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Multiomics Studies on Metabolism Changes in Alcohol-Associated Liver Disease.
- Source :
-
Journal of proteome research [J Proteome Res] 2024 Nov 01; Vol. 23 (11), pp. 4962-4972. Date of Electronic Publication: 2024 Oct 17. - Publication Year :
- 2024
-
Abstract
- Metabolic dysfunction in the liver represents a predominant feature in the early stages of alcohol-associated liver disease (ALD). However, the mechanisms underlying this are only partially understood. To investigate the metabolic characteristics of the liver in ALD, we did a relative quantification of polar metabolites and lipids in the liver of mice with experimental ALD using untargeted metabolomics and untargeted lipidomics. A total of 99 polar metabolites had significant abundance alterations in the livers of alcohol-fed mice. Pathway analysis revealed that amino acid metabolism was the most affected by alcohol in the mouse liver. Metabolites involved in glycolysis and the TCA cycle were decreased, while glycerol 3-phosphate (G3P) and long-chain fatty acids were increased. Relative quantification of lipids unveiled an upregulation of multiple lipid classes, suggesting that alcohol consumption drives metabolism toward lipid synthesis. Results from enzyme expression and activity detection indicated that the decreased activity of mitochondrial glycerol 3-phosphate dehydrogenase contributed to the disordered metabolism.
- Subjects :
- Animals
Mice
Glycerophosphates metabolism
Glycerolphosphate Dehydrogenase metabolism
Glycerolphosphate Dehydrogenase genetics
Glycolysis
Male
Fatty Acids metabolism
Citric Acid Cycle
Mice, Inbred C57BL
Amino Acids metabolism
Metabolome
Ethanol metabolism
Multiomics
Liver Diseases, Alcoholic metabolism
Liver Diseases, Alcoholic pathology
Metabolomics methods
Liver metabolism
Lipid Metabolism
Lipidomics methods
Subjects
Details
- Language :
- English
- ISSN :
- 1535-3907
- Volume :
- 23
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Journal of proteome research
- Publication Type :
- Academic Journal
- Accession number :
- 39418671
- Full Text :
- https://doi.org/10.1021/acs.jproteome.4c00451