Reversal of cocaine-conditioned place preference and mesocorticolimbic Zif268 expression by social interaction in rats

被引:92
作者
Fritz, Michael
El Rawas, Rana
Salti, Ahmad [2 ]
Klement, Sabine
Bardo, Michael T. [3 ]
Kemmler, Georg
Dechant, Georg [2 ]
Saria, Alois
Zernig, Gerald [1 ]
机构
[1] Med Univ Innsbruck, Dept Gen Psychiat & Social Psychiat, Expt Psychiat Unit, A-6020 Innsbruck, Austria
[2] Med Univ Innsbruck, Inst Neurosci, A-6020 Innsbruck, Austria
[3] Univ Kentucky, Ctr Drug Abuse Res Translat, Lexington, KY 40506 USA
基金
奥地利科学基金会;
关键词
Cocaine; conditioned place preference; relapse; social interaction; substance dependence; zif268; NUCLEUS-ACCUMBENS CORE; DOPAMINE TRANSPORTER; DRUG-ADDICTION; REWARD; RECEPTORS; REINSTATEMENT; SYSTEMS; MODEL; METHAMPHETAMINE; ACETYLCHOLINE;
D O I
10.1111/j.1369-1600.2010.00285.x
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
Little is known how social interaction, if offered as an alternative to drug consumption, affects neural circuits involved in drug reinforcement and substance dependence. Conditioned place preference (CPP) for cocaine (15 mg/kg i.p.) or social interaction (15 minutes) as an alternative stimulus was investigated in male Sprague-Dawley rats. Four social interaction episodes with a male adult conspecific completely reversed cocaine CPP and were even able to prevent reacquisition of cocaine CPP. Social interaction also reversed cocaine CPP-induced expression of the immediate-early gene zif268 in the nucleus accumbens shell, the central and basolateral amygdala and the ventral tegmental area. These findings suggest that social interaction, if offered in a context that is clearly distinct from the previously drug-associated ones, may profoundly decrease the incentive salience of drug-associated contextual stimuli. The novel experimental design facilitates the neurobiological investigation of this phenomenon which may be beneficial for human drug users in treatment.
引用
收藏
页码:273 / 284
页数:12
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