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Studies indicate that the anabolic nandrolone decanoate (Deca-Durabolin(r)) can modulate cell cycle regulation, but little is known about its effects on muscle cells. We examined whether Deca-Durabolin(r) treatment enhances the effects of endurance exercise on muscle mitochondrial biogenesis during recovery from aerobic exercise. Eighteen male recreational cyclists, in whom a previous bout of endurance exercise elicited an apparent increase in mitochondrial biogenesis measured by an oxidative phosphorylation assay, were supplemented with (a) 10 mg/kg (decanoate) and (b) 400 mg/kg (Durabolin(r)) every last two days for 2 wk. For an eight week training period, each experimental group completed two sets of six-fibre resistance exercises each day. One set was comprised of a single eccentric (eccentric) exercise and the second set was comprised of a single concentric (centre-locked) exercise as per the protocol. Training lasted 8 h. Training-induced mitochondrial biogenesis during an eight-week period was assessed, using an oxidative phosphorylation (Pi; oxidation) enzyme immunometric assay. It was determined that both conditions caused a significant decrease in Pi (0.27 ± 0.13 mU/m/min increase) during the second phase of endurance exercise compared to that in the first training time point (0.10 ± 0.04mU/m/min decrease). In addition, a dose-dependent enhancement of Pi during one- and two-set conditions was observed. These findings indicate that during an eight-week cycling training program, the administration of Deca-Durabolin(r) can modulate cell cycle regulation, which is possible because the two drugs have differing pharmacology. They also indicate that there may be potential to reduce muscle damage and oxidative stress in response to exercise.Similar articles: