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培养的大鼠颗粒细胞孕烯醇酮生物合成:促卵泡激素和促性腺激素释放激素的调节作用

Pregnenolone biosynthesis by cultured rat granulosa cells: modulation by follicle-stimulating hormone and gonadotropin-releasing hormone.

作者信息

Jones P B, Hsueh A J

出版信息

Endocrinology. 1982 Sep;111(3):713-21. doi: 10.1210/endo-111-3-713.

Abstract

The mechanism by which GnRH inhibits ovarian progesterone production was investigated by studying the GnRH modulation of pregnenolone biosynthesis in cultured rat granulosa cells. Granulosa cells from hypophysectomized, estrogen-treated rats were incubated for 2 days with various hormones in vitro. Pregnenolone production was measured in the presence of cyanoketone, which inhibits the conversion of pregnenolone to progesterone. FSH stimulated pregnenolone production in a dose-dependent manner (ED50, 4.47 ng/ml). Concomitant treatment with GnRH resulted in a dose-dependent decrease in FSH-stimulated pregnenolone production (ID50, 6.3 x 10(-9) M; maximal decrease, approximately 50%). In contrast, treatment with high doses of GnRH alone stimulated pregnenolone production (ED50, 2.95 x 10(-8) M) reaching a maximal level of about 10% that induced by FSH. Treatment with a GnRH antagonist, [Ac-D-Phe1, D-pCl-Phe2, D-Trp3,6]GnRH, did not affect either basal or FSH-stimulated pregnenolone production, but blocked both inhibitory and stimulatory effects of GnRH. The addition of 25-hydroxycholesterol, a soluble substrate for side-chain cleavage enzymes, enhanced FSH-stimulated pregnenolone production, but failed to overcome the inhibitory action of GnRH. GnRH also inhibited progesterone production stimulated by 8-bromo-cAMP and cholera toxin. This action of GnRH, however, was not associated with an inhibition of pregnenolone biosynthesis, but appeared to be due to a preferential increase in the metabolism of progesterone to 20 alpha-hydroxypregn-4-en-3-one. Thus, in addition to the reported GnRH stimulation of progesterone metabolism to 20 alpha-hydroxypregn-4-en-3-one and the GnRH inhibition of FSH-stimulated 3 beta-hydroxysteroid dehydrogenase activity, the present results demonstrate that GnRH also inhibits FSH-stimulated pregnenolone biosynthesis, probably at the side-chain cleavage enzyme step.

摘要

通过研究促性腺激素释放激素(GnRH)对培养的大鼠颗粒细胞孕烯醇酮生物合成的调节作用,探讨了GnRH抑制卵巢孕酮生成的机制。将来自垂体切除、雌激素处理大鼠的颗粒细胞在体外与各种激素一起孵育2天。在存在氰基酮的情况下测量孕烯醇酮的生成,氰基酮可抑制孕烯醇酮向孕酮的转化。促卵泡激素(FSH)以剂量依赖性方式刺激孕烯醇酮生成(半数有效剂量[ED50],4.47 ng/ml)。同时用GnRH处理导致FSH刺激的孕烯醇酮生成呈剂量依赖性降低(半数抑制剂量[ID50],6.3×10⁻⁹ M;最大降低约50%)。相反,单独用高剂量GnRH处理刺激孕烯醇酮生成(ED50,2.95×10⁻⁸ M),达到FSH诱导水平的约10%的最大水平。用GnRH拮抗剂[Ac-D-苯丙氨酸¹,D-对氯苯丙氨酸²,D-色氨酸³,⁶]GnRH处理既不影响基础孕烯醇酮生成也不影响FSH刺激的孕烯醇酮生成,但阻断了GnRH的抑制和刺激作用。添加25-羟胆固醇(一种侧链裂解酶的可溶性底物)可增强FSH刺激的孕烯醇酮生成,但未能克服GnRH的抑制作用。GnRH还抑制8-溴环磷腺苷(8-bromo-cAMP)和霍乱毒素刺激的孕酮生成。然而,GnRH的这种作用与孕烯醇酮生物合成的抑制无关,似乎是由于孕酮向20α-羟基孕-4-烯-3-酮代谢的优先增加所致。因此,除了已报道的GnRH刺激孕酮代谢为20α-羟基孕-4-烯-3-酮以及GnRH抑制FSH刺激的3β-羟基类固醇脱氢酶活性外,目前的结果表明GnRH还抑制FSH刺激的孕烯醇酮生物合成,可能是在侧链裂解酶步骤。

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