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细胞内受体介导性腺类固醇对促性腺激素释放激素诱导的促黄体生成素释放的调节作用。

Intracellular receptors mediate gonadal steroid modulation of LHRH-induced LH release.

作者信息

Kamel F, Krey L C

出版信息

Mol Cell Endocrinol. 1982 Nov-Dec;28(3):471-86. doi: 10.1016/0303-7207(82)90140-x.

Abstract

Primary cultures of enzymatically dispersed rat pituitary cells were used to study the role of intracellular receptors in gonadal steroid modulation of LHRH-induced LH release. Nuclear receptors for both testosterone (T) and 17 beta-estradiol (E) were observed, with KD values of 6.3 and 0.1 nM respectively. Occupation of these receptors was correlated with modulation of LH secretion. The relationship between these two parameters was nonlinear, so that steroid effects on LH secretion were maximal when fewer than 50% of the receptors were occupied. The androgen antagonist cyproterone blocked both T binding to nuclear receptors and T inhibition of LH secretion. Similarly, the estrogen antagonist CI-628 blocked both E binding and E stimulation of LH secretion. In cultures derived from pseudohermaphrodite rats. T did not bind to nuclear receptors, nor did it inhibit LH secretion. These results, showing a relationship between occupation of nuclear receptors and modulation of LH secretion, suggest that steroid effects on LH secretion are mediated by these receptors.

摘要

使用酶分散的大鼠垂体细胞原代培养物来研究细胞内受体在性腺类固醇对促性腺激素释放激素(LHRH)诱导的促黄体生成素(LH)释放的调节中的作用。观察到睾酮(T)和17β-雌二醇(E)的核受体,其解离常数(KD)值分别为6.3和0.1 nM。这些受体的占据与LH分泌的调节相关。这两个参数之间的关系是非线性的,因此当少于50%的受体被占据时,类固醇对LH分泌的影响最大。雄激素拮抗剂环丙孕酮阻断了T与核受体的结合以及T对LH分泌的抑制。同样,雌激素拮抗剂CI-628阻断了E的结合以及E对LH分泌的刺激。在来自假两性畸形大鼠的培养物中,T不与核受体结合,也不抑制LH分泌。这些结果表明核受体的占据与LH分泌的调节之间存在关系,提示类固醇对LH分泌的影响是由这些受体介导的。

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