Literature DB >> 15642607

Evaluation of a simple model of ethanol drinking to intoxication in C57BL/6J mice.

Justin S Rhodes1, Karyn Best, John K Belknap, Deborah A Finn, John C Crabbe.   

Abstract

Because of intrinsic differences between humans and mice, no single mouse model can represent all features of a complex human trait such as alcoholism. It is therefore necessary to develop partial models. One important feature is drinking to the point where blood ethanol concentration (BEC) reaches levels that have measurable affects on physiology and/or behavior (>1.0 mg ethanol/ml blood). Most models currently in use examine relative oral self-administration from a bottle containing alcohol versus one containing water (two-bottle preference drinking), or oral operant self-administration. In these procedures, it is not clear when or if the animals drink to pharmacologically significant levels because the drinking is episodic and often occurs over a 24-h period. The aim of this study was to identify the optimal parameters and evaluate the reliability of a very simple procedure, taking advantage of a mouse genotype (C57BL/6J) that is known to drink large quantities of ethanol. We exchanged for the water bottle a solution containing ethanol in tap water for a limited period, early in the dark cycle, in the home cage. Mice regularly drank sufficient ethanol to achieve BEC>1.0 mg ethanol/ml blood. The concentration of ethanol offered (10%, 20% or 30%) did not affect consumption in g ethanol/kg body weight. The highest average BEC ( approximately 1.6 mg/ml) occurred when the water-to-ethanol switch occurred 3 h into the dark cycle, and when the ethanol was offered for 4 rather than 2 h. Ethanol consumption was consistent within individual mice, and reliably predicted BEC after the period of ethanol access. C57BL/6J mice from three sources provided equivalent data, while DBA/2J mice drank much less than C57BL/6J in this test. We discuss advantages of the model for high-throughput screening assays where the goal is to find other genotypes of mice that drink excessively, or to screen drugs for their efficacy in blocking excessive drinking.

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Year:  2005        PMID: 15642607     DOI: 10.1016/j.physbeh.2004.10.007

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  414 in total

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Authors:  Helen M Kamens; Constanza Silva; Colette Peck; Carley N Miller
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2.  Persistent escalation of alcohol drinking in C57BL/6J mice with intermittent access to 20% ethanol.

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3.  The role of connexin-36 gap junctions in alcohol intoxication and consumption.

Authors:  Scott C Steffensen; Katie D Bradley; David M Hansen; Jeffrey D Wilcox; Rebecca S Wilcox; David W Allison; Collin B Merrill; Jeffrey G Edwards
Journal:  Synapse       Date:  2010-12-28       Impact factor: 2.562

Review 4.  Preclinical studies of alcohol binge drinking.

Authors:  John C Crabbe; R Adron Harris; George F Koob
Journal:  Ann N Y Acad Sci       Date:  2011-01       Impact factor: 5.691

5.  A limited access mouse model of prenatal alcohol exposure that produces long-lasting deficits in hippocampal-dependent learning and memory.

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7.  Levetiracetam results in increased and decreased alcohol drinking with different access procedures in C57BL/6J mice.

Authors:  Eric W Fish; Abigail E Agoglia; Michael C Krouse; R Grant Muller; J Elliott Robinson; C J Malanga
Journal:  Behav Pharmacol       Date:  2014-02       Impact factor: 2.293

8.  Medial prefrontal cortex neuropeptide Y modulates binge-like ethanol consumption in C57BL/6J mice.

Authors:  Stacey L Robinson; Isabel M Marrero; Carlos A Perez-Heydrich; Marian T Sepulveda-Orengo; Kathryn J Reissner; Todd E Thiele
Journal:  Neuropsychopharmacology       Date:  2019-01-07       Impact factor: 7.853

9.  Alcohol exposure inhibits adult neural stem cell proliferation.

Authors:  Joannalee C Campbell; Tamara Stipcevic; Roberto E Flores; Canelda Perry; Tod E Kippin
Journal:  Exp Brain Res       Date:  2014-04-26       Impact factor: 1.972

10.  Pharmacological inhibition of Receptor Protein Tyrosine Phosphatase β/ζ (PTPRZ1) modulates behavioral responses to ethanol.

Authors:  Rosalía Fernández-Calle; Marta Vicente-Rodríguez; Miryam Pastor; Esther Gramage; Bruno Di Geronimo; José María Zapico; Claire Coderch; Carmen Pérez-García; Amy W Lasek; Beatriz de Pascual-Teresa; Ana Ramos; Gonzalo Herradón
Journal:  Neuropharmacology       Date:  2018-05-09       Impact factor: 5.250

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