Endocannabinoids and pain: spinal and peripheral analgesia in inflammation and neuropathy

被引:145
作者
Rice, ASC [1 ]
Farquhar-Smith, WP [1 ]
Nagy, I [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Surg Anaesthet & Intens Care, Dept Anaesthet,Pain Res Grp, London SW10 9NH, England
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2002年 / 66卷 / 2-3期
基金
英国医学研究理事会;
关键词
D O I
10.1054/plef.2001.0362
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Analgesia is an important physiological function of the endocannabinoid system and one of significant clinical relevance. This review discusses the analgesic effects of endocannabinoids at spinal and peripheral levels, firstly by describing the physiological framework for analgesia and secondly by reviewing the evidence for analgesic effects of endocannabinoids obtained using animal models of clinical pain conditions. In the spinal cord, CB1 receptors have been demonstrated in laminae of the dorsal horn intimately concerned with the processing of nociceptive information and the modulation thereof. Similarly, CB1 receptors have been demonstrated on the cell bodies of primary afferent neurones; however, the exact phenotype of cells which express this receptor requires further elucidation. Local administration, peptide release and electrophysiological studies support the concept of spinally mediated endocannabinoid-induced analgesia. Whilst a proportion of the peripheral analgesic effect of endocannabinoids can be attributed to a neuronal mechanism acting through CB1 receptors expressed by primary afferent neurones, the antiinflammatory actions of endocannabinoids, mediated through CB2 receptors, also appears to contribute to local analgesic effects. Possible mechanisms of this CB2-mediated effect include the attenuation of NGF-induced mast cell degranulation and of neutrophil accumulation, both of which are processes known to contribute to the generation of inflammatory hyperalgesia. The analgesic effects of cannabinoids have been demonstrated in models of somatic and visceral inflammatory pain and of neuropathic pain, the latter being an important area of therapeutic need. Analgesia is one of the principal therapeutic targets of cannabinoids. This review will discuss the analgesic effects of endocannabinoids in relation to two areas of therapeutic need, persistent inflammation and neuropathic pain. The more general aspects of the role of cannabinoids, endogenous and exogenous, in analgesia have been recently reviewed elsewhere (Rice, Curr Opi Invest Drugs 2001; 2:399-414; Pertwee, Prog Neurobil 2001; 63:569-611; Rice, Mackie, In: Evers A. S, ed. Anesthetic Pharmacology: Physiologic Principles and Clinical Practice. St. Louis: Harcourt Health Sciences, 2002). Since a major goal in the development of cannabinoid-based analgesics is to divorce the antinociceptive effects from the psychotrophic effects, the discussion will focus on the antinociceptive effects produced at the spinal cord and/or peripheral level as these areas are the most attractive targets in this regard. A mechanistic discussion of the 'framework' for analgesia will be followed by a description of studies examining the role of endocannabinoids in relieving pain; since the elucidation of these effects was undertaken using synthetic cannabinoids, reference will also be made to such studies, in the context of endocannabinoids. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:243 / 256
页数:14
相关论文
共 145 条
[21]   Control of pain initiation by endogenous cannabinoids [J].
Calignano, A ;
La Rana, G ;
Giuffrida, A ;
Piomelli, D .
NATURE, 1998, 394 (6690) :277-281
[22]   The cannabinoid CB1 receptor antagonist, SR141716A, selectively facilitates nociceptive responses of dorsal horn neurones in the rat [J].
Chapman, V .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 127 (08) :1765-1767
[23]  
Chapman V, 1997, PHARM PAIN, P235
[24]   ROLE OF PERI-AXONAL INFLAMMATION IN THE DEVELOPMENT OF THERMAL HYPERALGESIA AND GUARDING BEHAVIOR IN A RAT MODEL OF NEUROPATHIC PAIN [J].
CLATWORTHY, AL ;
ILLICH, PA ;
CASTRO, GA ;
WALTERS, ET .
NEUROSCIENCE LETTERS, 1995, 184 (01) :5-8
[25]   Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase [J].
Cravatt, BF ;
Demarest, K ;
Patricelli, MP ;
Bracey, MH ;
Giang, DK ;
Martin, BR ;
Lichtman, AH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9371-9376
[26]   ANANDAMIDE, AN ENDOGENOUS LIGAND OF THE CANNABINOID RECEPTOR, INDUCES HYPOMOTILITY AND HYPOTHERMIA IN-VIVO IN RODENTS [J].
CRAWLEY, JN ;
CORWIN, RL ;
ROBINSON, JK ;
FELDER, CC ;
DEVANE, WA ;
AXELROD, J .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1993, 46 (04) :967-972
[27]   Possible role of inflammatory mediators in tactile hypersensitivity in rat models of mononeuropathy [J].
Cui, JG ;
Holmin, S ;
Mathiesen, T ;
Meyerson, BA ;
Linderoth, B .
PAIN, 2000, 88 (03) :239-248
[28]   Endocannabinoids and fatty acid amides in cancer, inflammation and related disorders [J].
De Petrocellis, L ;
Melck, D ;
Bisogno, T ;
Di Marzo, V .
CHEMISTRY AND PHYSICS OF LIPIDS, 2000, 108 (1-2) :191-209
[29]   ISOLATION AND STRUCTURE OF A BRAIN CONSTITUENT THAT BINDS TO THE CANNABINOID RECEPTOR [J].
DEVANE, WA ;
HANUS, L ;
BREUER, A ;
PERTWEE, RG ;
STEVENSON, LA ;
GRIFFIN, G ;
GIBSON, D ;
MANDELBAUM, A ;
ETINGER, A ;
MECHOULAM, R .
SCIENCE, 1992, 258 (5090) :1946-1949
[30]   Levels, metabolism, and pharmacological activity of anandamide in CB1 cannabinoid receptor knockout mice:: Evidence for non-CB1, non-CB2 receptor-mediated actions of anandamide in mouse brain [J].
Di Marzo, V ;
Breivogel, CS ;
Tao, Q ;
Bridgen, DT ;
Razdan, RK ;
Zimmer, AM ;
Zimmer, A ;
Martin, BR .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (06) :2434-2444