Multiomics Studies on Metabolism Changes in Alcohol-Associated Liver Disease

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.

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Publication Details

Journal
Journal of Proteome Research
Published
2024-10-17
DOI
https://doi.org/10.1021/acs.jproteome.4c00451
Citations
2
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.77

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article

Multiomics Studies on Metabolism Changes in Alcohol-Associated Liver Disease

Liqing He, Craig J. McClain, Xinmin Yin, Xipeng Ma et al.
2 citations
Journal of Proteome Research
Liver Disease Diagnosis and Treatment
0.77
article

Multiomics Studies on Metabolism Changes in Alcohol-Associated Liver Disease

Liqing He, Craig J. McClain, Xinmin Yin, Xipeng Ma, Eugene G. Mueller, Michael A. Menze, Wenke Feng, Raobo Xu, Xiang Zhang, Seongho Kim
article en
2 citations

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.

Journal of Proteome ResearchVol. 23(11)
University of Louisville (US), Wayne State University (US), The Barbara Ann Karmanos Cancer Institute (US), Louisville VA Medical Center (US), University of Louisville Hospital (US)
U.S. Department of Veterans Affairs, National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, NIH Office of the Director, National Institute of General Medical Sciences
Good health and well-being, Zero hunger
Openalex Percentile: Top 25%
Liver Disease Diagnosis and Treatment
0.77
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