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EBF and PES team up to make burning fat even hotter:
This is a log for…
EBF: Adipose Annihilation V2
PES: Alphamine
Get those apps in. Looking for experienced, detailed loggers. US only!
To completely round out your fat burning arsenal we have both pre and post meal catalysts for fat burning, along with around the clock cortisol control. To start off this stack we have the most versatile non stimulant fat burner on the market:
Adipose Annihilation v2 Under the Spotlight
In this stack we have Adipose Annihilation V2, which is a non stimulant fat burner to enhance the way your body uses and gets fid of fuel. Synergy is the key to these remarkable results; AAv2’s ingredients complement one another to create “2 + 2 = 5” fat melting maximization. Hydroxycitric Acid and Acetyl-L-Carnitine in the FAT MOBILIZATION COMPLEX interact to mobilize and transport fat. Then the EBF ANNIHILATION COMPLEX takes over, as Fucoxanthin, Alpha Yohimbine, and Capsaicin combine to vanquish fat stores through PPARγ receptor antagonism. The Evodiamine, and Ginkgo Biloba Extract in AAv2 take body recomposition to a new level, boosting thermogenesis, regulating thyroid activity, and producing preferential glucose uptake.
Garcinia Cambogia 50% HCA (Hydroxycitric Acid) is a potent plant derivative with clinically proven lipid metabolism/oxidation potential [3]. Via inhibition of Malonyl Coenzyme A, the so called “building blocks” of fat, it blocks adipose production for upwards of twelve hours after a meal [4, 5]. As HCA stops creation of new fat cells, it simultaneously prompts adipose and liver tissue to oxidize bodily fat stores. By slowing gastric emptying, HCA lowers post-prandial glucose response [6]. Clinical supplementation with Garcinia Cambogia led to, “significantly reduced visceral, subcutaneous, and total fat areas compared with the placebo group,” and, moreover, no visceral fat regain after cessation of use [7]. Beyond this, in a hypocaloric environment – created when one begins to diet – HCA will also help limit muscular catabolism and breakdown [4]. Not only does HCA help prevent fat gain, HCA increases fatty acid oxidation and expression of GLUT-4 protein and glycogen supercompensation during physical activity [7,8].
HCA shown data that has displayed supercompensation of glycogen during physical exercise with increase fatty acid oxidation, but as well as showing increased expression of CD36 in the presence of a high carbohydrate meal showing that there is an increase in fatty acid oxidation while continuing to eat carbohydrates [14]. This fits in perfect for those who want to remain in the elusive fat burning zone after a high glycemic post workout carbohydrate meal.
Acetyl-L-Carnitine ALCAR assumes an essential duty in the FAT MOBILIZATION COMPLEX, activating and transporting fat cells for beta oxidation [8]. Its ability to support bodily energy metabolism and insulin response creates innumerable health benefits. One clinical study found that, “safely ameliorated arterial hypertension, insulin resistance, impaired glucose tolerance, and hypoadiponectinemia in subjects” [9]. ALCAR supplementation may help overcome leptin resistance; a hormonal shift often responsible for the metabolic slowdown and fat loss plateaus that dieters experience [10]. Marked increase in dopamine levels and prevention of stress-related hormonal depletion are additional benefits that ALCAR can provide to those in a caloric deficit, to make their diet quicker, easier, and more effective [11, 12].
Choline Bitratrate is a B Vitamin that prevents fat deposition in the liver, encourages liver fatty acid metabolism and increases subsequent oxidation [13, 14]. When paired with carnitine in medical trials, the two supplements fashioned synergistic improvements in fat mobilization. Fat is literally flushed out of the body, in the form of urinary acylcarnitines [15].
Fucoxanthin can restrict differentiation of preadipocytes to adipocytes by means of PPARγ down-regulation. Thus, this algae extract limits the opportunity that adipose cells have to form and accumulate in the body [16]. A cutting-edge supplement in the dieter’s arsenal, Fucoxanthin is rapidly garnering popularity as an uncoupler. Recent Hokkaido University trials found that Fucoxanthin augmented expression of mitochondrial uncoupling protein 1 (UCP1). In turn, UCP1 expression shrank abdominal white adipose tissue cells; resultant net body composition changes in Fucoxanthin-fed subjects were undeniably positive [17].
Alpha Yohimbine is a forceful α2 adrenergic antagonist; compared to standard Yohimbine, Alpha Yohimbine’s impact on α2B and α2C adrenoreceptors is three and four times more potent, respectively [18, 20]. As such, it capably enhances vasodilation/blood flow in adipose cells [19]. Because Alpha Yohimbine modulates α2C prevalent in the brain, epinephrine – along with concurrent nutrient utilization, thermogenesis, and energy metabolism – is maximally activated, whilst breakdown of serotonin, noradrenaline, and dopamine are controlled [20].
