乙醇代谢
新陈代谢
肝病
疾病
酒精性肝病
医学
计算生物学
化学
生物信息学
生理学
生物
内科学
肝硬化
作者
Liqing He,Raobo Xu,Xipeng Ma,Xinmin Yin,Eugene G. Mueller,Wenke Feng,Michael A. Menze,Seongho Kim,Craig J. McClain,Xiang Zhang
标识
DOI:10.1021/acs.jproteome.4c00451
摘要
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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