Kühn-Velten N, Bunse T, Schürer N, Staib W
Hoppe Seylers Z Physiol Chem. 1984 Jul;365(7):773-9. doi: 10.1515/bchm2.1984.365.2.773.
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.
研究了雄激素可能通过睾丸内反馈机制控制大鼠睾丸组织自身生物合成的一个可能作用位点。结果表明,孕酮(Ks = 0.45微摩尔)和睾酮(Ks = 14.7微摩尔)均可诱导微粒体细胞色素P - 450的光谱变化;这些光谱效应并非相加性的,因此两种类固醇可能作用于同一细胞色素P - 450种类。睾酮对孕酮与可溶性微粒体蛋白结合的竞争性抑制作用(Ki = 10.0微摩尔)以及孕酮向雄激素转化的竞争性抑制作用(Ki = 14.3微摩尔)的观察结果支持了这一假设。得出的结论是,大鼠睾丸雄激素生物合成不仅通过垂体 - 睾丸轴受到反馈调节,而且雄激素还直接作用于依赖孕酮结合细胞色素P - 450的微粒体反应。