Department of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Pharmaceuticals (Basel). 2012 Feb 2;5(2):114-32. doi: 10.3390/ph5020114.
In the last decade, considerable evidence as accumulated to support the development of Transient Receptor Potential Vanilloid 1 (TRPV1) antagonists for the treatment of various chronic pain conditions. Whereas there is a widely accepted rationale for the development of TRPV1 antagonists for the treatment of various inflammatory pain conditions, their development for indications of chronic pain, where conditions of tactical, mechanical and spontaneous pain predominate, is less clear. Preclinical localization and expression studies provide a firm foundation for the use of molecules targeting TRPV1 for conditions of bone pain, osteoarthritis and neuropathic pain. Selective TRPV1 antagonists weakly attenuate tactile and mechanical hypersensivity and are partially effective for behavioral and electrophysiological endpoints that incorporate aspects of spontaneous pain. While initial studies with TRPV1 antagonist in normal human subjects indicate a loss of warm thermal perception, clinical studies assessing allelic variants suggests that TRPV1 may mediate other sensory modalities under certain conditions. The focus of this review is to summarize the current perspectives of TRPV1 for the treatment of conditions beyond those with a primary thermal sensitivity.
在过去的十年中,积累了相当多的证据支持开发瞬时受体电位香草素 1(TRPV1)拮抗剂来治疗各种慢性疼痛病症。尽管开发 TRPV1 拮抗剂治疗各种炎症性疼痛病症有广泛接受的理论基础,但它们在以慢性疼痛为指征的情况下的开发,其中战术性、机械性和自发性疼痛占主导地位,就不那么清楚了。临床前定位和表达研究为靶向 TRPV1 治疗骨痛、骨关节炎和神经病理性疼痛的分子提供了坚实的基础。选择性 TRPV1 拮抗剂可减弱触觉和机械性超敏反应,对包含自发性疼痛方面的行为和电生理终点的部分有效。虽然在正常人类受试者中进行的 TRPV1 拮抗剂的初步研究表明,温热感觉丧失,但评估等位基因变异的临床研究表明,在某些情况下,TRPV1 可能介导其他感觉模式。本综述的重点是总结 TRPV1 在治疗原发性热敏感性以外的病症的最新观点。