Literature DB >> 11274710

Cocaine induces conditioned place preference and increases locomotor activity in male Japanese quail.

N Levens1, C K Akins.   

Abstract

The conditioned place preference (CPP) procedure is a popular method used for testing the rewarding properties of human drugs of abuse. Most CPP studies utilize mammalian models. However, avian species have better visual systems than rodent species, and because the cues that become associated with human drug-taking behavior are often visual, Aves might serve as an alternative animal model for investigating drugs of abuse. In three experiments, we examined the locomotor stimulant and rewarding effects of cocaine in adult male Japanese quail. In Experiment 1, cocaine increased locomotor activity relative to saline. In addition, behavioral sensitization was evident across repeated injections. In Experiment 2, CPP was established after six pairings of cocaine. Finally, the dopamine D(2) receptor subtype antagonist eticlopride did not attenuate acquisition of cocaine CPP in Experiment 3. Rather, subjects receiving pretreatment of eticlopride demonstrated a place preference for the cocaine-paired context. In contrast, pretreatment of eticlopride reduced cocaine-induced locomotor activity. The findings suggest that drug-reward processes may be highly conserved across species and that birds may serve as a viable model for investigating drug-reward processes especially with regard to the ability of cocaine to become associated with visual cues.

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Year:  2001        PMID: 11274710     DOI: 10.1016/s0091-3057(00)00439-1

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


  11 in total

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6.  Female Japanese quail with high levels of estradiol demonstrate cocaine-induced conditioned place preference.

Authors:  Karin E Gill; Anna R Reynolds; Mark A Prendergast; Chana K Akins
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Journal:  Pharmacol Biochem Behav       Date:  2007-10-09       Impact factor: 3.533

10.  Zebrafish reward mutants reveal novel transcripts mediating the behavioral effects of amphetamine.

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