assessed before and 90 minutes after eating.

The researchers said the results didn't vary by dose, so they combined the data for the analysis.

Crandall also noted that her group had independent tests of the composition of the tablets to confirm that they delivered the indicated dose of resveratrol. She and colleagues found that after four weeks of resveratrol supplements, fasting plasma glucose was unchanged, but both peak post-meal glucose and three-hour glucose area under the curve declined (185 mg/dL versus 166 mg/dL, and 469 versus 428, respectively, P=0.001).

Measures of insulin sensitivity improved (P=0.03), although insulin secretion was unchanged, which indicates that the major effect was on insulin resistance, Crandall said.

There was also a trend toward improved post-meal endothelial function, but blood, lipids, and body weight remained unchanged.

Crandall concluded that the preliminary study shows resveratrol improves insulin resistance and post-meal blood glucose, especially in older patients with impaired glucose tolerance, but the findings need to be confirmed in larger analyses.


Crandall JP, et al "Resveratrol improves glucose metabolism in older adults with IGT" ADA 2010; Abstract 736-P.
 
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3beta-hydroxyurs-12-en-28-oic-acid/Ursolic Acid

Ursolic acid is a pentacyclic triterpene acid, used in cosmetics,[2] that is also capable of inhibiting various types of cancer cells by inhibiting the STAT3 activation pathway[3][4] and human fibrosarcoma cells by reducing the expression of matrix metalloproteinase-9 by acting through the glucocorticoid receptor. As medicine, it is well tolerated and can be used topically and orally.[citation needed]
Ursolic acid is present in many plants, including apples, basil, bilberries, cranberries, elder flower, peppermint, rosemary, lavender, oregano, thyme, hawthorn, prunes. Apple peels contain high quantity of ursolic acid and related compounds which are responsible for the anti-cancer activity of apple. Ursolic acid can also serve as a starting material for synthesis of more potent bioactive derivatives, such as anti-tumor agents.[5]
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http://www.ncbi.nlm.nih.gov/pubmed/18192087

Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition.
Gnoatto SC, Dassonville-Klimpt A, Da Nascimento S, Galéra P, Boumediene K, Gosmann G, Sonnet P, Moslemi S.

Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul (UFRGS), Av. Ipiranga 2752, Porto Alegre 90610-000, RS, Brazil.
Abstract
The inhibitory potency of ursolic acid extracted from Ilex paraguariensis, a plant used in South American population for a tea preparation known as maté, and its derivatives to inhibit aromatase activity was assessed and compared to a phytoestrogen apigenin and a steroidal aromatase inhibitor 4-hyroxyandrostenedione (4-OHA). Among all compounds tested only ursolic acid 1 showed an efficient and dose-dependent aromatase inhibition with IC50 value of 32 microM as did apigenin (IC50=10 microM), whereas IC50 value of 4-OHA was 0.8 microM. Our results show that the incorporation of a metallocene moiety into the ursolic acid derivatives decreases the aromatase inhibition. Moreover, comparison of the structure/inhibitory potency relationship of compounds indicates that the presence of cycle A and the configuration of C3-OH and C17-COOH seems to be more favourable to recognize the active site of aromatase and to block its activity.
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http://www.ncbi.nlm.nih.gov/pubmed/17238068

Aromatase inhibitors from Urtica dioica roots.
Gansser D, Spiteller G.

Lehrstuhl Organische Chemie I, Universität Bayreuth, NW I, Universitätsstrasse 30, D-95440 Bayreuth, Germany.
Abstract
Methanolic extracts of stinging nettle (Urtica dioica L.) roots were investigated for aromatase inhibition. Enzyme inhibition was detected only after appropriate chromatographic separation. Inhibitory effects on aromatase could be demonstrated in vitro for a variety of compounds belonging to different classes. The following compounds developed weak to moderate activity: secoisolariciresinol, oleanolic and ursolic acid, (9Z,11E)-13-hydroxy-9,11-octadecadienoic acid, and 14-octacosanol (5). Inhibitory effects on aromatase have been known to date neither for pentacyclic triterpenes nor for secondary fatty alcohols. The potential physiological significance of the above findings is discussed. Compound 5 is a previously unknown constituent of plants.
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Lots of anti-cancer abstracts:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2738836/
http://cancerres.aacrjournals.org/content/63/15/4375.abstract

Pharmacology of oleanolic acid and ursolic acid

Jie Liu
Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160-7417, USA
Received 30 June 1995; Revised 11 September 1995; accepted 12 September 1995. Available online 21 April 2004.
Abstract
Oleanolic acid and ursolic acid are triterpenoid compounds that exist widely in food, medicinal herbs and other plants. This review summarizes the pharmacological studies on these two triterpenoids. Both oleanolic acid and ursolic acid are effective in protecting against chemically induced liver injury in laboratory animals. Oleanolic acid has been marketed in China as an oral drug for human liver disorders. The mechanism of hepatoprotection by these two compounds may involve the inhibition of toxicant activation and the enhancement of the body defense systems. Oleanolic acid and ursolic acid have also been long-recognized to have antiinflammatory and antihyperlipidemic properties in laboratory animals, and more research is warranted to develop a therapy for patients. Recently, both compounds have been noted for their antitumor-promotion effects, which are stimulating additional research in this field. Oleanolic acid and ursolic acid are relatively non-toxic, and have been used in cosmetics and health products. The possible mechanisms for the pharmacological effects and the prospects for these two compounds are discussed.
Author Keywords: Oleanolic acid; Ursol
 
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UFC time!!!
and what a disappointment it was.... I'm not sure Bisping v Akiyama as a headliner is going to be anymore exciting. Nothing on the horizon until Brock/Cain or Aldo/Manny if you're into WEC. Which Aldo will rape.

Great posts Poison!!! :notworthy:
 
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It...SUCKED. CB was great, that's it. :quadbarrelrollintoguillotinescramble:
 
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It...SUCKED. CB was great, that's it. :quadbarrelrollintoguillotinescramble:
CB and Mitrione were the best fights of the night. When Meathead was my favorite part of the card, it's a bad day.

