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Pioglitazone retrieves hepatic antioxidant DNA repair in a mice model of high fat diet

机译:吡格列酮在高脂饮食小鼠模型中恢复肝脏抗氧化剂DNA的修复

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摘要

BackgroundPioglitazone was reported to improve hepatic steatosis and necroinflammation in human studies. To investigate whether the hepato-protective effect of pioglitazone was associated with an improvement of antioxidant defense mechanism, oxidative DNA damage and repair activity were determined in a high fat diet model. Male C57BL/6 mice were respectively fed with a 30% fat diet, the same diet with pioglitazone 100 mg/kg/day, or a chow diet as control for 8 weeks. Tissue oxidative stress was indicated by malondialdehyde concentration. Oxidative DNA damage was detected by immunohistochemical 8-oxoG staining. Enzymatic antioxidant defense was detected by the real-time PCR of superoxide dismutase (Sod1, Sod2) and DNA glycosylase (Ogg1, MutY). Oxidative DNA repair was detected by immunohistochemical staining and western blotting of OGG1 expression.
机译:背景在人体研究中据报道吡格列酮可改善肝脂肪变性和坏死性炎症。为了研究吡格列酮的肝保护作用是否与抗氧化防御机制的改善有关,在高脂饮食模型中确定了氧化DNA损伤和修复活性。雄性C57BL / 6小鼠分别饲喂30%的脂肪饮食,相同的吡格列酮100 mg / kg /天的饮食或作为对照的普通饮食,持续8周。通过丙二醛浓度指示组织氧化应激。通过免疫组织化学8-oxoG染色检测到氧化性DNA损伤。通过实时PCR检测超氧化物歧化酶(Sod1,Sod2)和DNA糖基化酶(Ogg1,MutY)的酶促抗氧化防御能力。通过免疫组化染色和OGG1表达的Western印迹检测氧化性DNA修复。

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