The ability of testosterone, androsterone, 5α-androstane-3α,17β-diol, and 5α-androstane-3β,17β-diol to prevent the castration-induced rise in serum gonadotropin levels was investigated in immature male rats. Rats castrated at 30 days of age were treated once per day by subcutaneous injection of 12.5–100 μg of the steroid per 100 g body weight per day for 3 days, beginning on the day of castration. The animals were sacrificed 24 h after the last injection. Testosterone propionate, androsterone propionate, and 5α-androstane-3α,17β-diol dipropionate were also tested at the approximate molar equivalent of 100 μg of the free alcohol form per 100 g body weight per day.Testosterone propionate and 5α-androstane-3α,17β-diol were the only compounds tested that prevented the castration induced rise in luteinizing hormone (LH) concentrations. Testosterone propionate also inhibited the rise in follicle stimulating hormone (FSH) concentrations whereas 5α-androstane-3α,17β-diol inhibited the rise in FSH in one but not in another experiment. These were the only compounds tested that affected serum FSH concentrations.The lower doses of testosterone tested significantly increased serum LH, but not FSH concentrations compared to castrate control animals. The highest dose tested partially inhibited the rise in serum LH concentrations.Both androsterone and androsterone propionate maintained ventral prostate weights. Although neither compound prevented the castration induced rise in serum LH, two groups receiving androsterone had serum LH concentrations significantly lower than the castrate control group.5α-Androstane-3β,17β-diol and 5α-androstane-3α,17β-diol dipropionate failed to maintain ventral prostate weights or prevent the rise in serum gonadotropin levels.These results indicate that 5α-androstane-3α,17β-diol is capable of preventing the castration induced rise in serum LH concentrations in the immature male rat and thus may participate in the regulation of LH secretion in these animals.