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Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice
Adverse early-life conditions induce persistent disturbances that give rise to negative emotional states. Therefore, early life stress confers increased vulnerability to substance use disorders, mainly during adolescence as the brain is still developing. In this study, we investigated the consequenc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5147915/ https://www.ncbi.nlm.nih.gov/pubmed/27936186 http://dx.doi.org/10.1371/journal.pone.0167483 |
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author | Gracia-Rubio, Irene Martinez-Laorden, Elena Moscoso-Castro, Maria Milanés, M. Victoria Laorden, M. Luisa Valverde, Olga |
author_facet | Gracia-Rubio, Irene Martinez-Laorden, Elena Moscoso-Castro, Maria Milanés, M. Victoria Laorden, M. Luisa Valverde, Olga |
author_sort | Gracia-Rubio, Irene |
collection | PubMed |
description | Adverse early-life conditions induce persistent disturbances that give rise to negative emotional states. Therefore, early life stress confers increased vulnerability to substance use disorders, mainly during adolescence as the brain is still developing. In this study, we investigated the consequences of maternal separation, a model of maternal neglect, on the psychotropic effects of cocaine and the neuroplasticity of the dopaminergic system. Our results show that mice exposed to maternal separation displayed attenuated behavioural sensitization, while no changes were found in the rewarding effects of cocaine in the conditioned place preference paradigm and in the reinforcing effects of cocaine in the self-administration paradigm. The evaluation of neuroplasticity in the striatal dopaminergic pathways revealed that mice exposed to maternal separation exhibited decreased protein expression levels of D2 receptors and increased levels of the transcriptional factor Nurr1. Furthermore, animals exposed to maternal separation and treated with cocaine exhibited increased DA turnover and protein expression levels of DAT and D2R, while decreased Nurr1 and Pitx3 protein expression levels were observed when compared with saline-treated mice. Taken together, our data demonstrate that maternal separation caused an impairment of cocaine-induced behavioural sensitization possibly due to a dysfunction of the dopaminergic system, a dysfunction that has been proposed as a factor of vulnerability for developing substance use disorders. |
format | Online Article Text |
id | pubmed-5147915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51479152016-12-28 Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice Gracia-Rubio, Irene Martinez-Laorden, Elena Moscoso-Castro, Maria Milanés, M. Victoria Laorden, M. Luisa Valverde, Olga PLoS One Research Article Adverse early-life conditions induce persistent disturbances that give rise to negative emotional states. Therefore, early life stress confers increased vulnerability to substance use disorders, mainly during adolescence as the brain is still developing. In this study, we investigated the consequences of maternal separation, a model of maternal neglect, on the psychotropic effects of cocaine and the neuroplasticity of the dopaminergic system. Our results show that mice exposed to maternal separation displayed attenuated behavioural sensitization, while no changes were found in the rewarding effects of cocaine in the conditioned place preference paradigm and in the reinforcing effects of cocaine in the self-administration paradigm. The evaluation of neuroplasticity in the striatal dopaminergic pathways revealed that mice exposed to maternal separation exhibited decreased protein expression levels of D2 receptors and increased levels of the transcriptional factor Nurr1. Furthermore, animals exposed to maternal separation and treated with cocaine exhibited increased DA turnover and protein expression levels of DAT and D2R, while decreased Nurr1 and Pitx3 protein expression levels were observed when compared with saline-treated mice. Taken together, our data demonstrate that maternal separation caused an impairment of cocaine-induced behavioural sensitization possibly due to a dysfunction of the dopaminergic system, a dysfunction that has been proposed as a factor of vulnerability for developing substance use disorders. Public Library of Science 2016-12-09 /pmc/articles/PMC5147915/ /pubmed/27936186 http://dx.doi.org/10.1371/journal.pone.0167483 Text en © 2016 Gracia-Rubio 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gracia-Rubio, Irene Martinez-Laorden, Elena Moscoso-Castro, Maria Milanés, M. Victoria Laorden, M. Luisa Valverde, Olga Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice |
title | Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice |
title_full | Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice |
title_fullStr | Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice |
title_full_unstemmed | Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice |
title_short | Maternal Separation Impairs Cocaine-Induced Behavioural Sensitization in Adolescent Mice |
title_sort | maternal separation impairs cocaine-induced behavioural sensitization in adolescent mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5147915/ https://www.ncbi.nlm.nih.gov/pubmed/27936186 http://dx.doi.org/10.1371/journal.pone.0167483 |
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