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Green Tea Polyphenols Ameliorate the Early Renal Damage Induced by a High-Fat Diet via Ketogenesis/SIRT3 Pathway.

Oxidative medicine and cellular longevity
January 1, 2017
Weijie Yi et al. (13 authors)
Journal ArticleAnimal StudyMolecular Study
Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
green tea polyphenols (GTPs)
decrease
increased renal oxidative stress
Wistar rats fed a high-fat diet
-
ameliorated
#1
green tea polyphenols (GTPs)
decrease
loss of renal function
Wistar rats fed a high-fat diet
-
ameliorated
#2
green tea polyphenols (GTPs)
increase
renal ketogenesis
Wistar rats fed a high-fat diet
-
restored
#3
green tea polyphenols (GTPs)
increase
SIRT3 expression and activity levels
Wistar rats fed a high-fat diet
-
restored
#4
high-fat diet (HFD)
decrease
renal ketogenesis
Wistar rats
-
reduced
#5
high-fat diet (HFD)
decrease
SIRT3 expression and activity levels
Wistar rats
-
reduced
#6
GTP treatment
increase
HMGCS2 expression
HEK293 cells
-
could upregulate
#7
GTP treatment
increase
SIRT3 expression
HEK293 cells
-
could upregulate
#8
HMGCS2 transfection
decrease
4-hydroxy-2-nonenal (4-HNE) level
HEK293 cells
-
reduced
#9
HMGCS2 transfection
decrease
acetyl-MnSOD (K122)/MnSOD ratio
HEK293 cells
-
reduced
#10
Abstract

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 CONCLUSION: The ketogenesis/SIRT3 pathway mediates the renoprotection of GTPs against the oxidative stress induced by an HFD.

Medical Subject Headings (MeSH)
AldehydesAnimalsBlood GlucoseBody WeightCholesterolDiet, High-FatForkhead Box Protein O3HEK293 CellsHumansHydroxymethylglutaryl-CoA SynthaseInsulinKidneyMaleOxidative StressPolyphenolsRatsRats, WistarSirtuin 3Superoxide DismutaseTea
Study Links
PubMed ID28814987
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