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Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption

BACKGROUND: Alcoholic cardiomyopathy (CMP) is one of the major complications of chronic excessive alcohol consumption. The pathogenic mechanisms implicated are diverse, inducing functional and structural changes in the myocardium. Insulin-like Growth Factor 1 (IGF-1) plays an important role in modul...

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Autores principales: Borrisser-Pairó, Francesc, Antúnez, Emilia, Tobías, Ester, Fernández-Solà, Joaquim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375930/
https://www.ncbi.nlm.nih.gov/pubmed/25984322
http://dx.doi.org/10.1186/2050-490X-1-3
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author Borrisser-Pairó, Francesc
Antúnez, Emilia
Tobías, Ester
Fernández-Solà, Joaquim
author_facet Borrisser-Pairó, Francesc
Antúnez, Emilia
Tobías, Ester
Fernández-Solà, Joaquim
author_sort Borrisser-Pairó, Francesc
collection PubMed
description BACKGROUND: Alcoholic cardiomyopathy (CMP) is one of the major complications of chronic excessive alcohol consumption. The pathogenic mechanisms implicated are diverse, inducing functional and structural changes in the myocardium. Insulin-like Growth Factor 1 (IGF-1) plays an important role in modulating the cell cycle, and helps the differentiation and proliferation of cardiac tissue inhibiting apoptosis. Experimental studies have suggested the role of IGF-1 in alcohol-induced cardiac damage. The aim of the present study was to determine the effect of chronic alcohol consumption on IGF-1 myocardial expression and to compare this expression in cases of hypertension and other cardiac diseases. METHODS: We studied heart samples from human organ donors: 10 healthy donors, 16 with hypertension, 23 with chronic alcohol consumption and 7 with other causes of cardiac disease. IGF-1 myocardial expression was evaluated with a specific immunohistochemistry assay using a semi-quantitative method. RESULTS: A significant decrease in IGF-1 myocardial expression was observed comparing all the cases included with control donors. This decrease in IGF-1 myocardial expression was significantly lower in the group of donors with chronic alcohol consumption compared to controls. On group evaluation according to the presence of CMP, donors with chronic alcohol consumption without CMP presented significantly lower IGF-1 expression than controls, whereas donors with chronic alcohol consumption with CMP showed a downward trend without achieving significance. CONCLUSIONS: Chronic alcohol consumption significantly reduces IGF-1 myocardial expression. This decrease induced by alcohol is partially compensated in the presence of structural myocardial damage.
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spelling pubmed-43759302015-05-16 Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption Borrisser-Pairó, Francesc Antúnez, Emilia Tobías, Ester Fernández-Solà, Joaquim Regen Med Res Research BACKGROUND: Alcoholic cardiomyopathy (CMP) is one of the major complications of chronic excessive alcohol consumption. The pathogenic mechanisms implicated are diverse, inducing functional and structural changes in the myocardium. Insulin-like Growth Factor 1 (IGF-1) plays an important role in modulating the cell cycle, and helps the differentiation and proliferation of cardiac tissue inhibiting apoptosis. Experimental studies have suggested the role of IGF-1 in alcohol-induced cardiac damage. The aim of the present study was to determine the effect of chronic alcohol consumption on IGF-1 myocardial expression and to compare this expression in cases of hypertension and other cardiac diseases. METHODS: We studied heart samples from human organ donors: 10 healthy donors, 16 with hypertension, 23 with chronic alcohol consumption and 7 with other causes of cardiac disease. IGF-1 myocardial expression was evaluated with a specific immunohistochemistry assay using a semi-quantitative method. RESULTS: A significant decrease in IGF-1 myocardial expression was observed comparing all the cases included with control donors. This decrease in IGF-1 myocardial expression was significantly lower in the group of donors with chronic alcohol consumption compared to controls. On group evaluation according to the presence of CMP, donors with chronic alcohol consumption without CMP presented significantly lower IGF-1 expression than controls, whereas donors with chronic alcohol consumption with CMP showed a downward trend without achieving significance. CONCLUSIONS: Chronic alcohol consumption significantly reduces IGF-1 myocardial expression. This decrease induced by alcohol is partially compensated in the presence of structural myocardial damage. BioMed Central 2013-10-01 /pmc/articles/PMC4375930/ /pubmed/25984322 http://dx.doi.org/10.1186/2050-490X-1-3 Text en © Borrisser-Pairó et al.; licensee BioMed Central Ltd. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Borrisser-Pairó, Francesc
Antúnez, Emilia
Tobías, Ester
Fernández-Solà, Joaquim
Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
title Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
title_full Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
title_fullStr Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
title_full_unstemmed Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
title_short Insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
title_sort insulin-like growth factor 1 myocardial expression decreases in chronic alcohol consumption
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375930/
https://www.ncbi.nlm.nih.gov/pubmed/25984322
http://dx.doi.org/10.1186/2050-490X-1-3
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