Literature DB >> 34933049

Independent of differences in taste, B6N mice consume less alcohol than genetically similar B6J mice, and exhibit opposite polarity modulation of tonic GABAAR currents by alcohol.

Chloe M Erikson1, Kevin T Douglas1, Talia O Thuet1, Ben D Richardson2, Claudia Mohr1, Hiroko Shiina3, Josh S Kaplan4, David J Rossi5.   

Abstract

Genetic differences in cerebellar sensitivity to alcohol (EtOH) influence EtOH consumption phenotype in animal models and contribute to risk for developing an alcohol use disorder in humans. We previously determined that EtOH enhances cerebellar granule cell (GC) tonic GABAAR currents in low EtOH consuming rodent genotypes, but suppresses it in high EtOH consuming rodent genotypes. Moreover, pharmacologically counteracting EtOH suppression of GC tonic GABAAR currents reduces EtOH consumption in high alcohol consuming C57BL/6J (B6J) mice, suggesting a causative role. In the low EtOH consuming rodent models tested to date, EtOH enhancement of GC tonic GABAAR currents is mediated by inhibition of neuronal nitric oxide synthase (nNOS) which drives increased vesicular GABA release onto GCs and a consequent enhancement of tonic GABAAR currents. Consequently, genetic variation in nNOS expression across rodent genotypes is a key determinant of whether EtOH enhances or suppresses tonic GABAAR currents, and thus EtOH consumption. We used behavioral, electrophysiological, and immunocytochemical techniques to further explore the relationship between EtOH consumption and GC GABAAR current responses in C57BL/6N (B6N) mice. B6N mice consume significantly less EtOH and achieve significantly lower blood EtOH concentrations than B6J mice, an outcome not mediated by differences in taste. In voltage-clamped GCs, EtOH enhanced the GC tonic current in B6N mice but suppressed it in B6J mice. Immunohistochemical and electrophysiological studies revealed significantly higher nNOS expression and function in the GC layer of B6N mice compared to B6Js. Collectively, our data demonstrate that despite being genetically similar, B6N mice consume significantly less EtOH than B6J mice, a behavioral difference paralleled by increased cerebellar nNOS expression and opposite EtOH action on GC tonic GABAAR currents in each genotype. Published by Elsevier Ltd.

Entities:  

Keywords:  Alcohol use disorder; Cerebellum; GABA; Genetic predilection; nNOS

Mesh:

Substances:

Year:  2021        PMID: 34933049      PMCID: PMC9208337          DOI: 10.1016/j.neuropharm.2021.108934

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.273


  45 in total

1.  Compromised pontocerebellar and cerebellothalamocortical systems: speculations on their contributions to cognitive and motor impairment in nonamnesic alcoholism.

Authors:  Edith V Sullivan
Journal:  Alcohol Clin Exp Res       Date:  2003-09       Impact factor: 3.455

2.  Differential effects of ethanol on serum GABAergic 3alpha,5alpha/3alpha,5beta neuroactive steroids in mice, rats, cynomolgus monkeys, and humans.

Authors:  Patrizia Porcu; Todd K O'Buckley; Sarah E Alward; Soomin C Song; Kathleen A Grant; Harriet de Wit; A Leslie Morrow
Journal:  Alcohol Clin Exp Res       Date:  2009-12-17       Impact factor: 3.455

3.  Functional topography of the cerebellum for motor and cognitive tasks: an fMRI study.

Authors:  Catherine J Stoodley; Eve M Valera; Jeremy D Schmahmann
Journal:  Neuroimage       Date:  2011-08-31       Impact factor: 6.556

4.  Oral sensation of ethanol in a primate model III: responses in the lingual branch of the trigeminal nerve of Macaca mulatta.

Authors:  Vicktoria Danilova; Göran Hellekant
Journal:  Alcohol       Date:  2002-01       Impact factor: 2.405

5.  Chemosensory factors influencing alcohol perception, preferences, and consumption.

Authors:  Alexander A Bachmanov; Stephen W Kiefer; Juan Carlos Molina; Michael G Tordoff; Valerie B Duffy; Linda M Bartoshuk; Julie A Mennella
Journal:  Alcohol Clin Exp Res       Date:  2003-02       Impact factor: 3.455

6.  Ethanol-induced changes in body sway in men at high alcoholism risk.

Authors:  M A Schuckit
Journal:  Arch Gen Psychiatry       Date:  1985-04

7.  Consumption of sweet, salty, sour, and bitter solutions by selectively bred alcohol-preferring and alcohol-nonpreferring lines of rats.

Authors:  R B Stewart; R N Russell; L Lumeng; T K Li; J M Murphy
Journal:  Alcohol Clin Exp Res       Date:  1994-04       Impact factor: 3.455

8.  Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake.

Authors:  Valerie B Duffy; Andrew C Davidson; Judith R Kidd; Kenneth K Kidd; William C Speed; Andrew J Pakstis; Danielle R Reed; Derek J Snyder; Linda M Bartoshuk
Journal:  Alcohol Clin Exp Res       Date:  2004-11       Impact factor: 3.455

9.  Nitric oxide synthase expression reveals compartments of cerebellar granule cells and suggests a role for mossy fibers in their development.

Authors:  K Schilling; H H Schmidt; S L Baader
Journal:  Neuroscience       Date:  1994-04       Impact factor: 3.590

10.  Family history of alcoholism and the human brain response to oral sucrose.

Authors:  William J A Eiler; Mario Dzemidzic; Christina M Soeurt; Claire R Carron; Brandon G Oberlin; Robert V Considine; Jaroslaw Harezlak; David A Kareken
Journal:  Neuroimage Clin       Date:  2017-12-12       Impact factor: 4.881

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