Sex-Specific Metabolic Effects of Dietary Folate Withdrawal in Wild-Type and Aldh1l1 Knockout Mice

• Published in: Metabolites Vol. 12; no. 5; p. 454
• Main Authors: Sharma, Jaspreet, Rushing, Blake R, Hall, Madeline S, Helke, Kristi L, McRitchie, Susan L, Krupenko, Natalia I, Sumner, Susan J, Krupenko, Sergey A
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 18.05.2022; MDPI
• Subjects: Aldh1l1 knockout; Automation; Biosynthesis; Carbon dioxide; Diet; dietary folate restriction; Enzymes; Females; folate metabolism; Folic acid; Formyltetrahydrofolate dehydrogenase; Genotypes; Hematology; Homogenization; Laboratory animals; Liver; Males; Metabolic pathways; Metabolism; Metabolites; Metabolomics; NADP; Nutrient deficiency; Plasma; Proteins; Tetrahydrofolic acid; Tumors; untargeted metabolomics; Vitamin B; Vitamin deficiency; United States > US; Aldh1l1 knockout; untargeted metabolomics; dietary folate restriction; folate metabolism; plasma; liver
• ISSN: 2218-1989; 2218-1989
• DOI: 10.3390/metabo12050454

ALDH1L1 (10-formyltetrahydrofolate dehydrogenase), an enzyme of folate metabolism, is highly expressed in the liver. It regulates the overall flux of folate-bound one-carbon groups by converting 10-formyltetrahydrofolate to tetrahydrofolate and CO in a NADP -dependent reaction. Our previous study revealed that knockout (KO) mice have an altered liver metabotype with metabolic symptoms of folate deficiency when fed a standard chow diet containing 2 ppm folic acid. Here we performed untargeted metabolomic analysis of liver and plasma of KO and wild-type (WT) male and female mice fed for 16 weeks either standard or folate-deficient diet. OPLS-DA, a supervised multivariate technique that was applied to 6595 and 10,678 features for the liver and plasma datasets, respectively, indicated that genotype and diet, alone or in combination, gave distinct metabolic profiles in both types of biospecimens. A more detailed analysis of affected metabolic pathways based on most confidently identified metabolites in the liver and plasma (OL1 and OL2a ontology level) indicated that the dietary folate restriction itself does not fully recapitulate the metabolic effect of the KO. Of note, dietary folate withdrawal enhanced the metabolic perturbations linked to the ALDH1L1 loss only for a subset of metabolites. Importantly, both the ALDH1L1 loss and dietary folate deficiency produced sex-specific metabolic effects.