PUBLICATION

Conjugation of Pea Peptides and D-Xylose via Maillard Glycosylation and Its Functionality to Antagonize Alcohol-Induced Liver Injury in Zebrafish

Authors
Li, G., Liu, X., Diao, S., Zheng, X.
ID
ZDB-PUB-250814-16
Date
2025
Source
Nutrients   17: (Journal)
Registered Authors
Keywords
Maillard glycosylation, antagonize alcohol-induced liver injury, pea glycopeptides, pea peptides
MeSH Terms
  • Peptides*/chemistry
  • Peptides*/pharmacology
  • Liver/drug effects
  • Liver/metabolism
  • Liver/pathology
  • Protein Hydrolysates/chemistry
  • Protein Hydrolysates/pharmacology
  • Liver Diseases, Alcoholic*/metabolism
  • Liver Diseases, Alcoholic*/prevention & control
  • Pisum sativum*/chemistry
  • Animals
  • Malondialdehyde/metabolism
  • Zebrafish
  • Disease Models, Animal
  • Xylose*/chemistry
  • Xylose*/pharmacology
  • Antioxidants/pharmacology
  • Ethanol
  • Maillard Reaction
  • Pea Proteins*/chemistry
  • Pea Proteins*/pharmacology
  • Glycosylation
  • Oxidative Stress/drug effects
PubMed
40806154 Full text @ Nutrients
Abstract
In this study, the preparation of pea glycopeptides based on the Maillard glycosylation pathway (PPH-M) and its antagonistic mechanism against alcoholic liver injury in zebrafish were studied.
The results showed that the conjugation of D-xylose significantly improved the antioxidant activity of pea protein hydrolysates (PPHs). The structural characterization indicated that PPH was successfully covalent binding to D-xylose, which was mainly manifested as a stretching vibration change in Fourier transform infrared spectroscopy (FTIR) and molecular size increase. Scanning electron microscopy (SEM) and zeta potential also confirmed the covalently bound of the two. In addition, a model of alcohol-induced liver injury in zebrafish was established. Through the intervention of different doses of PPH-M, it was found that the intervention of PPH-M could significantly increase superoxide dismutase (SOD) activity, reduce malondialdehyde (MDA) content, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) activity, and significantly improve alcohol-induced liver injury in zebrafish. The protective effect of PPH-M was also confirmed by liver pathology and fluorescence microscopy. Finally, reverse transcription-polymerase chain reaction (qRT-PCR) results indicated that PPH-M could significantly regulate the expression level of antioxidant-related mRNA. PPH-M could also regulate the expression of the Keap1/Nrf2 signaling pathway and up-regulated glutathione synthesis signaling pathway to antagonize alcohol-induced liver injury in zebrafish.
This study revealed the mechanism of PPH-M antagonized alcoholic liver injury and laid a theoretical foundation for its development as functional foods.
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