内源性大麻素与外周性疼痛

G. L. Rana, Roberta Maria Lobello, D. Piomelli, A. Calignano
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引用次数: 0

摘要

几个世纪以来,大麻一直被用于治疗疼痛,然而,临床研究并没有对大麻及其成分的镇痛效果产生统一的看法Δ9-tetrahydrocannabinol (Δ9-THC)。大麻素受体的两种内源性配体anandamide和2-花生四烯酰基甘油的发现引起了人们对这些分子在调节疼痛感知中的可能作用的兴趣。观察到的镇痛作用是通过定位于大脑的大麻素受体介导的,该受体与去甲肾上腺素能和κ-阿片系统相互作用;在脊髓中,调节伤害性知觉,在外周感觉神经元上调节传入刺激。阿南多巴胺是一种有效的抗痛觉药物,作用于中枢和外周神经元,调节疼痛感知和起始。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endocannabinoids and Peripheral Pain
For centuries cannabis has been used for the management of pain, however, clinical studies have not led to a uniform idea regarding the analgesic effectiveness of cannabis and its constituent Δ9-tetrahydrocannabinol (Δ9-THC). The discovery of anandamide and 2-arachidonylglycerol, two endogenous ligands for cannabinoid receptors, has aroused interest about the possible role for these molecules in modulation of pain perception. The analgesic effects observed are mediated through cannabinoid receptors, localized in the brain, that interact with the noradrenergic and κ-opioid system; in the spinal cord, modulating the nociceptive perception, and on peripheral sensory neurons regulating the afferent stimulations. Anandamide is an effective antinociceptive agent, acting centrally as well as on peripheral neurons, modulating pain perception and initiation.
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