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Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage

Naltrexone, an antagonist of μ-opioid receptors, is clinically used as adjuvant therapy of alcohol dishabituation. The aim of the present work was to test the effect of 1 mg/kg body weight of naltrexone to revert oxidative stress-related biochemical alterations, in the hippocampus and serum of chron...

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Autores principales: Almansa, Inmaculada, Barcia, Jorge M., López-Pedrajas, Rosa, Muriach, María, Miranda, María, Romero, Francisco Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864183/
https://www.ncbi.nlm.nih.gov/pubmed/24363821
http://dx.doi.org/10.1155/2013/296898
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author Almansa, Inmaculada
Barcia, Jorge M.
López-Pedrajas, Rosa
Muriach, María
Miranda, María
Romero, Francisco Javier
author_facet Almansa, Inmaculada
Barcia, Jorge M.
López-Pedrajas, Rosa
Muriach, María
Miranda, María
Romero, Francisco Javier
author_sort Almansa, Inmaculada
collection PubMed
description Naltrexone, an antagonist of μ-opioid receptors, is clinically used as adjuvant therapy of alcohol dishabituation. The aim of the present work was to test the effect of 1 mg/kg body weight of naltrexone to revert oxidative stress-related biochemical alterations, in the hippocampus and serum of chronic alcoholic adult rats. Malondialdehyde concentration was increased and glutathione peroxidase activity was decreased in hippocampus and serum of alcohol-treated rats. Naltrexone treatment restored these alterations. The in vitro antioxidant ability of Ntx could not justify these effects considering the doses used. Thus this apparent protective effect of Ntx can only be attributed to its pharmacological effects, as herein discussed.
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spelling pubmed-38641832013-12-22 Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage Almansa, Inmaculada Barcia, Jorge M. López-Pedrajas, Rosa Muriach, María Miranda, María Romero, Francisco Javier Oxid Med Cell Longev Research Article Naltrexone, an antagonist of μ-opioid receptors, is clinically used as adjuvant therapy of alcohol dishabituation. The aim of the present work was to test the effect of 1 mg/kg body weight of naltrexone to revert oxidative stress-related biochemical alterations, in the hippocampus and serum of chronic alcoholic adult rats. Malondialdehyde concentration was increased and glutathione peroxidase activity was decreased in hippocampus and serum of alcohol-treated rats. Naltrexone treatment restored these alterations. The in vitro antioxidant ability of Ntx could not justify these effects considering the doses used. Thus this apparent protective effect of Ntx can only be attributed to its pharmacological effects, as herein discussed. Hindawi Publishing Corporation 2013 2013-12-01 /pmc/articles/PMC3864183/ /pubmed/24363821 http://dx.doi.org/10.1155/2013/296898 Text en Copyright © 2013 Inmaculada Almansa et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Almansa, Inmaculada
Barcia, Jorge M.
López-Pedrajas, Rosa
Muriach, María
Miranda, María
Romero, Francisco Javier
Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage
title Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage
title_full Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage
title_fullStr Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage
title_full_unstemmed Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage
title_short Naltrexone Reverses Ethanol-Induced Rat Hippocampal and Serum Oxidative Damage
title_sort naltrexone reverses ethanol-induced rat hippocampal and serum oxidative damage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3864183/
https://www.ncbi.nlm.nih.gov/pubmed/24363821
http://dx.doi.org/10.1155/2013/296898
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