Literature DB >> 3659102

Chronic ethanol tolerance through free-choice drinking in the P line of alcohol-preferring rats.

G J Gatto1, J M Murphy, M B Waller, W J McBride, L Lumeng, T K Li.   

Abstract

The objective of this study was to determine if the selectively bred P line of alcohol-preferring rats would develop behavioral (neuronal) tolerance with free-choice drinking of ethanol. Adult, male P rats were divided into four groups. One group (FCE) received food, water and a 10% (v/v) ethanol solution ad lib, while the control group (C) had only food and water. The other two groups received either a liquid diet containing 5% (v/v) ethanol (LDE) or a control liquid diet (LDC). All groups were kept on their respective feeding regimens for 14 days. The mean (+/- SEM) ethanol intakes for the FCE and LDE groups were 6.8 +/- 0.5 and 9.9 +/- 0.4 g ethanol/kg body wt./day, respectively. A shock-motivated jumping task was used to test for tolerance. Each rat received an IP injection of 2.5 g ethanol/kg and was tested every 15 minutes for recovery to a criterion of 75% of the performance level achieved with training. All rats were tested twice, once on the day before beginning their feeding regimens (day 0) and again 14 days later. Tolerance was assessed from differences in time of recovery to criterion performance and in blood alcohol concentrations (BACs) at recovery on day 0 vs. day 14. The mean recovery times for the C, FCE, LDC, and LDE groups on day 0 were 177 +/- 6, 170 +/- 6, 143 +/- 10 and 153 +/- 13 minutes, respectively, and the BACs were 219 +/- 6, 222 +/- 5, 220 +/- 19 and 214 +/- 6 mg%, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1987        PMID: 3659102     DOI: 10.1016/0091-3057(87)90021-9

Source DB:  PubMed          Journal:  Pharmacol Biochem Behav        ISSN: 0091-3057            Impact factor:   3.533


  22 in total

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

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Review 3.  A Genetic Animal Model of Alcoholism for Screening Medications to Treat Addiction.

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Review 4.  Rat animal models for screening medications to treat alcohol use disorders.

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5.  The benzodiazepine inverse agonist RO19-4603 exerts prolonged and selective suppression of ethanol intake in alcohol-preferring (P) rats.

Authors:  H L June; J M Murphy; J J Mellor-Burke; L Lumeng; T K Li
Journal:  Psychopharmacology (Berl)       Date:  1994-07       Impact factor: 4.530

6.  Early ethanol and water consumption: accumulating experience differentially regulates drinking pattern and bout parameters in male alcohol preferring (P) vs. Wistar and Sprague Dawley rats.

Authors:  Alexey V Azarov; Donald J Woodward
Journal:  Physiol Behav       Date:  2013-10-02

7.  Early ethanol and water intake: choice mechanism and total fluid regulation operate in parallel in male alcohol preferring (P) and both Wistar and Sprague Dawley rats.

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8.  Differences in the hypothermic response to ethanol in rats selectively bred for oral ethanol preference and nonpreference.

Authors:  R B Stewart; D L Kurtz; M Zweifel; T K Li; J C Froehlich
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

Review 9.  Animal models for medications development targeting alcohol abuse using selectively bred rat lines: neurobiological and pharmacological validity.

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10.  Sex and age differences in heavy binge drinking and its effects on alcohol responsivity following abstinence.

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Journal:  Pharmacol Biochem Behav       Date:  2013-01-16       Impact factor: 3.533

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