Vega M, Devoto L, Castro O, Kohen P
Department of Cell Biology and Genetics, School of Medicine, University of Chile, Santiago.
J Clin Endocrinol Metab. 1994 Aug;79(2):466-9. doi: 10.1210/jcem.79.2.8045965.
To assess the role of estradiol (E2) upon progesterone (P4) synthesis, a well defined human midluteal cell system was used. A dose-dependent inhibition of P4 synthesis with and without hCG was induced by E2. In addition, E2 had a dose related cumulative effect on pregnenolone as compared with control experiments (2-fold, P < 0.05) as well as in hCG-stimulated conditions (3-fold, P < 0.005). On the other hand, the concentrations of 20 alpha-hydroxyprogesterone obtained in all experimental conditions were similar to control values, indicating that the catabolism of P4 was not modified. 3 beta-Hydroxysteroid dehydrogenase activity was significantly diminished (P < 0.05) in the presence of E2. Finally, the kinetic studies on P4 synthesis from pregnenolone showed a competitive type of inhibition with a K1 of 2.22 x 10(-6) mol/L. These data indicate an inhibition of 3 beta-hydroxysteroid dehydrogenase on human corpus luteum by E2.
为评估雌二醇(E2)对孕酮(P4)合成的作用,使用了一个明确的人黄体中期细胞系统。E2对有无hCG时的P4合成均产生剂量依赖性抑制。此外,与对照实验相比,E2对孕烯醇酮有剂量相关的累积效应(2倍,P<0.05),在hCG刺激条件下也是如此(3倍,P<0.005)。另一方面,在所有实验条件下获得的20α-羟孕酮浓度与对照值相似,表明P4的分解代谢未发生改变。在E2存在的情况下,3β-羟基类固醇脱氢酶活性显著降低(P<0.05)。最后,对孕烯醇酮合成P4的动力学研究显示为竞争性抑制类型,K1为2.22×10(-6)mol/L。这些数据表明E2对人黄体中的3β-羟基类固醇脱氢酶有抑制作用。