The way CB rolled and counter-rolled his way into locking that guillotine was effing artwork. His stock just went way up with me.
 
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I hate Mitrione. :lol: I'd jump at the chance to get in the ring with him, if only to enjoy TRYING to smash him in the face.

CB? Artwork, is right.
 
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Hibiscus

http://www.ncbi.nlm.nih.gov/pubmed/17688164

Nig Q J Hosp Med. 2007 Jan-Mar;17(1):5-7.
Anabolic effect of Hibiscus rosasinensis Linn. leaf extracts in immature albino male rats.
Olagbende-Dada SO, Ezeobika EN, Duru FI.

Department of Pharmacognosy, Faculty of Pharmacy, College of Medicine, University of Lagos, Idi-Araba, Lagos, Nigeria.
Abstract
Many plants remedies have been employed in solving man's health needs especially the nutritive value which enhances health living. Aphrodisiac plants are plants with anabolic properties i.e. they help in protein synthesis and enhances sexual abilities in males. They are also known as androgenic plants because their properties are similar to that of androgen a male hormone. Cold aqueous extract of Hibiscus rosasinensis leaves is reported by local traditional practioners in Western Nigeria to be aphrodisiac.

OBJECTIVE: To investigate the anabolic properties of Hibiscus rosasinensis.

MATERIALS AND METHOD: Three groups (8/group) of immature male rats of known weights were administered equal doses of aqueous (cold and hot) and alcoholic extracts of Hibiscus rosasinensis leaves for 8 weeks. The gain in body and isolated sexual organs (testis, epididymis, seminal vesicle and prostate) weights were determined after treatment and compared to the value obtained from a fourth untreated group which served as the control. Section through the testes of both the treated and untreated rats were also examined microscopically and displayed as a photomicrograph for comparism. All data were statistically analysed and displaced in graphic form.

RESULTS: Over the 8 weeks of treatment, the control, the cold aqueous extract dosed, hot aqueous extract dosed and alcoholic extract dosed rats gained 8%, 15%, 18% and 22% in body weights respectively. The increase in the weight of testis, epididymis, seminal vesicle and prostate of the alcoholic extract dosed rats was 19%, 30%, 31% and 40% respectively.

CONCLUSION: The anabolic effect of the leaf extracts of H. rosasinensis is hereby established. More work needs to be done on these leaf extracts to know their effect on the gonadotrophin hormones which regulate the activity of the androgens in relation to spermatogenesis.
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http://www.ncbi.nlm.nih.gov/pubmed/10465653

Effects of aqueous extracts of Hibiscus macranthus and Basella alba in mature rat testis function.
Moundipa FP, Kamtchouing P, Koueta N, Tantchou J, Foyang NP, Mbiapo FT.

Laboratory of Nutrition and Biochemical Toxicology, Faculty of Sciences, University of Yaounde, Cameroon.
Abstract
Mature male albino Wistar rats (180-220 g) were given by gastric intubation Hibiscus macranthus Hochst A ex Rich (Malvaceae) and Basella alba L. (Basellaceae) aqueous extract from both fresh and dry leaves, at a dose equivalent to 0.720 or 0.108 g of plant, respectively per kg body weight. This was to evaluate their effects on male reproductive function. Control groups were treated equally, but given water instead of the extract. After the treatment periods, animals were killed, their blood collected, the testes and some annex glands removed for histological and biochemical analysis. Results showed that the extract from fresh leaves significantly increased the body weight of rats by 17% from day 7 as compared to controls, whereas the increase was less pronounced (4%) when the rats were given dry leaf extract. The weight of seminal vesicles of rats given the extracts also increased after 15 days. The histological analysis of testis showed abundant spermatozoa in the lumen of the seminiferous tubulus from day 7 in rats fed with the extract when compared to the controls. The serum level of testosterone was significantly increased on the 15th day by 80% in rats given both types of extracts compared to the controls. Testis of treated rats showed high testosterone production in vitro (136 and 62%, respectively for treated and control after 15 days, compared to those of 3 days). Activity of prostatic acid phosphatase was high in prostate, testis and serum of treated rats in all experimental period. From these findings and observation, it was concluded that the aqueous extract of H. macranthus and B. alba had anabolizing and virilizing effects.

PMID: 10465653 [PubMed - indexed for MEDLINE]

Publication Types, MeSH Terms, Substan
-----

http://www.ncbi.nlm.nih.gov/pubmed/20645783

Neuroprotective effect of Hibiscus rosa sinensis in an oxidative stress model of cerebral post-ischemic reperfusion injury in rats.
Nade VS, Kawale LA, Dwivedi S, Yadav AV.

M.V.P.S. College of Pharmacy, Gangapur Road, Shivaji Nagar, Nashik-422 002, Maharashtra, India. [email protected]
Abstract
CONTEXT: The ischemic brain lesions induced in rats by temporary occlusion of the bilateral common carotid arteries and restoration of blood flow to an ischemic brain region is associated with generation of reactive oxygen species with consequent reperfusion injury.

OBJECTIVE: The present study investigated the neuroprotective potential of Hibiscus rosa sinensis L. (Malvaceae) in a bilateral common carotid artery (BCCA) occlusion model of global cerebral ischemic reperfusion.

MATERIALS AND METHODS: The animals underwent 30 min BCCA occlusion and 45 min reperfusion. The methanol extract of H. sinensis (100, 200, 300 mg/kg/day for 6 days, p.o.) was administered 30 min before induction of BCCA occlusion.

RESULTS: The bilateral common carotid artery occlusion resulted in increase in lipid peroxidation, and reduction in superoxide dismutase (SOD), catalase (CAT) and glutathione reductase (GSH) activity. The extract attenuated the ischemic reperfusion-induced increase in lipid peroxidation and fall in SOD, CAT, and GSH levels. The cerebral hypoperfusion caused a propensity towards anxiety and was accompanied by deficits of learning and memory. The extract ameliorated anxiety and there was improvement of learning and memory. Discussion: The administration of H. sinensis prevented the oxidative stress and the biochemical changes associated with cerebral ischemic reperfusion injury. The mechanism of such protection of H. sinensis may be due to cerebral adaptation, through augmentation of cellular antioxidants such as GSH, SOD and CAT. The results suggest the protective role of H. sinensis in ischemic reperfusion injury.

