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Publication : Enhanced and delayed stress-induced alcohol drinking in mice lacking functional CRH1 receptors.

First Author  Sillaber I Year  2002
Journal  Science Volume  296
Issue  5569 Pages  931-3
PubMed ID  11988580 Mgi Jnum  J:76358
Mgi Id  MGI:2179180 Doi  10.1126/science.1069836
Citation  Sillaber I, et al. (2002) Enhanced and delayed stress-induced alcohol drinking in mice lacking functional CRH1 receptors. Science 296(5569):931-3
abstractText  There is a relation between stress and alcohol drinking. We show that the corticotropin-releasing hormone (CRH) system that mediates endocrine and behavioral responses to stress plays a role in the control of long-term alcohol drinking. In mice lacking a functional CRH1 receptor, stress leads to enhanced and progressively increasing alcohol intake. The effect of repeated stress on alcohol drinking behavior appeared with a delay and persisted throughout life. It was associated with an up-regulation of the N-methyl-d-aspartate receptor subunit NR2B. Alterations in the CRH1 receptor gene and adaptional changes in NR2B subunits may constitute a genetic risk factor for stress-induced alcohol drinking and alcoholism.
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