BCAAs vs. L-Leucine
- 02-01-2006, 02:33 AM
BCAAs vs. L-Leucine
Ok... I'm still learning about BCAAs, but from what I've read so far the MOST benefit seems to be coming from... so my question is has anyone Megadosed(30-50g) Bulk ? Are there any potential problems with that? Would it be more beneficial?...I know its cheaper... just wondering your thoughts on this
- 02-01-2006, 02:56 AM
02-01-2006, 02:57 AM
02-01-2006, 04:12 AM
I've read somewhere about throwing off the bcaa balance if you only supplement leucine, now if it was from a research article or just somebody trying to push their product I can't recallOriginally Posted by mrmoose63
02-01-2006, 04:19 AM
Would throwing off BCAA balance still hold true with a high protein diet? and if they are off balance what consequences does that entail?
02-01-2006, 08:44 AM
02-01-2006, 11:34 AM
Nandi (Karl) at CEM (cuttingedgemuscle) was a big proponent of leucine and wrote about it frequently.
02-01-2006, 12:58 PM
If you are getting enough protein then there's no point in even using BCAA beyond the additional calories you get. There is something called the "muscle full" phenom where continually flooding the blood stream w leucine/BCAA doesn't do anything for additional mTOR stimulation. BCAA are a deal where a deficiency kicks your ass but an excess does little for you beyond the benefit of the increased calories.Originally Posted by mrmoose63
02-01-2006, 01:04 PM
Yes - see below for article from 04'.Originally Posted by TheCrownedOne
By Karl Hoffmann
While reserch shows that BCAAs promote anabolism in general, leucine has been shown to be the most anabolic of the BCAAs, functioning in a way similar to growth factors such as insulin and IGF-1. Hence one can conclude that the higher the ratio of leucine to the other BCAAS is in a particular amino acid supplement, the greater the anabolic reponse will be. See factor, aside from its effects as a simple nutrient. So something like a 4g:2g:2g (g=grams) ratio of leucine, isoleucine,and valine would ensure adequate supply of leucine, but still allow for absorption of the other (less anabolic but still important) BCAAs.
The Role of Branched-Chain Amino Acids in Fatigue Resistance
The branched-chain amino acids isoleucine, leucine, and valine are widely used among athletes for their protein sparing effect.
L-leucine is also known as 2-amino-4-methylvaleric acid, alpha-aminoisocaproic acid and (S)-2-amino-4-methylpentanoic acid. It is abbreviated as Leu or by its one letter abbreviation L. Its molecular formula is C6H13NO2, and its molecular weight is 131.17 daltons.
L-isoleucine is also known as 2-amino-3-methylvaleric acid, alpha-amino-beta-methylvaleric acid and (2S, 3S)-2-amino-3-methylpentanoic acid. It is abbreviated as Ile or by its one letter abbreviation I. Its molecular formula is C 6H13NO2, and its molecular weight is 131.17 daltons.
L-valine is also known as 2-aminoisovaleric acid, 2-amino-3-methylbutyric acid, alpha-aminoisovaleric acid and (S)-2-amino-3-methylbutanoic acid. It is abbreviated as Val, and its one letter abbreviation is V. Its molecular formula is C5H11NO2, and its molecular weight is 117.15 daltons.
A number of studies have shown that branched chain amino acids exert both an anabolic and ergogenic effect.
