Khairatkar-Joshi Neelima, Szallasi Arpad
Biological Research, Glenmark Research Center, Navi Mumbai 400709, India.
Trends Mol Med. 2009 Jan;15(1):14-22. doi: 10.1016/j.molmed.2008.11.004. Epub 2008 Dec 25.
The capsaicin receptor TRPV1 (transient receptor potential cation channel, subfamily V, member 1) is a polymodal nociceptor whose expression is upregulated in several painful disorders. At present, potent small molecule TRPV1 antagonists are undergoing clinical trials in patients with chronic pain. Clinical development of TRPV1 antagonists is, however, facing new challenges. Many drug candidates evoke a febrile reaction that varies among patients. We speculate that TRPV1 gene polymorphism might be an underlying cause of the inter-subject variability in pain sensation and response to TRPV1 antagonists. This newly understood and yet to be fully validated aspect of pain suggests that pain management based on regulating the TRPV1 receptor might require a personalized approach for effective clinical outcome. Here, we provide our perspectives on current progress in targeting TRPV1.
辣椒素受体TRPV1(瞬时受体电位阳离子通道,V亚家族,成员1)是一种多模式伤害感受器,其表达在多种疼痛性疾病中上调。目前,强效小分子TRPV1拮抗剂正在慢性疼痛患者中进行临床试验。然而,TRPV1拮抗剂的临床开发正面临新的挑战。许多候选药物会引发发热反应,且在患者之间存在差异。我们推测TRPV1基因多态性可能是个体间疼痛感觉和对TRPV1拮抗剂反应差异的潜在原因。这种对疼痛新认识且尚未完全验证的方面表明,基于调节TRPV1受体的疼痛管理可能需要个性化方法以获得有效的临床结果。在此,我们对靶向TRPV1的当前进展发表我们的观点。