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Publication : Several behavioral traits relevant for alcoholism are controlled by ɣ2 subunit containing GABA<sub>A</sub> receptors on dopamine neurons in mice.

First Author  Stojakovic A Year  2018
Journal  Neuropsychopharmacology Volume  43
Issue  7 Pages  1548-1556
PubMed ID  29463910 Mgi Jnum  J:273923
Mgi Id  MGI:6282859 Doi  10.1038/s41386-018-0022-z
Citation  Stojakovic A, et al. (2018) Several behavioral traits relevant for alcoholism are controlled by 2 subunit containing GABAA receptors on dopamine neurons in mice. Neuropsychopharmacology 43(7):1548-1556
abstractText  The risk factors for developing alcohol addiction include impulsivity, high sensitivity to the rewarding action of ethanol, and low sensitivity to its sedative and intoxicating effects. Genetic variation in GABAA receptor subunits, including the 2 subunit (Gabrg2), affects the risk for developing alcoholism. Alcohol directly potentiates GABAA receptors and activates the mesolimbic dopamine system. Here, we deleted Gabrg2 selectively in dopamine cells of adult mice. The deletion resulted in elevated firing of dopamine neurons and made them less sensitive to drugs acting at GABAA receptors. At the behavioral level, the deletion increased exploratory behavior and augmented both correct and incorrect responding in the go/no-go task, a test often used to assay the response inhibition component of impulsivity. In addition, conditioned place preference to alcohol, but not to cocaine or morphine, was increased. Ethanol-induced locomotor activation was enhanced in the mice lacking Gabrg2 on dopaminergic cells, whereas the sedative effect of alcohol was reduced. Finally, the alcohol drinking, but not the alcohol preference, at a high concentration was increased in the mutant mice. In summary, deletion of Gabrg2 on dopamine cells induced several behavioral traits associated with high risk of developing alcoholism. The findings suggest that mice lacking Gabrg2 on dopaminergic cells could be used as models for individuals at high risk for developing alcoholism and that GABAA receptors on dopamine cells are protective against the development of excessive alcohol drinking.
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