For example, one study showed that BCAA administration post exercise resulted in an approximately 30% decrease amino acid efflux from skeletal muscle. The authors concluded that BCAAs exert a post training protein-sparing effect on muscle tissue (4). These results have been verified in numerous other studies. It is now believed that BCAAs act through a specific pathway, the so-called signal transduction p70(S6k) pathway in skeletal muscle (5). p70(S6k) is believed to control growth-related protein synthesis (5). There is also some evidence that branched chain amino acids are preferentially broken down for fuel during exercise, arguing for BCAA supplementation to offset this effect. If this is the case, this might be one mechanism where BCAA supplementation would hold off fatigue. Leucine seems particularly critical in stimulating overall protein synthesis. Leucine mediated signaling results in a stimulation of initiation of mRNA translation and involves increases in the phosphorylation status of the translational repression 4E-BP1 and the ribosomal protein S6 kinase S6K1mentioned above. It also requires sustained activation of the mammalian target of rapamycin (mTOR) protein kinase, a field of active research. Leucine, however, also signals to stimulate protein synthesis in skeletal muscle by a mammalian target of rapamycin protein kinase independent (i.e. rapamycin insensitive) pathway, suggesting that the amino acid may signal for protein synthesis through multiple pathways.
Interestingly, insulin is believed to exert at least part of its anabolic effect by activating the same p70(Sk6) pathway as leucine, but via different upstream channels. This argues for an additive role between elevated insulin levels and elevated BCAA levels in the promotion of anabolism.
There is another mechanism whereby BCAAs might prevent fatigue. We mentioned that BCAAs are used for fuel during exercise. As these amino acids become depleted, the ratio of tryptophan to BCAAs in the plasma rises (6). It turns out that tryptophan and BCAAs compete for the same amino acid transporter into the brain. The excess tryptophan in the brain is converted to serotonin, which induces a feeling of lethargy and fatigue. (Recall that tryptophan was widely used as a sleep aid.)
Interestingly men may have a greater need for BCAA supplementation than women. It is well established that women rely more on fat oxidation and less on glycogen and amino oxidation that do men during exercise. The BCAA leucine seems to be preferentially used among the amino acids as a fuel substrate in men (7).
TNF-alpha and BCAAs
Tumor necrosis factor alpha (TNF-alpha) is a cytokine produced by immune cells in the body called monocytes and macrophages. TNF exerts a number of deleterious effects on the body, including muscle wasting, and locally produced igf-1 suppression, and general fatigue. While usually associated with illness, TNF-alpha levels are also high in hypogonadal patients and overtrained athletes. In one study, lipopolysachharide, a bacterial toxin that elevates TNF-alpha, was administered to rats. One group of rats was fed citrulline malate, and one group served as controls. The citrulline malate group performed much better on treadmill tests and exhibited less overall fatigue that did the controls (8).
These results may be of significance to overtrained athletes in whom TNF-alpha is elevated, and in anabolic steroid using athletes who are essentially hypogonadal post cycle. Citrulline malate may help alleviate the fatigue associated with both these conditions.
BCAAs may suppress TNF-alpha and its damaging effects on muscle tissue as well. In one study in animals, TNF-alpha was administered and diaphragm tissue was examined post mortem. Chronic TNF-alpha treatment produced a significant decline in the synthesis of all types of myofibrillar proteins, namely heavy chain myosin, light chain myosin and G-actin. TNF-alpha impaired peptide-chain initiation in diaphragm muscle was reversed by the branched-chain amino acids (BCAA) therapy of TNF-alpha treated rats. The authors concluded that
"These findings indicate a significant [inhibitory] role for TNF-alpha in the translational regulation of protein synthesis in skeletal muscle [which is reversed by BCAA administration ] (9) We see here a potential additive or even synergistic effect between citrulline malate and BCAAs in fighting muscle loss due to cytokines like TNF-alpha which are associated with illness, overtraining, and post anabolic steroid use."
In addition to blocking the muscle wasting catabolic effects of pro-inflammatory cytokines, BCAAs also seem to fight a tug of war with catabolic glucocorticoids. This suggests that under conditions such as stress or overtraining, BCAAs might help alleviate the catabolic effects of cortisol (10).
Leucine activates system A amino acid transport in skeletal muscle cells.
