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促性腺激素释放激素的作用机制。

Mechanism of action of gonadotropin releasing hormone.

作者信息

Conn P M, Staley D, Harris C, Andrews W V, Gorospe W C, McArdle C A, Huckle W R, Hansen J

出版信息

Annu Rev Physiol. 1986;48:495-513. doi: 10.1146/annurev.ph.48.030186.002431.

Abstract

GnRH interacts with a plasma membrane receptor to provoke gonadotropin release, as well as regulate numbers of its own receptor and target cell responsiveness. Receptor numbers are altered in different physiological states of the animal. Microaggregation of the GnRH receptor mimics all known actions of the releasing hormone, and therefore is viewed as an early step in the molecular mechanism of hormone action. Internalized hormone is neither necessary nor sufficient for stimulation of known releasing hormone actions. Evidence summarized in the present work suggests that Ca2+ serves a role as a second messenger for GnRH-stimulated gonadotropin release, and that it may be involved in receptor up-regulation in response to the releasing hormone. In the former role, diacylglycerols by their action on protein kinase C, in a fashion independent of the Ca2+ -calmodulin system, may act as a signal amplifier.

摘要

促性腺激素释放激素(GnRH)与质膜受体相互作用,引发促性腺激素释放,并调节其自身受体的数量以及靶细胞的反应性。在动物的不同生理状态下,受体数量会发生改变。GnRH受体的微聚集模拟了释放激素的所有已知作用,因此被视为激素作用分子机制的早期步骤。内化的激素对于刺激已知的释放激素作用既非必要条件也不充分。本研究总结的证据表明,Ca2+作为GnRH刺激促性腺激素释放的第二信使发挥作用,并且它可能参与了对释放激素的受体上调过程。在前一种作用中,二酰基甘油通过对蛋白激酶C的作用,以一种独立于Ca2+-钙调蛋白系统的方式,可能充当信号放大器。

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