Lipidomic profiling of the hepatic esterified fatty acid composition in diet-induced nonalcoholic fatty liver disease in genetically diverse Collaborative Cross mice

• Published in: The Journal of nutritional biochemistry Vol. 109; p. 109108
• Main Authors: Nagumalli, Suresh K., Willett, Rose A., de Conti, Aline, Tryndyak, Volodymyr P., Avigan, Mark I., da Costa, Gonçalo Gamboa, Beland, Frederick A., Rusyn, Ivan, Pogribny, Igor P.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.11.2022
• Subjects: Animals; Choline; Collaborative Cross Mice; Diet and dietary lipids; Diet, High-Fat - adverse effects; Disease Models, Animal; Fatty Acids; Fatty Acids, Monounsaturated; Fatty Acids, Nonesterified; Fatty Acids, Unsaturated; Fatty liver; Female; Folic Acid; Lipidomics; Liver; Male; Mice; Mouse genetics; Non-alcoholic Fatty Liver Disease - etiology; Nonalcoholic fatty liver disease; Sucrose; Diet and dietary lipids; Lipidomics; Nonalcoholic fatty liver disease; Fatty liver; Fatty acids; Mouse genetics
• ISSN: 0955-2863; 1873-4847
• DOI: 10.1016/j.jnutbio.2022.109108

Non-alcoholic fatty liver disease (NAFLD), one of the most common forms of chronic liver disease, is characterized by the excessive accumulation of lipid species in hepatocytes. Recent studies have indicated that in addition to the total lipid quantities, changes in lipid composition are a determining factor in hepatic lipotoxicity. Using ultra-high performance liquid chromatography coupled with electrospray tandem mass spectrometry, we analyzed the esterified fatty acid composition in 24 strains of male and female Collaborative Cross (CC) mice fed a high fat/high sucrose (HF/HS) diet for 12 weeks. Changes in lipid composition were found in all strains after the HF/HS diet, most notably characterized by increases in monounsaturated fatty acids (MUFA) and decreases in polyunsaturated fatty acids (PUFA). Similar changes in MUFA and PUFA were observed in a choline- and folate-deficient (CFD) mouse model of NAFLD, as well as in hepatocytes treated in vitro with free fatty acids. Analysis of fatty acid composition revealed that alterations were accompanied by an increase in the estimated activity of MUFA generating SCD1 enzyme and an estimated decrease in the activity of PUFA generating FADS1 and FADS2 enzymes. PUFA/MUFA ratios were inversely correlated with lipid accumulation in male and female CC mice fed the HF/HS diet and with morphological markers of hepatic injury in CFD diet-fed mouse model of NAFLD. These results demonstrate that different models of NAFLD are characterized by similar changes in the esterified fatty acid composition and that alterations in PUFA/MUFA ratios may serve as a diagnostic marker for NAFLD severity.