Modulation of the endocannabinoid system: Therapeutic potential against cocaine dependence

被引:16
作者
Tanda, Glanluigi [1 ]
机构
[1] Natl Inst Drug Abuse, Psychobiol Sect, Medicat Discovery Res Branch, Natl Inst Hlth,Dept Hlth & Human Serv, Baltimore, MD 21224 USA
关键词
cannabinoids; cocaine; addiction; behavior;
D O I
10.1016/j.phrs.2007.09.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dependence on cocaine is still a main unresolved medical and social concern, and in spite of research efforts, no pharmacological therapy against cocaine dependence is yet available. Recent studies have shown that the endocannabinoid system participates in specific stages and aspects of drug dependence in general, and some of this evidence suggests an involvement of the cannabinoid system in cocaine effects. For example, cocaine administration has been shown to alter brain endocannabinoid levels, and the endocannabinoid system has been involved in long-term modifications of brain processes that might play a role in neuro/behavioral effects of psychostimulant drugs like cocaine. Human studies show that marijuana dependence is frequently associated with cocaine dependence, and that the cannabinoid receptor CNR1 gene polymorphism might be related to cocaine addiction. This article will review the main papers in the field showing how a modulation of different components of the cannabinoid system might interact with some of the neurobiological/behavioral effects of cocaine related to its reinforcing effects, evaluated in preclinical models or in clinical settings. The goal of this review will be to provide insights into the complex picture of cocaine abuse and addiction, and to extrapolate from such endocannabinoid-cocaine interactions useful information to test the therapeutic potential of cannabinoid ligands and endocannabinoid-level enhancers against cocaine dependence for future preclinical/clinical trials. Published by Elsevier Ltd.
引用
收藏
页码:406 / 417
页数:12
相关论文
共 170 条
[1]   Cannabis and other illicit drugs: Comorbid use and abuse/dependence in males and females [J].
Agrawal, A ;
Neale, MC ;
Prescott, CA ;
Kendler, KS .
BEHAVIOR GENETICS, 2004, 34 (03) :217-228
[2]   Postdischarge cannabis use and its relationship to cocaine, alcohol, and heroin use: A prospective study [J].
Aharonovich, E ;
Liu, XH ;
Samet, S ;
Nunes, E ;
Waxman, R ;
Hasin, D .
AMERICAN JOURNAL OF PSYCHIATRY, 2005, 162 (08) :1507-1514
[3]   Effects of the cannabinoid receptor agonist CP 55,940 and the cannabinoid receptor antagonist SR 141716 on intracranial self-stimulation in Lewis rats [J].
Arnold, JC ;
Hunt, GE ;
McGregor, LS .
LIFE SCIENCES, 2001, 70 (01) :97-108
[4]   Effects of pre-exposure and co-administration of the cannabinoid receptor agonist CP 55,940 on behavioral sensitization to cocaine [J].
Arnold, JC ;
Topple, AN ;
Hunt, GE ;
McGregor, IS .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 354 (01) :9-16
[5]   A critique of fixed and progressive ratio schedules used to examine the neural substrates of drug reinforcement [J].
Arnold, JM ;
Roberts, DCS .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 57 (03) :441-447
[6]   (AAT)n repeat in the cannabinoid receptor gene (CNR1):: association with cocaine addiction in an African-Caribbean population [J].
Ballon, N ;
Leroy, S ;
Roy, C ;
Bourdel, MC ;
Charles-Nicolas, A ;
Krebs, MO ;
Poirier, MF .
PHARMACOGENOMICS JOURNAL, 2006, 6 (02) :126-130
[7]  
BANERJEE SP, 1975, J PHARMACOL EXP THER, V194, P74
[8]   Direct inhibition by cannabinoids of human 5-HT3A receptors:: probable involvement of an allosteric modulatory site [J].
Barann, M ;
Molderings, G ;
Brüss, M ;
Bönisch, H ;
Urban, BW ;
Göthert, M .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 137 (05) :589-596
[9]   Conditioned place preference: what does it add to our preclinical understanding of drug reward? [J].
Bardo, MT ;
Bevins, RA .
PSYCHOPHARMACOLOGY, 2000, 153 (01) :31-43
[10]   Evidence for novel cannabinoid receptors [J].
Begg, M ;
Pacher, P ;
Bátkai, S ;
Osei-Hyiaman, D ;
Offertáler, L ;
Mo, FM ;
Liu, H ;
Kunos, G .
PHARMACOLOGY & THERAPEUTICS, 2005, 106 (02) :133-145