Capsicium Annum 8% Capsaicinoids increases energy expenditure and metabolic rate through multiple pathways [21, 22]. Studies claim, “capsaicin also inhibited the expression of PPARγ, C/EBPα, and leptin, but induced up-regulation of adiponectin at the protein level. These results demonstrate that capsaicin efficiently induces apoptosis and inhibits adipogenesis in 3T3-L1 preadipocytes and adipocytes” [23]. PPARγ modulation causes the bulk of adipose loss to be exhibited on ugly abdominal fat stores [24]. Capsaicinoid dosage in V2.0’s EBF ANNIHILATION COMPLEX has been reduced to .5mg per pill, resulting in similar increased post-ingestion glycerol and blood FFA levels seen in V1.0, without the potential for heartburn-like side-effects [25].
Evodiamine is an essential new addition to the re-formulated AAv2. This ingredient “mimics the characteristic anti-obese effects induced by capsaicin” to “induce heat loss and heat production at the same time and dissipate food energy, preventing the accumulation of perivisceral fat and the body weight increase” [26]. Inclusion of Evodiamine has reduced the required amount of Capsaicinoids in V2.0’s proprietary blend – this reduction, in turn will maintain all the effectiveness of the original formulation, without the potential for occurrence of heartburn at higher Capsaicinoid dosages. A recent medical study found that Evodiamine’s ability to inhibit adipocyte differentiation and limit fat gain – unlike Capsaicin - is not reliant on a mechanism of action involving uncoupling protein-1 (UCP1) thermogenesis [27]. Therefore, utilization of these two ingredients together can produce similar and cumulative effects by channeling multiple bodily pathways.
Ginko Biloba Extract is a compound that contains naturally-occurring flavonoids such as Kaempferol and Quercetin. Kaempferol is known to promote overall body/mind wellness through antioxidant, anti-inflammatory, cardioprotective, and neuroprotective activities [28]. Significant improvements in insulin-stimulated glucose uptake can be provided via Kaempferol supplementation, due to an ability to “act at multiple targets to ameliorate hyperglycemia, including by acting as partial agonists of PPARγ”; this partial PPARγ modulation “activates some (insulin sensitization), but not all (adipogenesis), PPARγ-signaling pathways” [29, 31]. Furthermore, in a separate FDA-sponsored study, both Kaempferol and Quercetin were proven to “down-regulate the adipogenesis-related transcriptional factors PPARγ, C/EBP-α and SREBP-1 and to inhibit adipocyte differentiation during the early stage” [30]. Couple this mechanism of action with Kaempferol’s known capacity to regulate D2-mediated thyroid activity (T3 production), and the result is truly astounding cumulative 2+2=5 fat-burning potential [32].
Now let’s take a look at the other side of the coin…the strongest stimmed fat burner on the market.
This is a log for…
EBF: Adipose Annihilation V2
PES: Alphamine
Get those apps in. Looking for experienced, detailed loggers. US only!
To completely round out your fat burning arsenal we have both pre and post meal catalysts for fat burning, along with around the clock cortisol control. To start off this stack we have the most versatile non stimulant fat burner on the market:
Adipose Annihilation v2 Under the Spotlight
In this stack we have Adipose Annihilation V2, which is a non stimulant fat burner to enhance the way your body uses and gets fid of fuel. Synergy is the key to these remarkable results; AAv2’s ingredients complement one another to create “2 + 2 = 5” fat melting maximization. Hydroxycitric Acid and Acetyl-L-Carnitine in the FAT MOBILIZATION COMPLEX interact to mobilize and transport fat. Then the EBF ANNIHILATION COMPLEX takes over, as Fucoxanthin, Alpha Yohimbine, and Capsaicin combine to vanquish fat stores through PPARγ receptor antagonism. The Evodiamine, and Ginkgo Biloba Extract in AAv2 take body recomposition to a new level, boosting thermogenesis, regulating thyroid activity, and producing preferential glucose uptake.
Garcinia Cambogia 50% HCA (Hydroxycitric Acid) is a potent plant derivative with clinically proven lipid metabolism/oxidation potential [3]. Via inhibition of Malonyl Coenzyme A, the so called “building blocks” of fat, it blocks adipose production for upwards of twelve hours after a meal [4, 5]. As HCA stops creation of new fat cells, it simultaneously prompts adipose and liver tissue to oxidize bodily fat stores. By slowing gastric emptying, HCA lowers post-prandial glucose response [6]. Clinical supplementation with Garcinia Cambogia led to, “significantly reduced visceral, subcutaneous, and total fat areas compared with the placebo group,” and, moreover, no visceral fat regain after cessation of use [7]. Beyond this, in a hypocaloric environment – created when one begins to diet – HCA will also help limit muscular catabolism and breakdown [4]. Not only does HCA help prevent fat gain, HCA increases fatty acid oxidation and expression of GLUT-4 protein and glycogen supercompensation during physical activity [7,8].
HCA shown data that has displayed supercompensation of glycogen during physical exercise with increase fatty acid oxidation, but as well as showing increased expression of CD36 in the presence of a high carbohydrate meal showing that there is an increase in fatty acid oxidation while continuing to eat carbohydrates [14]. This fits in perfect for those who want to remain in the elusive fat burning zone after a high glycemic post workout carbohydrate meal.