Just as glucose uptake into cells is dependent upon a family of so called GLUT (Glucose Transporters), amino acids are transported into cells by a distinct family of transporters. One main transport system is the so-called System A. In vitro studies have shown that leucine upregulates System A transporters, allowing for greater entry of a number of amino acids into muscle cells (11). It should be noted that one of the anabolic effects of IGF-1 is believed to be upregulation of this same transport system. So in this sense leucine may share at least one of the anabolic effects associated with insulin like growth factor.
So we have seen that amino acids, and leucine in particular are capable of activating signal transduction pathways in an almost hormone like manner. They are much more than simple nutrients in this regard. To quote from one recent review,
"The protein kinase mTOR is a common intermediate in both nutrient and hormone signal transduction pathways. Signaling through mTOR is enhanced by nutrients and anabolic hormones, such as insulin or IGF-I and repressed by elevation of cAMP or activation of AMPK suggesting that one function of mTOR is to integrate the anabolic response to nutrients and insulin and the catabolic response to counter-regulatory hormones, such as glucagon...Although other amino acids have been shown to increase signaling through mTOR, leucine is arguably the most potent of the amino acids in activating the pathway." (12)
The importance of leucine to post resistance exercise recovery is highlighted in another recently published study where participants undertook a bout of resistance exercise and were fed either carbohydrates alone, carbohydrates plus whey protein, or a combination of carbs, whey and leucine (13). Subjects received a beverage volume of 3 ml.kg-1 every 30 minutes to ensure a given dose of 0.3 g carbohydrate.kg-1 (50% as glucose and 50% as maltodextrin) and 0.2 g.kg-1 of a protein hydrolysate [whey] every h, with or without the addition of 0.1 g.kg-1.h-1 leucine. To quote from the report, “Mixed muscle [protein synthesis rate], measured over a 6h period of post-exercise recovery, was significantly greater in the CHO+PRO+leu trial compared to the CHO, with intermediate values observed in the CHO+PRO trial. We conclude that the co-ingestion of protein and leucine stimulates muscle protein synthesis and optimizes whole-body protein balance when compared to the intake of carbohydrate only.”
(1) Blomstrand E, Saltin B. BCAA intake affects protein metabolism in muscle after but not during exercise in humans. Am J Physiol Endocrinol Metab 2001 Aug;281(2):E365-74
(2) Karlsson HK, Nilsson PA, Nilsson J, Chibalin AV, Zierath JR, Blomstrand E. Branched-chain amino acids increase p70S6k phosphorylation in human skeletal muscle after resistance exercise. Am J Physiol Endocrinol Metab. 2004 Jul;287(1):E1-7
(3) Blomstrand E, Celsing F, Newsholme EA. Changes in plasma concentrations of aromatic and branched-chain amino acids during sustained exercise in man and their possible role in fatigue. Acta Physiol Scand 1988 May;133(1):115-21
(4) Lamont LS, McCullough AJ, Kalhan SC. Gender differences in the regulation of amino acid metabolism. J Appl Physiol. 2003 Sep;95(3):1259-65
(5) Verleye M, Heulard I, Stephens JR, Levy RH, Gillardin JM. Effects of citrulline malate on bacterial lipopolysaccharide induced endotoxemia in rats. Arzneimittelforschung 1995 Jun;45(6):712-5
(6) Cheema IR, Hermann C, Postell S, Barnes P. Effect of chronic excess of tumour necrosis factor-alpha on contractile proteins in rat skeletal muscle. Cytobios. 2000;103(404):169-76.
(7) Liu Z, Jahn LA, Long W, Fryburg DA, Wei L, Barrett EJ. Branched chain amino acids activate messenger ribonucleic acid translation regulatory proteins in human skeletal muscle, and glucocorticoids blunt this action. J Clin Endocrinol Metab 2001 May;86(5):2136-43.
(8) McDowell HE, Christie GR, Stenhouse G, Hundal HS. Leucine activates system A amino acid transport in L6 rat skeletal muscle cells. Am J Physiol. 1995 Nov;269(5 Pt 1):C1287-94.
