Brain-Specific Inactivation of the Crhr1 Gene Inhibits Post-Dependent and Stress-Induced Alcohol Intake, but Does Not Affect Relapse-Like Drinking

被引:47
作者
Molander, Anna [1 ]
Vengeliene, Valentina [1 ]
Heilig, Markus [2 ]
Wurst, Wolfgang [3 ,4 ,5 ,6 ]
Deussing, Jan M. [3 ]
Spanagel, Rainer [1 ]
机构
[1] Heidelberg Univ, Cent Inst Mental Hlth, Inst Psychopharmacol, D-6800 Mannheim, Germany
[2] NIAAA, Lab Clin & Translat Studies, Bethesda, MD USA
[3] Max Planck Inst Psychiat, D-80804 Munich, Germany
[4] German Res Ctr Environm Hlth, Helmholtz Ctr, Munich, Germany
[5] Tech Univ Weihenstephan, Inst Dev Genet, Munich, Germany
[6] DZNE Demenzzentrum, Munich, Germany
关键词
alcoholism; stress; relapse; post-dependent drinking; alcohol deprivation effect (ADE); conditional Crhr1(NestinCre)-knockout mice; CORTICOTROPIN-RELEASING-FACTOR; RECEPTOR ANTAGONIST ANTALARMIN; ANXIETY-RELATED BEHAVIOR; PITUITARY-ADRENAL AXIS; INDUCED INCREASES; ETHANOL DRINKING; PROTRACTED ABSTINENCE; REDUCED ANXIETY; ANIMAL-MODEL; MICE LACKING;
D O I
10.1038/npp.2011.297
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Corticotropin-releasing hormone (CRH) and its receptor, CRH receptor-1 (CRHR1), have a key role in alcoholism. Especially, post-dependent and stress-induced alcohol intake involve CRH/CRHR1 signaling within extra-hypothalamic structures, but a contribution of the hypothalamic-pituitary-adrenal (HPA) axis activity might be involved as well. Here we examined the role of CRHR1 in various drinking conditions in relation to HPA and extra-HPA sites, and studied relapse-like drinking behavior in the alcohol deprivation model (ADE). To dissect CRH/CRHR1 extra-HPA and HPA signaling on a molecular level, a conditional brain-specific Crhr1-knockout (Crhr1(NestinCre)) and a global knockout mouse line were studied for basal alcohol drinking, stress-induced alcohol consumption, deprivation-induced intake, and escalated alcohol consumption in the post-dependent state. In a second set of experiments, we tested CRHR1 antagonists in the ADE model. Stress-induced augmentation of alcohol intake was lower in Crhr1(NestinCre) mice as compared with control animals. Crhr1 NestinCre mice were also resistant to escalation of alcohol intake in the post-dependent state. Contrarily, global Crhr1 knockouts showed enhanced stress-induced alcohol consumption and a more pronounced escalation of intake in the post-dependent state than their control littermates. Basal intake and deprivation-induced intake were unaltered in both knockout models when compared with their respective controls. In line with these findings, CRHR1 antagonists did not affect relapse-like drinking after a deprivation period in rats. We conclude that CRH/CRHR1 extra-HPA and HPA signaling may have opposing effects on stress-related alcohol consumption. CRHR1 does not have a role in basal alcohol intake or relapse-like drinking situations with a low stress load. Neuropsychopharmacology (2012) 37, 1047-1056; doi: 10.1038/npp.2011.297; published online 23 November 2011
引用
收藏
页码:1047 / 1056
页数:10
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