4.7 Article

Effect of dopamine receptor antagonists on renewal of cocaine seeking by reexposure to drug-associated contextual cues

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NEUROPSYCHOPHARMACOLOGY
卷 27, 期 6, 页码 1006-1015

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ELSEVIER SCIENCE INC
DOI: 10.1016/S0893-133X(02)00356-1

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conditioning; occasion setting; context; drug self-administration; raclopride; reinstatement; relapse; SCH 23390

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We recently found that in rats trained to self-administer a heroin-cocaine mixture, exposure to the drug self-administration environment, after extinction of the drug-reinforced behavior in a different context, leads to renewal of drug seeking. Here we further explored the role of contextual stimuli in drug seeking by characterizing the effect of drug-associated environmental stimuli on renewal of cocaine seeking. We also investigated whether activation of dopamine receptors contributes to context-induced renewal of cocaine seeking by testing the effects of selective D1-like (SCH 23390) and D2-like (raclopride) receptor antagonists. Rats were trained for 10 days to self-administer cocaine by pressing a lever. Next, lever pressing was extinguished in the presence of the discrete cues associated with cocaine infusions for 10 days in a context that was distinctively different from the drug-taking context. On the test days, rats were pretreated with SCH 23390 (0, 5 or 10 mug/kg) or raclopride (0, 50 or 100 mug/kg) and nonreinforced lever-pressing behavior was determined either in the extinction context (Control group) or the cocaine-associated context (Renewal group). Consistent with our previous report, cocaine seeking was renewed when rats were exposed to the drug-associated context after extinction in a different context. Furthermore, pretreatment with the D1-like or the D2-like receptor antagonists attenuated context-induced renewal of cocaine seeking. These data suggest that activation of dopamine receptors is involved in reinstatement of cocaine seeking induced by exposure to the drug self-administration context. (C) 2002 American College of Neuropsychopharmacology. Published by Elsevier Science Inc.

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