Literature DB >> 24290311

Scheduled access alcohol drinking by alcohol-preferring (P) and high-alcohol-drinking (HAD) rats: modeling adolescent and adult binge-like drinking.

Richard L Bell1, Zachary A Rodd2, Eric A Engleman2, Jamie E Toalston2, William J McBride2.   

Abstract

Binge alcohol drinking continues to be a public health concern among today's youth and young adults. Moreover, an early onset of alcohol use, which usually takes the form of binge drinking, is associated with a greater risk for developing alcohol use disorders. Given this, it is important to examine this behavior in rat models of alcohol abuse and dependence. Toward that end, the objective of this article is to review findings on binge-like drinking by selectively bred alcohol-preferring (P) and high-alcohol-drinking (HAD) lines of rats. As reviewed elsewhere in this special issue, the P line meets all, and the HAD line meets most, of the proposed criteria for an animal model of alcoholism. One model of binge drinking is scheduled ethanol access during the dark cycle, which has been used by our laboratory for over 20 years. Our laboratory has also adopted a protocol involving the concurrent presentation of multiple ethanol concentrations. When this protocol is combined with limited access, ethanol intake is maximized yielding blood ethanol levels (BELs) in excess, sometimes greatly in excess, of 80 mg%. By extending these procedures to include multiple scheduled ethanol access sessions during the dark cycle for 5 consecutive days/week, P and HAD rats consume in 3 or 4 h as much as, if not more than, the amount usually consumed in a 24 h period. Under certain conditions, using the multiple scheduled access procedure, BELs exceeding 200 mg% can be achieved on a daily basis. An overview of findings from studies with other selectively bred, inbred, and outbred rats places these findings in the context of the existing literature. Overall, the findings support the use of P and HAD rats as animal models to study binge-like alcohol drinking and reveal that scheduled access procedures will significantly increase ethanol intake by other rat lines and strains as well.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Animal model of alcoholism; Blood alcohol concentration; Discrete bout; Drinking-in-the-dark; Excessive intake; Extreme drinking; Limited access; Loss-of-control drinking; Nocturnal drinking

Mesh:

Substances:

Year:  2013        PMID: 24290311      PMCID: PMC4007416          DOI: 10.1016/j.alcohol.2013.10.004

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  89 in total

1.  Effects of concurrent access to a single concentration or multiple concentrations of ethanol on ethanol intake by periadolescent high-alcohol-drinking rats.

Authors:  Richard L Bell; Zachary A Rodd; Cathleen C Hsu; Lawrence Lumeng; Ting-Kai Li; James M Murphy; William J McBride
Journal:  Alcohol       Date:  2004-06       Impact factor: 2.405

Review 2.  Animal models of neuropsychiatric disorders.

Authors:  Eric J Nestler; Steven E Hyman
Journal:  Nat Neurosci       Date:  2010-09-27       Impact factor: 24.884

3.  Early-onset drug use and risk of later drug problems.

Authors:  J C Anthony; K R Petronis
Journal:  Drug Alcohol Depend       Date:  1995-11       Impact factor: 4.492

4.  Relationship between level of consumption and harms in assessing drink cut-points for alcohol research: Commentary on "Many college freshmen drink at levels far beyond the binge threshold" by white et Al.

Authors:  Henry Wechsler; Toben F Nelson
Journal:  Alcohol Clin Exp Res       Date:  2006-06       Impact factor: 3.455

5.  Demonstration of lever pressing for oral ethanol by rats with no prior training or ethanol experience.

Authors:  P Hyytiä; J D Sinclair
Journal:  Alcohol       Date:  1989 Mar-Apr       Impact factor: 2.405

6.  Genetic selection for high and low alcohol consumption in a limited-access paradigm.

Authors:  A D Lê; Y Israel; W Juzytsch; B Quan; S Harding
Journal:  Alcohol Clin Exp Res       Date:  2001-11       Impact factor: 3.455

Review 7.  Overview of the past contributions of animal models and their changing place in psychiatry.