CONCLUSION: This study indicates the beneficial role of H. sinensis in cerebrovascular insufficiency states and dementia.

PMID: 20645783 [PubMed - in process]
-----
 
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http://www.ncbi.nlm.nih.gov/pubmed

Zhong Yao Cai. 2004 Jul;27(7):504-6.
[Effects of osthol on androgen level and nitric oxide synthase activity in castrate rats]
[Article in Chinese]

Yuan J, Xie J, Li A, Zhou F.

Guangxi College of TCM, Nanning 530001.
Abstract
OBJECTIVE: To investigate the effects of osthol on androgen level and nitric oxide synthase (NOS) activity in castrate rats.

METHODS: Immature castrate male rats were treated with osthol daily for 20 d. The levels of testosterone(T), luteinizing hormone (LH) and follicle stimulating hormone (FSH) in serum and the activity of NOS, the nitric monoxide (NO) level in penis tissue were determined.

RESULTS: T( P < 0.05), LH( P < 0.05) and FSH( P < 0.01) were significantly increased at the high dose of osthol treatment. The high and low dose of osthol treatment significantly enhanced the activity of NOS (P < 0.01).

CONCLUSION: Osthol could increase androgen, gonadotropin and nitric oxide synthase (NOS) activity. It suggested that osthol had androgen-like effect and gonadotropin-like effect.
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http://www.fasebj.org/cgi/content/meeting_abstract/21/6/A1165

The vasorelaxation effect of osthole, derived from Radix Angelicae Pubescentis, in porcine coronary artery

MatthewLai Yin Chan 1,2, Wendy Keung1, Dennis K.Y. Yeung1, Susan W.S. Leung1, C. M. Che2 and Ricky Y.K. Man1
1 Pharmacology, The University of Hong Kong, 21 Sassoon Road, 2/F, Laboratory Block, HKSAR, Hong Kong,
2 Chemistry, The University of Hong Kong, Chong Yuet Ming Chemistry Building, Pokfulam Road, HKSAR, Hong Kong

ABSTRACT

Radix Angelicae Pubescentis is a traditional Chinese medicine used to treat thrombosis. Osthole, a coumarin from Angelica pubescens, possesses antiarrhythmic activity. The vascular effects of Angelica pubescens extract (APE) and osthole, as well as their underlying signaling pathways, were investigated in isolated porcine coronary artery rings contracted with U46619.

APE (20–80 µg/ml) dose-dependently relaxed endothelium-intact and endothelium-disrupted arterial rings to a similar extent. Osthole induced relaxation in endothelium-intact rings with a lower threshold concentration (< 10 µM) than in endothelium-disrupted rings (> 10 µM). In the presence of L-NAME (a nitric oxide synthase inhibitor) or ODQ (a soluble guanylyl cyclase inhibitor), relaxation to osthole in endothelium-intact rings was similar to that in endothelium-disrupted rings. Neither APE- nor osthole-induced relaxation was inhibited by SQ22536 (an adenylyl cyclase inhibitor).

Our results demonstrated that APE acted directly on vascular smooth muscle to induce relaxation, whereas osthole acted on both endothelium and smooth muscle for relaxation. The endothelium-dependent relaxation of osthole was mediated through nitric oxide-cGMP signaling cascade. Mechanisms other than cAMP signaling pathway appeared to be responsible for endothelium-independent relaxation effect of APE and osthole.
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http://www.ncbi.nlm.nih.gov/pubmed/19682441

Chem Biol Interact. 2009 Oct 30;181(3):309-15. Epub 2009 Aug 12.
Osthole, a potential antidiabetic agent, alleviates hyperglycemia in db/db mice.
Liang HJ, Suk FM, Wang CK, Hung LF, Liu DZ, Chen NQ, Chen YC, Chang CC, Liang YC.

Department of Food Science, Yuanpei University, HsinChu, Taiwan.
Abstract
Osthole is an agent isolated from Cnidium monnieri (L.) Cusson and Angelica pubescens and has been used to treat several diseases, including metabolic syndromes. To investigate the hypoglycemic effects of osthole in diabetic db/db mice and the underlying mechanisms of these effects by in vitro assay, diabetic db/db mice and cell experiments were utilized to understand its possible effects. Osthole significantly activated both PPARalpha and PPARgamma in a dose-dependent manner based on the results of the transition transfection assay. The activation of PPARalpha and PPARgamma by osthole also resulted in an increase in the expression of PPAR target genes such as PPAR itself, adipose fatty acid-binding protein 2, acyl-CoA synthetases, and carnitine palmitoyltransferase-1A. In vitro results suggested that osthole might be a dual PPARalpha/gamma activator, but its chemical structure differed from that of the thiazolidinedione class of antidiabetic drugs. In addition, osthole markedly activated the AMP-activated protein kinase and its downstream acetyl CoA carboxylase molecules by increasing their phosphorylation levels. Finally, obese diabetic db/db mice were treated with osthole by different administered routes, and osthole was found to markedly reduce blood glucose level. Interestingly, osthole did not reduce the blood insulin or lipid levels, two phenomena that did occur in animals treated with insulin sensitizers like PPAR agonists. These results suggest that osthole can alleviate hyperglycemia and could be potentially developed into a novel drug for treatment of diabetes mellitus.

PMID: 19682441 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/20717873

Planta Med. 2010 Aug 17. [Epub ahead of print]
Osthole Ameliorates Insulin Resistance by Increment of Adiponectin Release in High-Fat and High-Sucrose-Induced Fatty Liver Rats.
Qi Z, Xue J, Zhang Y, Wang H, Xie M.