(9) Kimball SR, Jefferson LS. Amino acids as regulators of gene expression. Nutr Metab (Lond). 2004 Aug 17;1(1):3
(10) Koopman R, Wagenmakers AJ, Manders RJ, Zorenc AH, Senden JM, Gorselink M, Keizer HA, van Loon LJ. The combined ingestion of protein and free leucine with carbohydrate increases post-exercise muscle protein synthesis in vivo in male subjects. Am J Physiol Endocrinol Metab. 2004 Nov 23
(11) Holecek M. Relation between glutamine, branched-chain amino acids, and protein metabolism. Nutrition. 2002 Feb;18(2):130-3
(12) Nakata M, Yada T. Endocrinology: nitric oxide-mediated insulin secretion in response to citrulline in islet beta-cells. Pancreas. 2003 Oct;27(3):209-13
Copyright 2004 by Karl Hoffmann
02-01-2006, 01:18 PM
Thats great info but a lot happened in 2005 and 2006
Branched-Chain Amino Acids as Fuels and Anabolic Signals in Human Muscle
ABSTRACT During exercise, there is an increase in amino acid (AA) oxidation accompanied by a depression in whole-body protein synthesis and an increase in protein breakdown. Leucine oxidation increases in proportion to energy expenditure, but the total contribution of BCAA to fuel provision during exercise is minor and insufficient to increase dietary protein requirements. When investigating the effects of AA on the control of muscle protein synthesis (MPS), we showed that increased availability of mixed AAs caused a rise in human MPS to about the same extent as complete meals. Leucine alone (and to some extent other essential, but not nonessential, AAs) can stimulate MPS for a short period, suggesting that leucine acts as a signal as well as a substrate. MPS stimulation by infused AAs shows tachyphylaxis, returning to basal rates after 2 h, possibly explaining why chronically elevated leucine delivery does not elevate MPS clinically. Increased availability of essential amino acids (EAAs) results in dose-related responses of MPS, but, in elderly subjects, there is blunted sensitivity and responsiveness associated with decreased total RNA and mRNA for signaling proteins and signaling activity. Increases of MPS due to EAAs are associated with elevation of signaling activity in the mammalian target of rapamycin (mTOR)/p70 ribosomal subunit S6 kinase eukaryotic initiation factor 4 binding protein 1 pathway, without requiring rises of plasma insulin availability above 10 mU/mL. However, at insulin of ,5 mU/mL, AAs appear to stimulate MPS without increasing mTOR signaling. Further increasing availability of insulin to postprandial values increases signaling activity, but has no further effect on MPS. J. Nutr. 136: 264S–268S, 2006
02-01-2006, 01:20 PM
And what exactly has happened since 2004?Originally Posted by Jay Mc
And, do you happen to understand who you are trying to discredit? Nandi is kind of legend in this stuff...
Your credentials would be?
02-01-2006, 01:22 PM
additional research into the nature of how leucine influences protein synthesis, as per the abstract I posted.Originally Posted by houseman
and I agree nandi is rad and brilliant and all that. I'm just saying since his untimely passing a lot of new information has come out.
02-01-2006, 01:25 PM
So in terms of that study... supping with EAAs are more beneficial at stimulating protein synthesis than leucine? ...maybe I'm reading it wrong
02-01-2006, 01:29 PM
02-01-2006, 01:33 PM
I believe that this study is referring to aerobic/ednurance exercise rather than resistance exercise if I am not mistaken as the result of resistance exercise is increased protein synthesis but an even greater increase in protein breakdown resulting in a negative balance (in the fasted state). It may be possible that it can be equally applied to resistance exercise but I am not too sure.Originally Posted by Jay Mc
02-01-2006, 01:40 PM
According to those authors as long as you have adequate dietary intake of protein you'll be set up. There is research that shows utilization of amino acids becomes more efficient in trained people, that coupled witht he data showing prolonged infussion fails to continually increase protein synthesis and the transient nature of the effect when it does occur makes the concept of supplementing to increase protein synthesis seem less probable than it seemed in the past.Originally Posted by mrmoose63
I have a degree in biology and chemistry and I'm currently a medstudent. That doesn't make me an expert on exercise or nutrition but it does mean I have access to every journal in the world and am pretty adept at reading technical articles.
