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Current Pharmaceutical Biotechnology

Author(s): Gaurav Gopal Naik, Ankit Uniyal, Deepak Chouhan, Vinod Tiwari and Alakh N. Sahu*

DOI: 10.2174/1389201022666210719155931

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Natural Products and some Semi-synthetic Analogues as Potential TRPV1 Ligands for Attenuating Neuropathic Pain

Page: [766 - 786] Pages: 21

  • * (Excluding Mailing and Handling)

Abstract

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.

Keywords: TRPV1 channels, neuropathic pain, natural products, semi-synthetic analogues, agonists, antagonists.

Graphical Abstract

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