Department of Pharmacology, Medical College of Soochow University, Suzhou, Jiangsu Province, China.
Abstract
The objectives of this study were to determine the effect of osthole on the insulin resistance (IR) in high-fat and high-sucrose-induced fatty liver rats and to investigate its potential mechanisms. The rat model was established by orally feeding high-fat and high-sucrose emulsion by gavage for 9 weeks. The experimental rats were treated with osthole 5 and 10 mg/kg, lipanthyl 30 mg/kg, and rosiglitazone 4 mg/kg after oral high-fat and high-sucrose emulsion for 6 weeks and were sacrificed 4 weeks after administration. The total cholesterol (TC), triglycerides (TG), and free fatty acids (FFA) in serum and hepatic tissue, fasting blood glucose (FBG), fasting serum insulin (FINS), serum adiponectin, and liver weight were measured. The homeostasis model assessment of insulin resistance (HOMA-IR) and coefficient of hepatic weight were calculated. The results showed that after treatment with osthole, the serum levels of TC, TG, and FFA, the contents of TG and FFA in hepatic tissue, and body weight gain were lowered, especially in the osthole 10 mg/kg group (p < 0.05 or p < 0.01). Moreover, the histological evaluation of liver specimens demonstrated that the steatosis and inflammation in liver in osthole-treated groups were improved, especially in the 10 mg/kg group (p < 0.05). Importantly, the levels of FBG, FINS, and HOMA-IR in the osthole 10 mg/kg group were decreased (p < 0.01), while the level of serum adiponectin in the osthole-treated groups, like PPAR alpha agonist lipanthyl and PPAR gamma agonist rosiglitazone, was increased (p < 0.05). These results revealed that osthole could improve the IR induced by high-fat and high-sucrose emulsion in fatty liver rats, and its mechanism might be associated with increment of adiponectin release via activation of PPAR alpha/ gamma pathway.

PMID: 20717873 [PubMed - as supplied by publisher]
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http://www.ncbi.nlm.nih.gov/pubmed/20362569

Eur J Pharmacol. 2010 Jun 25;636(1-3):96-101. Epub 2010 Apr 1.
Osthole improves chronic cerebral hypoperfusion induced cognitive deficits and neuronal damage in hippocampus.
Ji HJ, Hu JF, Wang YH, Chen XY, Zhou R, Chen NH.

Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China.
Abstract
This study is to investigate the effects of osthole on cognitive impairment and neuronal degeneration in hippocampus induced by chronic cerebral hypoperfusion in rats, as well as the potential mechanism. Permanent occlusion of bilateral common carotid arteries (2VO) induced severe cognitive deficits tested by the water maze task, along with oxidative stress and neuronal loss in hippocampus. Oral administration of osthole for 3 weeks markedly attenuated cognitive deficits and neuronal damage. Biochemical experiments revealed that osthole decreased the production of malondialdehyde (MDA) and significantly increased the activities of Glutathione Peroxidase (GPx) and Catalase. Western blot analyses indicated that osthole prevented the downregulation of bcl-2 expression and upregulation of bax expression, which resulted in decreasing bax/bcl-2 ratio in hippocampus of 2VO rats. Additionally, osthole effectively alleviated the activation of caspase-3 induced by permanent occlusion of bilateral common carotid arteries. The observed results in present study suggest that osthole exhibits therapeutic potential for vascular dementia, which is most likely related, at least in part, to its antioxidation and anti-apoptotic actions.

PMID: 20362569 [PubMed - indexed for MEDLINE]
-----

http://www.ncbi.nlm.nih.gov/pubmed/10799242

J Urol. 2000 Jun;163(6):1975-80.
Effect of the plant-extract osthole on the relaxation of rabbit corpus cavernosum tissue in vitro.
Chen J, Chiou WF, Chen CC, Chen CF.

Institute of Clinical Medicine, National Yang-Ming University, and National Research Institute of Chinese Medicine, Taipei, Taiwan, Republic of China.
Abstract
PURPOSE: We investigated the cavernosal relaxant effect of osthole, a coumarin isolated from Cnidium monnier (L.) Cusson which has been long used in China as a herbal medicine to improve male sexual dysfunction.

MATERIALS AND METHODS: Strips of rabbit corpus cavernosum were precontracted with phenylephrine. Corporal relaxation evoked by osthole was then determined in the absence and presence of nitric oxide synthase inhibitor (L-NAME), soluble guanylate cyclase inhibitor (ODQ), cyclooxygenase inhibitor (indomethacin), tetradotoxin, and after endothelium deprivation.

RESULTS: Corpus cavernosal strips showed relaxation in response to osthole (0.1 approximately 30 microM) in a dose-dependent manner. These effects were reduced partially but significantly by pretreatment with L-NAME, ODQ and by endothelial disruption. However, they were not affected by indomethacin and tetradotoxin treatment. Osthole pretreatment (from 1 to 30 microM) enhanced the sodium nitroprusside (0.3 microM)-induced relaxation of corpus cavernosum in a dose-dependent manner to a maximum of 3 times the pretreatment level at 30 microM osthole. However, this effect was abolished in the presence of zaprinast. Additionally, a higher concentration of osthole (30 microM) also enhanced forskolin-induced relaxation.

CONCLUSION: The data suggested that osthole possesses a relaxant effect on rabbit corpus cavernosal tissues which is attributable to the release of NO from sinusoidal endothelium and to the potentiation of the cGMP and/or cAMP signal mediating relaxation of cavernosal smooth muscle by inhibiting phosphodiesterase.

PMID: 10799242 [PubMed - indexed for MEDLINE]
-----

http://www.ncbi.nlm.nih.gov/pubmed/19101603

Food Chem Toxicol. 2009 Mar;47(3):525-9. Epub 2008 Dec 7.
Protective effect of the extracts from Cnidium officinale against oxidative damage induced by hydrogen peroxide via antioxidant effect.
Jeong JB, Park JH, Lee HK, Ju SY, Hong SC, Lee JR, Chung GY, Lim JH, Jeong HJ.

