Modulation of GABAA receptor activity by phosphorylation and receptor trafficking:: implications for the efficacy of synaptic inhibition

被引:223
作者
Kittler, JT
Moss, SJ
机构
[1] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[2] UCL, Dept Pharmacol, London WC1E 6BT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/S0959-4388(03)00064-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fast synaptic inhibition in the brain is largely mediated by GABA(A) receptors. These ligand-gated ion channels are crucial in the control of cell and network activity. Therefore, modulating their function or cell surface stability will have major consequences for neuronal excitation. It has become clear that the stability and activity of GABAA receptors at synapses can be dynamically modulated by receptor trafficking and phosphorylation. Here, we discuss these regulatory mechanisms, and their consequences for the efficacy of GABAA receptor mediated synaptic inhibition.
引用
收藏
页码:341 / 347
页数:7
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