Coman Oana Andreia, Paunescu Horia, Coman Laurentiu, Badarau Anca, Fulga Ion
"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
J Med Life. 2008 Oct-Dec;1(4):365-75.
Natural cannabinoids have been used for centuries for their psychotropic properties, but their possible therapeutic implications in analgesia have been recently documented. The present review intended to make an analysis of the neuroanatomy and physiology of the cannabinoid system (receptors, functions, agents acting on these receptors) and of its implications in neuropathic pain. There were also described the complex phenomena implicated in the generation and maintenance of neuropathic pain, by high lightening the implications of endogenous cannabinoids in this complex of painful conditions. The pharmacological analgesia test proves of cannabinoid implication in neuropathic pain was sustained by many studies presented in this paper. Therapeutic approaches using natural and synthetic cannabinoid receptor agonists were reviewed. Therapeutic perspectives in neuropathic pain might involve the development of new agents that influence the cannabinoid system. Thus, peripheral acting cannabinoid 1 receptors agonists, selective cannabinoid 2 receptor agonists and also modulators of endocannabinoids metabolism might be a way to success in the treatment of this complex entity called neuropathic pain.
天然大麻素因其精神活性特性已被使用了几个世纪,但它们在镇痛方面可能的治疗意义最近已有文献记载。本综述旨在分析大麻素系统的神经解剖学和生理学(受体、功能、作用于这些受体的药物)及其在神经性疼痛中的意义。还描述了与神经性疼痛的产生和维持相关的复杂现象,强调了内源性大麻素在这种疼痛状况中的作用。本文中介绍的许多研究支持了大麻素与神经性疼痛相关的药理镇痛试验。综述了使用天然和合成大麻素受体激动剂的治疗方法。神经性疼痛的治疗前景可能涉及开发影响大麻素系统的新型药物。因此,外周作用的大麻素1受体激动剂、选择性大麻素2受体激动剂以及内源性大麻素代谢调节剂可能是成功治疗这种称为神经性疼痛的复杂病症的一种方法。