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培养的产后视交叉上核神经元中GABAA反应的药理学特性。

Pharmacological characteristics of GABAA responses in postnatal suprachiasmatic neurons in culture.

作者信息

Kawahara F, Saito H, Katsuki H

机构信息

Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Neurosci Lett. 1993 Sep 17;160(1):45-8. doi: 10.1016/0304-3940(93)90913-6.

DOI:10.1016/0304-3940(93)90913-6
PMID:8247331
Abstract

The suprachiasmatic nucleus (SCN) is considered to be an endogenous circadian pacemaker. Previous studies have suggested functional roles of gamma-aminobutyric acid (GABA) in the control of circadian rhythms. In this study, the responses to applied GABA in cultured SCN neurons dissociated from postnatal rat hypothalamus were investigated using whole-cell voltage-clamp techniques. GABA and muscimol induced a large current response (EC50 values 5.3 and 1.6 microM, respectively), which was blocked by the GABAA antagonist bicuculline. This current response was also blocked by Zn2+ (0.5-50 microM) in a concentration-dependent manner, but was not potentiated by diazepam (10 microM) or ethanol (21 mM). These characteristics seem to correspond to those of GABAA receptors that lack gamma-type subunits.

摘要

视交叉上核(SCN)被认为是内源性昼夜节律起搏器。先前的研究表明γ-氨基丁酸(GABA)在昼夜节律控制中具有功能作用。在本研究中,使用全细胞膜片钳技术研究了从新生大鼠下丘脑分离的培养SCN神经元对施加的GABA的反应。GABA和蝇蕈醇诱导了大的电流反应(EC50值分别为5.3和1.6 microM),该反应被GABAA拮抗剂荷包牡丹碱阻断。这种电流反应也被Zn2+(0.5 - 50 microM)以浓度依赖性方式阻断,但未被地西泮(10 microM)或乙醇(21 mM)增强。这些特征似乎与缺乏γ型亚基的GABAA受体的特征相符。

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