College of Natural Sciences, Andong National University, Andong, Republic of Korea.
Abstract
The dried rhizomes of Cnidium officinale are used as herbal drugs in the treatment of pain, inflammation, menstrual disturbance and antivitamin deficiency disease, and also act as a blood pressure depressant. In addition, there are several reports suggesting that they have pharmacological properties to tumor metastasis and angiogenesis, and that they act as an inhibitor of high glucose-induced proliferation of glomerular mesangial cells. However, little has been known about the functional role of the extracts from C. officinale on oxidative DNA damage and apoptosis caused by ROS. In this work, we have investigated the DPPH radical, hydroxyl radical and intracellular ROS scavenging capacity, and Fe(2+) chelating activity of the extracts from C. officinale. In addition, we evaluated whether the extracts are capable of reducing H(2)O(2)-induced DNA and cell damage in the human skin fibroblast cell. These extracts showed a dose-dependent free-radical scavenging capacity and a protective effect on DNA damage and the lipid peroxidation causing the cell damage by ROS. These antioxidant activities and inhibitory effects of the extracts on DNA and cell damage may further explain that C. officinale is useful as a herbal medicine for cancer chemoprevention.
 
VolcomX311

VolcomX311

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You've got mail on your synephrine inquisition. Real mail, not PM.
 
MAxximal

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any chance for a "carb and sugar" FREE version?
 
MAxximal

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that'd be one hard powder to swallow, but I like the way you think.
ASGT is amazing but right now i can`t use (No Carb Diet) and maybe the carbs in form of (Soluble Fiber and Insoluble Fiber)...?
 
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ASGT is amazing but right now i can`t use (No Carb Diet) and maybe the carbs in form of (Soluble Fiber and Insoluble Fiber)...?
I'm on a no carb diet as well, outside of vegetables and the occasional fruit.
 
MAxximal

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I'm on a no carb diet as well, outside of vegetables and the occasional fruit.
Sweet Bud!

damn man 7g carbs + 4g Sugar = 11g!!!! i see people with 12g a day of carbs and can continue in Ketosis
 
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Synephrine

http://www.ncbi.nlm.nih.gov/pubmed/12939122

J Med. 2002;33(1-4):247-64.
Citrus aurantium as a thermogenic, weight-reduction replacement for ephedra: an overview.
Preuss HG, DiFerdinando D, Bagchi M, Bagchi D.

Department of Physiology, Medicine and Pathology, Georgetown University Medical Center, Washington, DC 20057, USA. [email protected]
Abstract
Obesity is a serious health problem throughout the world. More than half of U.S. adults are overweight (61%) and more than a quarter (26%) of U.S. adults are obese. The inability of many individuals to keep their weight in check by diet and exercise has created a need for additional therapeutic means to combat obesity. Despite great effort, the pharmaceutical industry has not come up with the solution; because most weight-loss drugs to date have serious adverse effects to health and well-being. The theory that beta agonists, especially beta 3 agonists, can affect body weight and fat mass is well accepted. Ephedrine has proven time and time again that it is an effective weight loss agent through its ability to increase thermogenesis and quench appetite. However, the publicity concerning adverse reactions has led to its gradual withdrawal from use by many despite the perceived consequences of obesity. Many companies are now substituting Citrus aurantium for ephedra in their formulations. Citrus aurantium, an agent containing beta agonists, has been reported to aid in weight loss in two studies and increase thermogenesis, at least to some extent, in three studies. Colker et al. (1999) reported that in a double-blind, placebo-controlled, randomized study the subjects receiving a combination of Citrus aurantium, caffeine and St John's Wort, lost significant amounts of total body weight while on a strict diet and exercise. Those in the placebo and control groups who also were on the same restricted diet did not. However, intergroup analysis showed no statistical significance among the weight changes in the three groups. In contrast, the loss of fat mass in the test group was significantly greater compared to the placebo and control groups. Jones describes an open labeled study performed on 9 women. The subjects showed a mean of 0.94 kg lost during the first week when no product was given and 2.40 kg during the second week when a Citrus aurantium product was taken. Body weight losses were statistically greater during the second week compared to the first week. Since most clinicians would agree that the most weight loss should occur initially coinciding with a greater fluid loss during the first week, these differences are even more remarkable. Three studies reported increased metabolic rates when ingesting Citrus aurantium products, however, at least two of these studies were acute. At present, Citrus aurantium may be the best thermogenic substitute for ephedra. However, more studies are needed to establish this definitively.

PMID: 12939122 [PubMed - indexed for MEDLINE]
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http://cat.inist.fr/?aModele=afficheN&cpsidt=1726318

Effects of Citrus aurantium extract, caffeine, and St. John's Wort on body fat loss, lipid levels, and mood states in overweight healthy adults
Auteur(s) / Author(s)
COLKER C. M. (1) ; KALMAN D. S. (2) ; TORINA G. C. (1) ; PERLIS T. (3) ; STREET C. (4) ;
Affiliation(s) du ou des auteurs / Author(s) Affiliation(s)
(1) Greenwich Hospital, Greenwich, Connecticut, ETATS-UNIS
(2) Peak Wellness, Greenwich, Connecticut, ETATS-UNIS
(3) National Drug Research Institute, New York, New York, ETATS-UNIS
(4) TSI University Laboratories, Houston, Texas, ETATS-UNIS
Résumé / Abstract
The purpose of this study was to determine the effects of Citrus aurantium extract (an indirect beta-sympathicomimetic agent), caffeine, and St. John's Wort on body composition, metabolic variables, plasma lipid levels, and mood states in overweight healthy adults. In a double-masked, randomized, placebo-controlled study, 23 subjects with a body-mass index >25 kg/m2 were assigned to 1 of 3 groups. Group A received C aurantium extract 975 mg, caffeine 528 mg, and St. John's Wort 900 mg daily; group B received a maltodextrin placebo; and group C received nothing and served as the control group. For 6 weeks, subjects were instructed by a registered dietitian on how to follow an 1800-kcal/d American Heart Association Step One diet and performed a 3-day/week circuit training exercise program under the supervision of an exercise physiologist. During the exercise sessions, subjects achieved approximately 70% of age-predicted maximum heart rate. Compared with subjects in the placebo and control groups, subjects in the treatment group lost a significant amount of body weight (1.4 kg). They also lost a significant amount of body fat (an average change of 2.9%). In terms of actual fat loss, group A lost a significant amount (3.1 kg), whereas the control group demonstrated a tendency toward fat loss. No significant changes were noted in the results of the Profile of Mood States questionnaire for fatigue or vigor in any of the 3 groups. Group A experienced a decrease, which did not reach statistical significance, of both plasma cholesterol and triglycerides. No significant changes in blood pressure, heart rate, electrocardiographic findings, serum chemistries, or urinalysis findings were noted in any of the groups. Based on these results, it was concluded that the combination of C aurantium extract, caffeine, and St. John's Wort is safe and effective when combined with mild caloric restriction and exercise for promoting both body weight and fat loss in healthy overweight adults.
Revue / Journal Title
 

