Sites of positive allosteric modulation by neurosteroids on ionotropic y-aminobutyric acid receptor subunits

被引:29
作者
Ueno, S
Tsutsui, M
Toyohira, Y
Minami, K
Yanagihara, N
机构
[1] Univ Occupat & Environm Hlth, Sch Med, Dept Pharmacol, Fukuoka 8078555, Japan
[2] Univ Occupat & Environm Hlth, Sch Med, Dept Anesthesiol, Fukuoka 8078555, Japan
来源
FEBS LETTERS | 2004年 / 566卷 / 1-3期
基金
日本学术振兴会;
关键词
GABA(A) receptor; GABA(C) receptor; glycine receptor; neurosteroid; chimera; Xenopus oocyte;
D O I
10.1016/j.febslet.2004.04.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurosteroids are known as allosteric modulators of ionotropic gamma-aminobutyric acid (GABA) receptors. Here, we investigated sites of positive allosteric modulation by allotetrahydrodeoxycorticosterone (5alpha-THDOC) at GABA receptors using the technique of chimeragenesis and the Xenopus oocyte expression system. Our findings have demonstrated that the region from transmembrane segment (TM) 4 to the C-terminus of the GABA(A) receptor alpha1 subunit is crucial for the action of 50alpha-THDOC, but insufficient for the action of another neurosteroid allopregnanolone, suggesting that a specific region critical for neurosteroid action at GABA receptors exists in the domain between TM4 and the C-terminus of GABA receptor subunits. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:213 / 217
页数:5
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