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Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice
The recreational drugs, alcohol and 3,4-Methylenedioxymethamphetamine (MDMA, “Ecstasy”) have both been shown to cause immune activation in vivo, and they are linked to cognitive impairment and anxiety-like behaviors in rodents. The neuronal effects of these drugs in the hippocampal area, an area tha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643963/ https://www.ncbi.nlm.nih.gov/pubmed/26566284 http://dx.doi.org/10.1371/journal.pone.0142978 |
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author | Johansson, Emily M. García-Gutiérrez, María S. Moscoso-Castro, María Manzanares, Jorge Valverde, Olga |
author_facet | Johansson, Emily M. García-Gutiérrez, María S. Moscoso-Castro, María Manzanares, Jorge Valverde, Olga |
author_sort | Johansson, Emily M. |
collection | PubMed |
description | The recreational drugs, alcohol and 3,4-Methylenedioxymethamphetamine (MDMA, “Ecstasy”) have both been shown to cause immune activation in vivo, and they are linked to cognitive impairment and anxiety-like behaviors in rodents. The neuronal effects of these drugs in the hippocampal area, an area that has been a focus of studies aiming to explain the mechanisms underlying anxiety related-disorders, remains poorly understood. Therefore we investigated the specific inflammatory impact of alcohol and MDMA on this area of the brain and on a hippocampal-related behavioral task. We centered our study on two inflammatory factors linked to anxiety-related disorders, namely Interleukin-1β (IL-1β) and brain-derived neurotrophic factor (BDNF). We subjected drug-consuming mice to a battery of behavioral tests to evaluate general activity, anxiety-like and depressive-live behaviors. We then introduced them to a contextual fear discrimination task and immune-related effects were examined by immunohistochemical and biochemical studies. Our results suggest that there is a relationship between the induction of immune activated pathways by voluntary alcohol consumption and a high-dose MDMA. Furthermore, the ability of mice to perform a contextual fear discrimination task was impaired by drug consumption and we report long term inflammatory alterations in the hippocampus even several weeks after drug intake. This information will be helpful for discovering new selective drug targets, and to develop treatments and preventive approaches for patients with anxiety-related disorders. |
format | Online Article Text |
id | pubmed-4643963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46439632015-11-18 Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice Johansson, Emily M. García-Gutiérrez, María S. Moscoso-Castro, María Manzanares, Jorge Valverde, Olga PLoS One Research Article The recreational drugs, alcohol and 3,4-Methylenedioxymethamphetamine (MDMA, “Ecstasy”) have both been shown to cause immune activation in vivo, and they are linked to cognitive impairment and anxiety-like behaviors in rodents. The neuronal effects of these drugs in the hippocampal area, an area that has been a focus of studies aiming to explain the mechanisms underlying anxiety related-disorders, remains poorly understood. Therefore we investigated the specific inflammatory impact of alcohol and MDMA on this area of the brain and on a hippocampal-related behavioral task. We centered our study on two inflammatory factors linked to anxiety-related disorders, namely Interleukin-1β (IL-1β) and brain-derived neurotrophic factor (BDNF). We subjected drug-consuming mice to a battery of behavioral tests to evaluate general activity, anxiety-like and depressive-live behaviors. We then introduced them to a contextual fear discrimination task and immune-related effects were examined by immunohistochemical and biochemical studies. Our results suggest that there is a relationship between the induction of immune activated pathways by voluntary alcohol consumption and a high-dose MDMA. Furthermore, the ability of mice to perform a contextual fear discrimination task was impaired by drug consumption and we report long term inflammatory alterations in the hippocampus even several weeks after drug intake. This information will be helpful for discovering new selective drug targets, and to develop treatments and preventive approaches for patients with anxiety-related disorders. Public Library of Science 2015-11-13 /pmc/articles/PMC4643963/ /pubmed/26566284 http://dx.doi.org/10.1371/journal.pone.0142978 Text en © 2015 Johansson 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 Johansson, Emily M. García-Gutiérrez, María S. Moscoso-Castro, María Manzanares, Jorge Valverde, Olga Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice |
title | Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice |
title_full | Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice |
title_fullStr | Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice |
title_full_unstemmed | Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice |
title_short | Reduced Contextual Discrimination following Alcohol Consumption or MDMA Administration in Mice |
title_sort | reduced contextual discrimination following alcohol consumption or mdma administration in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643963/ https://www.ncbi.nlm.nih.gov/pubmed/26566284 http://dx.doi.org/10.1371/journal.pone.0142978 |
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