Lacroix E, Eechaute W, Leusen I
Arch Int Physiol Biochim. 1981 Feb;89(1):75-80. doi: 10.3109/13813458109069140.
The role of a direct or a hypophysis-mediated influence of increased testosterone levels in the effects of a long-term high-dose HCG administration (10 IU/day) upon the 7 alpha-hydroxylation and 5 alpha-reduction activities of incubated testes of mature rats was investigated. Administration of high doses of HCG to hypophysectomized rats resulted in the same metabolic changes as in normal rats, namely, a large decrease in the 7 alpha-hydroxylation and an increase in the 5 alpha-reduction processes. Administration of testosterone-propionate (0.2 mg and 20 mg/day) for several days to hypophysectomized rats and to normal rats receiving and substitutive dose of 1 IU HCG/day, did not modify the testicular metabolization pattern. These findings indicate that the decrease in testicular 7 alpha-hydroxylation activity induced by long-term administration of high doses of HCG is probably not mediated by the hypophysis nor by the extracellular testosterone levels.
研究了长期高剂量注射人绒毛膜促性腺激素(10国际单位/天)对成熟大鼠睾丸7α-羟化和5α-还原活性的影响中,睾酮水平升高的直接作用或垂体介导作用的角色。对垂体切除的大鼠注射高剂量人绒毛膜促性腺激素,导致了与正常大鼠相同的代谢变化,即7α-羟化大幅降低,5α-还原过程增加。对垂体切除的大鼠以及接受1国际单位/天替代剂量人绒毛膜促性腺激素的正常大鼠连续几天注射丙酸睾酮(0.2毫克和20毫克/天),并未改变睾丸代谢模式。这些发现表明,长期高剂量注射人绒毛膜促性腺激素诱导的睾丸7α-羟化活性降低可能既不是由垂体介导,也不是由细胞外睾酮水平介导。