Literature DB >> 12798969

Effects of concurrent access to a single concentration or multiple concentrations of ethanol on the intake of ethanol by male and female periadolescent alcohol-preferring (P) rats.

Richard L Bell1, Zachary A Rodd-Henricks, Kelly A Kuc, Lawrence Lumeng, Ting Kai Li, James M Murphy, William J McBride.   

Abstract

The objectives of this study were to assess the effects of access to different concentrations of ethanol and sex of the animal on ethanol consumption during periadolescence [postnatal days (PNDs) 30-60] in alcohol-preferring (P) rats. On PND 28, female and male P pups were single housed in hanging stainless steel cages with ad libitum access to water and food. Beginning on PND 30, the rats were also given access to either a single concentration [15% volume/volume (vol./vol.)] or multiple concentrations [10%, 20%, and 30% (vol./vol.)] of ethanol. Differences between sex (male vs. female) and ethanol conditions (single concentration vs. multiple concentrations), for the average amount of ethanol consumed for each week (starting on PND 33) of access, were examined. Analyses of the data for ethanol drinking revealed significant (P<.025) main effects of week and ethanol condition, as well as a significant weekxethanol condition interaction. For the first week, both male and female P pups consumed more ethanol under the multiple-ethanol-concentration condition than under the single-ethanol-concentration condition. However, across the second through fourth weeks, this pattern was seen only in female P pups. When preference for one concentration of ethanol over the other concentrations was assessed, it was found that male P pups tended to choose the 30% concentration over the 10% and 20% concentrations, whereas female P pups did not display a preference. The findings of this study corroborate previous work indicating that periadolescent P rats readily acquire high-ethanol-drinking behavior and that, similar to adult P rats, concurrent access to multiple concentrations of ethanol further enhances ethanol intake. These findings suggest to us that innate genetically influenced mechanisms promoting high ethanol intake are present at this stage of development.

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Year:  2003        PMID: 12798969     DOI: 10.1016/s0741-8329(03)00022-3

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


  19 in total

1.  Reinforcing properties and neurochemical response of ethanol within the posterior ventral tegmental area are enhanced in adulthood by periadolescent ethanol consumption.

Authors:  Jamie E Toalston; Gerald A Deehan; Sheketha R Hauser; Eric A Engleman; Richard L Bell; James M Murphy; William A Truitt; William J McBride; Zachary A Rodd
Journal:  J Pharmacol Exp Ther       Date:  2014-08-22       Impact factor: 4.030

2.  Long-term risk preference and suboptimal decision making following adolescent alcohol use.

Authors:  Nicholas A Nasrallah; Tom W H Yang; Ilene L Bernstein
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-21       Impact factor: 11.205

3.  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

4.  Varenicline Reduces Alcohol Intake During Repeated Cycles of Alcohol Reaccess Following Deprivation in Alcohol-Preferring (P) Rats.

Authors:  Janice C Froehlich; Emily R Nicholson; Julian E Dilley; Nick J Filosa; Logan C Rademacher; Teal N Smith
Journal:  Alcohol Clin Exp Res       Date:  2017-07-10       Impact factor: 3.455

Review 5.  Rat animal models for screening medications to treat alcohol use disorders.

Authors:  Richard L Bell; Sheketha R Hauser; Tiebing Liang; Youssef Sari; Antoniette Maldonado-Devincci; Zachary A Rodd
Journal:  Neuropharmacology       Date:  2017-02-16       Impact factor: 5.250

6.  Modeling binge-like ethanol drinking by peri-adolescent and adult P rats.

Authors:  Richard L Bell; Zachary A Rodd; Rebecca J Smith; Jamie E Toalston; Kelle M Franklin; William J McBride
Journal:  Pharmacol Biochem Behav       Date:  2011-07-29       Impact factor: 3.533

7.  The reinforcing properties of ethanol are quantitatively enhanced in adulthood by peri-adolescent ethanol, but not saccharin, consumption in female alcohol-preferring (P) rats.

Authors:  Jamie E Toalston; Gerald A Deehan; Sheketha R Hauser; Eric A Engleman; Richard L Bell; James M Murphy; William J McBride; Zachary A Rodd
Journal:  Alcohol       Date:  2015-05-22       Impact factor: 2.405

Review 8.  The emergence of gonadal hormone influences on dopaminergic function during puberty.

Authors:  Cynthia Kuhn; Misha Johnson; Alex Thomae; Brooke Luo; Sidney A Simon; Guiying Zhou; Q David Walker
Journal:  Horm Behav       Date:  2009-11-10       Impact factor: 3.587

Review 9.  Scheduled access alcohol drinking by alcohol-preferring (P) and high-alcohol-drinking (HAD) rats: modeling adolescent and adult binge-like drinking.

Authors:  Richard L Bell; Zachary A Rodd; Eric A Engleman; Jamie E Toalston; William J McBride
Journal:  Alcohol       Date:  2013-10-31       Impact factor: 2.405

10.  Effects of ceftriaxone on ethanol, nicotine or sucrose intake by alcohol-preferring (P) rats and its association with GLT-1 expression.

Authors:  Youssef Sari; Jamie E Toalston; P S S Rao; Richard L Bell
Journal:  Neuroscience       Date:  2016-04-07       Impact factor: 3.590

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