Literature DB >> 27083122

The role of dose and restriction state on morphine-, cocaine-, and LiCl-induced suppression of saccharin intake: A comprehensive analysis.

Robert C Twining1, Christopher S Freet2, Robert A Wheeler1, Christian G Reich1, Dennie A Tompers1, Sarah E Wolpert1, Patricia S Grigson1.   

Abstract

Rats avoid intake of a taste cue when paired with a drug of abuse or with the illness-inducing agent, lithium chloride (LiCl). Although progress has been made, it is difficult to compare the suppressive effects of abused agents and LiCl on intake of a gustatory conditioned stimulus (CS) because of the cross-laboratory use of different CSs, different unconditioned stimuli (USs), and different doses of the drugs, different conditioning regimens, and different restriction states. Here we have attempted to unify these variables by comparing the suppressive effects of a range of doses of morphine, cocaine, and LiCl on intake of a saccharin CS using a common regimen in non-restricted, food restricted, or water restricted male Sprague-Dawley rats. The results showed that, while the putatively aversive agent, LiCl, was effective in suppressing intake of the taste cue across nearly all doses, regardless of restriction state, the suppressive effects of both morphine and cocaine were greatly reduced when evaluated in either food or water restricted rats. Greater sensitivity to drug was revealed, at very low doses, when testing occurred in the absence of need (i.e., when the rats were non-restricted). Together, these results provide the first uniform and comprehensive analysis of the suppressive effects of morphine, cocaine, and LiCl as a function of dose and restriction state. In the present case, the suppressive effects of morphine and cocaine are found to differ from those of LiCl and, in some respects, from one another as well.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Conditioned taste aversion; Contrast; Drugs of abuse; Natural rewards; Reward comparison

Mesh:

Substances:

Year:  2016        PMID: 27083122      PMCID: PMC4867279          DOI: 10.1016/j.physbeh.2016.03.037

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  66 in total

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Journal:  Behav Neurosci       Date:  1991-12       Impact factor: 1.912

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Journal:  Brain Res       Date:  2000-04-28       Impact factor: 3.252

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Authors:  C M Ferrari; D A O'Connor; A L Riley
Journal:  Pharmacol Biochem Behav       Date:  1991-02       Impact factor: 3.533

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Journal:  Psychopharmacologia       Date:  1973

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Authors:  P S Grigson; K Cornelius; D S Wheeler
Journal:  Pharmacol Biochem Behav       Date:  2001 May-Jun       Impact factor: 3.533

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Journal:  Pharmacol Biochem Behav       Date:  1978-06       Impact factor: 3.533

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Authors:  M Nachman; D Lester; J Le Magnen
Journal:  Science       Date:  1970-06-05       Impact factor: 47.728

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Journal:  Pharmacol Biochem Behav       Date:  1986-04       Impact factor: 3.533

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Journal:  Brain Res       Date:  1978-03-24       Impact factor: 3.252

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  3 in total

1.  Female rats exhibit less avoidance than male rats of a cocaine-, but not a morphine-paired, saccharin cue.

Authors:  Christopher B Jenney; Jinju Dasalla; Patricia S Grigson
Journal:  Brain Res Bull       Date:  2017-09-09       Impact factor: 4.077

2.  Short-term memory reactivation of a weak CS-US association promotes long-term memory persistence in conditioned odor aversion.

Authors:  Jorge Tovar-Díaz; Jean-Pascal Morín; Jorge Eduardo Ríos-Carrillo; Hilda Sánchez de Jesús; Gabriel Roldán-Roldán
Journal:  Learn Mem       Date:  2021-04-15       Impact factor: 2.460

3.  Glucagon-like peptide-1 receptor agonist, exendin-4, reduces reinstatement of heroin-seeking behavior in rats.

Authors:  Joaquin E Douton; Corinne Augusto; Brooke Stoltzfus; Nurgul Carkaci-Salli; Kent E Vrana; Patricia S Grigson
Journal:  Behav Pharmacol       Date:  2021-06-01       Impact factor: 2.293

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