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In dietinduced obese mice, NNMTi treatment significantly reduced liver weight, liver volume, and hepatic triglyceride levels, alleviated hepatic steatosis and inflammatory infiltration, downregulated inflammatory factors (such as TNF and IL6) and lipogenic genes (such as FAS), and upregulated lipolytic genes (such as ATGL) in the liver

This loss of translocase function was accompanied by increased externalization of PS, a key eat-me signal that flags cells for recognition and phagocytosis by macrophages

UFe and FFA treatments restored shoot and root biomass, improved relative water content, and stabilized the membrane integrity by reducing electrolyte leakage and lipid peroxidation

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We then measured 0.3 l of each sample using a 1 l Hamilton syringe (Hamilton, 80135) and extracted these volumes in 20 l of a 75:25:0.1 HPLC grade acetonitrilemethanolformic acid extraction mix with the following labelled stable isotope internal standards: 2 H 9 -choline (DLM-549), 13 C 4 -3-hydroxybutyrate (CLM-3853), 13 C 6 , 15 N 2 -cystine (CNLM-4244), 13 C 3 -lactate (485926, Sigma-Aldrich), 13 C 6 -glucose (CLM-1396), 13 C 3 -serine (CLM-1574), 13 C 2 -glycine (CLM-1017), 13 C 5 -hypoxanthine (CLM-8042), 13 C 2 , 15 N-taurine (CNLM-10253), 13 C 3 -glycerol (CLM-1510), 2 H 3 -creatinine (DLM-3653), 13 C 10 -kynurenic acid (80445, Sigma-Aldrich), 13 C 10 , 15 N 5 -adenosine (CNLM-3806), 13 C 8 -indole-3-carboxaldehyde (CLM-10745), 15 N 4 -inosine (NLM-4264), 13 C 10 -kynurenine (CLM-9884) and 13 C 4 -methylmalonic acid (CLM-9426)