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The mechanisms behind the reduction in muscle pyruvate dehydrogenase complex (PDC)-controlled carbohydrate (CHO) oxidation during chronic high-fat dietary intake are poorly understood, as is the basis of CHO oxidation restoration during muscle contraction. C2C12 myotubes were treated with (300 μM) palmitate or without (control) for 16 h in the presence and absence of electrical pulse stimulation (EPS, 11.5 V, 1 Hz, 2 ms). Compared to control, palmitate reduced cell glucose uptake ( p &lt; 0.05), PDC activity ( p &lt; 0.01), acetylcarnitine accumulation ( p &lt; 0.05) and glucose-derived mitochondrial ATP production ( p &lt; 0.01) and increased pyruvate dehydrogenase kinase isoform 4 (PDK4) ( p &lt; 0.01), peroxisome proliferator-activated receptor alpha (PPARα) ( p &lt; 0.01) and peroxisome proliferator-activated receptor delta (PPARδ) ( p &lt; 0.01) proteins, and reduced the whole-cell p -FOXO1/t-FOXO1 (Forkhead Box O1) ratio ( p &lt; 0.01). EPS rescued palmitate-induced inhibition of CHO oxidation, reflected by increased glucose uptake ( p &lt; 0.01), PDC activity ( p &lt; 0.01) and glucose-derived mitochondrial ATP production ( p &lt; 0.01) compared to palmitate alone. EPS was also associated with less PDK4 ( p &lt; 0.01) and PPARδ ( p &lt; 0.01) proteins, and lower nuclear p -FOXO1/t-FOXO1 ratio normalised to the cytoplasmic ratio, but with no changes in PPARα protein. Collectively, these data suggest PPARδ, and FOXO1 transcription factors increased PDK4 protein in the presence of palmitate, which limited PDC activity and flux, and blunted CHO oxidation and glucose uptake. Conversely, EPS rescued these metabolic events by modulating the same transcription factors.

international journal of molecular sciences

PPARδ and FOXO1 Mediate Palmitate-Induced Inhibition of Muscle Pyruvate Dehydrogenase Complex and CHO Oxidation, Events Reversed by Electrical Pulse Stimulation