Literature DB >> 15528008

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

Richard L Bell1, Zachary A Rodd, Cathleen C Hsu, Lawrence Lumeng, Ting-Kai Li, James M Murphy, William J McBride.   

Abstract

The objectives of the current study were to assess the effects of access to different concentrations of ethanol and sex of the animal on ethanol consumption of high-alcohol-drinking (HAD-1 and HAD-2) rats during adolescence [postnatal days (PNDs) 30 through 60]. At the beginning of adolescence (PND 30), the rats were given concurrent access to either a single concentration [15% volume/volume (vol./vol.)] or multiple concentrations [10%, 20%, and 30% (vol./vol.)] of ethanol and water. Analyses of ethanol consumption data revealed significant (P < .025) main effects of line, ethanol condition, and week, and a significant line by sex by ethanol condition by week interaction. For the first week, both male and female HAD-1 and HAD-2 rats 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 primarily in male and female HAD-1 rats and to a lesser degree in female HAD-2 rats. In general, female rats consumed more fluids than consumed by male rats, and male rats displayed a higher preference for ethanol over water ratio than observed for their female counterparts. In addition, in comparison with HAD-2 rats, HAD-1 rats drank more ethanol and displayed a higher preference for ethanol ratio. Overall, the current study results indicate that, compared with access to a single concentration (which is used in most studies), concurrent access to multiple concentrations of ethanol produced significantly higher ethanol intakes in periadolescent HAD rats, supporting the suggestion that this ethanol drinking condition would have a greater impact on neuronal development. In addition, although the replicate lines were selectively bred by using the same criteria and foundation stock, the higher ethanol intakes of the HAD-1 line, compared with intakes for the HAD-2 line, seen in the current study support the suggestion that there are some differences in their genetic make-up, affecting ethanol intake, which are expressed during periadolescence.

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Year:  2004        PMID: 15528008     DOI: 10.1016/j.alcohol.2004.06.001

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


  20 in total

1.  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

Review 2.  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

3.  Chronic alcohol drinking alters neuronal dendritic spines in the brain reward center nucleus accumbens.

Authors:  Feng C Zhou; Bruce Anthony; Kenneth W Dunn; W Brent Lindquist; Zao C Xu; Ping Deng
Journal:  Brain Res       Date:  2007-01-02       Impact factor: 3.252

4.  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

5.  Effect of sex on ethanol consumption and conditioned taste aversion in adolescent and adult rats.

Authors:  Nicole L Schramm-Sapyta; Reynold Francis; Andrea MacDonald; Colby Keistler; Lauren O'Neill; Cynthia M Kuhn
Journal:  Psychopharmacology (Berl)       Date:  2013-10-26       Impact factor: 4.530

6.  Nicotinic receptor ligands reduce ethanol intake by high alcohol-drinking HAD-2 rats.

Authors:  Richard L Bell; Bill J A Eiler; Jason B Cook; Shafiqur Rahman
Journal:  Alcohol       Date:  2009-12       Impact factor: 2.405

Review 7.  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

8.  Effects of short deprivation and re-exposure intervals on the ethanol drinking behavior of selectively bred high alcohol-consuming rats.

Authors:  Richard L Bell; Zachary A Rodd; Jonathon A Schultz; Caron L Peper; Lawrence Lumeng; James M Murphy; William J McBride
Journal:  Alcohol       Date:  2008-05-16       Impact factor: 2.405

9.  Alcohol enhances unprovoked 22-28 kHz USVs and suppresses USV mean frequency in High Alcohol Drinking (HAD-1) male rats.

Authors:  Neha Thakore; James M Reno; Rueben A Gonzales; Timothy Schallert; Richard L Bell; W Todd Maddox; Christine L Duvauchelle
Journal:  Behav Brain Res       Date:  2016-01-21       Impact factor: 3.332

10.  Differential effects of chronic ethanol consumption and withdrawal on homer/glutamate receptor expression in subregions of the accumbens and amygdala of P rats.

Authors:  Ilona Obara; Richard L Bell; Scott P Goulding; Cindy M Reyes; Lindsay A Larson; Alexis W Ary; William A Truitt; Karen K Szumlinski
Journal:  Alcohol Clin Exp Res       Date:  2009-08-10       Impact factor: 3.455

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