PSIV-B-34 Late-Breaking: Targeted metabolomics analysis reveals that dietary super-nutritional selenium regulates energy metabolism homeostasis in pig liver

摘要

Energy metabolism is a major mechanism of power reduction needed to maintain the redox state in an organism. By using a selenium (Se)-deficiency model we have previously demonstrated that Se can shift glycolysis by regulating the redox state in pig skeletal muscle. How dietary super-nutritional Se affects the energy metabolism in pig liver remains unknown. In the present study, super-nutritional Se supplementation (as selenomethionine) effects on liver selenoprotein expression and energy metabolite profiles in pigs were evaluated. In total, 36 castrated male pigs (Duroc × Landrace × Yorkshire, 62.3 ± 3.3 kg) were randomly assigned to two treatment groups with six replicates of three pigs per replicate. The two treatment groups received the same basal diet supplemented with different levels of selenomethionine: Se adequate (Se-A, 0.25 mg Se/kg) and Se supra-nutritional (2.5 mg Se/kg) for 60 days. Animals were then scarified and their livers were sampled for Se content, selenotranscriptome, and energy-targeted metabolite profile analysis. Super-nutritional Se supplementation increased the levels of serum fasting glucose, insulin, and free fatty acid levels (P < 0.05), as well as elevated the total Se liver content (P < 0.05). Glutathione peroxidase 4 mRNA expression was upregulated, while thioredoxin reductase 1 and selenoprotein W mRNA expression levels were downregulated in the super-nutritional Se group. LC-MS-based target metabolomics showed that high Se supplementation increased the levels of most metabolites involved in glycolysis, pentose phosphate pathway, tricarboxylic acid cycle, and acylcarnitine metabolism. These results indicated that dietary super-nutritional Se can regulate energy metabolism homeostasis in the pig liver.