4.5 Article

High fat high fructose diet induces mild oxidative stress and reorganizes intermediary metabolism in male mouse liver: Alpha-ketoglutarate effects

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ELSEVIER
DOI: 10.1016/j.bbagen.2022.130226

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Alpha-ketoglutarate; Antioxidant enzymes; Fructose; Glycolysis; Oxidative stress; Liver

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  1. Vitalii Derkachov

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This study investigated the effects of a high fat high fructose diet (HFFD) on mouse liver and found that it activated fructolysis and glycolysis, induced inflammation and oxidative stress. Additionally, supplementation with alpha-ketoglutarate (AKG) had weak modulating effects on HFFD-induced oxidative stress and changes in energetics in mouse liver.
Background: Diets rich in fats and/or carbohydrates are used to study obesity and related metabolic complications. We studied the effects of a high fat high fructose diet (HFFD) on intermediary metabolism and the development of oxidative stress in mouse liver and tested the ability of alpha-ketoglutarate to prevent HFFDinduced changes.Methods: Male mice were fed a standard diet (10% kcal fat) or HFFD (45% kcal fat, 15% kcal fructose) with or without addition of 1% alpha-ketoglutarate (AKG) in drinking water for 8 weeks.Results: The HFFD had no effect on body mass but activated fructolysis and glycolysis and induced inflammation and oxidative stress with a concomitant increase in activity of antioxidant enzymes in the mouse liver. HFFD-fed mice also showed lower mRNA levels of pyruvate dehydrogenase kinase 4 (PDK4) and slightly increased intensity of mitochondrial respiration in liver compared to mice on the standard diet. No significant effects of HFFD on transcription of PDK2 and PGC1 alpha, a peroxisome proliferator-activated receptor co-activator-1 alpha, or protein levels of p-AMPK, an active form of AMP-activated protein kinase, were found. The addition of AKG to HFFD decreased oxidized glutathione levels, did not affect levels of lipid peroxides and PDK4 transcripts but increased activities of hexokinase and phosphofructokinase in mouse liver.Conclusions: Supplementation with AKG had weak modulating effects on HFFD-induced oxidative stress and changes in energetics in mouse liver. General significance: Our research expands the understanding of diet-induced metabolic switching and elucidates further roles of alpha-ketoglutarate as a metabolic regulator.

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