The cloned capsaicin receptor integrates multiple pain-producing stimuli

被引:2567
作者
Tominaga, M
Caterina, MJ
Malmberg, AB
Rosen, TA
Gilbert, H
Skinner, K
Raumann, BE
Basbaum, AI
Julius, D [1 ]
机构
[1] Univ Calif San Francisco, Dept Mol & Cellular Pharmacol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, W M Keck Fdn Ctr Integrat Neurosci, San Francisco, CA 94143 USA
关键词
D O I
10.1016/S0896-6273(00)80564-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Capsaicin, the main pungent ingredient in "hot" chili peppers, elicits burning pain by activating specific (vanilloid) receptors on sensory nerve endings. The cloned vanilloid receptor (VR1) is a cation channel that is also activated by noxious heat. Here, analysis of heat-evoked single channel currents in excised membrane patches suggests that heat gates VR1 directly. We also show that protons decrease the temperature threshold for VR1 activation such that even moderately acidic conditions (pH less than or equal to 5.9) activate VR1 at room temperature. VR1 can therefore be viewed as a molecular integrator of chemical and physical stimuli that elicit pain. Immunocytochemical analysis indicates that the receptor is located in a neurochemically heterogeneous population of small diameter primary afferent fibers. A role for VR1 in injury-induced hypersensitivity at the level of the sensory neuron is presented.
引用
收藏
页码:531 / 543
页数:13
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