Knockin mice with ethanol-insensitive alpha1-containing gamma-aminobutyric acid type A receptors display selective alterations in behavioral responses to ethanol

• Published in: The Journal of pharmacology and experimental therapeutics 2006-10, Vol.319 (1), p.219-227
• Main Authors: Werner, David F, Blednov, Yuri A, Ariwodola, Olusegun J, Silberman, Yuval, Logan, Exazevia, Berry, Raymond B, Borghese, Cecilia M, Matthews, Douglas B, Weiner, Jeffrey L, Harrison, Neil L, Harris, R Adron, Homanics, Gregg E
• Format: Article
• Language: English
• Subjects: Animals; Behavior, Animal - drug effects; Body Temperature - drug effects; Ethanol - administration & dosage; Ethanol - blood; Ethanol - pharmacology; Etomidate - pharmacology; Female; Hippocampus - physiology; Male; Maze Learning - drug effects; Mice; Mice, Inbred C57BL; Motor Activity - drug effects; Quinine - administration & dosage; Receptors, GABA-A - chemistry; Receptors, GABA-A - drug effects; Receptors, GABA-A - physiology; Reflex - drug effects; Saccharin - administration & dosage; Structure-Activity Relationship
• ISSN: 0022-3565

Despite the pervasiveness of alcohol (ethanol) use, it is unclear how the multiple molecular targets for ethanol contribute to its many behavioral effects. The function of GABA type A receptors (GABA(A)-Rs) is altered by ethanol, but there are multiple subtypes of these receptors, and thus far, individual subunits have not been definitively linked with specific behavioral actions. The alpha1 subunit of the GABA(A)-R is the most abundant alpha subunit in the brain, and the goal of this study was to determine the role of receptors containing this subunit in alcohol action. We designed an alpha1 subunit with serine 270 to histidine and leucine 277 to alanine mutations that was insensitive to potentiation by ethanol yet retained normal GABA sensitivity and constructed knockin mice containing this mutant subunit. Hippocampal slice recordings from these mice indicated that the mutant receptors were less sensitive to ethanol's potentiating effects. Behaviorally, we observed that mutant mice recovered more quickly from the motor-impairing effects of ethanol and etomidate, but not pentobarbital, and showed increased anxiolytic effects of ethanol. No differences were observed in ethanol-induced hypnosis, locomotor stimulation, cognitive impairment, or in ethanol preference and consumption. Overall, these studies demonstrate that the postsynaptic effects of ethanol at GABAergic synapses containing the alpha1 subunit are important for specific ethanol-induced behavioral effects.