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Different Expression of Mitochondrial and Endoplasmic Reticulum Stress Genes in Epicardial Adipose Tissue Depends on Coronary Atherosclerosis
H. Kratochvílová, M. Mráz, BJ. Kasperová, D. Hlaváček, J. Mahrík, I. Laňková, A. Cinkajzlová, Z. Matloch, Z. Lacinová, J. Trnovská, P. Ivák, P. Novodvorský, I. Netuka, M. Haluzík
Language English Country Switzerland
Document type Journal Article
Grant support
IN 00023001
Health, Czech Republic - conceptual development of research organization ("Institute for Clinical and Experimental Medicine - IKEM
NV19-02-00118
Ministry of Health of the Czech Republic
RVO VFN64165
Ministry of Health, Czech Republic
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
33926122
DOI
10.3390/ijms22094538
Knihovny.cz E-resources
- MeSH
- Endoplasmic Reticulum genetics metabolism MeSH
- Gene Expression genetics MeSH
- Muscle, Skeletal metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger genetics MeSH
- Mitochondria genetics metabolism MeSH
- Myocardium metabolism MeSH
- Coronary Artery Disease genetics physiopathology MeSH
- Pericardium metabolism MeSH
- Subcutaneous Fat metabolism MeSH
- Aged MeSH
- Gene Expression Profiling methods MeSH
- Endoplasmic Reticulum Stress genetics physiology MeSH
- Transcriptome genetics MeSH
- Adipose Tissue metabolism MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
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.
Department of Oncology and Metabolism University of Sheffield Sheffield S0114 UK
Shackleton Department of Anaesthesia UHS NHS UK Southampton General Hospital Southampton SO14 UK
References provided by Crossref.org
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