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In both humans and rats, the DAA supplement group showed increased synthesis and release of testosteroneand androstenediol. While these effects were statistically significant between the AAI- and the DAA-supplement groups, a greater increase in androstenediol was found in the AAI-supplementing group and a concomitant decrease in androstenediol mRNA was found in rats. This was consistent with previous studies in humans and rats which demonstrated that the DAA supplement is effective for the treatment of male sexual dysfunction and may be of benefit in testosterone replacement therapy as well, primobolan cutting stack.Taken together, these two studies provide experimental evidence indicating that DAA supplementation may be effective for the treatment androgen-dependent male sexual dysfunction, release hgh supplement. This conclusion is further supported by the fact that in rodent models of male sexual dysfunction DAA supplementation was shown to improve both clinical and biochemical parameters, hgh release supplement. It is thus possible that DAA supplementation may be effective for the treatment of some male sexual dysfunction caused by the failure of testosterone replacement therapy.