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High-fat diet-induced changes in liver thioredoxin and thioredoxin reductase as a novel feature of insulin resistance

机译:高脂饮食诱导肝脏硫氧还蛋白和硫氧还蛋白还原酶的变化是胰岛素抵抗的新特征

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摘要

High-fat diet (HFD) can induce oxidative stress. Thioredoxin (Trx) and thioredoxin reductase (TrxR) are critical antioxidant proteins but how they are affected by HFD remains unclear. Using HFD-induced insulin-resistant mouse model, we show here that liver Trx and TrxR are significantly decreased, but, remarkably, the degree of their S-acylation is increased after consuming HFD. These HFD-induced changes in Trx/TrxR may reflect abnormalities of lipid metabolism and insulin signaling transduction. HFD-driven accumulation of 4-hydroxynonenal is another potential mechanism behind inactivation and decreased expression of Trx/TrxR. Thus, we propose HFD-induced impairment of liver Trx/TrxR as major contributor to oxidative stress and as a novel feature of insulin resistance.
机译:高脂饮食(HFD)可以诱发氧化应激。硫氧还蛋白(Trx)和硫氧还蛋白还原酶(TrxR)是关键的抗氧化剂蛋白,但如何影响HFD尚不清楚。使用HFD诱导的胰岛素抵抗小鼠模型,我们在这里显示肝脏Trx和TrxR显着降低,但值得注意的是,食用HFD后它们的S-酰化程度增加。这些HFD诱导的Trx / TrxR变化可能反映了脂质代谢和胰岛素信号转导的异常。 HFD驱动的4-羟基壬烯醛积累是失活和Trx / TrxR表达降低的另一个潜在机制。因此,我们提出HFD诱导的肝Trx / TrxR损伤是氧化应激的主要贡献者,也是胰岛素抵抗的新特征。

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