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大麻素CB2受体介导的急慢性疼痛模型中的抗伤害感受作用。

Cannabinoid CB2 receptor-mediated anti-nociception in models of acute and chronic pain.

作者信息

Jhaveri Maulik D, Sagar Devi R, Elmes Steven J R, Kendall David A, Chapman Victoria

机构信息

Institute of Neuroscience, School of Biomedical Sciences, University of Nottingham, Nottingham, UK.

出版信息

Mol Neurobiol. 2007 Aug;36(1):26-35. doi: 10.1007/s12035-007-8007-7. Epub 2007 Oct 2.

Abstract

The endocannabinoid system consists of cannabinoid CB(1) and CB(2) receptors, endogenous ligands and their synthesising/metabolising enzymes. Cannabinoid receptors are present at key sites involved in the relay and modulation of nociceptive information. The analgesic effects of cannabinoids have been well documented. The usefulness of nonselective cannabinoid agonists can, however, be limited by psychoactive side effects associated with activation of CB(1) receptors. Following the recent evidence for CB(2) receptors existing in the nervous system and reports of their up-regulation in chronic pain states and neurodegenerative diseases, much research is now aimed at shedding light on the role of the CB(2) receptor in human disease. Recent studies have demonstrated anti-nociceptive effects of selective CB(2) receptor agonists in animal models of pain in the absence of CNS side effects. This review focuses on the analgesic potential of CB(2) receptor agonists for inflammatory, post-operative and neuropathic pain states and discusses their possible sites and mechanisms of action.

摘要

内源性大麻素系统由大麻素CB(1)和CB(2)受体、内源性配体及其合成/代谢酶组成。大麻素受体存在于参与伤害性信息传递和调节的关键部位。大麻素的镇痛作用已有充分记录。然而,非选择性大麻素激动剂的效用可能会受到与CB(1)受体激活相关的精神活性副作用的限制。随着最近有证据表明CB(2)受体存在于神经系统中,以及有报道称它们在慢性疼痛状态和神经退行性疾病中上调,现在许多研究旨在阐明CB(2)受体在人类疾病中的作用。最近的研究表明,选择性CB(2)受体激动剂在动物疼痛模型中具有抗伤害感受作用,且无中枢神经系统副作用。本综述重点关注CB(2)受体激动剂对炎症性、术后和神经性疼痛状态的镇痛潜力,并讨论其可能的作用部位和作用机制。

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