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首页> 外文期刊>Toxicology and Applied Pharmacology >Effects of dapagliflozin and statins attenuate renal injury and liver steatosis in high-fat/high-fructose diet-induced insulin resistant rats
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Effects of dapagliflozin and statins attenuate renal injury and liver steatosis in high-fat/high-fructose diet-induced insulin resistant rats

机译:Dapagliflozin和他汀类药物在高脂肪/高果糖饮食诱导的胰岛素抗性大鼠中衰减肾损伤和肝脏脂肪变性的影响

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摘要

High-fat high-fructose diet (HFF) in obesity can induce dyslipidemia and lipid accumulation both in kidney and liver which related to insulin resistance and lipotoxicity-induced cellular damage. We investigated whether dapagliflozin with or without atorvastatin could improve lipid accumulation-induced kidney and liver injury in HFF-induced insulin resistant rats. Male Wistar rats were fed with HFF for 16 weeks and then received drug treatments for 4 weeks; vehicle, dapagliflozin, atorvastatin and dapagliflozin plus atorvastatin treatment groups. HFF rats demonstrated insulin resistance, dyslipidemia, liver injury and renal dysfunction associated with impaired renal lipid metabolism and lipid accumulation. Dapagliflozin and combination treatment could improve HFF-induced insulin resistance, lipogenesis and lipotoxicity-related renal oxidative stress, inflammation, fibrosis and apoptosis leading to kidney dysfunction recovery. Liver injury-associated inflammation was also improved by these two regimens. Notably, the reduced lipid accumulation in liver and kidney that linked to an improvement of lipid oxidation was prominent in the combination treatment. Therefore, dapagliflozin combined with atorvastatin treatment exert the beneficial effects on lipid metabolism and lipotoxicity in liver and kidney injury via the attenuation of oxidative stress, fibrosis and apoptosis in insulin resistant model.
机译:肥胖症中的高脂肪高果糖饮食(HFF)可以诱导肾病和肝脏中的血脂积累,患有胰岛素抵抗和脂毒性诱导的细胞损伤。我们调查了具有或不含阿托伐他汀的Dapagliflozin可以改善HFF诱导的胰岛素抗性大鼠的脂质积累诱导的肾脏和肝损伤。雄性Wistar大鼠用HFF喂食16周,然后接受药物治疗4周;车辆,Dapagliflozin,阿托伐他汀和Dapagliflozin Plus Atorvastatin治疗组。 HF大鼠显示出胰岛素抵抗,血脂血症,肝损伤和肾功能障碍与肾脏脂质代谢和脂质积累有损相关。 Dapagliflozin和组合治疗可以提高HFF诱导的胰岛素抵抗,脂肪生成和脂毒性相关的肾氧化应激,炎症,纤维化和凋亡,导致肾功能障碍回收。通过这两个方案还改善了肝损伤相关的炎症。值得注意的是,与脂质氧化改善有关的肝脏和肾脏的降低的脂质积累在组合治疗中突出。因此,Dapagliflozin联合阿托伐他汀治疗对胰岛素抗性,胰岛素抗性模型中氧化应激,纤维化和凋亡的衰减来对肝脏和肾损伤的脂质代谢和脂肪毒性的有益作用。

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