Preti Delia, Saponaro Giulia, Szallasi Arpad
Department of Chemical & Pharmaceutical Sciences, University of Ferrara, Italy.
Pharm Pat Anal. 2015;4(2):75-94. doi: 10.4155/ppa.14.60.
The transient receptor potential ankyrin 1 (TRPA1) channel is an irritant sensor highly expressed on nociceptive neurons. The clinical use of TRPA1 antagonists is based on the concept that TRPA1 is active during disease states like neuropathic pain. Indeed, in Phase 2a proof-of-concept studies the TRPA1 antagonist GRC17536 has shown efficacy in patients with painful diabetic neuropathy. Moreover, animal studies suggest that the therapeutic value of TRPA1 antagonists extends beyond pain to pruritus, asthma and cough with limited safety concerns. This review provides a comprehensive overview of the patent literature (since 2007) on small-molecule inhibitors of the TRPA1 channel. Despite the clear progress, many unanswered questions remain. Future advancement to Phase 3 studies will assess the real translational potential of this research field.
瞬时受体电位锚蛋白1(TRPA1)通道是一种在伤害性神经元上高度表达的刺激传感器。TRPA1拮抗剂的临床应用基于这样一种概念,即TRPA1在诸如神经性疼痛等疾病状态下处于激活状态。事实上,在2a期概念验证研究中,TRPA1拮抗剂GRC17536已在疼痛性糖尿病神经病变患者中显示出疗效。此外,动物研究表明,TRPA1拮抗剂的治疗价值不仅限于疼痛,还扩展到瘙痒、哮喘和咳嗽,且安全性问题有限。本综述全面概述了(自2007年以来)关于TRPA1通道小分子抑制剂的专利文献。尽管取得了明显进展,但仍有许多问题未得到解答。未来进入3期研究将评估该研究领域的实际转化潜力。