Center for Clinical Pharmacology, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000 Leuven, Belgium.
Laboratory of Endometrium, Endometriosis and Reproductive Medicine, Department of Development and Regeneration, KU Leuven, 3000 Leuven, Belgium.
Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:655-677. doi: 10.1146/annurev-pharmtox-010919-023238. Epub 2020 Sep 25.
Chronic pain treatment remains a sore challenge, and in our aging society, the number of patients reporting inadequate pain relief continues to grow. Current treatment options all have their drawbacks, including limited efficacy and the propensity of abuse and addiction; the latter is exemplified by the ongoing opioid crisis. Extensive research in the last few decades has focused on mechanisms underlying chronic pain states, thereby producing attractive opportunities for novel, effective and safe pharmaceutical interventions. Members of the transient receptor potential (TRP) ion channel family represent innovative targets to tackle pain sensation at the root. Three TRP channels, TRPV1, TRPM3, and TRPA1, are of particular interest, as they were identified as sensors of chemical- and heat-induced pain in nociceptor neurons. This review summarizes the knowledge regarding TRP channel-based pain therapies, including the bumpy road of the clinical development of TRPV1 antagonists, the current status of TRPA1 antagonists, and the future potential of targeting TRPM3.
慢性疼痛治疗仍然是一个棘手的挑战,在我们这个老龄化的社会中,报告疼痛缓解不足的患者人数持续增加。目前的治疗选择都有其缺点,包括疗效有限以及滥用和成瘾的倾向;后者的例子就是持续的阿片类药物危机。在过去几十年中,大量研究集中在慢性疼痛状态的机制上,从而为新型、有效和安全的药物干预提供了有吸引力的机会。瞬时受体电位 (TRP) 离子通道家族的成员代表了从根本上解决疼痛感觉的创新靶点。TRPV1、TRPM3 和 TRPA1 这三种 TRP 通道特别引人关注,因为它们被确定为伤害感受器神经元中化学和热诱导疼痛的传感器。这篇综述总结了基于 TRP 通道的疼痛治疗的知识,包括 TRPV1 拮抗剂临床开发的坎坷道路、TRPA1 拮抗剂的现状以及靶向 TRPM3 的未来潜力。
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