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Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running

BACKGROUND: Rats lever-press for access to running wheels suggesting that wheel running by itself is reinforcing. Furthermore, pairings of an episode of wheel running and subsequent confinement in a specific environment can establish a conditioned place preference (CPP). This finding implies that th...

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Autores principales: Trost, Alexandra, Hauber, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239394/
https://www.ncbi.nlm.nih.gov/pubmed/25407014
http://dx.doi.org/10.1186/s12868-014-0124-4
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author Trost, Alexandra
Hauber, Wolfgang
author_facet Trost, Alexandra
Hauber, Wolfgang
author_sort Trost, Alexandra
collection PubMed
description BACKGROUND: Rats lever-press for access to running wheels suggesting that wheel running by itself is reinforcing. Furthermore, pairings of an episode of wheel running and subsequent confinement in a specific environment can establish a conditioned place preference (CPP). This finding implies that the reinforcing effects of wheel running outlast the actual occurrence of physical activity, a phenomenon referred to as aftereffect of wheel running. Aftereffect-induced CPP involves Pavlovian conditioning, i.e. repeated pairings of the aftereffect of wheel running with a specific environment creates a learned association between aftereffect and environment and, in turn, a preference for that environment. Given the involvement of dopamine systems in mediating effects of Pavlovian stimuli on appetitive behavior, a role of dopamine in mediating aftereffect-induced CPP seems plausible. Here we assessed whether the mixed D1/D2 receptor antagonist flupenthixol (0.25 mg/kg, i.p.) can block the expression of an aftereffect-induced CPP. RESULTS: In line with earlier studies, our results demonstrate that rats displayed a conditioned preference for environments paired with the aftereffect of wheel running and further show that the magnitude of CPP was not related to the wheel running rate. Furthermore, we found that flupenthixol (0.25 mg/kg, i.p.) reduced locomotor activity but did not attenuate the expression of an aftereffect-induced CPP. CONCLUSION: The expression of a CPP produced by the aftereffect of wheel running seems not to depend on dopamine D1/D2 receptor activation.
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spelling pubmed-42393942014-11-21 Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running Trost, Alexandra Hauber, Wolfgang BMC Neurosci Research Article BACKGROUND: Rats lever-press for access to running wheels suggesting that wheel running by itself is reinforcing. Furthermore, pairings of an episode of wheel running and subsequent confinement in a specific environment can establish a conditioned place preference (CPP). This finding implies that the reinforcing effects of wheel running outlast the actual occurrence of physical activity, a phenomenon referred to as aftereffect of wheel running. Aftereffect-induced CPP involves Pavlovian conditioning, i.e. repeated pairings of the aftereffect of wheel running with a specific environment creates a learned association between aftereffect and environment and, in turn, a preference for that environment. Given the involvement of dopamine systems in mediating effects of Pavlovian stimuli on appetitive behavior, a role of dopamine in mediating aftereffect-induced CPP seems plausible. Here we assessed whether the mixed D1/D2 receptor antagonist flupenthixol (0.25 mg/kg, i.p.) can block the expression of an aftereffect-induced CPP. RESULTS: In line with earlier studies, our results demonstrate that rats displayed a conditioned preference for environments paired with the aftereffect of wheel running and further show that the magnitude of CPP was not related to the wheel running rate. Furthermore, we found that flupenthixol (0.25 mg/kg, i.p.) reduced locomotor activity but did not attenuate the expression of an aftereffect-induced CPP. CONCLUSION: The expression of a CPP produced by the aftereffect of wheel running seems not to depend on dopamine D1/D2 receptor activation. BioMed Central 2014-11-19 /pmc/articles/PMC4239394/ /pubmed/25407014 http://dx.doi.org/10.1186/s12868-014-0124-4 Text en © Trost and Hauber; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Trost, Alexandra
Hauber, Wolfgang
Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
title Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
title_full Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
title_fullStr Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
title_full_unstemmed Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
title_short Dopamine D1/D2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
title_sort dopamine d1/d2 receptors do not mediate the expression of conditioned place preference induced by the aftereffect of wheel running
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239394/
https://www.ncbi.nlm.nih.gov/pubmed/25407014
http://dx.doi.org/10.1186/s12868-014-0124-4
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