Department of Pharmaceutical Engineering & Technology, Indian Institute of Technology (BHU) Varanasi, Varanasi, UP, India.
Curr Pharm Biotechnol. 2022;23(6):766-786. doi: 10.2174/1389201022666210719155931.
Natural products and leads inspired by them have acted as a probe for successful drug discovery for many decades. Pain is an obnoxious sensory and emotional experience associated with potential tissue damage. It affects the quality of life of patients to a greater extent. Despite the availability of several agents targeting TRP receptors, none of them can proficiently alleviate neuropathic pain. TRPV1 is a prospective target for treating neuropathic pain as it is recognized to modulate the pain circuitry at the periphery and the central level. In this review, we have discussed several natural molecules, such as Capsaicinoids, Capsinoids, Piperine, Eugenol, Scutigeral, Ginsenosides, Cinnamaldehyde, Camphor, Shogaol, Gingerols, Zingerone, Allicin, Evodiamine, Allylisothiocyanate, Cannabidiol, Ricinoleic acid, Isovelleral, Capsazepine, Thapsigargin, Pellitorine, Yohimbine, Curcumin and some semi-synthetic analogues that activate TRPV1 channels and consequently, can be further harnessed for the treatment of neuropathic pain.
天然产物及其衍生药物作为探针,在过去几十年中为药物研发的成功做出了重要贡献。疼痛是一种与潜在组织损伤相关的令人不快的感觉和情绪体验,它在更大程度上影响着患者的生活质量。尽管有几种针对 TRP 受体的药物,但没有一种能够有效地缓解神经性疼痛。TRPV1 是治疗神经性疼痛的一个有前途的靶点,因为它被认为可以调节外周和中枢水平的疼痛回路。在这篇综述中,我们讨论了几种天然分子,如辣椒素类、辣椒素类、胡椒碱、丁香酚、Scutigeral、人参皂苷、肉桂醛、樟脑、姜辣素、姜醇、香草醛、大蒜素、吴茱萸碱、异硫氰酸烯丙酯、大麻二酚、蓖麻油酸、异缬草酸、辣椒素、他普汀、白屈菜红碱、育亨宾、姜黄素和一些半合成类似物,它们可以激活 TRPV1 通道,因此可以进一步用于治疗神经性疼痛。