Serum hormone quantification Serum levels of testosterone,

DHT, and E2 were determined by enzyme-linked immunosorbent assay (ELISA) using commercially available kits (Alpha Diagnostic, San Antonio, USA). Briefly, reference controls, standards and samples were aliquoted in triplicate into separate wells pre-incubated with horseradish peroxidase (HRP)-conjugated primary antibodies specific for either testosterone, DHT, or E2. After washing, reference controls, standards, and sample wells were incubated with tetramethylbenzidine and gently agitated. CH5424802 research buy After 10 min, the HRP-substrate colorimetric reaction was stopped with 0.16 M H2SO4, and the absorbance at 450 nm of each well was evaluated using a spectrophotometer. Statistical analysis To evaluate the significance of possible group differences in steroid hormone levels within treatment groups, a 2 (high versus low dose) × 4 (sample time point) one-way repeated measures Analysis of Variance (ANOVA) was conducted. LY3039478 molecular weight To evaluate statistically significant differences in steroid hormone levels between treatment groups, a two-way ANOVA was used. Differences in steroid hormone concentrations were considered clinically significant when the probability of a Type I error was less than 0.05. Results and discussion Total

testosterone levels tend to decline as men age [7]. Given that natural 5α-reductase/aromatase inhibitors, such as AX, may increase serum testosterone [9,18,19], we set out to determine if Resettin® was capable of increasing serum testosterone levels in sedentary men. To that end, a randomized controlled clinical dose comparison study of Resettin® was completed. Body weight, blood pressure, and tolerance The average baseline body weight of participants within the 800 mg/day placebo and Resettin®/MyTosterone™ treatment groups

were 88.3 kg and 93 kg, respectively. The average baseline body weight of participants within 1200 mg/day placebo and Resettin®/MyTosterone™ treatment VX-689 cost groups were 103.7 kg and 95.8 kg, respectively. Results indicated that there were no clinically significant changes in average Endonuclease body weight over the duration of the study. The average baseline systolic diastolic blood pressure ratios were 120 mmHg over 82 mmHg in the 800 mg/day placebo control group, 125 mmHg over 83 mmHg in the 800 mg/day Resettin®/MyTosterone™ treatment group, 122 mmHg over 82 mmHg in the 1200 mg/day placebo control group and 122 mmHg over 81 mmHg in the 1200 mg/day Resettin®/MyTosterone™ treatment group. No significant changes in systolic or diastolic blood pressure were observed over the course of the study. Owing to the significant safety profile and tolerability of AX as well as the other constituent compounds of Resettin®, there were no reports of adverse side effects during the study.