BrYmAsTeR17

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Excellent detail. Really looking forward to trying ASGT and this evidence just makes me want it more!
 
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ASGT is definitely a sick prorduct!! Always LOVED using it.

ASGT+Natadrol+GHenerate+Slin= Ultimate Recomp Stack

:redeemerwhore:
 
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Concerning that last abstract: I would avoid St. John's Wort. The stuff is a dramatic agonist for Cyp3A; so taking it will greatly decrease the circulating half-life of any other "drug-like" substances you may be taking.

ASGT does not contain St. John's Wort, though, so we got nothing to worry about.
 

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Sounds like an awesome product! Thanks for all the info! I'll def have to try this out!
 
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Sweet Bud!

damn man 7g carbs + 4g Sugar = 11g!!!! i see people with 12g a day of carbs and can continue in Ketosis
ASGT has 7g of carbs total, not 12g. Within that 7g is 4g of sugar. The other 3g are detrose and waxy maize.
 
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Creatine

I'm sure this is somewhat redundant, as we all know what creatine does. Here are some alternative benefits:

http://www.ncbi.nlm.nih.gov/pubmed/18708688

Int J Sport Nutr Exerc Metab. 2008 Aug;18(4):389-98.
Effect of creatine supplementation and resistance-exercise training on muscle insulin-like growth factor in young adults.
Burke DG, Candow DG, Chilibeck PD, MacNeil LG, Roy BD, Tarnopolsky MA, Ziegenfuss T.

Department of Human Kinetics, St. Francis Xavier University, Antigonish, NS, Canada.
Abstract
The purpose of this study was to compare changes in muscle insulin-like growth factor-I (IGF-I) content resulting from resistance-exercise training (RET) and creatine supplementation (CR). Male (n=24) and female (n=18) participants with minimal resistance-exercise-training experience (=1 year) who were participating in at least 30 min of structured physical activity (i.e., walking, jogging, cycling) 3-5 x/wk volunteered for the study. Participants were randomly assigned in blocks (gender) to supplement with creatine (CR: 0.25 g/kg lean-tissue mass for 7 days; 0.06 g/kg lean-tissue mass for 49 days; n=22, 12 males, 10 female) or isocaloric placebo (PL: n=20, 12 male, 8 female) and engage in a whole-body RET program for 8 wk. Eighteen participants were classified as vegetarian (lacto-ovo or vegan; CR: 5 male, 5 female; PL: 3 male, 5 female). Muscle biopsies (vastus lateralis) were taken before and after the intervention and analyzed for IGF-I using standard immunohistochemical procedures. Stained muscle cross-sections were examined microscopically and IGF-I content quantified using image-analysis software. Results showed that RET increased intramuscular IGF-I content by 67%, with greater accumulation from CR (+78%) than PL (+54%; p=.06). There were no differences in IGF-I between vegetarians and nonvegetarians. These findings indicate that creatine supplementation during resistance-exercise training increases intramuscular IGF-I concentration in healthy men and women, independent of habitual dietary routine.

PMID: 18708688 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/19490606

J Int Soc Sports Nutr. 2009 Jun 2;6:13.
Creatine supplementation enhances muscle force recovery after eccentrically-induced muscle damage in healthy individuals.
Cooke MB, Rybalka E, Williams AD, Cribb PJ, Hayes A.

Exercise Metabolism Unit, Centre for Ageing, Rehabilitation, Exercise and Sport, School of Biomedical and Health Sciences, Victoria University, Melbourne, Australia. [email protected].
Abstract
ABSTRACT:

BACKGROUND: Eccentric exercise-induced damage leads to reductions in muscle force, increased soreness, and impaired muscle function. Creatine monohydrate's (Cr) ergogenic potential is well established; however few studies have directly examined the effects of Cr supplementation on recovery after damage. We examined the effects of Cr supplementation on muscle proteins and force recovery after eccentrically-induced muscle damage in healthy individuals.

METHODS: Fourteen untrained male participants (22.1 +/- 2.3 yrs, 173 +/- 7.7 cm, 76.2 +/- 9.3 kg) were randomly separated into 2 supplement groups: i) Cr and carbohydrate (Cr-CHO; n = 7); or ii) carbohydrate (CHO; n = 7). Participants consumed their supplement for a period of 5 days prior to, and 14 days following a resistance exercise session. Participants performed 4 sets of 10 eccentric-only repetitions at 120% of their maximum concentric 1-RM on the leg press, leg extension and leg flexion exercise machine. Plasma creatine kinase (CK) and lactate dehydrogenase (LDH) activity were assessed as relevant blood markers of muscle damage. Muscle strength was examined by voluntary isokinetic knee extension using a Cybex dynamometer. Data were analyzed using repeated measures ANOVA with an alpha of 0.05.

RESULTS: The Cr-supplemented group had significantly greater isokinetic (10% higher) and isometric (21% higher) knee extension strength during recovery from exercise-induced muscle damage. Furthermore, plasma CK activity was significantly lower (by an average of 84%) after 48 hrs (P < 0.01), 72 hrs (P < 0.001), 96 hrs (P < 0.0001), and 7 days (P < 0.001) recovery in the Cr-supplemented group.

