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Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol

Ethanol abuse is linked to several acute and chronic injuries that can lead to health problems. Ethanol addiction is one of the most severe diseases linked to the abuse of this drug. Symptoms of ethanol addiction include compulsive substance intake and withdrawal syndrome. Stress exposure has an imp...

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Autores principales: Morais-Silva, G., Fernandes-Santos, J., Moreira-Silva, D., Marin, M.T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681418/
https://www.ncbi.nlm.nih.gov/pubmed/26628398
http://dx.doi.org/10.1590/1414-431X20155009
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author Morais-Silva, G.
Fernandes-Santos, J.
Moreira-Silva, D.
Marin, M.T.
author_facet Morais-Silva, G.
Fernandes-Santos, J.
Moreira-Silva, D.
Marin, M.T.
author_sort Morais-Silva, G.
collection PubMed
description Ethanol abuse is linked to several acute and chronic injuries that can lead to health problems. Ethanol addiction is one of the most severe diseases linked to the abuse of this drug. Symptoms of ethanol addiction include compulsive substance intake and withdrawal syndrome. Stress exposure has an important role in addictive behavior for many drugs of abuse (including ethanol), but the consequences of stress and ethanol in the organism when these factors are concomitant results in a complex interaction. We investigated the effects of concomitant, chronic administration of ethanol and stress exposure on the withdrawal and consumption of, as well as the preference for, ethanol in mice. Male Swiss mice (30–35 g, 8-10 per group) were exposed to an ethanol liquid diet as the only source of food for 15 days. In the final 5 days, they were exposed to forced swimming stress. Twelve hours after removal of the ethanol liquid diet, animals were evaluated for ethanol withdrawal by measuring anxiety-related behaviors and locomotor activity. Twenty-four hours after evaluation of ethanol withdrawal, they were evaluated for voluntary consumption of ethanol in a “three-bottle choice” paradigm. Mice exposed to chronic consumption of ethanol had decreased locomotor activity during withdrawal. Contrary to our expectations, a concomitant forced swimming stress did not aggravate ethanol withdrawal. Nevertheless, simultaneous ethanol administration and stress exposure increased voluntary consumption of ethanol, mainly solutions containing high concentrations of ethanol. These results showed that stressful situations during ethanol intake may aggravate specific addiction-related behaviors.
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spelling pubmed-46814182015-12-28 Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol Morais-Silva, G. Fernandes-Santos, J. Moreira-Silva, D. Marin, M.T. Braz J Med Biol Res Biomedical Sciences Ethanol abuse is linked to several acute and chronic injuries that can lead to health problems. Ethanol addiction is one of the most severe diseases linked to the abuse of this drug. Symptoms of ethanol addiction include compulsive substance intake and withdrawal syndrome. Stress exposure has an important role in addictive behavior for many drugs of abuse (including ethanol), but the consequences of stress and ethanol in the organism when these factors are concomitant results in a complex interaction. We investigated the effects of concomitant, chronic administration of ethanol and stress exposure on the withdrawal and consumption of, as well as the preference for, ethanol in mice. Male Swiss mice (30–35 g, 8-10 per group) were exposed to an ethanol liquid diet as the only source of food for 15 days. In the final 5 days, they were exposed to forced swimming stress. Twelve hours after removal of the ethanol liquid diet, animals were evaluated for ethanol withdrawal by measuring anxiety-related behaviors and locomotor activity. Twenty-four hours after evaluation of ethanol withdrawal, they were evaluated for voluntary consumption of ethanol in a “three-bottle choice” paradigm. Mice exposed to chronic consumption of ethanol had decreased locomotor activity during withdrawal. Contrary to our expectations, a concomitant forced swimming stress did not aggravate ethanol withdrawal. Nevertheless, simultaneous ethanol administration and stress exposure increased voluntary consumption of ethanol, mainly solutions containing high concentrations of ethanol. These results showed that stressful situations during ethanol intake may aggravate specific addiction-related behaviors. Associação Brasileira de Divulgação Científica 2015-11-27 /pmc/articles/PMC4681418/ /pubmed/26628398 http://dx.doi.org/10.1590/1414-431X20155009 Text en 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 work is properly cited.
spellingShingle Biomedical Sciences
Morais-Silva, G.
Fernandes-Santos, J.
Moreira-Silva, D.
Marin, M.T.
Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
title Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
title_full Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
title_fullStr Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
title_full_unstemmed Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
title_short Concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
title_sort concomitant stress potentiates the preference for, and consumption of, ethanol induced by chronic pre-exposure to ethanol
topic Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681418/
https://www.ncbi.nlm.nih.gov/pubmed/26628398
http://dx.doi.org/10.1590/1414-431X20155009
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