TRPV1 and TRPA1 channels in inflammatory pain: elucidating mechanisms

被引：13

作者：

Brain, Susan D. ^{[1
,2
]}

机构：

[1] Kings Coll London, Div Cardiovasc, BHF Ctr Cardiovasc Excellence, London SE1 9NH, England

[2] Kings Coll London, Sect Integrat Biomed, London SE1 9NH, England

来源：

ANIMAL MODELS: THEIR VALUE IN PREDICTING DRUG EFFICACY AND TOXICITY | 2011年 / 1245卷

基金：

英国生物技术与生命科学研究理事会;

关键词：

hyperalgesia; pain; TRP channels; mice; INVOLVEMENT; NEURONS;

D O I：

10.1111/j.1749-6632.2011.06326.x

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];

摘要：

Transient receptor potential (TRP) receptors are ion channels that mediate pain and inflammation. We provide evidence for the distinct roles of TRPV1 and TRPA1 in arthritis.

引用

页码：36 / 37

页数：2

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