I just recently finished an article about all this for avant's magazine mind and muscle. It will be out in march.
Until then, here are some places to read.
With regard to #3 keep in mind that duringg exercise prot synth is impossible (due to complicated molecular stuff you probably don't care about). So post exercise prot synth is very low, doubling something very low still doesn't give you anything amazing, ESPECIALLY compared to 4 hours later when stuff REALLY goes into high gear and you see the bulk of your adaptation.
1. Norton LE, Layman DK. Leucine regulates translation initiation of protein synthesis in skeletal muscle after exercise. J Nutr. 2006 Feb;136(2):533S-7S. PMID: 16424142
2. Rennie MJ, Bohe J, Smith K, Wackerhage H, Greenhaff P. Branched-chain amino acids as fuels and anabolic signals in human muscle. J Nutr. 2006 Jan;136(1):264S-8S. PMID: 16365095
3. Blomstrand E, Eliasson J, Karlsson HK, Kohnke R. Branched-chain amino acids activate key enzymes in protein synthesis after physical exercise. J Nutr. 2006 Jan;136(1):269S-73S. PMID: 16365096
4. Glass DJ. Skeletal muscle hypertrophy and atrophy signaling pathways. Int J Biochem Cell Biol. 2005 Oct;37(10):1974-84. PMID: 16087388
5. Rose AJ, Broholm C, Kiillerich K, Finn SG, Proud CG, Rider MH, Richter EA, Kiens B. Exercise rapidly increases eukaryotic elongation factor 2 phosphorylation in skeletal muscle of men. J Physiol. 2005 Nov 15;569(Pt 1):223-8. Epub 2005 Oct 6. PMID: 16210351
6. Mechanical signal transduction in skeletal muscle growth and adaptation. J Appl Physiol. 2005 May;98(5):1900-8. PMID: 15829723
02-01-2006, 01:41 PM
02-01-2006, 02:47 PM
Originally Posted by The Godfather
That article is actually a review of the current research on molecular signalling and how leucine ties in.
The nerdy side of me eats up the molecular research stuff. LOVE IT! But the practical bodybuilder side of me realizes it has little application because everyone already knows how to get big: eat, lift, sleep, repeat.
A doubling of protein synthesis from basal rates or in the post workout window sounds great. DOUBLED WOW! But consider this: 2x something really small isn't that big a deal. Look at protein synthesis about 4-12 hours post workout and its increased WAY more than 2x over basal. Thats the kind of protein synthesis you need to put on muscle.
We know to stimulate max protein synthesis you need three things: protein, insulin, and exercise. Just tweaking one part of that equation isn't going to do near as much if you hit all three. So BCAA have a big influence on signalling, but just upping BCAA isn't going to make you huge. Just keeping high insulin isn't going to make you huge (well fat maybe). Just exercising isn't enough. You need all three and you can only hit them so hard before your just wasting your time.
10-18-2007, 03:57 PM
In short without cut and pasting a huge research article. Simply Google "Leucine + insulin release" and you'll get all the researched science you'll ever want on Leucine. Do yourselves a favor, skip over to "Conclusion." The Intro, methods, procedures sections of any research article are full of jabber that mainly concern scientific peer review panels. Maybe read the intro, but the title of the research article should summarize the intro anyway.
01-13-2008, 09:25 AM
Leucine shouldn't be used in a prolonged manner anyway.
It should only be used just before/during/and IMMEDIATE post training to optimize the benefits. Other proteins are better choices outside this training session window.
Prolonging leucine intake as stated in the above citation is not only unbeneficial but also counter productive. Leucine ONLY during training....
01-13-2008, 10:02 AM
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