Tackling the Link Between Stress and Alcohol

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引用次数: 1

Abstract

The chances of developing alcoholism throughout one's life are determined by a genetic predisposition and an individual's reaction to lifetime events, such a stress. The corticotropin-releasing hormone (CRH) system regulates endocrine responses to stress and mediates stress-related behavior. To better understand the molecular and cellular mechanism underlying stress-induced alcohol drinking Sillaber et al. created knockout mice lacking CRH1 receptors. Crhr1−/− mice did not differ from wild-type mice in their basal alcohol intake and preference. However, after repeated stress episodes, the knockout mice gradually increased their alcohol consumption and kept it elevated for the rest of their life. This change in drinking behavior was accompanied by enhanced protein levels of the NR2B subunit of the N-methyl-D-aspartate receptor. I. Sillaber, G. Rammes, S. Zimmermann, B. Mahal, W. Zieglgänsberger, W. Wurst, F. Holsboer, R. Spanagel, Enhanced and delayed stress-induced alcohol drinking in mice lacking functional CRH1 receptors. Science 296, 931-933 (2002). [Abstract] [Full Text]
解决压力和酒精之间的联系
一个人一生中患上酒精中毒的几率是由遗传倾向和个人对生活事件(如压力)的反应决定的。促肾上腺皮质激素释放激素(CRH)系统调节对应激的内分泌反应,并介导应激相关行为。为了更好地理解应激性饮酒的分子和细胞机制,Sillaber等人创造了缺乏CRH1受体的敲除小鼠。Crhr1−/−小鼠在基础酒精摄入量和偏好方面与野生型小鼠没有差异。然而,在反复的应激事件后,基因敲除小鼠逐渐增加了酒精摄入量,并在其余生中保持高水平。这种饮酒行为的改变伴随着n -甲基- d -天冬氨酸受体NR2B亚基蛋白水平的提高。I. Sillaber, G. Rammes, S. Zimmermann, B. Mahal, W. Zieglgänsberger, W. Wurst, F. Holsboer, R. Spanagel,缺乏功能性CRH1受体的小鼠应激诱导饮酒的增强和延迟。科学296,931-933(2002)。【摘要】【全文】
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