Cargando…

Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward

It is well established that cocaine induces an increase of dendritic spines density in some brain regions. However, few studies have addressed the role of this neuroplastic changes in cocaine rewarding effects and have often led to contradictory results. So, we hypothesized that using a rigorous tim...

Descripción completa

Detalles Bibliográficos
Autores principales: Marie, Nicolas, Canestrelli, Corinne, Noble, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260254/
https://www.ncbi.nlm.nih.gov/pubmed/22272316
http://dx.doi.org/10.1371/journal.pone.0030241
_version_ 1782221469892214784
author Marie, Nicolas
Canestrelli, Corinne
Noble, Florence
author_facet Marie, Nicolas
Canestrelli, Corinne
Noble, Florence
author_sort Marie, Nicolas
collection PubMed
description It is well established that cocaine induces an increase of dendritic spines density in some brain regions. However, few studies have addressed the role of this neuroplastic changes in cocaine rewarding effects and have often led to contradictory results. So, we hypothesized that using a rigorous time- and subject-matched protocol would demonstrate the role of this spine increase in cocaine reward. We designed our experiments such as the same animals (rats) were used for spine analysis and behavioral studies. Cocaine rewarding effects were assessed with the conditioned place preference paradigm. Spines densities were measured in the two subdivisions of the nucleus accumbens (NAcc), core and shell. We showed a correlation between the increase of spine density in NAcc core and shell and cocaine rewarding effects. Interestingly, when cocaine was administered in home cages, spine density was increase in NAcc core only. With anisomycin, a protein synthesis inhibitor, injected in the core we blocked spine increase in core and shell and also cocaine rewarding effects. Strikingly, whereas injection of this inhibitor in the shell immediately after conditioning had no effect on neuroplasticity or behavior, its injection 4 hours after conditioning was able to block neuroplasticity in shell only and cocaine-induced place preference. Thus, it clearly appears that the neuronal plasticity in the NAcc core is essential to induce plasticity in the shell, necessary for cocaine reward. Altogether, our data revealed a new mechanism in the NAcc functioning where a neuroplasticity transfer occurred from core to shell.
format Online
Article
Text
id pubmed-3260254
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32602542012-01-23 Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward Marie, Nicolas Canestrelli, Corinne Noble, Florence PLoS One Research Article It is well established that cocaine induces an increase of dendritic spines density in some brain regions. However, few studies have addressed the role of this neuroplastic changes in cocaine rewarding effects and have often led to contradictory results. So, we hypothesized that using a rigorous time- and subject-matched protocol would demonstrate the role of this spine increase in cocaine reward. We designed our experiments such as the same animals (rats) were used for spine analysis and behavioral studies. Cocaine rewarding effects were assessed with the conditioned place preference paradigm. Spines densities were measured in the two subdivisions of the nucleus accumbens (NAcc), core and shell. We showed a correlation between the increase of spine density in NAcc core and shell and cocaine rewarding effects. Interestingly, when cocaine was administered in home cages, spine density was increase in NAcc core only. With anisomycin, a protein synthesis inhibitor, injected in the core we blocked spine increase in core and shell and also cocaine rewarding effects. Strikingly, whereas injection of this inhibitor in the shell immediately after conditioning had no effect on neuroplasticity or behavior, its injection 4 hours after conditioning was able to block neuroplasticity in shell only and cocaine-induced place preference. Thus, it clearly appears that the neuronal plasticity in the NAcc core is essential to induce plasticity in the shell, necessary for cocaine reward. Altogether, our data revealed a new mechanism in the NAcc functioning where a neuroplasticity transfer occurred from core to shell. Public Library of Science 2012-01-17 /pmc/articles/PMC3260254/ /pubmed/22272316 http://dx.doi.org/10.1371/journal.pone.0030241 Text en Marie et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Marie, Nicolas
Canestrelli, Corinne
Noble, Florence
Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward
title Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward
title_full Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward
title_fullStr Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward
title_full_unstemmed Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward
title_short Transfer of Neuroplasticity from Nucleus Accumbens Core to Shell Is Required for Cocaine Reward
title_sort transfer of neuroplasticity from nucleus accumbens core to shell is required for cocaine reward
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260254/
https://www.ncbi.nlm.nih.gov/pubmed/22272316
http://dx.doi.org/10.1371/journal.pone.0030241
work_keys_str_mv AT marienicolas transferofneuroplasticityfromnucleusaccumbenscoretoshellisrequiredforcocainereward
AT canestrellicorinne transferofneuroplasticityfromnucleusaccumbenscoretoshellisrequiredforcocainereward
AT nobleflorence transferofneuroplasticityfromnucleusaccumbenscoretoshellisrequiredforcocainereward