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

被引:79
作者
Jhaveri, Maulik D. [1 ]
Sagar, Devi R. [1 ]
Elmes, Steven J. R. [1 ]
Kendall, David A. [1 ]
Chapman, Victoria [1 ]
机构
[1] Univ Nottingham, Sch Biomed Sci, Inst Neurosci, Nottingham NG7 2RD, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
CB2; receptor; cannabinoid; nociception; neuropathic pain; inflammatory pain; postoperative pain; preclinical; electrophysiology; weight bearing;
D O I
10.1007/s12035-007-8007-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The endocannabinoid system consists of cannabinoid CB1 and CB2 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 CB1 receptors. Following the recent evidence for CB2 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 CB2 receptor in human disease. Recent studies have demonstrated anti-nociceptive effects of selective CB2 receptor agonists in animal models of pain in the absence of CNS side effects. This review focuses on the analgesic potential of CB2 receptor agonists for inflammatory, post-operative and neuropathic pain states and discusses their possible sites and mechanisms of action.
引用
收藏
页码:26 / 35
页数:10
相关论文
共 86 条
[1]   Expression of the cannabinoid CB2 receptor in the rat cerebellum: An immunohistochemical study [J].
Ashton, JC ;
Friberg, D ;
Darlington, CL ;
Smith, PF .
NEUROSCIENCE LETTERS, 2006, 396 (02) :113-116
[2]   CB2 receptor-mediated antihyperalgesia: possible direct involvement of neural mechanisms [J].
Beltramo, M ;
Bernardini, N ;
Bertorelli, R ;
Campanella, M ;
Nicolussi, E ;
Fredduzzi, S ;
Reggiani, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (06) :1530-1538
[3]  
Benito C, 2003, J NEUROSCI, V23, P11136
[4]   Characterization of a rat model of incisional pain [J].
Brennan, TJ ;
Vandermeulen, EP ;
Gebhart, GF .
PAIN, 1996, 64 (03) :493-501
[5]   Control of pain initiation by endogenous cannabinoids [J].
Calignano, A ;
La Rana, G ;
Giuffrida, A ;
Piomelli, D .
NATURE, 1998, 394 (6690) :277-281
[6]   Differential expression of the CB2 cannabinoid receptor by rodent macrophages and macrophage-like cells in relation to cell activation [J].
Carlisle, SJ ;
Marciano-Cabral, F ;
Staab, A ;
Ludwick, C ;
Cabral, GA .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2002, 2 (01) :69-82
[7]   Cultured rat microglial cells synthesize the endocannabinoid 2-arachidonylglycerol, which increases proliferation via a CB2 receptor-dependent mechanism [J].
Carrier, EJ ;
Kearn, CS ;
Barkmeier, AJ ;
Breese, NM ;
Yang, WQ ;
Nithipatikom, K ;
Pfister, SL ;
Campbell, WB ;
Hillard, CJ .
MOLECULAR PHARMACOLOGY, 2004, 65 (04) :999-1007
[8]   CLONING AND SEQUENCING OF A CDNA-ENCODING THE MOUSE BRAIN-TYPE CANNABINOID RECEPTOR PROTEIN [J].
CHAKRABARTI, A ;
ONAIVI, ES ;
CHAUDHURI, G .
DNA SEQUENCE, 1995, 5 (06) :385-388
[9]  
Chapman Victoria, 2003, Reviews in Analgesia, V7, P25, DOI 10.3727/000000003783992991
[10]   CB1 and CB2 cannabinoid receptors are implicated in inflammatory pain [J].
Clayton, N ;
Marshall, FH ;
Bountra, C ;
O'Shaughnessy, CT .
PAIN, 2002, 96 (03) :253-260