Oxidative Medicine and Cellular Longevity · 2017 · 34 citations · 37 references
Life SciencesBiochemistryNutritional SciencesMetabolic RegulationMetabolismRenal PathophysiologyKetone Body MetabolismRenal DiseaseRenal Molecular PhysiologyHek293 Cell ExpressionImpaired Kidney FunctionKetone Body SignalingOxidative Stress InjuryOxidative Stress MitigationRenal Oxidative StressRenoprotective EffectsTea Polyphenols
Scope . Several reports in the literature have suggested the renoprotective effects of ketone bodies and green tea polyphenols (GTPs). Our previous study found that GTP consumption could elevate the renal expression of the ketogenic rate‐limiting enzyme, which was decreased by a high‐fat diet (HFD) in rats. Here, we investigated whether ketogenesis can mediate renoprotection by GTPs against an HFD. Methods and Results . Wistar rats were fed a standard or HFD with or without GTPs for 18 weeks. The renal oxidative stress level, kidney function, renal expression, and activity levels of mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA (HMG‐CoA) synthase 2 (HMGCS2) and sirtuin 3(SIRT3) were detected. The increased renal oxidative stress and the loss of renal function induced by the HFD were ameliorated by GTPs. Renal ketogenesis and SIRT3 expression and activity levels, which were reduced by the HFD, were restored by GTPs. In vitro, HEK293 cells were transfected with the eukaryotic expression plasmid pcDNA HMGCS2. GTP treatment could upregulate HMGCS2 and SIRT3 expression. Although SIRT3 expression was not affected by HMGCS2 transfection, the 4‐hydroxy‐2‐nonenal (4‐HNE) level and the acetyl‐MnSOD (K122)/MnSOD ratio were reduced in HMGCS2‐transfected cells in the context of H 2 O 2 . Conclusion . The ketogenesis/SIRT3 pathway mediates the renoprotection of GTPs against the oxidative stress induced by an HFD.
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