Authors:  W T McKinney
Journal:  Semin Clin Neuropsychiatry       Date:  2001-01

8.  Expression of the gene encoding the ghrelin receptor in rats selected for differential alcohol preference.

Authors:  Sara Landgren; Jörgen A Engel; Petri Hyytiä; Henrik Zetterberg; Kaj Blennow; Elisabet Jerlhag
Journal:  Behav Brain Res       Date:  2011-03-15       Impact factor: 3.332

9.  Selective breeding of rats differing in voluntary ethanol consumption.

Authors:  A Bisaga; W Kostowski
Journal:  Pol J Pharmacol       Date:  1993 Jul-Aug

10.  Circadian drinking rhythms and blood alcohol levels in two rat lines developed for their alcohol consumption.

Authors:  J Aalto
Journal:  Alcohol       Date:  1986 Jan-Feb       Impact factor: 2.405

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  35 in total

1.  Neural Firing in the Prefrontal Cortex During Alcohol Intake in Alcohol-Preferring "P" Versus Wistar Rats.

Authors:  David N Linsenbardt; Christopher C Lapish
Journal:  Alcohol Clin Exp Res       Date:  2015-08-06       Impact factor: 3.455

2.  Voluntary Binge Consumption of Ethanol in a Sweetened, Chocolate-Flavored Solution by Male and Female Adolescent Sprague Dawley Rats.

Authors:  Dominika Hosová; Linda Patia Spear
Journal:  Alcohol Clin Exp Res       Date:  2017-02-14       Impact factor: 3.455

3.  Effects of chronic intermittent ethanol exposure and withdrawal on neuroblastoma cell transcriptome.

Authors:  Jeanette N McClintick; Kriti Thapa; Yunlong Liu; Xiaoling Xuei; Howard J Edenberg
Journal:  Alcohol       Date:  2020-01-07       Impact factor: 2.405

Review 4.  How Imaging Glutamate, γ-Aminobutyric Acid, and Dopamine Can Inform the Clinical Treatment of Alcohol Dependence and Withdrawal.

Authors:  Ansel T Hillmer; Graeme F Mason; Lisa M Fucito; Stephanie S O'Malley; Kelly P Cosgrove
Journal:  Alcohol Clin Exp Res       Date:  2015-10-28       Impact factor: 3.455

5.  Alcohol-preferring P rats emit spontaneous 22-28 kHz ultrasonic vocalizations that are altered by acute and chronic alcohol experience.

Authors:  James M Reno; Neha Thakore; Rueben Gonzales; Timothy Schallert; Richard L Bell; W Todd Maddox; Christine L Duvauchelle
Journal:  Alcohol Clin Exp Res       Date:  2015-04-01       Impact factor: 3.455

6.  Reduction of alcohol drinking of alcohol-preferring (P) and high-alcohol drinking (HAD1) rats by targeting phosphodiesterase-4 (PDE4).

Authors:  Kelle M Franklin; Sheketha R Hauser; Amy W Lasek; Jeanette McClintick; Zheng-Ming Ding; William J McBride; Richard L Bell
Journal:  Psychopharmacology (Berl)       Date:  2015-01-15       Impact factor: 4.530

7.  Alcohol-naïve USVs distinguish male HAD-1 from LAD-1 rat strains.

Authors:  Nitish Mittal; Neha Thakore; James M Reno; Richard L Bell; W Todd Maddox; Timothy Schallert; Christine L Duvauchelle
Journal:  Alcohol       Date:  2017-09-14       Impact factor: 2.405

Review 8.  A Genetic Animal Model of Alcoholism for Screening Medications to Treat Addiction.

Authors:  R L Bell; S Hauser; Z A Rodd; T Liang; Y Sari; J McClintick; S Rahman; E A Engleman
Journal:  Int Rev Neurobiol       Date:  2016-03-21       Impact factor: 3.230

9.  Pharmacologically Counteracting a Phenotypic Difference in Cerebellar GABAA Receptor Response to Alcohol Prevents Excessive Alcohol Consumption in a High Alcohol-Consuming Rodent Genotype.

Authors:  Josh Steven Kaplan; Michelle A Nipper; Ben D Richardson; Jeremiah Jensen; Melinda Helms; Deborah Ann Finn; David James Rossi
Journal:  J Neurosci       Date:  2016-08-31       Impact factor: 6.167

10.  Homer2 within the nucleus accumbens core bidirectionally regulates alcohol intake by both P and Wistar rats.

Authors:  Arshad Haider; Nicholas C Woodward; Kevin D Lominac; Arianne D Sacramento; Matthias Klugmann; Richard L Bell; Karen K Szumlinski
Journal:  Alcohol       Date:  2015-07-21       Impact factor: 2.405

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