Direct effect of androgens on progesterone binding and metabolism in rat testis microsomes.

N Kühn-Velten, T Bunse, N Schürer, W Staib
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引用次数: 7

Abstract

A possible site of action at which androgens may control their own biosynthesis in rat testicular tissue in terms of an intratesticular feedback mechanism is investigated. It is shown that both progesterone (Ks = 0.45 microM) and testosterone (Ks = 14.7 microM) induce spectral changes at microsomal cytochrome P-450; these spectral effects are not additive and therefore both steroids may act on the same species of cytochrome P-450. This hypothesis is supported by the observation of competitive inhibition by testosterone of progesterone binding to solubilized microsomal proteins (Ki = 10.0 microM) and of progesterone conversion to androgens (Ki = 14.3 microM). It is concluded that rat testicular androgen biosynthesis is subject to feedback regulation not only via the pituitary-testicular axis but also by direct action of androgens on microsomal reactions dependent on progesterone-binding cytochrome P-450.

雄激素对大鼠睾丸微粒体孕酮结合及代谢的直接影响。
研究了雄激素通过睾丸内反馈机制控制其自身在大鼠睾丸组织中的生物合成的可能作用位点。结果表明,黄体酮(Ks = 0.45 μ m)和睾酮(Ks = 14.7 μ m)均可诱导微粒体细胞色素P-450的光谱变化;这些光谱效应不是相加的,因此两种类固醇可能作用于相同种类的细胞色素P-450。这一假设得到了睾酮竞争性抑制孕酮与溶解微粒体蛋白结合(Ki = 10.0微米)和孕酮转化为雄激素(Ki = 14.3微米)的观察的支持。由此可见,大鼠睾丸雄激素的生物合成不仅受垂体-睾丸轴的反馈调节,而且还受雄激素对依赖于孕激素结合细胞色素P-450的微粒体反应的直接作用。
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