Literature DB >> 20590397

What aspects of human alcohol use disorders can be modeled using selectively bred rat lines?

J C Froehlich1.   

Abstract

The use of selective breeding to produce animal models for the study of alcohol abuse and alcoholism represents one of the major advances in the field of alcohol research. Rats selectively bred for alcohol preference and alcohol nonpreference have been useful to both preclinical and clinical investigators in the alcohol research community for studying the behavioral, neurobiological, and molecular basis of alcohol drinking, for identifying the genes that may contribute to the development of alcohol abuse and alcoholism, and for evaluating the utility of drugs aimed at reducing alcohol intake and preventing alcohol relapse. Rats selectively bred for alcohol preference (alcohol preferring or "P" line) have enhanced responsiveness to the low dose reinforcing effects of alcohol, less aversion to moderate/high doses of alcohol, and are able to develop tolerance to the aversive effects of alcohol more rapidly and to maintain tolerance longer than rats selectively bred for alcohol nonpreference (alcohol nonpreferring or "NP" line). The increased potency of low-dose alcohol as a reinforcer for P rats might be expected to foster and maintain alcohol drinking. Weaker aversion to the pharmacological effects of moderate/high doses of alcohol in the P line would allow P rats to drink more alcohol than NP rats before the postingestional effects become aversive. Rapid induction of tolerance to the aversive effects of alcohol with repeated bouts of voluntary alcohol drinking, as well as persistence of alcohol tolerance in rats of the P line might serve to maintain alcohol drinking. These are powerful mechanisms that may serve to promote and maintain a high alcohol drinking behavior. Although these rat lines have been used to address several characteristics of excessive alcohol consumption in humans, they have not yet been used to model several aspects of human alcohol use disorders. New applications of these selectively bred rat lines are discussed which may further our understanding of the factors contributing to alcohol abuse and alcoholism.

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Year:  2010        PMID: 20590397     DOI: 10.3109/10826084.2010.482424

Source DB:  PubMed          Journal:  Subst Use Misuse        ISSN: 1082-6084            Impact factor:   2.164


  9 in total

1.  Combining naltrexone and prazosin in a single oral medication decreases alcohol drinking more effectively than does either drug alone.

Authors:  Janice C Froehlich; Brett J Hausauer; Dennis D Rasmussen
Journal:  Alcohol Clin Exp Res       Date:  2013-07-22       Impact factor: 3.455

2.  Prazosin Reduces Alcohol Intake in an Animal Model of Alcohol Relapse.

Authors:  Janice C Froehlich; Brett Hausauer; Stephen Fischer; Bradley Wise; Dennis D Rasmussen
Journal:  Alcohol Clin Exp Res       Date:  2015-08       Impact factor: 3.455

3.  Effects of prazosin, an α1-adrenergic receptor antagonist, on the seeking and intake of alcohol and sucrose in alcohol-preferring (P) rats.

Authors:  Terril L Verplaetse; Dennis D Rasmussen; Janice C Froehlich; Cristine L Czachowski
Journal:  Alcohol Clin Exp Res       Date:  2011-10-07       Impact factor: 3.455

4.  Tolcapone suppresses ethanol intake in alcohol-preferring rats performing a novel cued access protocol.

Authors:  Aqilah M McCane; Cristine L Czachowski; Christopher C Lapish
Journal:  Alcohol Clin Exp Res       Date:  2014-09       Impact factor: 3.455

5.  A Combination of Naltrexone + Varenicline Retards the Expression of a Genetic Predisposition Toward High Alcohol Drinking.

Authors:  Janice C Froehlich; Stephen M Fischer; Emily R Nicholson; Julian E Dilley; Nicholas J Filosa; Teal N Smith; Logan C Rademacher
Journal:  Alcohol Clin Exp Res       Date:  2017-02-09       Impact factor: 3.455

Review 6.  Rodent models of alcoholic liver disease: of mice and men.

Authors:  Elizabeth Brandon-Warner; Laura W Schrum; C Max Schmidt; Iain H McKillop
Journal:  Alcohol       Date:  2012-09-07       Impact factor: 2.405

7.  Differential effects of quinine adulteration of alcohol on seeking and drinking.

Authors:  Aqilah M McCane; Curtis D Auterson; Michael J DeLory; Christopher C Lapish; Cristine L Czachowski
Journal:  Alcohol       Date:  2021-01-16       Impact factor: 2.405

8.  COMT Inhibition Alters Cue-Evoked Oscillatory Dynamics during Alcohol Drinking in the Rat.

Authors:  A M McCane; S Ahn; L L Rubchinsky; S S Janetsian-Fritz; D N Linsenbardt; C L Czachowski; C C Lapish
Journal:  eNeuro       Date:  2018-10-31

9.  Behavioral Profiles of Adolescent Alcohol-Preferring/Non-preferring (P/NP) and High/Low Alcohol-Drinking (HAD/LAD) Rats Are Dependent on Line but Not Sex.

Authors:  Stina Lundberg; Erika Roman; Richard L Bell
Journal:  Front Neurosci       Date:  2022-01-13       Impact factor: 4.677

  9 in total

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