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Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis

The aim of our study was to analyze mitochondrial and endoplasmic reticulum (ER) gene expression profiles in subcutaneous (SAT) and epicardial (EAT) adipose tissue, skeletal muscle, and myocardium in patients with and without CAD undergoing elective cardiac surgery. Thirty-eight patients, 27 with (C...

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Autores principales: Kratochvílová, Helena, Mráz, Miloš, Kasperová, Barbora J., Hlaváček, Daniel, Mahrík, Jakub, Laňková, Ivana, Cinkajzlová, Anna, Matloch, Zdeněk, Lacinová, Zdeňka, Trnovská, Jaroslava, Ivák, Peter, Novodvorský, Peter, Netuka, Ivan, Haluzík, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123607/
https://www.ncbi.nlm.nih.gov/pubmed/33926122
http://dx.doi.org/10.3390/ijms22094538
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author Kratochvílová, Helena
Mráz, Miloš
Kasperová, Barbora J.
Hlaváček, Daniel
Mahrík, Jakub
Laňková, Ivana
Cinkajzlová, Anna
Matloch, Zdeněk
Lacinová, Zdeňka
Trnovská, Jaroslava
Ivák, Peter
Novodvorský, Peter
Netuka, Ivan
Haluzík, Martin
author_facet Kratochvílová, Helena
Mráz, Miloš
Kasperová, Barbora J.
Hlaváček, Daniel
Mahrík, Jakub
Laňková, Ivana
Cinkajzlová, Anna
Matloch, Zdeněk
Lacinová, Zdeňka
Trnovská, Jaroslava
Ivák, Peter
Novodvorský, Peter
Netuka, Ivan
Haluzík, Martin
author_sort Kratochvílová, Helena
collection PubMed
description The aim of our study was to analyze mitochondrial and endoplasmic reticulum (ER) gene expression profiles in subcutaneous (SAT) and epicardial (EAT) adipose tissue, skeletal muscle, and myocardium in patients with and without CAD undergoing elective cardiac surgery. Thirty-eight patients, 27 with (CAD group) and 11 without CAD (noCAD group), undergoing coronary artery bypass grafting and/or valvular surgery were included in the study. EAT, SAT, intercostal skeletal muscle, and right atrium tissue and blood samples were collected at the start and end of surgery; mRNA expression of selected mitochondrial and ER stress genes was assessed using qRT-PCR. The presence of CAD was associated with decreased mRNA expression of most of the investigated mitochondrial respiratory chain genes in EAT, while no such changes were seen in SAT or other tissues. In contrast, the expression of ER stress genes did not differ between the CAD and noCAD groups in almost any tissue. Cardiac surgery further augmented mitochondrial dysfunction in EAT. In our study, CAD was associated with decreased expression of mitochondrial, but not endoplasmic reticulum stress genes in EAT. These changes may contribute to the acceleration of coronary atherosclerosis.
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spelling pubmed-81236072021-05-16 Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis Kratochvílová, Helena Mráz, Miloš Kasperová, Barbora J. Hlaváček, Daniel Mahrík, Jakub Laňková, Ivana Cinkajzlová, Anna Matloch, Zdeněk Lacinová, Zdeňka Trnovská, Jaroslava Ivák, Peter Novodvorský, Peter Netuka, Ivan Haluzík, Martin Int J Mol Sci Article The aim of our study was to analyze mitochondrial and endoplasmic reticulum (ER) gene expression profiles in subcutaneous (SAT) and epicardial (EAT) adipose tissue, skeletal muscle, and myocardium in patients with and without CAD undergoing elective cardiac surgery. Thirty-eight patients, 27 with (CAD group) and 11 without CAD (noCAD group), undergoing coronary artery bypass grafting and/or valvular surgery were included in the study. EAT, SAT, intercostal skeletal muscle, and right atrium tissue and blood samples were collected at the start and end of surgery; mRNA expression of selected mitochondrial and ER stress genes was assessed using qRT-PCR. The presence of CAD was associated with decreased mRNA expression of most of the investigated mitochondrial respiratory chain genes in EAT, while no such changes were seen in SAT or other tissues. In contrast, the expression of ER stress genes did not differ between the CAD and noCAD groups in almost any tissue. Cardiac surgery further augmented mitochondrial dysfunction in EAT. In our study, CAD was associated with decreased expression of mitochondrial, but not endoplasmic reticulum stress genes in EAT. These changes may contribute to the acceleration of coronary atherosclerosis. MDPI 2021-04-26 /pmc/articles/PMC8123607/ /pubmed/33926122 http://dx.doi.org/10.3390/ijms22094538 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kratochvílová, Helena
Mráz, Miloš
Kasperová, Barbora J.
Hlaváček, Daniel
Mahrík, Jakub
Laňková, Ivana
Cinkajzlová, Anna
Matloch, Zdeněk
Lacinová, Zdeňka
Trnovská, Jaroslava
Ivák, Peter
Novodvorský, Peter
Netuka, Ivan
Haluzík, Martin
Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
title Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
title_full Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
title_fullStr Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
title_full_unstemmed Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
title_short Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
title_sort different expression of mitochondrial and endoplasmic reticulum stress genes in epicardial adipose tissue depends on coronary atherosclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123607/
https://www.ncbi.nlm.nih.gov/pubmed/33926122
http://dx.doi.org/10.3390/ijms22094538
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