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人体睾丸的体外类固醇代谢研究I:雌激素对孕酮代谢的影响。

In vitro steroid metabolic studies in human testes I: Effects of estrogen on progesterone metabolism.

作者信息

Rodriguez-Rigau L J, Tcholakian R K, Smith K D, Steinberger E

出版信息

Steroids. 1977 Jun;29(6):771-86. doi: 10.1016/0039-128x(77)90121-0.

Abstract

A technique of incubation of testicular tissue in vitro with radiolabeled precursors was applied in the investigation of the steroid biosynthesis by testes of four young men after long-term, high-dose estrogen treatment. A positive correlation between plasma and testicular steroid levels, and in vitro capacity of the testes to metabolize progesterone was demonstrated. Estrogen administration produced a very significant inhibition of plasma and testicular levels of testosterone. The in vitro synthesis of testosterone from progesterone was very severely impaired; especially 17alpha-hydroxylation of progesterone. 20alpha-hydroxysteroid-dehydrogenase activity was found to be increased after estrogen treatment, both in vivo and in vitro. These findings suggest that testicular 17alpha-hydroxylase activity (and possibly also 17-20 lyase activity) is either under gonadotropin regulation, or is directly suppressed by estrogen. This could result by decreased enzyme synthesis, direct enzyme inhibition or affectation of the cofactors or cytochromes necessary for the enzymatic activity. 20alpha-reduction of C21-steroids would represent an alternative pathway for their catabolism, not regulated by gonadotropin or not affected by estrogen, that would be significant in situations with reduced 17alpha-hydroxylase activity.

摘要

一种用放射性标记前体体外孵育睾丸组织的技术被应用于研究四名长期接受高剂量雌激素治疗的年轻男性睾丸的类固醇生物合成。血浆和睾丸类固醇水平之间以及睾丸体外代谢孕酮的能力之间存在正相关。给予雌激素对血浆和睾丸中的睾酮水平产生了非常显著的抑制作用。孕酮体外合成睾酮的过程受到严重损害;尤其是孕酮的17α-羟化。雌激素治疗后,体内和体外的20α-羟类固醇脱氢酶活性均升高。这些发现表明,睾丸17α-羟化酶活性(可能还有17-20裂解酶活性)要么受促性腺激素调节,要么直接被雌激素抑制。这可能是由于酶合成减少、酶直接抑制或影响酶活性所需的辅因子或细胞色素所致。C21类固醇的20α-还原将代表其分解代谢的另一条途径,不受促性腺激素调节或不受雌激素影响,在17α-羟化酶活性降低的情况下具有重要意义。

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