TRPs and pain

被引:120
作者
Dai, Yi [1 ,2 ,3 ]
机构
[1] Hyogo Univ Hlth Sci, Sch Pharm, Dept Pharmacotherapy & Oriental Med, Chuo Ku, 1-3-6 Minatojima, Kobe, Hyogo 6508530, Japan
[2] Hyogo Coll Med, Dept Anat & Neurosci, Nishinomiya, Hyogo 6638501, Japan
[3] Hyogo Coll Med, Chinese Med Confucius Inst, Tradit Med Res Ctr, Kobe, Hyogo 6508530, Japan
关键词
Pain; Nociception; TRP channel; Neuropathy; Peripheral inflammation; RECEPTOR POTENTIAL A1; ROOT GANGLION NEURONS; PRIMARY AFFERENT NEURONS; RAT GENICULATE GANGLION; PRIMARY SENSORY NEURONS; HEAT-EVOKED ACTIVATION; SPINAL NERVE LIGATION; DORSAL-HORN NEURONS; ION-CHANNEL TRPA1; CAPSAICIN-RECEPTOR;
D O I
10.1007/s00281-015-0526-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nociception is the process of transmission of painful signals by nociceptors in the primary afferent nerve fibers, which specifically respond to noxious stimuli. These noxious stimuli are detected by nociceptors and converted into electrical signals, which are then transmitted to the spinal cord, thalamus, and the cerebral cortex, where pain is finally sensed. Transient receptor potential (TRP) ion channels have emerged as a family of evolutionarily conserved ligand-gated ion channels that function as molecular detectors of physical stimuli. Several member of this family, at least six channels from three TRP family subtypes (TRPV1-4, TRPM8, and TRPA1), are expressed in nociceptors, where they act as transducers for signals from thermal, chemical, and mechanical stimuli and play crucial roles in the generation and development of pathological pain perception. This review focuses on the increasing evidence of TRP channel involvement and contribution in nociceptive pain and the pain hypersensitivity associated with peripheral inflammation or neuropathy, and on the renewed interest in targeting TRP channels for pain relief.
引用
收藏
页码:277 / 291
页数:15
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