CONCLUSION: The major finding of this investigation was a significant improvement in the rate of recovery of knee extensor muscle function after Cr supplementation following injury.
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http://www.ncbi.nlm.nih.gov/pubmed/11079535

Ann Neurol. 2000 Nov;48(5):723-9.
Dietary supplement creatine protects against traumatic brain injury.
Sullivan PG, Geiger JD, Mattson MP, Scheff SW.

Sanders-Brown Center on Aging, University of Kentucky, Lexington 40536-0230, USA.
Abstract
Creatine, one of the most common food supplements used by individuals at almost every level of athleticism, promote gains in performance, strength, and fat-free mass. Recent experimental findings have demonstrated that creatine affords significant neuroprotection against ischemic and oxidative insults. The present experiments investigated the possible effect of creatine dietary supplementation on brain tissue damage after experimental traumatic brain injury. Results demonstrate that chronic administration of creatine ameliorated the extent of cortical damage by as much as 36% in mice and 50% in rats. Protection seems to be related to creatine-induced maintenance of mitochondrial bioenergetics. Mitochondrial membrane potential was significantly increased, intramitochondrial levels of reactive oxygen species and calcium were significantly decreased, and adenosine triphosphate levels were maintained. Induction of mitochondrial permeability transition was significantly inhibited in animals fed creatine. This food supplement may provide clues to the mechanisms responsible for neuronal loss after traumatic brain injury and may find use as a neuroprotective agent against acute and delayed neurodegenerative processes.

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PMID: 11079535 [PubMed - indexed for MEDLINE]

Publication Types, MeSH Terms, Substances, Grant Support
LinkOut - more resources

MMA/boxers/football players, etc, pay attention. ^^^ ;)

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http://www.ncbi.nlm.nih.gov/sites/entrez

Eur Heart J. 1998 Apr;19(4):617-22.
The effect of dietary creatine supplementation on skeletal muscle metabolism in congestive heart failure.
Andrews R, Greenhaff P, Curtis S, Perry A, Cowley AJ.

Department of Cardiovascular Medicine, University Hospital, Nottingham, U.K.
Comment in:

Eur Heart J. 1998 Apr;19(4):533-4.
Abstract
AIMS: To assess the effects of dietary creatine supplementation on skeletal muscle metabolism and endurance in patients with chronic heart failure.

METHODS: A forearm model of muscle metabolism was used, with a cannula inserted retrogradely into an antecubital vein of the dominant forearm. Maximum voluntary contraction was measured using handgrip dynanometry. Subjects performed handgrip exercise, 5 s contraction followed by 5 s rest for 5 min at 25%, 50%, and 75% of maximum voluntary contraction or until exhaustion. Blood was taken at rest and 0 and 2 min after exercise for measurement of lactate and ammonia. After 30 min the procedure was repeated with fixed workloads of 7 kg, 14 kg and 21 kg. Patients were assigned to creatine 20 g daily or matching placebo for 5 days and returned after 6 days for repeat study.

RESULTS: Contractions (median (25th, 75th interquartiles)) until exhaustion at 75% of maximum voluntary contraction increased after creatine treatment (8 (6, 14) vs 14 (8, 17), P = 0.025) with no significant placebo effect. Ammonia per contraction at 75% maximum voluntary contraction (11.6 mumol/l/contraction (8.3, 15.7) vs 8.9 mumol/l/contraction (5.9, 10.8), P = 0.037) and lactate per contraction at 75% maximum voluntary contraction (0.32 mmol/l/contraction (0.28, 0.61) vs 0.27 mmol/l/contraction (0.19, 0.49), P = 0.07) fell after creatine but not after placebo.

CONCLUSIONS: Creatine supplementation in chronic heart failure augments skeletal muscle endurance and attenuates the abnormal skeletal muscle metabolic response to exercise.

PMID: 9597411 [PubMed - indexed for MEDLINE]Free Article
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http://www.ncbi.nlm.nih.gov/pubmed/19741313

lin J Sport Med. 2009 Sep;19(5):399-404.
Three weeks of creatine monohydrate supplementation affects dihydrotestosterone to testosterone ratio in college-aged rugby players.
van der Merwe J, Brooks NE, Myburgh KH.

Department of Physiological Sciences, Stellenbosch University, Stellenbosch, South Africa.
Comment in:

Clin J Sport Med. 2010 May;20(3):220; author reply 220-2.
Abstract
OBJECTIVE: This study investigated resting concentrations of selected androgens after 3 weeks of creatine supplementation in male rugby players. It was hypothesized that the ratio of dihydrotestosterone (DHT, a biologically more active androgen) to testosterone (T) would change with creatine supplementation.

DESIGN: Double-blind placebo-controlled crossover study with a 6-week washout period.

SETTING: Rugby Institute in South Africa.

PARTICIPANTS: College-aged rugby players (n = 20) volunteered for the study, which took place during the competitive season.

INTERVENTIONS: Subjects loaded with creatine (25 g/day creatine with 25 g/day glucose) or placebo (50 g/day glucose) for 7 days followed by 14 days of maintenance (5 g/day creatine with 25 g/day glucose or 30 g/day glucose placebo).

MAIN OUTCOME MEASURES: Serum T and DHT were measured and ratio calculated at baseline and after 7 days and 21 days of creatine supplementation (or placebo). Body composition measurements were taken at each time point.

RESULTS: After 7 days of creatine loading, or a further 14 days of creatine maintenance dose, serum T levels did not change. However, levels of DHT increased by 56% after 7 days of creatine loading and remained 40% above baseline after 14 days maintenance (P < 0.001). The ratio of DHT:T also increased by 36% after 7 days creatine supplementation and remained elevated by 22% after the maintenance dose (P < 0.01).

CONCLUSIONS: Creatine supplementation may, in part, act through an increased rate of conversion of T to DHT. Further investigation is warranted as a result of the high frequency of individuals using creatine supplementation and the long-term safety of alterations in circulating androgen composition. STATEMENT OF

CLINICAL RELEVANCE: Although creatine is a widely used ergogenic aid, the mechanisms of action are incompletely understood, particularly in relation to dihydrotestosterone, and therefore the long-term clinical safety cannot be guaranteed.

