The role and mechanism of action of menthol in topical analgesic products

薄荷醇 止痛药 TRPM8型 瞬时受体电位通道 药理学 医学 作用机理 伤害感受器 类阿片 麻醉 化学 伤害 受体 内科学 TRPV1型 有机化学 体外 生物化学
作者
Joseph V. Pergolizzi,Robert Taylor,Jo Ann LeQuang,Robert B. Raffa
出处
期刊:Journal of Clinical Pharmacy and Therapeutics [Wiley]
卷期号:43 (3): 313-319 被引量:57
标识
DOI:10.1111/jcpt.12679
摘要

Menthol has been used as a non-opioid pain reliever since ancient times. A modern understanding of its molecular mechanism of action could form the basis for generating targets for discovery of novel non-opioid analgesic drugs.The PubMed database was queried using search words related to menthol, pain and analgesia. The results were limited to relevant preclinical studies and clinical trials and reviews published in English during the past 5 years, which yielded 31 reports. The bibliographies of these articles were sources of additional supporting articles.Menthol is a selective activator of transient receptor potential melastatin-8 (TRPM8) channels and is also a vasoactive compound. As a topical agent, it acts as a counter-irritant by imparting a cooling effect and by initially stimulating nociceptors and then desensitizing them. Topically applied menthol may also activate central analgesic pathways. At high concentrations, menthol may generate cold allodynia.Recent elucidation of TRPM8 channels has provided a molecular basis for understanding the molecular action of menthol and its ability to produce both a cooling sensation and reduction in pain associated with a wide variety of pain(ful) conditions. The more modern mechanistic understanding of menthol and its pharmacologic mechanism of action may lead to an expanded role for this substance in the search for replacements for opioid analgesics, particularly those that can be applied topically.
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