Acetyl-L-Carnitine ALCAR assumes an essential duty in the FAT MOBILIZATION COMPLEX, activating and transporting fat cells for beta oxidation [8]. Its ability to support bodily energy metabolism and insulin response creates innumerable health benefits. One clinical study found that, “safely ameliorated arterial hypertension, insulin resistance, impaired glucose tolerance, and hypoadiponectinemia in subjects” [9]. ALCAR supplementation may help overcome leptin resistance; a hormonal shift often responsible for the metabolic slowdown and fat loss plateaus that dieters experience [10]. Marked increase in dopamine levels and prevention of stress-related hormonal depletion are additional benefits that ALCAR can provide to those in a caloric deficit, to make their diet quicker, easier, and more effective [11, 12].
Choline Bitratrate is a B Vitamin that prevents fat deposition in the liver, encourages liver fatty acid metabolism and increases subsequent oxidation [13, 14]. When paired with carnitine in medical trials, the two supplements fashioned synergistic improvements in fat mobilization. Fat is literally flushed out of the body, in the form of urinary acylcarnitines [15].
Fucoxanthin can restrict differentiation of preadipocytes to adipocytes by means of PPARγ down-regulation. Thus, this algae extract limits the opportunity that adipose cells have to form and accumulate in the body [16]. A cutting-edge supplement in the dieter’s arsenal, Fucoxanthin is rapidly garnering popularity as an uncoupler. Recent Hokkaido University trials found that Fucoxanthin augmented expression of mitochondrial uncoupling protein 1 (UCP1). In turn, UCP1 expression shrank abdominal white adipose tissue cells; resultant net body composition changes in Fucoxanthin-fed subjects were undeniably positive [17].
Alpha Yohimbine is a forceful α2 adrenergic antagonist; compared to standard Yohimbine, Alpha Yohimbine’s impact on α2B and α2C adrenoreceptors is three and four times more potent, respectively [18, 20]. As such, it capably enhances vasodilation/blood flow in adipose cells [19]. Because Alpha Yohimbine modulates α2C prevalent in the brain, epinephrine – along with concurrent nutrient utilization, thermogenesis, and energy metabolism – is maximally activated, whilst breakdown of serotonin, noradrenaline, and dopamine are controlled [20].
Capsicium Annum 8% Capsaicinoids increases energy expenditure and metabolic rate through multiple pathways [21, 22]. Studies claim, “capsaicin also inhibited the expression of PPARγ, C/EBPα, and leptin, but induced up-regulation of adiponectin at the protein level. These results demonstrate that capsaicin efficiently induces apoptosis and inhibits adipogenesis in 3T3-L1 preadipocytes and adipocytes” [23]. PPARγ modulation causes the bulk of adipose loss to be exhibited on ugly abdominal fat stores [24]. Capsaicinoid dosage in V2.0’s EBF ANNIHILATION COMPLEX has been reduced to .5mg per pill, resulting in similar increased post-ingestion glycerol and blood FFA levels seen in V1.0, without the potential for heartburn-like side-effects [25].
Evodiamine is an essential new addition to the re-formulated AAv2. This ingredient “mimics the characteristic anti-obese effects induced by capsaicin” to “induce heat loss and heat production at the same time and dissipate food energy, preventing the accumulation of perivisceral fat and the body weight increase” [26]. Inclusion of Evodiamine has reduced the required amount of Capsaicinoids in V2.0’s proprietary blend – this reduction, in turn will maintain all the effectiveness of the original formulation, without the potential for occurrence of heartburn at higher Capsaicinoid dosages. A recent medical study found that Evodiamine’s ability to inhibit adipocyte differentiation and limit fat gain – unlike Capsaicin - is not reliant on a mechanism of action involving uncoupling protein-1 (UCP1) thermogenesis [27]. Therefore, utilization of these two ingredients together can produce similar and cumulative effects by channeling multiple bodily pathways.
Ginko Biloba Extract is a compound that contains naturally-occurring flavonoids such as Kaempferol and Quercetin. Kaempferol is known to promote overall body/mind wellness through antioxidant, anti-inflammatory, cardioprotective, and neuroprotective activities [28]. Significant improvements in insulin-stimulated glucose uptake can be provided via Kaempferol supplementation, due to an ability to “act at multiple targets to ameliorate hyperglycemia, including by acting as partial agonists of PPARγ”; this partial PPARγ modulation “activates some (insulin sensitization), but not all (adipogenesis), PPARγ-signaling pathways” [29, 31]. Furthermore, in a separate FDA-sponsored study, both Kaempferol and Quercetin were proven to “down-regulate the adipogenesis-related transcriptional factors PPARγ, C/EBP-α and SREBP-1 and to inhibit adipocyte differentiation during the early stage” [30]. Couple this mechanism of action with Kaempferol’s known capacity to regulate D2-mediated thyroid activity (T3 production), and the result is truly astounding cumulative 2+2=5 fat-burning potential [32].
Now let’s take a look at the other side of the coin…the strongest stimmed fat burner on the market.