TRP channels as emerging targets for pain therapeutics

被引:32
|
作者
Broad, Lisa M. [1 ]
Mogg, Adrian J. [1 ]
Beattie, Ruth E. [1 ]
Ogden, Ann-Marie [2 ]
Blanco, Maria-Jesus [2 ]
Bleakman, David [2 ]
机构
[1] Eli Lilly & Co, Lilly Res Ctr, Windlesham GU20 6PH, Surrey, England
[2] Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
关键词
nociception; pain; pain therapeutics; thermo-TRP; TRP channels; VANILLOID RECEPTOR TRPV1; POTENTIAL CATION CHANNELS; DORSAL-ROOT GANGLION; MICE LACKING; CAPSAICIN-RECEPTOR; ION CHANNELS; MECHANICAL HYPERALGESIA; NOCICEPTIVE NEURONS; COLD HYPERALGESIA; BODY-TEMPERATURE;
D O I
10.1517/14728220802616620
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The transient receptor potential (TRP) superfamily of ion channels are a large and diverse group that have received increased attention in recent years. The sub-family of thermo-TRPs which are regulated by temperature, among other physical and chemical stimuli, are of particular interest for the development of potential pain therapeutics. Objective/methods: We review the advances in the field in recent years, focusing on a rationale for pain therapy and potential challenges associated with these targets. Results/conclusions: Vanilloid-type TRP 1 (TRPV1) is the most well studied and advanced member of the family, with selective agonists and antagonists already in clinical use or development, respectively. Among other thermo-TRPs (including TRPV2 - 4, Ankyrin type TRP 1 (TRPA1) and melastatin type TRP 8 (TRPM8)), TRPA1 and TRPM8 are emerging as promising novel pain targets.
引用
收藏
页码:69 / 81
页数:13
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