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Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei
The experience of social stress during adolescence is associated with higher vulnerability to drug use. Increases in the acquisition of cocaine self-administration, in the escalation of cocaine-seeking behavior, and in the conditioned rewarding effects of cocaine have been observed in rodents expose...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203396/ https://www.ncbi.nlm.nih.gov/pubmed/30365534 http://dx.doi.org/10.1371/journal.pone.0206421 |
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author | Rodríguez-Arias, Marta Montagud-Romero, Sandra Guardia Carrión, Ana María Ferrer-Pérez, Carmen Pérez-Villalba, Ana Marco, Eva López Gallardo, Meritxell Viveros, María-Paz Miñarro, José |
author_facet | Rodríguez-Arias, Marta Montagud-Romero, Sandra Guardia Carrión, Ana María Ferrer-Pérez, Carmen Pérez-Villalba, Ana Marco, Eva López Gallardo, Meritxell Viveros, María-Paz Miñarro, José |
author_sort | Rodríguez-Arias, Marta |
collection | PubMed |
description | The experience of social stress during adolescence is associated with higher vulnerability to drug use. Increases in the acquisition of cocaine self-administration, in the escalation of cocaine-seeking behavior, and in the conditioned rewarding effects of cocaine have been observed in rodents exposed to repeated social defeat (RSD). In addition, prolonged or severe stress induces a proinflammatory state with microglial activation and increased cytokine production. The aim of the present work was to describe the long-term effects induced by RSD during adolescence on the neuroinflammatory response and synaptic structure by evaluating different glial and neuronal markers. In addition to an increase in the conditioned rewarding effects of cocaine, our results showed that RSD in adolescence produced inflammatory reactivity in microglia that is prolonged into adulthood, affecting astrocytes and neurons of two reward-processing areas of the brain (the prelimbic cortex, and the nucleus accumbens core). Considered as a whole these results suggest that social stress experience modulates vulnerability to suffer a loss of glia-supporting functions and neuronal functional synaptic density due to drug consumption in later life. |
format | Online Article Text |
id | pubmed-6203396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62033962018-11-19 Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei Rodríguez-Arias, Marta Montagud-Romero, Sandra Guardia Carrión, Ana María Ferrer-Pérez, Carmen Pérez-Villalba, Ana Marco, Eva López Gallardo, Meritxell Viveros, María-Paz Miñarro, José PLoS One Research Article The experience of social stress during adolescence is associated with higher vulnerability to drug use. Increases in the acquisition of cocaine self-administration, in the escalation of cocaine-seeking behavior, and in the conditioned rewarding effects of cocaine have been observed in rodents exposed to repeated social defeat (RSD). In addition, prolonged or severe stress induces a proinflammatory state with microglial activation and increased cytokine production. The aim of the present work was to describe the long-term effects induced by RSD during adolescence on the neuroinflammatory response and synaptic structure by evaluating different glial and neuronal markers. In addition to an increase in the conditioned rewarding effects of cocaine, our results showed that RSD in adolescence produced inflammatory reactivity in microglia that is prolonged into adulthood, affecting astrocytes and neurons of two reward-processing areas of the brain (the prelimbic cortex, and the nucleus accumbens core). Considered as a whole these results suggest that social stress experience modulates vulnerability to suffer a loss of glia-supporting functions and neuronal functional synaptic density due to drug consumption in later life. Public Library of Science 2018-10-26 /pmc/articles/PMC6203396/ /pubmed/30365534 http://dx.doi.org/10.1371/journal.pone.0206421 Text en © 2018 Rodríguez-Arias 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 Rodríguez-Arias, Marta Montagud-Romero, Sandra Guardia Carrión, Ana María Ferrer-Pérez, Carmen Pérez-Villalba, Ana Marco, Eva López Gallardo, Meritxell Viveros, María-Paz Miñarro, José Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
title | Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
title_full | Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
title_fullStr | Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
title_full_unstemmed | Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
title_short | Social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
title_sort | social stress during adolescence activates long-term microglia inflammation insult in reward processing nuclei |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203396/ https://www.ncbi.nlm.nih.gov/pubmed/30365534 http://dx.doi.org/10.1371/journal.pone.0206421 |
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