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雌激素、 kisspeptin、GPR54与排卵前促黄体生成素激增

Oestrogen, kisspeptin, GPR54 and the pre-ovulatory luteinising hormone surge.

作者信息

Clarkson J, Herbison A E

机构信息

Department of Neurobiology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

出版信息

J Neuroendocrinol. 2009 Mar;21(4):305-11. doi: 10.1111/j.1365-2826.2009.01835.x.

DOI:10.1111/j.1365-2826.2009.01835.x
PMID:19207812
Abstract

Ovulation is central to mammalian fertility, yet the precise mechanism through which oestrogen triggers the gonadotrophin-releasing hormone (GnRH) surge that generates the pre-ovulatory luteinising hormone (LH) surge has remained elusive. The recent discovery that kisspeptin-GPR54 signalling is an essential regulator of the neuroendocrine axis at puberty has led investigators to evaluate the role of kisspeptin in the pre-ovulatory GnRH surge mechanism. Kisspeptin neurones are known to express oestrogen and progesterone receptors and have their cell bodies located in brain regions implicated in the positive-feedback mechanism in several mammalian species. In rodents, kisspeptin neurones located in the rostral periventricular area of the third ventricle (RP3V) are positively regulated by oestrogen and most likely are activated by oestrogen at the time of positive feedback. A similar scenario appears to exist for a sub-population of kisspeptin neurones located in the mediobasal hypothalamus of sheep and primates. The majority of GnRH neurones express GPR54, and kisspeptin causes an intense electrical activation of these cells. In concordance with this, kisspeptin administration in vivo results in an abrupt and prolonged release of LH in all mammalian species examined to date. Functional evidence from immunoneutralisation and knockout studies suggests that RP3V kisspeptin neurones projecting to GnRH neurones are an essential component of the surge mechanism in rodents. Taken together, the studies undertaken to date provide substantial evidence in support of a key role of kisspeptin-GPR54 signalling in the generation of the oestrogen-induced pre-ovulatory surge mechanism in mammals.

摘要

排卵是哺乳动物生育能力的核心,但雌激素触发促性腺激素释放激素(GnRH)激增从而引发排卵前促黄体生成素(LH)激增的确切机制仍不清楚。最近发现, kisspeptin-GPR54信号传导是青春期神经内分泌轴的重要调节因子,这促使研究人员评估kisspeptin在排卵前GnRH激增机制中的作用。已知kisspeptin神经元表达雌激素和孕激素受体,其细胞体位于几个哺乳动物物种中与正反馈机制相关的脑区。在啮齿动物中,位于第三脑室室周吻侧区(RP3V)的kisspeptin神经元受雌激素正向调节,很可能在正反馈时被雌激素激活。在绵羊和灵长类动物的中基底下丘脑的一部分kisspeptin神经元中似乎也存在类似情况。大多数GnRH神经元表达GPR54,kisspeptin可引起这些细胞强烈的电激活。与此一致的是,迄今为止,在所有接受检测的哺乳动物物种中,体内注射kisspeptin都会导致LH突然且持续释放。免疫中和及基因敲除研究的功能证据表明,投射到GnRH神经元的RP3V kisspeptin神经元是啮齿动物激增机制的重要组成部分。综上所述,迄今为止进行的研究提供了大量证据,支持kisspeptin-GPR54信号传导在哺乳动物雌激素诱导的排卵前激增机制的产生中起关键作用。

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