Author:
Yako Hideji,Niimi Naoko,Kato Ayako,Takaku Shizuka,Tatsumi Yasuaki,Nishito Yasumasa,Kato Koichi,Sango Kazunori
Abstract
AbstractPyruvate 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.
Funder
the Ministry of Education, Science, Sports, Culture and Technology of Japan
the Cooperative Research Project Program of the Medical Institute of Bioregulation, Kyushu University
the Nukada Institute for Medical and Biological Research
Sumitomo Dainippon Pharma Co., Ltd.
Publisher
Springer Science and Business Media LLC
Cited by
22 articles.
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