Citation

Yang AR, Liu J, Yi HS, Warnock KT, Wang M, June HL, Puche AC, Elnabawi A, Sieghart W, Aurelian L, June HL. Front. Neurosci. 2011; 5(online): 123.

Affiliation

Neuropsychopharmacology Laboratory, Department of Psychiatry, Division of Alcohol and Drug Abuse, School of Medicine, University of Maryland Baltimore, MD, USA.

Copyright

(Copyright © 2011, Frontiers Research Foundation)

DOI

10.3389/fnins.2011.00123

PMID

22022305

PMCID

PMC3195989

Abstract

Binge drinking, frequently referred to clinically as problem or hazardous drinking, is a pattern of excessive alcohol intake characterized by blood alcohol levels ≥0.08 g% within a 2-h period. Here, we show that overexpression of α1 subunits of the GABA(A) receptor contributes to binge drinking, and further document that this involvement is related to the neuroanatomical localization of α1 receptor subunits. Using a herpes simplex virus amplicon vector to deliver small interference RNA (siRNA), we showed that siRNA specific for the α1 subunit (pHSVsiLA1) caused profound, long-term, and selective reduction of gene expression, receptor density, and binge drinking in high-alcohol drinking rats when delivered into the ventral pallidum (VP). Scrambled siRNA (pHSVsiNC) delivered similarly into the VP failed to alter gene expression, receptor density, or binge drinking. Silencing of the α1 gene in the VP, however, failed to alter binge sucrose or water intake. These results, along with our prior research, provide compelling evidence that the α1-containing GABA(A) receptor subunits are critical in the regulation of binge-like patterns of excessive drinking. Collectively, these data may be useful in the development of gene-based and novel pharmacological approaches for the treatment of excessive drinking.

Language: en