TREK-1, a K+ channel involved in polymodal pain perception

被引:313
作者
Alloui, Abdelkrim
Zimmermann, Katharina
Mamet, Julien
Duprat, Fabrice
Noel, Jacques
Chemin, Jean
Guy, Nicolas
Blondeau, Nicolas
Voilley, Nicolas
Rubat-Coudert, Catherine
Borsotto, Marc
Romey, Georges
Heurteaux, Catherine
Reeh, Peter
Eschalier, Alain
Lazdunski, Michel
机构
[1] Univ Nice, CNRS, Inst Pharmacol Mol & Cellulaire, Inst Paul Hamel, F-06560 Valbonne, France
[2] CHU, Fac Med, INSERM, Lab Pharmacol Med EA 3848, Clermont Ferrand, France
[3] Univ Erlangen Nurnberg, Dept Physiol & Pathophysiol, Erlangen, Germany
关键词
pain; potassium channel; TREK-1;
D O I
10.1038/sj.emboj.7601116
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
The TREK-1 channel is a temperature-sensitive, osmosensitive and mechano-gated K+ channel with a regulation by Gs and Gq coupled receptors. This paper demonstrates that TREK-1 qualifies as one of the molecular sensors involved in pain perception. TREK-1 is highly expressed in small sensory neurons, is present in both peptidergic and non-peptidergic neurons and is extensively colocalized with TRPV1, the capsaicin-activated nonselective ion channel. Mice with a disrupted TREK-1 gene are more sensitive to painful heat sensations near the threshold between anoxious warmth and painful heat. This phenotype is associated with the primary sensory neuron, as polymodal C-fibers were found to be more sensitive to heat in single fiber experiments. Knockout animals are more sensitive to low threshold mechanical stimuli and display an increased thermal and mechanical hyperalgesia in conditions of inflammation. They display a largely decreased pain response induced by osmotic changes particularly in prostaglandin E2-sensitized animals. TREK-1 appears as an important ion channel for polymodal pain perception and as an attractive target for the development of new analgesics.
引用
收藏
页码:2368 / 2376
页数:9
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