Modulation of glutamate receptor functions by glutathione

被引:75
作者
Oja, SS
Janáky, R
Varga, V
Saransaari, P
机构
[1] Univ Tampere, Sch Med, Tampere Brain Res Ctr, FIN-33101 Tampere, Finland
[2] Tampere Univ Hosp, Dept Clin Physiol, Tampere, Finland
[3] Univ Debrecen, Dept Anim Physiol, Debrecen, Hungary
基金
芬兰科学院;
关键词
D O I
10.1016/S0197-0186(00)00031-0
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
In addition to its well-known antioxidant effects, glutathione apparently has an additional double role in the central nervous system as a neurotransmitter and neuromodulator. A number of recent neurochemical, neuropharmacological and electrophysiological studies have yielded evidence on both functions. As an excitatory neurotransmitter, glutathione depolarizes neurons by acting as ionotropic receptors of its own which are different from any other excitatory amino acid receptors. As a neuromodulator, it displaces ionotropic glutamate receptor ligands from their binding sites and regulates calcium influx through N-methyl-D-asyartate receptor-governed ionophores. In brain slices glutathione has been shown to regulate the release of other transmitters, e.g., gamma-aminobutyrate and dopamine, mediated by N-methyl-D-aspartate receptors. In the present article, we review recent findings on the neuromodulatory actions of glutathione and discuss possible physiological and pathophysiological consequences. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:299 / 306
页数:8
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