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Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction

BACKGROUND: Gender can influence post-infarction cardiac remodeling. OBJECTIVE: To evaluate whether gender influences left ventricular (LV) remodeling and integrin-linked kinase (ILK) after myocardial infarction (MI). METHODS: Female and male Wistar rats were assigned to one of three groups: sham, m...

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Autores principales: Sofia, Renato Rodrigues, Serra, Andrey Jorge, Silva, Jose Antonio, Antonio, Ednei Luiz, Manchini, Martha Trindade, de Oliveira, Fernanda Aparecida Alves, Teixeira, Vicente Paulo Castro, Tucci, Paulo José Ferreira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150663/
https://www.ncbi.nlm.nih.gov/pubmed/25098374
http://dx.doi.org/10.5935/abc.20140113
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author Sofia, Renato Rodrigues
Serra, Andrey Jorge
Silva, Jose Antonio
Antonio, Ednei Luiz
Manchini, Martha Trindade
de Oliveira, Fernanda Aparecida Alves
Teixeira, Vicente Paulo Castro
Tucci, Paulo José Ferreira
author_facet Sofia, Renato Rodrigues
Serra, Andrey Jorge
Silva, Jose Antonio
Antonio, Ednei Luiz
Manchini, Martha Trindade
de Oliveira, Fernanda Aparecida Alves
Teixeira, Vicente Paulo Castro
Tucci, Paulo José Ferreira
author_sort Sofia, Renato Rodrigues
collection PubMed
description BACKGROUND: Gender can influence post-infarction cardiac remodeling. OBJECTIVE: To evaluate whether gender influences left ventricular (LV) remodeling and integrin-linked kinase (ILK) after myocardial infarction (MI). METHODS: Female and male Wistar rats were assigned to one of three groups: sham, moderate MI (size: 20-39% of LV area), and large MI (size: ≥40% of LV area). MI was induced by coronary occlusion, and echocardiographic analysis was performed after six weeks to evaluate MI size as well as LV morphology and function. Real-time RT-PCR and Western blot were used to quantify ILK in the myocardium. RESULTS: MI size was similar between genders. MI resulted in systolic dysfunction and enlargement of end-diastolic as well as end-systolic dimension of LV as a function of necrotic area size in both genders. Female rats with large MI showed a lower diastolic and systolic dilatation than the respective male rats; however, LV dysfunction was similar between genders. Gene and protein levels of ILK were increased in female rats with moderate and large infarctions, but only male rats with large infarctions showed an altered ILK mRNA level. A negative linear correlation was evident between LV dimensions and ILK expression in female rats with large MI. CONCLUSIONS: Post-MI ILK expression is altered in a gender-specific manner, and higher ILK levels found in females may be sufficient to improve LV geometry but not LV function.
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spelling pubmed-41506632014-09-04 Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction Sofia, Renato Rodrigues Serra, Andrey Jorge Silva, Jose Antonio Antonio, Ednei Luiz Manchini, Martha Trindade de Oliveira, Fernanda Aparecida Alves Teixeira, Vicente Paulo Castro Tucci, Paulo José Ferreira Arq Bras Cardiol Original Articles BACKGROUND: Gender can influence post-infarction cardiac remodeling. OBJECTIVE: To evaluate whether gender influences left ventricular (LV) remodeling and integrin-linked kinase (ILK) after myocardial infarction (MI). METHODS: Female and male Wistar rats were assigned to one of three groups: sham, moderate MI (size: 20-39% of LV area), and large MI (size: ≥40% of LV area). MI was induced by coronary occlusion, and echocardiographic analysis was performed after six weeks to evaluate MI size as well as LV morphology and function. Real-time RT-PCR and Western blot were used to quantify ILK in the myocardium. RESULTS: MI size was similar between genders. MI resulted in systolic dysfunction and enlargement of end-diastolic as well as end-systolic dimension of LV as a function of necrotic area size in both genders. Female rats with large MI showed a lower diastolic and systolic dilatation than the respective male rats; however, LV dysfunction was similar between genders. Gene and protein levels of ILK were increased in female rats with moderate and large infarctions, but only male rats with large infarctions showed an altered ILK mRNA level. A negative linear correlation was evident between LV dimensions and ILK expression in female rats with large MI. CONCLUSIONS: Post-MI ILK expression is altered in a gender-specific manner, and higher ILK levels found in females may be sufficient to improve LV geometry but not LV function. Sociedade Brasileira de Cardiologia 2014-08 /pmc/articles/PMC4150663/ /pubmed/25098374 http://dx.doi.org/10.5935/abc.20140113 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Sofia, Renato Rodrigues
Serra, Andrey Jorge
Silva, Jose Antonio
Antonio, Ednei Luiz
Manchini, Martha Trindade
de Oliveira, Fernanda Aparecida Alves
Teixeira, Vicente Paulo Castro
Tucci, Paulo José Ferreira
Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction
title Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction
title_full Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction
title_fullStr Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction
title_full_unstemmed Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction
title_short Gender-Based Differences in Cardiac Remodeling and ILK Expression after Myocardial Infarction
title_sort gender-based differences in cardiac remodeling and ilk expression after myocardial infarction
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150663/
https://www.ncbi.nlm.nih.gov/pubmed/25098374
http://dx.doi.org/10.5935/abc.20140113
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