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Article
Nature Neuroscience  8, 339 - 345 (2005)
Published online: 6 February 2005; | doi:10.1038/nn1398

Alcohol-induced motor impairment caused by increased extrasynaptic GABAA receptor activity

H Jacob Hanchar1, 3, Paul D Dodson2, 3, Richard W Olsen1, Thomas S Otis2 & Martin Wallner1

1  Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California, Los Angeles, California 90095, USA.

2  Department of Neurobiology, David Geffen School of Medicine, University of California, Los Angeles, California 90095, USA.

3  These authors contributed equally to this work.

Correspondence should be addressed to Martin Wallner mwallner@mednet.ucla.edu or Thomas S Otis otist@ucla.edu
Neuronal mechanisms underlying alcohol intoxication are unclear. We find that alcohol impairs motor coordination by enhancing tonic inhibition mediated by a specific subtype of extrasynaptic GABAA receptor (GABAR), alpha6beta3delta, expressed exclusively in cerebellar granule cells. In recombinant studies, we characterize a naturally occurring single-nucleotide polymorphism that causes a single amino acid change (R100Q) in alpha6 (encoded in rats by the Gabra6 gene). We show that this change selectively increases alcohol sensitivity of alpha6beta3delta GABARs. Behavioral and electrophysiological comparisons of Gabra6 100R/100R and Gabra6 100Q/100Q rats strongly suggest that alcohol impairs motor coordination by enhancing granule cell tonic inhibition. These findings identify extrasynaptic GABARs as critical targets underlying low-dose alcohol intoxication and demonstrate that subtle changes in tonic inhibition in one class of neurons can alter behavior.

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Nature Neuroscience
ISSN: 1097-6256
EISSN: 1546-1726
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