Well whatever the reason, the dosing scheme is still ridiculous.
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Well whatever the reason, the dosing scheme is still ridiculous.
At first I thought they added it just to add stuff like AndroFactory did, but BBG may be onto something else
I designed 5-Alpha Test and have said many times that it was a 25mg tablet of epiandrosterone plus 500mcg's of methylcobalamin.
Alpha Hard is not intended for under the tongue.
Hai
Is anyone else selling a blend of both isomers? Last I checked this was the only product.
No...you are the only one selling both isomers, which is why I ordered a bottle to try. But I have to say, customer service at Forerunner is severely lacking. I have questions and I've emailed them a couple times and I have yet to hear back.
I want to know why it says to dose one pill per hour for three hours in the a.m. and then the same thing in the p.m? What is the point of dosing like that? Why can't they be taken all three at once in the a.m. and then again all three at once in the p.m? The way it is instructed seems cumbersome and a bit annoying to have to dose it that way. I asked this same thing in an email to customer service and to another email that I had found and I don't get a response?
Not too impressive thus far.
junk email folder? Check there.
For both an acute effect (Preworkout)as well as the overall benefits of agmatine supplementation.
J. Biol. Chem., 2014 vol. 289(14) pp. 9710-29
The molecular and metabolic influence of long term agmatine consumption
Nissim, I; Horyn, O; Daikhin, Y; Chen, P; Li, C; Wehrli, SL; Nissim, I; Yudkoff, M
Agmatine (AGM), a product of arginine decarboxylation, influences multiple physiologic and metabolic functions. However, the mechanism(s) of action, the impact on whole body gene expression and metabolic pathways, and the potential benefits and risks of long term AGM consumption are still a mystery. Here, we scrutinized the impact of AGM on whole body metabolic profiling and gene expression and assessed a plausible mechanism(s) of AGM action. Studies were performed in rats fed a high fat diet or standard chow. AGM was added to drinking water for 4 or 8 weeks. We used (13)C or (15)N tracers to assess metabolic reactions and fluxes and real time quantitative PCR to determine gene expression. The results demonstrate that AGM elevated the synthesis and tissue level of cAMP. Subsequently, AGM had a widespread impact on gene expression and metabolic profiling including (a) activation of peroxisomal proliferator-activated receptor-α and its coactivator, PGC1α, and (b) increased expression of peroxisomal proliferator-activated receptor-γ and genes regulating thermogenesis, gluconeogenesis, and carnitine biosynthesis and transport. The changes in gene expression were coupled with improved tissue and systemic levels of carnitine and short chain acylcarnitine, increased β-oxidation but diminished incomplete fatty acid oxidation, decreased fat but increased protein mass, and increased hepatic ureagenesis and gluconeogenesis but decreased glycolysis. These metabolic changes were coupled with reduced weight gain and a curtailment of the hormonal and metabolic derangements associated with high fat diet-induced obesity. The findings suggest that AGM elevated the synthesis and levels of cAMP, thereby mimicking the effects of caloric restriction with respect to metabolic reprogramming.