The neuronal background K2P channels:: focus on TREK1

被引:374
作者
Honore, Eric [1 ]
机构
[1] Univ Nice Sophia Antipolis, CNRS, UMR 6097, Inst Pharmcol Mol & Cellulaire, F-06560 Valbonne, France
关键词
D O I
10.1038/nrn2117
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Two-pore-domain K+ (K-2P) channel subunits are made up of four transmembrane segments and two pore-forming domains that are arranged in tandem and function as either homo- or heterodimeric channels. This structural motif is associated with unusual gating properties, including background channel activity and sensitivity to membrane stretch. Moreover, K-2P channels are modulated by a variety of cellular lipids and pharmacological agents, including polyunsaturated fatty acids and volatile general anaesthetics. Recent in vivo studies have demonstrated that TREK1, the most thoroughly studied K-2P channel, has a key role in the cellular mechanisms of neuroprotection, anaesthesia, pain and depression.
引用
收藏
页码:251 / 261
页数:11
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