The effect of fructose exposure on amino acid metabolism among Chinese community residents and its possible multi-omics mechanisms

• Published in: Scientific reports Vol. 13; no. 1; p. 22704
• Main Authors: Rang, Ouyan, Qin, Xinru, Tang, Yonghong, Cao, Lin, Li, Guojuan, Liu, Xiaocheng, Zhong, Jing, Wang, Mu
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 19.12.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/553; 692/53; Amino Acids; Animals; China; Fructose; Fructose - adverse effects; Glutamine; Glutamine - metabolism; Humanities and Social Sciences; Humans; Hypertriglyceridemia; Hyperuricemia; Liver; Metabolic disorders; Metabolic networks; Metabolism; Metabolites; Metabolomics; multidisciplinary; Multiomics; Proteomes; Rats; Science; Science (multidisciplinary); Urea; γ-Aminobutyric acid; China
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-50069-5

The consumption of fructose has increased dramaticly during the last few decades, inducing a great increase in the risk of intrahepatic lipid accumulation, hypertriglyceridemia, hyperuricemia and cancer. However, the underlying mechanism has not yet been fully elucidated. Amino acid metabolism may play an important role in the process of the diseases caused by fructose, but there is still a lack of corresponding evidence. In present study, we provide an evidence of how fructose affects amino acids metabolism in 1895 ordinary residents in Chinese community using UPLC-QqQMS based amino acid targeted metabolomics and the underlying mechanism of fructose exposure how interferes with amino acid metabolism related genes and acetylated modification of proteome in the liver of rats model. We found people with high fructose exposure had higher levels of Asa, EtN, Asp, and Glu, and lower levels of 1MHis, PEtN, Arg, Gln, GABA, Aad, Hyl and Cys. The further mechanism study displayed amino acid metabolic genes of Aspa , Cndp1 , Dbt , Dmgdh, and toxic metabolites such as N -acetylethanolamines accumulation, interference of urea cycle, as well as acetylated modification of key enzymes in glutamine metabolic network and glutamine derived NEAAs synthesis pathway in liver may play important roles in fructose caused reprogramming in amino acid metabolism. This research provides novel insights of the mechanism of amino acid metabolic disorder caused by fructose and supplies new targets for clinical therapy.