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γ-氨基丁酸A(GABA(A))受体上的神经甾体结合位点。

Neurosteroid binding sites on GABA(A) receptors.

作者信息

Hosie Alastair M, Wilkins Megan E, Smart Trevor G

机构信息

University College London, Department of Pharmacology, Gower Street, London, WC1E 6BT.

出版信息

Pharmacol Ther. 2007 Oct;116(1):7-19. doi: 10.1016/j.pharmthera.2007.03.011. Epub 2007 Apr 21.

DOI:10.1016/j.pharmthera.2007.03.011
PMID:17560657
Abstract

Controlling neuronal excitability is vitally important for maintaining a healthy central nervous system (CNS) and this relies on the activity of type A gamma-aminobutyric acid (GABA(A)) neurotransmitter receptors. Given this role, it is therefore important to understand how these receptors are regulated by endogenous modulators in the brain and determine where they bind to the receptor. One of the most potent groups of modulators is the neurosteroids which regulate the activity of synaptic and extrasynaptic GABA(A) receptors. This level of regulation is thought to be physiologically important and its dysfunction may be relevant to numerous neurological conditions. The aim of this review is to summarise those studies that over the last 20 years have focussed upon finding the binding sites for neurosteroids on GABA(A) receptors. We consider the nature of steroid binding sites in other proteins where this has been determined at atomic resolution and how their generic features were mapped onto GABA(A) receptors to help locate 2 putative steroid binding sites. Altogether, the findings strongly suggest that neurosteroids do bind to discrete sites on the GABA(A) receptor and that these are located within the transmembrane domains of alpha and beta receptor subunits. The implications for neurosteroid binding to other inhibitory receptors such as glycine and GABA(C) receptors are also considered. Identifying neurosteroid binding sites may enable the precise pathophysiological role(s) of neurosteroids in the CNS to be established for the first time, as well as providing opportunities for the design of novel drug entities.

摘要

控制神经元兴奋性对于维持健康的中枢神经系统(CNS)至关重要,而这依赖于A型γ-氨基丁酸(GABA(A))神经递质受体的活性。鉴于此作用,了解这些受体如何受到脑内内源性调节剂的调节并确定它们在受体上的结合位置就显得尤为重要。最有效的调节剂组之一是神经甾体,它调节突触和突触外GABA(A)受体的活性。这种调节水平被认为在生理上很重要,其功能障碍可能与多种神经系统疾病有关。本综述的目的是总结过去20年中那些专注于寻找神经甾体在GABA(A)受体上结合位点的研究。我们考虑了其他蛋白质中甾体结合位点的性质,这些性质已在原子分辨率下确定,以及它们的一般特征如何映射到GABA(A)受体上以帮助定位2个假定的甾体结合位点。总之,这些发现强烈表明神经甾体确实与GABA(A)受体上的离散位点结合,并且这些位点位于α和β受体亚基的跨膜结构域内。还考虑了神经甾体与其他抑制性受体如甘氨酸和GABA(C)受体结合的意义。确定神经甾体结合位点可能首次使神经甾体在中枢神经系统中的精确病理生理作用得以确立,同时也为新型药物实体的设计提供机会。

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