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Lookup NU author(s): Professor Quentin AnsteeORCiD
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Alcohol-dependence is a common, complex and debilitating disorder with genetic and environmental influences. Here we show that alcohol consumption increases following mutations to the γ-aminobutyric acidA receptor (GABAAR) β1 subunit gene (Gabrb1). Using N-ethyl-N-nitrosourea mutagenesis on an alcohol-averse background (F1 BALB/cAnN x C3H/HeH), we develop a mouse model exhibiting strong heritable preference for ethanol resulting from a dominant mutation (L285R) in Gabrb1. The mutation causes spontaneous GABA ion channel opening and increases GABA sensitivity of recombinant GABAARs, coupled to increased tonic currents in the nucleus accumbens, a region long-associated with alcohol reward. Mutant mice work harder to obtain ethanol, and are more sensitive to alcohol intoxication. Another spontaneous mutation (P228H) in Gabrb1 also causes high ethanol consumption accompanied by spontaneous GABA ion channel opening and increased accumbal tonic current. Our results provide a new and important link between GABAAR function and increased alcohol consumption that could underlie some forms of alcohol abuse. Normal 0 false false false EN-GB X-NONE X-NONE
Author(s): Anstee QM, Knapp S, Maguire EP, Hosie AM, Thomas P, Mortensen M, Bhome R, Martinez A, Walker SE, Dixon CI, Ruparelia K, Montagnese S, Kuo YT, Herlihy A, Bell JD, Robinson I, Guerrini I, McQuillin A, Fisher EMC, Ungless MA, Gurling HMD, Morgan MY, Brown SDM, Stephens DN, Belelli D, Lambert J, Smart T, Thomas HC
Publication type: Article
Publication status: Published
Journal: Nature Communications
Year: 2013
Volume: 4
Pages: 1-11
Print publication date: 26/11/2013
ISSN (electronic): 2041-1723
Publisher: Nature Publishing Group
URL: http://dx.doi.org/10.1038/ncomms3816
DOI: 10.1038/ncomms3816
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