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Int J Mol Sci ; 22(5)2021 Feb 28.
Article in English | MEDLINE | ID: mdl-33670975

ABSTRACT

Excessive intake of fructose results in metabolic syndrome (MS) and kidney damage, partly mediated by its metabolism by fructokinase-C or ketohexokinase-C (KHK-C). Osthol has antioxidant properties, is capable of regulating adipogenesis, and inhibits KHK-C activity. Here, we examined the potential protective role of osthol in the development of kidney disease induced by a Western (high-fat/high-sugar) diet. Control rats fed with a high-fat/high-sugar diet were compared with two groups that also received two different doses of osthol (30 mg/kg/d or 40 mg/kg/d body weight BW). A fourth group served as a normal control and received regular chow. At the end of the follow-up, kidney function, metabolic markers, oxidative stress, and lipogenic enzymes were evaluated. The Western diet induced MS (hypertension, hyperglycemia, hypertriglyceridemia, obesity, hyperuricemia), a fall in the glomerular filtration rate, renal tubular damage, and increased oxidative stress in the kidney cortex, with increased expression of lipogenic enzymes and increased kidney KHK expression. Osthol treatment prevented the development of MS and ameliorated kidney damage by inhibiting KHK activity, preventing oxidative stress via nuclear factor erythroid 2-related factor (Nrf2) activation, and reducing renal lipotoxicity. These data suggest that the nutraceutical osthol might be an ancillary therapy to slow the progression of MS and kidney damage induced by a Western diet.


Subject(s)
Coumarins/pharmacology , Diet, Western/adverse effects , Fructokinases/antagonists & inhibitors , Kidney Diseases/prevention & control , Metabolic Syndrome/prevention & control , Animals , Coumarins/therapeutic use , Diet, Carbohydrate Loading/adverse effects , Diet, High-Fat/adverse effects , Fructokinases/metabolism , Fructose/metabolism , Kidney Diseases/etiology , Kidney Diseases/metabolism , Male , Metabolic Syndrome/etiology , Metabolic Syndrome/metabolism , NF-E2-Related Factor 2 , Oxidative Stress , Protective Agents/pharmacology , Protective Agents/therapeutic use , Rats , Rats, Wistar
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