TRPA1 mediates the inflammatory actions of environmental irritants and proalgesic agents

被引:1477
作者
Bautista, DM
Jordt, SE
Nikai, T
Tsuruda, PR
Read, AJ
Poblete, J
Yamoah, EN
Basbaum, AI
Julius, D [1 ]
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[2] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06520 USA
[3] Univ Calif San Francisco, Dept Anat & Physiol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, WM Keck Ctr Integrat Neurosci, San Francisco, CA 94143 USA
[5] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[6] Univ Calif Davis, Dept Otolaryngol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.cell.2006.02.023
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
TRPA1 is an excitatory ion channel targeted by pungent irritants from mustard and garlic. TRPA1 has been proposed to function in diverse sensory processes, including thermal (cold) nociception, hearing, and inflammatory pain. Using TRPA1-deficient mice, we now show that this channel is the sole target through which mustard oil and garlic activate primary afferent nociceptors to produce inflammatory pain. TRPA1 is also targeted by environmental irritants, such as acrolein, that account for toxic and inflammatory actions of tear gas, vehicle exhaust, and metabolic byproducts of chemotherapeutic agents. TRPA1-deficient mice display normal cold sensitivity and unimpaired auditory function, suggesting that this channel is not required for the initial detection of noxious cold or sound. However, TRPA1-deficient mice exhibit pronounced deficits in bradykinin-evoked nociceptor excitation and pain hypersensitivity. Thus, TRPA1 is an important component of the transduction machinery through which environmental irritants and endogenous proalgesic agents depolarize nociceptors, to elicit inflammatory pain.
引用
收藏
页码:1269 / 1282
页数:14
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