Effects of CP-154,526 on responding during extinction from cocaine self-administration in rats

被引:15
作者
Gurkovskaya, O
Goeders, NE
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Pharmacol & Therapeut, Shreveport, LA 71130 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Dept Psychiat, Shreveport, LA 71130 USA
关键词
cocaine; self-administration; conditioning; CRH (corticotropin releasing hormone); (rat);
D O I
10.1016/S0014-2999(01)01465-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Conditioned cues associated with cocaine induce craving and relapse. Although the role of corticotropin releasing hormone (CRH) in stress- and cocaine-induced relapse has been reported, its involvement in cue-induced behavior has not been established. Using responding during extinction as a model of cue-induced craving, we tested the effects of a selective CRH1 receptor antagonist, CP-154,526(butyl-ethyl-[2,5-dimethyl-7-(2,4,6-trimethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine). Rats were trained to respond on a multiple schedule of cocaine self-administration and food reinforcement. On extinction test days, saline was substituted for cocaine. Pretreatment with CP-154,526 (20 mg/kg, i.p.) decreased responding on the cocaine-associated lever during extinction, suggesting an involvement of CRH I receptors in cue-induced craving. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:53 / 56
页数:4
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