TRPV1 in neuropathic pain: from animal models to therapeutical prospects

被引:7
|
作者
Danigo, Aurore [1 ,2 ]
Magy, Laurent [1 ]
Demiot, Claire [1 ]
机构
[1] Fac Med & Pharm, EA 6309, F-87025 Limoges, France
[2] Ctr Reference Neuropathies Peripher Rares, Serv Neurol, F-87042 Limoges, France
来源
M S-MEDECINE SCIENCES | 2013年 / 29卷 / 6-7期
关键词
CAPSAICIN RECEPTOR TRPV1; PERIPHERAL-NERVE; SENSORY NEURONS; RESINIFERATOXIN; ACTIVATION; ANALOG; INFLAMMATION; EXPRESSION; CONDUCTION; CHANNELS;
D O I
10.1051/medsci/2013296012
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Since its cloning in 1997, functional and structural studies of TRPV1 have led to an improvement in our understanding of the mechanisms that underlie the transduction of noxious thermal and mechanical stimuli by sensory neurons. Because of its role in inflammatory processes and nociceptive pathways, TRPV1 has become an important target for neuropathic pain relief. Models of painful small-fiber sensory neuropathy were developed and several laboratories have progressed in the conception of TRPV1 agonists and antagonists. Patch and cream containing capsaicin, the most famous TRPV1 agonist, are commercialized to relieve neuropathic pain. Others agonists and TRPV1 antagonists are tested in clinical trials and new agents, "TRPV1 modulators", with fewer side effects are currently developed in experimental studies. lozenge
引用
收藏
页码:597 / 606
页数:10
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