Nimrod A
Mol Cell Endocrinol. 1977 Sep;8(3):189-99. doi: 10.1016/0303-7207(77)90091-0.
Metabolic transformations of progesterone in cultures of granulosa cells from immature hypophysectomized rats treated with diethylstilbestrol were studied in relation to the synergistic action of exogenous androgen and FSH on progestin (progesterone and 20alpha-dihydroprogesterone) accumulation. Androstenedione (Ad; 10 ng/ml) enhanced the sensitivity of rat granulosa cells to this steroidogenic action of FSH, lowering the threshold of the response from greater than 4 ng/ml (FSH alone) to 0.8 ng/ml in the presence of Ad. A synergistic effect with FSH was also shown by various 5alpha-androstane derivatives. They were, however, less effective than the parent delta4-3 keto androstenes. Progesterone underwent extensive 5alpha-reduction during culture, leading to accumulation of endogenous 5alpha-pregnane compounds, and to transformation of labelled progesterone into 5 alpha-reduced radiometabolites. These compounds corresponded in gas-liquid and thin-layer chromatographic behaviour to 3alpha-hydroxy-5alpha-pregnan-20-one, 20alpha-hydroxy-5alpha-pregnan-3-one and 5alpha-pregnane-3alpha,20alpha-diol. The rate of 5alpha-reduction of progestins was not affected by the presence of exogenous Ad (1 microgram/ml), ruling out the possibility that the effect of androgen on progestin accumulation depends on competitive inhibition of 5alpha-reductase. An involvement of androgen of thecal origin in the enhancement of the sensitivity of the FSH-responsive mechanism in granulosa cells is suggested.
研究了用己烯雌酚处理的未成熟去垂体大鼠颗粒细胞培养物中孕酮的代谢转化,及其与外源性雄激素和促卵泡激素(FSH)对孕激素(孕酮和20α-二氢孕酮)积累的协同作用之间的关系。雄烯二酮(Ad;10 ng/ml)增强了大鼠颗粒细胞对FSH这种促类固醇生成作用的敏感性,使反应阈值从单独使用FSH时大于4 ng/ml降至存在Ad时的0.8 ng/ml。各种5α-雄烷衍生物也显示出与FSH的协同作用。然而,它们的效果不如母体Δ4-3-酮雄烯。在培养过程中,孕酮经历了广泛的5α-还原,导致内源性5α-孕烷化合物的积累,并使标记的孕酮转化为5α-还原的放射性代谢产物。这些化合物在气液色谱和薄层色谱行为上与3α-羟基-5α-孕烷-20-酮、20α-羟基-5α-孕烷-3-酮和5α-孕烷-3α,20α-二醇相对应。孕激素的5α-还原速率不受外源性Ad(1 μg/ml)存在的影响,排除了雄激素对孕激素积累的作用取决于对5α-还原酶的竞争性抑制的可能性。提示卵泡膜来源的雄激素参与了颗粒细胞中FSH反应机制敏感性的增强。