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大脑γ-氨基丁酸受体

Cerebral GABA receptors.

作者信息

Kuriyama K

机构信息

Department of Pharmacology, Kyoto Prefectural University of Medicine, Japan.

出版信息

Alcohol Alcohol Suppl. 1994;2:181-6.

PMID:8974333
Abstract

GABA (gamma-aminobutyric acid) receptors in the brain have been classified into GABAA and GABAB types. The GABAA receptor is an ionotropic type that forms the GABA-gated Cl- channel. The structure of GABAA receptor has been intensively analyzed and found to consist of several subunits and the combination of these subunits is heterogeneous. Therefore, it is likely that multiple GABAA receptors are present and exert various inhibitory actions in the brain. On the other hand, the GABAB receptor, a metabotropic type, inhibits cAMP formation as well as inositol phosphates turnover. The inhibition of adenylyl cyclase activity is mediated by GTP-binding protein such as Gi and/or Go which is coupled with GABAB receptor. Studies of the purified GABAB receptor obtained by baclofen-affinity and immunoaffinity column chromatographic procedures have indicated that this receptor protein is approximately 80 kDa in molecular weight and heterogeneous as determined by SDS-polyacrylamide gel electrophoresis. Alcohol induces the activation of GABA-gated Cl- channel but this activation is found to be diminished following the establishment of alcohol dependence. Furthermore, alcohol dependence induces the increase of GABAB receptor binding, while suppressing the functional coupling between GABAB receptor and adenylyl cyclase, possibly altering the function of Gi/Go type of GTP-binding protein which is coupled to GABAB receptor in the brain. The pathophysiological significance of these changes in the establishment of alcohol dependence and/or alcohol withdrawal syndrome is also briefly discussed.

摘要

大脑中的γ-氨基丁酸(GABA)受体已被分为GABAA和GABAB两种类型。GABAA受体是一种离子型受体,可形成GABA门控氯离子通道。对GABAA受体的结构进行了深入分析,发现它由几个亚基组成,且这些亚基的组合具有异质性。因此,大脑中可能存在多种GABAA受体并发挥各种抑制作用。另一方面,代谢型的GABAB受体可抑制环磷酸腺苷(cAMP)的形成以及肌醇磷酸的周转。腺苷酸环化酶活性的抑制是由与GABAB受体偶联的诸如Gi和/或Go等GTP结合蛋白介导的。通过巴氯芬亲和柱色谱和免疫亲和柱色谱法获得的纯化GABAB受体的研究表明,该受体蛋白的分子量约为80 kDa,经十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定具有异质性。酒精可诱导GABA门控氯离子通道的激活,但在酒精依赖形成后,这种激活作用会减弱。此外,酒精依赖会导致GABAB受体结合增加,同时抑制GABAB受体与腺苷酸环化酶之间的功能偶联,这可能会改变大脑中与GABAB受体偶联的Gi/Go型GTP结合蛋白的功能。本文还简要讨论了这些变化在酒精依赖和/或酒精戒断综合征形成中的病理生理学意义。

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