Affiliation:
1. Department of Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, China
2. Guangxi Medical University, Nanning, China
3. Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, China
Abstract
Objectives:
Acute pancreatitis(AP) is a common digestive tract disease, often accompanied
by severe metabolic disorders, but there are no specific markers and treatment methods,
and the potential metabolic pathways behind it remain to be explored.
Methods:
Establish mild acute pancreatitis and severe acute pancreatitis models in rats and intervene
with antioxidant NAC. Analyze serum oxidative stress indicators and pathological changes
in pancreatic tissue. In addition, non-targeted metabolomics analysis of serum differential metabolites
between groups was conducted based on the LC/MS system.
Results:
The pathological score of the model group rats increased, and the levels of oxidative
stress factors ROS and MDA significantly increased, while the activity of the antioxidant enzyme
SOD decreased. After NAC intervention, oxidative stress damage in rats was alleviated.
Non-targeted metabolomics experiments suggest significant differences in serum metabolic profiles
among different groups of rats.
Conclusion:
Metabolomics results show that the obtained differential metabolites are expected to
become serum biomarkers for AP.
result:
In the untargeted metabolomics test, we found that there were obvious differences in serum metabolic profiles of rats. The MAP model group was compared with the NC group, we selected 7 significant differential metabolites, including PC, Tuftsin, etc. The comparison of the MAP + NAC intervention group with the MAP group yielded a total of five significantly differential metabolites, including 20-Deoxynarasin, VPGPR Enterostatin and 12-Ketoporrigenin et al. Compared with the SO group, 23 metabolites with significant differences were screened out in SAP group. The comparison of SAP + NAC intervention group with SAP model group selected 10 significantly different metabolites, including lipids (PC, PE), Physalolactone B, etc.. These metabolites are involved in complex pathophysiological processes such as oxidative stress and inflammation, involving various metabolic pathways such as glycerophospholipid metabolism, arachidonic acid metabolism, and pentose and glucuronate interconversions.
Publisher
Bentham Science Publishers Ltd.