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激素对子宫肌层肾上腺素能反应的调节:受体及其他方面。

Hormonal regulation myometrial adrenergic responses: the receptor and beyond.

作者信息

Roberts J M, Riemer R K, Bottari S P, Wu Y Y, Goldfien A

机构信息

Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco.

出版信息

J Dev Physiol. 1989 Mar;11(3):125-34.

PMID:2553793
Abstract

The contractile response of the uterus is modified by sex steroids. In rabbit uterus, oestrogen promotes alpha-adrenergically-mediated contraction, whilst progesterone treatment results in beta-adrenergic relaxation. Examination of the mechanisms responsible for these changing adrenergic responses with sex steroids reveals multiple sites of regulation. Oestrogen increases alpha 1-receptor concentration and the linkage of the receptor to phospholipase C. In addition to this direct effect to promote contraction, oestrogen also uncouples the beta-receptor from adenylate cyclase. Progesterone, conversely, promotes relaxation through beta-receptors by uncoupling alpha 2-receptors from inhibition of adenylate cyclase. Thus sex steroids can regulate specific agonist responses at and beyond the receptor.

摘要

子宫的收缩反应会受到性类固醇的调节。在兔子宫中,雌激素促进α-肾上腺素能介导的收缩,而孕激素处理则导致β-肾上腺素能松弛。研究性类固醇导致这些肾上腺素能反应变化的机制发现了多个调节位点。雌激素增加α1受体浓度以及受体与磷脂酶C的联系。除了这种促进收缩的直接作用外,雌激素还使β受体与腺苷酸环化酶解偶联。相反,孕激素通过使α2受体与对腺苷酸环化酶的抑制作用解偶联,从而通过β受体促进松弛。因此,性类固醇可以在受体水平及受体以外调节特定激动剂的反应。

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