作者: Erik H.F. Wong , L.M. Fredrik Leeb-Lundberg , Vivian I. Teichberg , Richard W. Olsen
DOI: 10.1016/0006-8993(84)91213-7
关键词: Muscimol 、 Nipecotic acid 、 Barbiturate 、 Biochemistry 、 GABA receptor antagonist 、 Bicuculline 、 GABA receptor 、 Pharmacology 、 Hexobarbital 、 GABA Uptake Inhibitors 、 Chemistry 、 Developmental biology 、 General Neuroscience 、 Molecular biology 、 Clinical neurology
摘要: Abstract γ-Aminobutyric acid (GABA) increases the rate of36Cl- efflux from preloaded rat hippocampal slices in a dose-dependent manner (EC50: 400 μM). This action has pharmacological specificity expected of activation GABA receptor that it is mimicked by agonists muscimol and 3-aminopropanesulfonic acid, blocked antagonists bicuculline picrotoxinin. uptake inhibitors, nipecotic 2, 4-diaminobutyric fail to increase36Cl- flux. Pentobarbital produces (EC50 = 1.5mM) with maximal response greater than GABA. The effect pentobarbital can be 1, 3-dimethylbutylbarbiturate, secobarbital, (+)hexobarbital but not (−)hexobarbital, other active barbiturates also potentiate Phenobarbital does have any independently or combination It suggested increases36Cl- permeability postsynaptic which turn functionally copupled barbiturate receptor.