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向基底外侧杏仁核注射 D-苯丙胺后可卡因寻求行为的增强恢复

Potentiated reinstatement of cocaine-seeking behavior following D-amphetamine infusion into the basolateral amygdala.

作者信息

Ledford Christopher C, Fuchs Rita A, See Ronald E

机构信息

Department of Physiology and Neuroscience, Medical University of South Carolina, Charleston, SC 29425, USA.

出版信息

Neuropsychopharmacology. 2003 Oct;28(10):1721-9. doi: 10.1038/sj.npp.1300249.

DOI:10.1038/sj.npp.1300249
PMID:12865896
Abstract

Reinstatement of extinguished drug-seeking behavior following chronic drug self-administration has been demonstrated in rats in the presence of conditioned cues. This experimental model of cue-induced relapse can be used to assess the neural circuitry involved in relapse. We have previously shown that blockade of dopamine D1 receptors in the basolateral amygdala (BLA) abolishes conditioned cue-induced reinstatement of cocaine-seeking behavior. The present study tested the hypothesis that D-amphetamine-induced facilitation of monoamine neurotransmission in the BLA would potentiate conditioned cue-induced reinstatement of extinguished drug-seeking behavior. During daily self-administration sessions over 10 consecutive days, rats pressed a lever to receive cocaine infusions (0.2 mg/0.05 ml) paired with a light+tone compound stimulus. Following self-administration, rats underwent daily extinction sessions, during which no stimuli were presented. On the test days, rats received intra-BLA D-amphetamine (10 or 30 micro g/side) or vehicle infusions followed by extinction or conditioned cue-induced reinstatement testing. D-amphetamine infusions did not alter extinction responding relative to vehicle infusions. During reinstatement testing, conditioned cue presentation significantly increased responding over extinction levels, and intra-BLA D-amphetamine produced a dose-dependent increase in lever responding relative to vehicle infusions. These findings suggest that enhanced monoamine tone in the BLA potentiates the motivational effect and/or salience of cocaine-paired cues during reinstatement.

摘要

在有条件线索存在的情况下,慢性药物自我给药后消退的觅药行为在大鼠中已得到证实。这种线索诱导复吸的实验模型可用于评估参与复吸的神经回路。我们之前已经表明,阻断基底外侧杏仁核(BLA)中的多巴胺D1受体可消除条件线索诱导的可卡因觅药行为的恢复。本研究检验了以下假设:D-苯丙胺诱导的BLA中单胺神经传递的促进作用会增强条件线索诱导的消退的觅药行为的恢复。在连续10天的每日自我给药过程中,大鼠按压杠杆以接受与光+音复合刺激配对的可卡因输注(0.2 mg/0.05 ml)。自我给药后,大鼠进行每日消退训练,在此期间不呈现刺激。在测试日,大鼠接受BLA内D-苯丙胺(10或30μg/侧)或溶剂输注,随后进行消退或条件线索诱导的复吸测试。与溶剂输注相比,D-苯丙胺输注并未改变消退反应。在复吸测试期间,条件线索呈现显著增加了相对于消退水平的反应,并且与溶剂输注相比,BLA内注射D-苯丙胺使杠杆反应产生了剂量依赖性增加。这些发现表明,BLA中单胺水平的增强会增强复吸过程中可卡因配对线索的动机效应和/或显著性。

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