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Lipidomic Profiles of the Heart and Circulation in Response to Exercise versus Cardiac Pathology: A Resource of Potential Biomarkers and Drug Targets.
- Source :
-
Cell reports [Cell Rep] 2018 Sep 04; Vol. 24 (10), pp. 2757-2772. - Publication Year :
- 2018
-
Abstract
- Exercise-induced heart growth provides protection against cardiovascular disease, whereas disease-induced heart growth leads to heart failure. These distinct forms of growth are associated with different molecular profiles (e.g., mRNAs, non-coding RNAs, and proteins), and targeting differentially regulated genes has therapeutic potential for heart failure. The effects of exercise on the cardiac and circulating lipidomes in comparison to disease are unclear. Lipidomic profiling was performed on hearts and plasma of mice subjected to swim endurance training or a cardiac disease model (moderate or severe pressure overload). Several sphingolipid species and phospholipids containing omega-3/6 fatty acids were distinctly altered in heart and/or plasma with exercise versus pressure overload. A subset of lipids was validated in an independent mouse model with heart failure and atrial fibrillation. This study highlights the adaptations that occur to lipid profiles in response to endurance training versus pathology and provides a resource to investigate potential therapeutic targets and biomarkers.<br /> (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Atrial Fibrillation blood
Atrial Fibrillation metabolism
Cardiomegaly blood
Cardiomegaly metabolism
Disease Models, Animal
Heart Failure blood
Heart Failure metabolism
Humans
Mice
Myocardium metabolism
Myocardium pathology
Phospholipids metabolism
Physical Conditioning, Animal
Sphingolipids blood
Sphingolipids metabolism
Biomarkers blood
Phospholipids blood
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 24
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 30184508
- Full Text :
- https://doi.org/10.1016/j.celrep.2018.08.017