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Damage of hippocampal neurons in rats with chronic alcoholism

Chronic alcoholism can damage the cytoskeleton and aggravate neurological deficits. However, the effect of chronic alcoholism on hippocampal neurons remains unclear. In this study, a model of chronic alcoholism was established in rats that were fed with 6% alcohol for 42 days. Endogenous hydrogen su...

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Autores principales: Du, Ailin, Jiang, Hongbo, Xu, Lei, An, Na, Liu, Hui, Li, Yinsheng, Zhang, Ruiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211203/
https://www.ncbi.nlm.nih.gov/pubmed/25368648
http://dx.doi.org/10.4103/1673-5374.141787
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author Du, Ailin
Jiang, Hongbo
Xu, Lei
An, Na
Liu, Hui
Li, Yinsheng
Zhang, Ruiling
author_facet Du, Ailin
Jiang, Hongbo
Xu, Lei
An, Na
Liu, Hui
Li, Yinsheng
Zhang, Ruiling
author_sort Du, Ailin
collection PubMed
description Chronic alcoholism can damage the cytoskeleton and aggravate neurological deficits. However, the effect of chronic alcoholism on hippocampal neurons remains unclear. In this study, a model of chronic alcoholism was established in rats that were fed with 6% alcohol for 42 days. Endogenous hydrogen sulfide content and cystathionine-beta-synthase activity in the hippocampus of rats with chronic alcoholism were significantly increased, while F-actin expression was decreased. Hippocampal neurons in rats with chronic alcoholism appeared to have a fuzzy nuclear membrane, mitochondrial edema, and ruptured mitochondrial crista. These findings suggest that chronic alcoholism can cause learning and memory decline in rats, which may be associated with the hydrogen sulfide/cystathionine-beta-synthase system, mitochondrial damage and reduced expression of F-actin.
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spelling pubmed-42112032014-11-03 Damage of hippocampal neurons in rats with chronic alcoholism Du, Ailin Jiang, Hongbo Xu, Lei An, Na Liu, Hui Li, Yinsheng Zhang, Ruiling Neural Regen Res Technical Updates Chronic alcoholism can damage the cytoskeleton and aggravate neurological deficits. However, the effect of chronic alcoholism on hippocampal neurons remains unclear. In this study, a model of chronic alcoholism was established in rats that were fed with 6% alcohol for 42 days. Endogenous hydrogen sulfide content and cystathionine-beta-synthase activity in the hippocampus of rats with chronic alcoholism were significantly increased, while F-actin expression was decreased. Hippocampal neurons in rats with chronic alcoholism appeared to have a fuzzy nuclear membrane, mitochondrial edema, and ruptured mitochondrial crista. These findings suggest that chronic alcoholism can cause learning and memory decline in rats, which may be associated with the hydrogen sulfide/cystathionine-beta-synthase system, mitochondrial damage and reduced expression of F-actin. Medknow Publications & Media Pvt Ltd 2014-09-01 /pmc/articles/PMC4211203/ /pubmed/25368648 http://dx.doi.org/10.4103/1673-5374.141787 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Updates
Du, Ailin
Jiang, Hongbo
Xu, Lei
An, Na
Liu, Hui
Li, Yinsheng
Zhang, Ruiling
Damage of hippocampal neurons in rats with chronic alcoholism
title Damage of hippocampal neurons in rats with chronic alcoholism
title_full Damage of hippocampal neurons in rats with chronic alcoholism
title_fullStr Damage of hippocampal neurons in rats with chronic alcoholism
title_full_unstemmed Damage of hippocampal neurons in rats with chronic alcoholism
title_short Damage of hippocampal neurons in rats with chronic alcoholism
title_sort damage of hippocampal neurons in rats with chronic alcoholism
topic Technical Updates
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211203/
https://www.ncbi.nlm.nih.gov/pubmed/25368648
http://dx.doi.org/10.4103/1673-5374.141787
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