2022
DOI: 10.1016/j.bbagen.2022.130226
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High fat high fructose diet induces mild oxidative stress and reorganizes intermediary metabolism in male mouse liver: Alpha-ketoglutarate effects

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Cited by 6 publications
(5 citation statements)
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“…In this context, the excess of energy substrates from different types of diet is associated with oxidative damage to macromolecules such as lipids (lipid peroxidation or lipid peroxidation) and proteins (carbonylation and/or nitration) because they increase the production of ROS, which alter the chemical structure and/or biological function, inducing cell death and consequent deleterious effects (Fernández-Sánchez et al, 2011). Bayliak et al (2022) have observed that male mice fed high-fat high-fructose diet (45% kcal fat, 15% kcal fructose) presented mild oxidative stress with higher activities of primary antioxidant enzymes namely CAT, glutathione peroxidase (GPx), and glutathione-S-transferase. In disagreement with the literature, our findings showed no significant differences between the experimental groups for the levels of MDA and carbonylated proteins in serum and adipose tissue, as well as, the activities of antioxidant enzymes (SOD and CAT) did not present alterations, demonstrating that dietary interventions did not lead to oxidative stress.…”
Section: Discussionmentioning
confidence: 99%
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“…In this context, the excess of energy substrates from different types of diet is associated with oxidative damage to macromolecules such as lipids (lipid peroxidation or lipid peroxidation) and proteins (carbonylation and/or nitration) because they increase the production of ROS, which alter the chemical structure and/or biological function, inducing cell death and consequent deleterious effects (Fernández-Sánchez et al, 2011). Bayliak et al (2022) have observed that male mice fed high-fat high-fructose diet (45% kcal fat, 15% kcal fructose) presented mild oxidative stress with higher activities of primary antioxidant enzymes namely CAT, glutathione peroxidase (GPx), and glutathione-S-transferase. In disagreement with the literature, our findings showed no significant differences between the experimental groups for the levels of MDA and carbonylated proteins in serum and adipose tissue, as well as, the activities of antioxidant enzymes (SOD and CAT) did not present alterations, demonstrating that dietary interventions did not lead to oxidative stress.…”
Section: Discussionmentioning
confidence: 99%
“…Bayliak et al ( 2022 ) have observed that male mice fed high‐fat high‐fructose diet (45% kcal fat, 15% kcal fructose) presented mild oxidative stress with higher activities of primary antioxidant enzymes namely CAT, glutathione peroxidase (GPx), and glutathione‐ S ‐transferase. In disagreement with the literature, our findings showed no significant differences between the experimental groups for the levels of MDA and carbonylated proteins in serum and adipose tissue, as well as, the activities of antioxidant enzymes (SOD and CAT) did not present alterations, demonstrating that dietary interventions did not lead to oxidative stress.…”
Section: Discussionmentioning
confidence: 99%
“…HF diet induces metabolic syndrome and simple steatosis, usually not spontaneously progressing toward NASH unless an additional stimulus is provided [ 42 ]. The HFF diet induces liver pathology prior to, or even in the absence of, obesity or insulin resistance in association with skeletal muscle extracellular lipid accumulation, inflammation, and autophagy [ 43 ] and mild oxidative stress [ 44 ]. The CC diet was developed to mimic the cholesterol-mediated insulin resistance, cardiovascular risk increase, and NASH; the CC diet produces steatosis, inflammation, HSC activation, and fibrosis; however, animals fed with this diet are not insulin-resistant; and tend to lose weight and have lower triglyceride levels, with respect to standard chow-fed mice [ 2 ].…”
Section: Discussionmentioning
confidence: 99%
“…Activities of hexokinase, phosphofructokinase, pyruvate kinase, lactate dehydrogenase, and glutamate dehydrogenase (GDH) were determined by monitoring NADP + reduction or NADH oxidation at 340 nm as described previously (Bayliak et al, 2022; Gospodaryov et al, 2020; Lylyk et al, 2018).…”
Section: Methodsmentioning
confidence: 99%