TRP Channels as Drug Targets to Relieve Itch

被引:60
|
作者
Xie, Zili [1 ]
Hu, Hongzhen [1 ]
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol, Ctr Study Itch, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
TRP channels; itch; pain; TRPA1; TRPV1; TRPV3; TRPV4; TRPM8; TRPC4; agonists; antagonists; RECEPTOR POTENTIAL CHANNELS; ATOPIC-DERMATITIS; LYSOPHOSPHATIDIC ACID; SKIN BARRIER; SPHINGOSINE; 1-PHOSPHATE; NEUROGENIC INFLAMMATION; CELLULAR MECHANISMS; INTERNATIONAL-UNION; SCRATCHING BEHAVIOR; PRURITUS RESEARCH;
D O I
10.3390/ph11040100
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Although acute itch has a protective role by removing irritants to avoid further damage, chronic itch is debilitating, significantly impacting quality of life. Over the past two decades, a considerable amount of stimulating research has been carried out to delineate mechanisms of itch at the molecular, cellular, and circuit levels. There is growing evidence that transient receptor potential (TRP) channels play important roles in itch signaling. The purpose of this review is to summarize our current knowledge about the role of TRP channels in the generation of itch under both physiological and pathological conditions, thereby identifying them as potential drug targets for effective anti-itch therapies.
引用
收藏
页数:20
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