(A) Modulation of gene expression by metabolites. (Left) mRNA expression of indicated genes (36B4: Rplp0 ribosomal protein, large, P0, HPRT: hypoxanthine guanine phosphoribosyl transferase, CYCS: cytochrome c, somatic, COX5B: cytochrome c oxidase subunit Vb, NDUFb5: NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 5, NR4A1 (or nur77): nuclear receptor subfamily 4, group A, member 1, PGC1a: peroxisome proliferator-activated receptor gamma, coactivator 1 alpha, HK2: hexokinase 2, PFKM: phosphofructokinase, muscle, MCAD: acyl-Coenzyme A dehydrogenase, medium chain, CD36: fatty–acid translocase, PDK4: pyruvate dehydrogenase kinase, isoenzyme 4) in C2C12 cells differentiated into myotubes 60 minutes after treating with the metabolite cocktail (black bars) versus control (white bars). The pooled metabolites consisted of glycerol, succinate, glucose-6-phosphate, pantothenate, and niacinamide. (Right) nr4a1 in cells 0, 60, and 240 minutes after treating with cocktail. ETC, electron transport chain. TFs, transcription factors, Glyc, glycolysis; FA, fatty acid transport. *P<0.05 vs. baseline values. (B) Modulation of gene expression by exercise. (Left) mRNA expression of nr4a1 in quadriceps 0, 30, and 240 minutes after running to maximum capacity. (Right) mRNA expression of PGC-1 α (ppargc1a) and PDK4 under the same conditions.