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Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience

Large preclinical evidence shows that exposure to social defeat (SD) increases vulnerability to drug abuse, increasing the consumption of ethanol. However, not all subjects are equally affected by the changes induced by stress. Previous reports have evidenced that the resilient phenotype to depressi...

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Autores principales: Reguilón, Marina D., Ferrer-Pérez, Carmen, Manzanedo, Carmen, Miñarro, José, Rodríguez-Arias, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591477/
https://www.ncbi.nlm.nih.gov/pubmed/34815986
http://dx.doi.org/10.1016/j.ynstr.2021.100413
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author Reguilón, Marina D.
Ferrer-Pérez, Carmen
Manzanedo, Carmen
Miñarro, José
Rodríguez-Arias, Marta
author_facet Reguilón, Marina D.
Ferrer-Pérez, Carmen
Manzanedo, Carmen
Miñarro, José
Rodríguez-Arias, Marta
author_sort Reguilón, Marina D.
collection PubMed
description Large preclinical evidence shows that exposure to social defeat (SD) increases vulnerability to drug abuse, increasing the consumption of ethanol. However, not all subjects are equally affected by the changes induced by stress. Previous reports have evidenced that the resilient phenotype to depressive-like behaviors after SD is associated with the resistant phenotype to cocaine-increased rewarding effects and the smaller neuroinflammatory response. The aim of the present study was to further clarify whether the resilient profile to depressive-like behavior also predicts a protection against the increase in ethanol intake induced by SD. The neuroinflammatory profile was studied after the end of the oral ethanol self-administration (SA) procedure, measuring levels of the pro-inflammatory cytokine IL-6 and the chemokine CX3CL1 or fractalkine in the striatum and prefrontal cortex. Previous studies have shown that environmental enrichment (EE) is an effective mechanism to dimish the detrimental effects of social stress. In a second study, we aimed to evaluate if EE housing before exposure to SD could potentiate resilience. Our results showed that mice with a phenotype susceptible to SD-induced depressive-like behaviors showed increased ethanol consumption and increased neuroinflammatory signaling. In contrast, despite the lack of effect on depressive-like behaviors, defeated mice previously housed under EE conditions did not show an increase in ethanol SA or an increase in immune response. To sum up, the resilient phenotype to SD develops at different levels, such as depressive-like behaviors, ethanol consumption and the neuroinflammatory response. Our results also point to the protective role of EE in potentiating resilience to SD effects.
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spelling pubmed-85914772021-11-22 Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience Reguilón, Marina D. Ferrer-Pérez, Carmen Manzanedo, Carmen Miñarro, José Rodríguez-Arias, Marta Neurobiol Stress Original Research Article Large preclinical evidence shows that exposure to social defeat (SD) increases vulnerability to drug abuse, increasing the consumption of ethanol. However, not all subjects are equally affected by the changes induced by stress. Previous reports have evidenced that the resilient phenotype to depressive-like behaviors after SD is associated with the resistant phenotype to cocaine-increased rewarding effects and the smaller neuroinflammatory response. The aim of the present study was to further clarify whether the resilient profile to depressive-like behavior also predicts a protection against the increase in ethanol intake induced by SD. The neuroinflammatory profile was studied after the end of the oral ethanol self-administration (SA) procedure, measuring levels of the pro-inflammatory cytokine IL-6 and the chemokine CX3CL1 or fractalkine in the striatum and prefrontal cortex. Previous studies have shown that environmental enrichment (EE) is an effective mechanism to dimish the detrimental effects of social stress. In a second study, we aimed to evaluate if EE housing before exposure to SD could potentiate resilience. Our results showed that mice with a phenotype susceptible to SD-induced depressive-like behaviors showed increased ethanol consumption and increased neuroinflammatory signaling. In contrast, despite the lack of effect on depressive-like behaviors, defeated mice previously housed under EE conditions did not show an increase in ethanol SA or an increase in immune response. To sum up, the resilient phenotype to SD develops at different levels, such as depressive-like behaviors, ethanol consumption and the neuroinflammatory response. Our results also point to the protective role of EE in potentiating resilience to SD effects. Elsevier 2021-11-03 /pmc/articles/PMC8591477/ /pubmed/34815986 http://dx.doi.org/10.1016/j.ynstr.2021.100413 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Reguilón, Marina D.
Ferrer-Pérez, Carmen
Manzanedo, Carmen
Miñarro, José
Rodríguez-Arias, Marta
Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience
title Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience
title_full Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience
title_fullStr Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience
title_full_unstemmed Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience
title_short Ethanol intake in male mice exposed to social defeat: Environmental enrichment potentiates resilience
title_sort ethanol intake in male mice exposed to social defeat: environmental enrichment potentiates resilience
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591477/
https://www.ncbi.nlm.nih.gov/pubmed/34815986
http://dx.doi.org/10.1016/j.ynstr.2021.100413
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