Lack of CB1 cannabinoid receptor impairs cocaine self-administration

被引:180
作者
Soria, G
Mendizábal, V
Touriño, C
Ledent, C
Parmentier, M
Maldonado, R
Valverde, O
机构
[1] Univ Pompeu Fabra, Lab Neurofarmacol, Dept Ciencies Expt & Salut, Barcelona 08003, Spain
[2] Inst Municipal Invest Med, E-08003 Barcelona, Spain
[3] Univ Libre Bruxelles, IRIBHM, Brussels, Belgium
关键词
CB1 cannabinoid receptor; self-administration; cocaine; knockout; in vivo microdialysis; dopamine;
D O I
10.1038/sj.npp.1300707
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acute rewarding properties are essential for the establishment of cocaine addiction, and multiple neurochemical processes participate in this complex behavior. In the present study, we used the self-administration paradigm to evaluate the role of CB1 cannabinoid receptors in several aspects of cocaine reward, including acquisition, maintenance, and motivation to seek the drug. For this purpose, both CB1 receptor knockout mice and wild-type littermates were trained to intravenously self-administer cocaine under different schedules. Several cocaine training doses (0.32, 1, and 3.2 mg/kg/infusion) were used in the acquisition studies. Only 25% of CB1 knockout mice vs 75% of their wild-type littermates acquired a reliable operant responding to self-administer the most effective dose of cocaine (1 mg/kg/ infusion), and the number of sessions required to attain this behavior was increased in knockout mice. Animals reaching the acquisition criteria were evaluated for the motivational strength of cocaine as a reinforcer under a progressive ratio schedule. The maximal effort to obtain a cocaine infusion was significantly reduced after the genetic ablation of CB1 receptors. A similar result was obtained after the pharmacological blockade of CB1 receptors with SR141716A in wild-type mice. Moreover, the cocaine dose-response curve was flattened in the knockout group, suggesting that the differences observed between genotypes were related to changes in the reinforcing efficacy of the training dose of cocaine. Self-administration for water and food was not altered in CB1 knockout mice in any of the reinforcement schedules used, which emphasizes the selective impairment of drug reinforcement in these knockout mice. Finally, cocaine effects on mesolimbic dopaminergic transmission were evaluated by in vivo microdialysis in these mice. Acute cocaine administration induced a similar enhancement in the extracellular levels of dopamine in the nucleus accumbens of both CB1 knockout and wild-type mice. This work clearly demonstrates that CB1 receptors play an important role in the consolidation of cocaine reinforcement, although are not required for its acute effects on mesolimbic dopaminergic transmission.
引用
收藏
页码:1670 / 1680
页数:11
相关论文
共 38 条
[1]   Selective inhibition of sucrose and ethanol intake by SR 141716, an antagonist of central cannabinoid (CB1) receptors [J].
Arnone, M ;
Maruani, J ;
Chaperon, F ;
Thiebot, MH ;
Poncelet, M ;
Soubrie, P ;
LeFur, G .
PSYCHOPHARMACOLOGY, 1997, 132 (01) :104-106
[2]   SR141716A reduces the reinforcing properties of heroin but not heroin-induced increases in nucleus accumbens dopamine in rats [J].
Caillé, S ;
Parsons, LH .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 18 (11) :3145-3149
[3]   Method for training operant responding and evaluating cocaine self-administration behavior in mutant mice [J].
Caine, SB ;
Negus, SS ;
Mello, NK .
PSYCHOPHARMACOLOGY, 1999, 147 (01) :22-24
[4]  
Carelli RM, 2000, J NEUROSCI, V20, P4255
[5]   Lack of CB1 cannabinoid receptors modifies nicotine behavioural responses, but not nicotine abstinence [J].
Castañé, A ;
Valjent, E ;
Ledent, C ;
Parmentier, M ;
Maldonado, R ;
Valverde, O .
NEUROPHARMACOLOGY, 2002, 43 (05) :857-867
[6]   A critical interaction between dopamine D2 receptors and endocannabinoids mediates the effects of cocaine on striatal GABAergic transmission [J].
Centonze, D ;
Battista, N ;
Rossi, S ;
Mercuri, NB ;
Finazzi-Agrò, A ;
Bernardi, G ;
Calabresi, P ;
Maccarrone, M .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (08) :1488-1497
[7]   Motivational responses to natural and drug rewards in rats with neonatal ventral hippocampal lesions: An animal model of dual diagnosis schizophrenia [J].
Chambers, RA ;
Self, DW .
NEUROPSYCHOPHARMACOLOGY, 2002, 27 (06) :889-905
[8]   Reinforcing and locomotor stimulant effects of cocaine are absent in mGluR5 null mutant mice [J].
Chiamulera, C ;
Epping-Jordan, MP ;
Zocchi, A ;
Marcon, C ;
Cottiny, C ;
Tacconi, S ;
Corsi, M ;
Orzi, F ;
Conquet, F .
NATURE NEUROSCIENCE, 2001, 4 (09) :873-874
[9]   SR141716, a central cannabinoid (CB1) receptor antagonist, blocks the motivational and dopamine-releasing effects of nicotine in rats [J].
Cohen, C ;
Perrault, G ;
Voltz, C ;
Steinberg, R ;
Soubrié, P .
BEHAVIOURAL PHARMACOLOGY, 2002, 13 (5-6) :451-463
[10]   Cannabinoid CB1 receptor knockout mice fail to self-administer morphine but not other drugs of abuse [J].
Cossu, G ;
Ledent, C ;
Fattore, L ;
Imperato, A ;
Böhme, GA ;
Parmentier, M ;
Fratta, W .
BEHAVIOURAL BRAIN RESEARCH, 2001, 118 (01) :61-65