O'Donnell L, Stanton P G, Wreford N G, Robertson D M, McLachlan R I
Prince Henry's Institute of Medical Research, Clayton, Australia.
Endocrinology. 1996 Jul;137(7):2703-10. doi: 10.1210/endo.137.7.8770889.
Testosterone (T) is required for spermatogenesis, particularly in the conversion of round spermatids between stages VII and VIII of spermatogenesis. T is generally thought to be the major androgen involved in adult spermatogenesis due to the high local concentration within the testis, whereas its more potent 5alpha-reduced metabolite dihydrotestosterone (DHT) is thought to be the active androgen in peripheral tissues. The current study investigated whether 5alpha-reduction of T to DHT is involved in the restoration of spermiogenesis in vivo in a setting in which testicular T levels were markedly reduced. Adult male rats were given 3-cm T plus 0.4-cm estradiol implants for 9 weeks to suppress serum LH and testicular T levels and thereby inhibit spermatogenesis. Increasing doses of T (3-, 6-, 10-, and 24-cm implants) were then given for 4 days to restore spermatogenesis in the presence or absence of a 5alpha-reductase inhibitor (L685,273). The hourly production rates of round spermatids in stages I-III, IV-VI, VII, and VIII were assessed using stereological techniques, and the conversion of round spermatids between stages VII and VIII was then assessed as an index of androgen action on spermiogenesis. Testicular androgen levels were measured by HPLC and RIA. The 5alpha-reductase inhibitor significantly suppressed (P < 0.05) the hourly production rate of round spermatids at the 3- and 6-cm T doses, but not at the 10- and 24-cm doses. The conversion of round spermatids between stages VII and VIII was suppressed (P < 0.05) by the inhibitor only at the 3- and 6-cm doses. The 5alpha-reductase inhibitor had no effect on testicular T levels, but suppressed (P < 0.05) DHT levels at the 6-, 10-, and 24-cm doses. We conclude that the 5alpha-reduction of T is involved in the restoration of spermiogenesis at the lower administered doses of T and that these data are the first description of a role for 5alpha-reduced androgens in adult spermatogenesis.
睾酮(T)对精子发生是必需的,特别是在精子发生的VII期和VIII期之间圆形精子细胞的转化过程中。由于睾丸内局部浓度较高,T通常被认为是参与成年男性精子发生的主要雄激素,而其活性更强的5α-还原代谢产物双氢睾酮(DHT)则被认为是外周组织中的活性雄激素。本研究调查了在睾丸T水平显著降低的情况下,T向DHT的5α-还原是否参与体内精子形成的恢复。成年雄性大鼠植入3厘米的T加0.4厘米的雌二醇9周,以抑制血清促黄体生成素(LH)和睾丸T水平,从而抑制精子发生。然后给予递增剂量的T(3厘米、6厘米、10厘米和24厘米的植入物)4天,以在有或无5α-还原酶抑制剂(L685,273)的情况下恢复精子发生。使用体视学技术评估I-III期、IV-VI期、VII期和VIII期圆形精子细胞的每小时产生率,然后将VII期和VIII期之间圆形精子细胞的转化作为雄激素对精子形成作用的指标进行评估。通过高效液相色谱法(HPLC)和放射免疫分析法(RIA)测量睾丸雄激素水平。5α-还原酶抑制剂在T剂量为3厘米和6厘米时显著抑制(P<0.05)圆形精子细胞的每小时产生率,但在10厘米和24厘米剂量时没有抑制作用。仅在3厘米和6厘米剂量时,抑制剂抑制(P<0.05)了VII期和VIII期之间圆形精子细胞的转化。5α-还原酶抑制剂对睾丸T水平没有影响,但在6厘米、10厘米和24厘米剂量时抑制(P<0.05)了DHT水平。我们得出结论,在较低的T给药剂量下,T的5α-还原参与了精子形成的恢复,并且这些数据首次描述了5α-还原雄激素在成年男性精子发生中的作用。