Soybean meal peptide Gly-Thr-Tyr-Trp could protect mice from acute alcoholic liver damage: A study of protein-protein interaction and proteomic analysis

Alcoholic liver disease (ALD) is a serious health threat. Soybean meal peptide (SMP) supplementation may protect against this damage; however, the potential mechanism underlying the specific sequence of SMPs is unclear. Protein-protein interaction and proteomic analyses are effective methods for stu...

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Veröffentlicht in:Food chemistry 2024-09, Vol.451, p.139337-139337, Article 139337
Hauptverfasser: Lyu, Siwen, Cai, Zhuanzhang, Yang, Qi, Liu, Jingbo, Yu, Yiding, Pan, Fengguang, Zhang, Ting
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Sprache:eng
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Zusammenfassung:Alcoholic liver disease (ALD) is a serious health threat. Soybean meal peptide (SMP) supplementation may protect against this damage; however, the potential mechanism underlying the specific sequence of SMPs is unclear. Protein-protein interaction and proteomic analyses are effective methods for studying functional ingredients in diseases. This study aimed to investigate the potential mechanism of action of the peptide Gly-Thr-Tyr-Trp (GTYW) on ALD using protein-protein interaction and proteomic analyses. These results demonstrate that GTYW influenced the targets of glutathione metabolism (glutathione-disulfide reductase, glutathione S-transferase pi 1, and glutathione S-transferase mu 2). It also regulated the expression of targets related to energy metabolism and amino acid conversion (trypsin-2, cysteine dioxygenase type-1, and F6SJM7). Amino acid and lipid metabolisms were identified based on Gene Ontology annotation. These results indicate that GTYW might affect alcohol-related liver disease signaling pathways. This study provides evidence of the protective and nutritional benefits of SMPs in ALD treatment. [Display omitted] •The protein expression could be influenced by GTYW.•GTYW might regulate the target proteins related to glutathione metabolism.•Diet supplement of GTYW could prevent the alcoholic liver damage of mice.•GTYW could affect the alcohol and amino acid metabolism pathways.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2024.139337