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Abstract
Pyruvate functions as a key molecule in energy production and as an antioxidant. The efficacy of pyruvate supplementation in diabetic retinopathy and nephropathy has been shown in animal models; however, its significance in the functional maintenance of neurons and Schwann cells under diabetic conditions remains unknown. We observed rapid and extensive cell death under high-glucose (> 10 mM) and pyruvate-starved conditions. Exposure of Schwann cells to these conditions led to a significant decrease in glycolytic flux, mitochondrial respiration and ATP production, accompanied by enhanced collateral glycolysis pathways (e.g., polyol pathway). Cell death could be prevented by supplementation with 2-oxoglutarate (a TCA cycle intermediate), benfotiamine (the vitamin B1 derivative that suppresses the collateral pathways), or the poly (ADP-ribose) polymerase (PARP) inhibitor, rucaparib. Our findings suggest that exogenous pyruvate plays a pivotal role in maintaining glycolysis–TCA cycle flux and ATP production under high-glucose conditions by suppressing PARP activity.
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Details
1 Tokyo Metropolitan Institute of Medical Science, Diabetic Neuropathy Project, Tokyo, Japan (GRID:grid.272456.0)
2 Aichi Gakuin University, School of Pharmacy, Laboratory of Medicine, Nagoya, Japan (GRID:grid.411253.0) (ISNI:0000 0001 2189 9594)
3 Tokyo Metropolitan Institute of Medical Science, Basic Technology Research Center, Tokyo, Japan (GRID:grid.272456.0)