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kisspeptins与雄性和雌性啮齿动物促性腺激素分泌的调控

Kisspeptins and the control of gonadotropin secretion in male and female rodents.

作者信息

Roa J, Castellano J M, Navarro V M, Handelsman D J, Pinilla L, Tena-Sempere M

机构信息

Department of Cell Biology, Physiology and Immunology, University of Córdoba, 14004 Córdoba, Spain.

出版信息

Peptides. 2009 Jan;30(1):57-66. doi: 10.1016/j.peptides.2008.08.009. Epub 2008 Aug 22.

Abstract

Kisspeptins, the products of KiSS-1 gene acting via G protein-coupled receptor 54 (GPR54), have recently emerged as fundamental gatekeepers of gonadal function by virtue of their ability to stimulate gonadotropin secretion. Indeed, since the original disclosure of the reproductive facet of the KiSS-1/GPR54 system, an ever-growing number of studies have substantiated the extraordinary potency of kisspeptins to elicit gonadotropin secretion in different mammalian species, under different physiologic and experimental conditions, and through different routes of administration. In this context, studies conducted in laboratory rodents have been enormously instrumental to characterize: (i) the primary mechanisms of action of kisspeptins in the control of gonadotropin secretion; (ii) the pharmacological consequences of acute vs. continuous activation of GPR54; (iii) the roles of specific populations of kisspeptin-producing neurons at the hypothalamus in mediating the feedback effects of sex steroids; (v) the function of kisspeptins in the generation of the pre-ovulatory surge of gonadotropins; and (iv) the influence of sex steroids on GnRH/gonadotropin responsiveness to kisspeptins. While some of those aspects of kisspeptin function will be covered elsewhere in this Special Issue, we summarize herein the most salient data, obtained in laboratory rodents, that have helped to define the physiologic roles and putative pharmacological implications of kisspeptins in the control of male and female gonadotropic axis.

摘要

亲吻素是KiSS-1基因的产物,通过G蛋白偶联受体54(GPR54)发挥作用,最近因其刺激促性腺激素分泌的能力而成为性腺功能的基本调控因子。事实上,自从最初揭示KiSS-1/GPR54系统的生殖方面以来,越来越多的研究证实了亲吻素在不同哺乳动物物种中、在不同生理和实验条件下以及通过不同给药途径引发促性腺激素分泌的非凡效力。在此背景下,在实验室啮齿动物身上进行的研究对于以下方面具有极大的帮助:(i)亲吻素在控制促性腺激素分泌中的主要作用机制;(ii)GPR54急性激活与持续激活的药理学后果;(iii)下丘脑特定亲吻素产生神经元群体在介导性类固醇反馈作用中的作用;(v)亲吻素在促性腺激素排卵前激增产生中的功能;以及(iv)性类固醇对GnRH/促性腺激素对亲吻素反应性的影响。虽然亲吻素功能的某些方面将在本期特刊的其他地方进行阐述,但我们在此总结在实验室啮齿动物身上获得的最显著数据,这些数据有助于确定亲吻素在控制雄性和雌性促性腺轴中的生理作用和假定的药理学意义。

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