Corticotropin-releasing factor-1 receptor antagonists decrease heroin self-administration in long- but not short-access rats

被引:66
作者
Greenwell, Thomas N. [1 ]
Funk, Cindy K. [1 ]
Cottone, Pietro [1 ]
Richardson, Heather N. [1 ]
Chen, Scott A. [1 ]
Rice, Kenner C. [1 ]
Zorrilla, Eric P. [1 ]
Koob, George F. [1 ]
机构
[1] Scripps Res Inst, Comm Neurobiol Addict Disorders, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
Addiction; antagonist; CRF; escalation; heroin; self-administration; CONDITIONED PLACE AVERSION; ETHANOL-DEPENDENT RATS; STRESS-INDUCED RELAPSE; OPIATE WITHDRAWAL; MORPHINE-WITHDRAWAL; STRIA TERMINALIS; BED NUCLEUS; NEUROBIOLOGICAL EVIDENCE; FEEDING PATTERNS; DRUG-ADDICTION;
D O I
10.1111/j.1369-1600.2008.00142.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
Dysregulation of the stress-related corticotropin-releasing factor (CRF) system has been implicated in the development of drug dependence. The present study examined the effects of administering CRF type 1 (CRF1) receptor antagonists on heroin self-administration in animals allowed short (1 hour) or long (8-12 hours) access to intravenous heroin self-administration sessions. The nonpeptide CRF1 antagonists MJL-1-109-2 (1 hour versus 8 hours access) or R121919 (1 hour versus 12 hours access) were systemically injected in both short- and long-access rats. MJL-1-109-2 (10 mg/kg) and R121919 (10 and 20 mg/kg) reduced heroin self-administration in long-access animals without altering heroin intake in short-access animals. Both MJL-1-109-2 and R121919 decreased first-hour intravenous heroin self-administration selectively in long-access rats, with R121919 decreasing cumulative heroin intake across the 12-hour session. The results demonstrate that blockade of the CRF-CRF1 receptor system attenuates the increased heroin intake of rats with extended access to the drug.
引用
收藏
页码:130 / 143
页数:14
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