PMID: 19741313 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/14507259

Clin Sci (Lond). 2004 Jan;106(1):99-106.
Creatine supplementation increases glycogen storage but not GLUT-4 expression in human skeletal muscle.
van Loon LJ, Murphy R, Oosterlaar AM, Cameron-Smith D, Hargreaves M, Wagenmakers AJ, Snow R.

Nutrition Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands. [email protected]
Abstract
It has been speculated that creatine supplementation affects muscle glucose metabolism in humans by increasing muscle glycogen storage and up-regulating GLUT-4 protein expression. In the present study, we assessed the effects of creatine loading and prolonged supplementation on muscle glycogen storage and GLUT-4 mRNA and protein content in humans. A total of 20 subjects participated in a 6-week supplementation period during which creatine or a placebo was ingested. Muscle biopsies were taken before and after 5 days of creatine loading (20 g.day(-1)) and after 6 weeks of continued supplementation (2 g.day(-1)). Fasting plasma insulin concentrations, muscle creatine, glycogen and GLUT-4 protein content as well as GLUT-4, glycogen synthase-1 (GS-1) and glycogenin-1 (Gln-1) mRNA expression were determined. Creatine loading significantly increased total creatine, free creatine and creatine phosphate content with a concomitant 18 +/- 5% increase in muscle glycogen content (P<0.05). The subsequent use of a 2 g.day(-1) maintenance dose for 37 days did not maintain total creatine, creatine phosphate and glycogen content at the elevated levels. The initial increase in muscle glycogen accumulation could not be explained by an increase in fasting plasma insulin concentration, muscle GLUT-4 mRNA and/or protein content. In addition, neither muscle GS-1 nor Gln-1 mRNA expression was affected. We conclude that creatine ingestion itself stimulates muscle glycogen storage, but does not affect muscle GLUT-4 expression.

PMID: 14507259 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/1269086

Circ Res. 1976 May;38(5 Suppl 1):I115-23.
Creatine and the control of muscle-specific protein synthesis in cardiac and skeletal muscle.
Ingwall JS.

Abstract
The observation that increased muscular activity leads to muscle hypertrophy is well known, but identification of the biochemical and physiological mechanisms by which this occurs remains an important problem. The hypothesis has been proposed that creatine, an end product of contraction, may be the chemical signal coupling increased muscular activity and increased contractile mass. Two muscle models have been used in experimental tests of this hypothesis: differentiating skeletal muscle cells in culture and the fetal mouse heart in organ culture. Using these culture models, it is possible to alter the intracellular creatine concentration and to measure the effect of increased creatine concentrations on the rates of synthesis and accumulation of both muscle-specific and nonspecific proteins. The results show that muscle-specific protein synthesis in both skeletal and cardiac muscle is selectively stimulated by creatine.

PMID: 1269086 [PubMed - indexed for MEDLINE]
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http://www.ncbi.nlm.nih.gov/pubmed/11581551

Med Sci Sports Exerc. 2001 Oct;33(10):1674-81.
Effects of oral creatine and resistance training on myosin heavy chain expression.
Willoughby DS, Rosene J.

Department of Kinesiology, Texas Christian University, Fort Worth, TX 76129, USA. [email protected]
Abstract
PURPOSE: This study examined 12 wk of creatine (Cr) supplementation and heavy resistance training on muscle strength and myosin heavy chain (MHC) isoform mRNA and protein expression.

METHODS: Twenty-two untrained male subjects were randomly assigned to either a control (CON), placebo (PLC), or Cr (CRT) group in a double-blind fashion. Muscle biopsies were obtained before and after 12 wk of heavy resistance training. PLC and CRT trained thrice weekly using three sets of 6-8 repetitions at 85-90% 1-RM on the leg press, knee extension, and knee curl exercises. CRT ingested 6 g.d-1 of Cr for 12 wk, whereas PLC consumed the equal concentration of placebo.

RESULTS: There were no significant differences for percent body fat (P > 0.05). However, for total body mass, fat-free mass, thigh volume, muscle strength, and myofibrillar protein, CRT and PLC exhibited significant increases after training when compared to CON (P < 0.05), whereas CRT was also significantly greater than PLC (P < 0.05). For Type I, IIa, and IIx MHC mRNA expression, CRT was significantly greater than CON and PLC, whereas PLC was greater than CON (P < 0.05). For MHC protein expression, CRT was significantly greater than CON and PLC for Type I and IIx (P < 0.05) but was equal to PLC for IIa.

CONCLUSION: Long-term Cr supplementation increases muscle strength and size, possibly as a result of increased MHC synthesis.

PMID: 11581551 [PubMed - indexed for MEDLINE]
 
VolcomX311

VolcomX311

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It makes me excited about being on creatine though :cheers:
 
Resolve

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The inclusion of the studies that don't pertain to creatine's effect on muscle are most interesting to me. It makes perfect sense that creatine would have a systemic impact, considering that creatine acts as a phosphate reservoir for ATP synthesis.
 
poison

poison

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The inclusion of the studies that don't pertain to creatine's effect on muscle are most interesting to me. It makes perfect sense that creatine would have a systemic impact, considering that creatine acts as a phosphate reservoir for ATP synthesis.
Resolve, I posted additional abstracts for most of the ASGT ingredients that have nothing to do with athletic performance, because I find that equally interesting. I very much prefer to take something that has a dual purpoise, or overall health benefits, NOT just athletic benefit, and this ASGT delivers in spades. It delivers performance enhancement, sure, but those same ingredients may fight cancer, obesity, aging, mental decline, disease, etc. That's a huge win for ASGT users.
 
oufinny

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The inclusion of the studies that don't pertain to creatine's effect on muscle are most interesting to me. It makes perfect sense that creatine would have a systemic impact, considering that creatine acts as a phosphate reservoir for ATP synthesis.
Hence why I take creatine year round.
 
poison

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Now you have even more reason to supplement creatine!
 

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