4.6 Article

Time-Course Lipidomics of Ornithine-Induced Severe Acute Pancreatitis Model Reveals the Free Fatty Acids Centered Lipids Dysregulation Characteristics

Journal

METABOLITES
Volume 13, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/metabo13090993

Keywords

lipidomics; severe acute pancreatitis; free fatty acids; triglycerides; ceramides

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The relationship between the type and intensities of lipids in blood and pancreas during severe acute pancreatitis (SAP) is still unclear. Through a rat model of SAP induced by ornithine injections, this study found changes in lipid profiles in both blood and pancreas. The levels of glycerophospholipids decreased while cholesterol esters increased in the pancreas. In the blood, specific carbon atom TAGs decreased while CERs increased in the pancreas. Moreover, TAGs with specific carbon atom numbers showed a significant increase during the repair phase in both blood and pancreas.
The relationship between the type and intensities of lipids of blood and pancreas and the pathological changes in the pancreas during severe acute pancreatitis (SAP) remains unclear. In our study, we employed a rat model of SAP induced through intraperitoneal ornithine injections. We collected serum and pancreas samples at various time points (0-144 h) for histopathological and biochemical assessments, followed by lipidomic analyses using LC-MS/MS or in situ mass spectrometry imaging (MSI) To discern changes over time or at specific points, we employed time-course and univariate analyses for lipid screening, respectively. Our findings indicated that the peak inflammation in the Orn-SAP model occurred within the 24-30 h timeframe, with evident necrosis emerging from 24 h onwards, followed by regeneration starting at 48 h. Time-course analysis revealed an overall decrease in glycerophospholipids (PEs, PCs, LPEs, LPCs), while CEs exhibited an increase within the pancreas. Univariate analysis unveiled a significant reduction in serum TAGs containing 46-51 carbon atoms at 24 h, and CERs in the pancreas significantly increased at 30 h, compared with 0 h. Moreover, a substantial rise in TAGs containing 56-58 carbon atoms was observed at 144 h, both in serum and pancreas. MSI demonstrated the CERs containing saturated mono-acyl chains of 16 and 18 carbon atoms influenced pancreatic regeneration. Tracing the origin of FFAs hydrolyzed from pancreatic glycerophospholipids and serum TAGs during the early stages of inflammation, as well as FFAs utilized for CEs and CERs synthesis during the repair phase, may yield valuable strategies for diagnosing and managing SAP.

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