Mifepristone in the Central Nucleus of the Amygdala Reduces Yohimbine Stress-Induced Reinstatement of Ethanol-Seeking

被引:149
作者
Simms, Jeffrey A. [1 ]
Haass-Koffler, Carolina L. [1 ,2 ]
Bito-Onon, Jade [1 ]
Li, Rui [1 ]
Bartlett, Selena E. [1 ]
机构
[1] Univ Calif San Francisco, Preclin Dev Grp, Ernest Gallo Clin & Res Ctr, Emeryville, CA 94608 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
mifepristone; yohimbine; reinstatement; ethanol; self-administration; corticosterone; CORTICOTROPIN-RELEASING-FACTOR; LONG-EVANS RATS; PITUITARY-ADRENAL AXIS; ANXIETY-LIKE BEHAVIOR; FACTOR MESSENGER-RNA; ALCOHOL-SEEKING; COCAINE-SEEKING; GLUCOCORTICOID-RECEPTORS; INDUCED RELAPSE; STEROID-HORMONE;
D O I
10.1038/npp.2011.268
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Chronic ethanol exposure leads to dysregulation of the hypothalamic-pituitary-adrenal axis, leading to changes in glucocorticoid release and function that have been proposed to maintain pathological alcohol consumption and increase vulnerability to relapse during abstinence. The objective of this study was to determine whether mifepristone, a glucocorticoid receptor antagonist, plays a role in ethanol self-administration and reinstatement. Male, Long-Evans rats were trained to self-administer either ethanol or sucrose in daily 30 min operant self-administration sessions using a fixed ratio 3 schedule of reinforcement. Following establishment of stable baseline responding, we examined the effects of mifepristone on maintained responding and yohimbine-induced increases in responding for ethanol and sucrose. Lever responding was extinguished in separate groups of rats and animals were tested for yohimbine-induced reinstatement and corticosterone release. We also investigated the effects of local mifepristone infusions into the central amygdala (CeA) on yohimbine-induced reinstatement of ethanol-and sucrose-seeking. In addition, we infused mifepristone into the basolateral amygdala (BLA) in ethanol-seeking animals as an anatomical control. We show that both systemic and intra-CeA (but not BLA) mifepristone administration suppressed yohimbine-induced reinstatement of ethanol-seeking, while only systemic injections attenuated sucrose-seeking. In contrast, baseline consumption, yohimbine-induced increases in responding, and circulating CORT levels were unaffected. The data indicate that the CeA plays an important role in the effects of mifepristone on yohimbine-induced reinstatement of ethanol-seeking. Mifepristone may be a valuable pharmacotherapeutic strategy for preventing relapse to alcohol use disorders and, as it is FDA approved, may be a candidate for clinical trials in the near future. Neuropsychopharmacology (2012) 37, 906-918; doi: 10.1038/npp.2011.268; published online 2 November 2011
引用
收藏
页码:906 / 918
页数:13
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