Literature DB >> 1599629

Ethanol tolerance developed during intoxicated operant performance in rats prevents subsequent ethanol-induced conditioned taste aversion.

D V Gauvin1, F A Holloway.   

Abstract

Four groups of Sprague-Dawley rats (n = 10 per group) were trained in a two-phase conditioning experiment. All rats were initially trained in an FR30 operant task (phase 1), and subsequently trained in a conditioned taste aversion (CTA) task. The groups of rats differed in their ETOH exposure. All rats received 2-week chronic exposure in phase 1. Two groups received chronic presession ETOH and, therefore, the opportunity for intoxicated practice; another group, yoked to this latter group, received postsession ETOH; the final group received presession saline injections. The presession ETOH groups were conditioned in the CTA task with either ETOH or saline; both increased their intakes of the conditioned tastant. The presession saline and the postsession ETOH groups received ETOH CTA; both developed a robust CTA. Thus, prior history of intoxicated practice under the operant task prevented the development of ETOH-induced CTA. We argue that ETOH exposure may be a necessary but not sufficient condition for tolerance to develop to the aversive attributes of ETOH.

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Year:  1992        PMID: 1599629     DOI: 10.1016/0741-8329(92)90029-a

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


  3 in total

Review 1.  Increases in ethanol ingestion by young rats following interaction with intoxicated siblings: a review.

Authors:  P S Hunt; R A Hallmark
Journal:  Integr Physiol Behav Sci       Date:  2001 Jul-Sep

2.  Tolerance to ethanol's effects on operant performance in rats: role of number and pattern of intoxicated practice opportunities.

Authors:  F A Holloway; R C Michaelis; R D Harland; J R Criado; D V Gauvin
Journal:  Psychopharmacology (Berl)       Date:  1992       Impact factor: 4.530

3.  Gender differences in ethanol preference and ingestion in rats. The role of the gonadal steroid environment.

Authors:  O F Almeida; M Shoaib; J Deicke; D Fischer; M H Darwish; V K Patchev
Journal:  J Clin Invest       Date:  1998-06-15       Impact factor: 14.808

  3 in total

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