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围产期大鼠卵巢对二丁酰环磷腺苷的反应性:体内存在抑制作用的证据。

Responsiveness of rat ovaries to dcAMP in the perinatal period: evidence for an inhibitory influence in vivo.

作者信息

Rouiller V, Gangnerau M N, Picon R

机构信息

Laboratoire de Physiologie du Développement, URA CNRS No. 307, Paris, France.

出版信息

J Steroid Biochem Mol Biol. 1991 Dec;39(6):953-7. doi: 10.1016/0960-0760(91)90355-9.

Abstract

The progesterone production by rat ovaries from 18-day-old fetuses to 6-day-old neonates was measured in vitro in the presence of dibutyryl cAMP (dcAMP, 1 mM). A pronounced decline was observed at the end of fetal life. The 5 alpha-reductase activity did not seem sufficient to explain this decrease. Preculture of the ovaries for 48 h in the basal medium enhanced responsiveness to the nucleotide. Addition of spironolactone, an inhibitor of 17 alpha-hydroxylase to dcAMP did not modify this evolution. 3 beta-hydroxysteroid dehydrogenase activity, detectable in fetal ovaries in the absence of dcAMP was also increased after preculture. In the presence of spironolactone and trilostane, the pregnenolone production showed the same evolution as progesterone and was also enhanced after culture. These results suggest the existence of inhibitory factor(s) present in vivo at the end of fetal life.

摘要

在存在二丁酰环磷酸腺苷(dcAMP,1 mM)的情况下,体外测定了18日龄胎儿至6日龄新生儿大鼠卵巢的孕酮生成。在胎儿期结束时观察到明显下降。5α-还原酶活性似乎不足以解释这种下降。卵巢在基础培养基中预培养48小时可增强对核苷酸的反应性。向dcAMP中添加17α-羟化酶抑制剂螺内酯不会改变这种变化。在没有dcAMP的情况下,胎儿卵巢中可检测到的3β-羟类固醇脱氢酶活性在预培养后也增加了。在存在螺内酯和曲洛司坦的情况下,孕烯醇酮的生成与孕酮表现出相同的变化,并且在培养后也增加了。这些结果表明在胎儿期结束时体内存在抑制因子。

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