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In vitro nonenzymatic glycation enhances the role of myoglobin as a source of oxidative stress.

机译:体外非酶糖基化增强了肌红蛋白作为氧化应激源的作用。

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Metmyoglobin (Mb) was glycated by glucose in a non-enzymatic in vitro reaction. Amount of iron release from the heme pocket of myoglobin was found to be directly related with the extent of glycation. After in vitro glycation, the unchanged Mb and glycated myoglobin (GMb) were separated by ion exchange (BioRex 70) chromatography, which eliminated free iron from the protein fractions. Separated fractions of Mb and GMb were converted to their oxy forms -MbO2 and GMbO2, respectively. H2O2-induced iron release was significantly higher from GMbO2 than that from MbO2. This free iron, acting as a Fenton reagent, might produce free radicals and degrade different cell constituents. To verify this possibility, degradation of different cell constituents catalyzed by these fractions in the presence of H2O2 was studied. GMbO2 degraded arachidonic acid, deoxyribose and plasmid DNA more efficiently than MbO2. Arachidonic acid peroxidation and deoxyribose degradation were significantly inhibited by desferrioxamine (DFO), mannitol and catalase. However, besides free iron-mediated free radical reactions, role of iron of higher oxidation states, formed during interaction of H2O2 with myoglobin might also be involved in oxidative degradation processes. Formation of carbonyl content, an index of oxidative stress, was higher by GMbO2. Compared to MbO2, GMbO2 was rapidly autooxidized and co-oxidized with nitroblue tetrazolium, indicating increased rate of Mb and superoxide radical formation in GMbO2. GMb exhibited more peroxidase activity than Mb, which was positively correlated with ferrylmyoglobin formation in the presence of H2O2. These findings correlate glycation-induced modification of myoglobin and a mechanism of increased formation of free radicals. Although myoglobin glycation is not significant within muscle cells, free myoglobin in circulation, if becomes glycated, may pose a serious threat by eliciting oxidative stress, particularly in diabetic patients.
机译:在非酶体外反应中,葡萄糖将糖化肌红蛋白(Mb)糖化。发现从肌红蛋白的血红素袋释放的铁量与糖基化程度直接相关。体外糖基化后,未离子化的Mb和糖化的肌红蛋白(GMb)通过离子交换色谱(BioRex 70)色谱分离,从而消除了蛋白质部分中的游离铁。 Mb和GMb的分离馏分分别转化为氧形式-MbO2和GMbO2。 H2O2引起的铁释放从GMbO2明显高于MbO2。用作Fenton试剂的这种游离铁可能产生自由基并降解不同的细胞成分。为了证实这种可能性,研究了在H 2 O 2存在下由这些级分催化的不同细胞成分的降解。 GMbO2比MbO2更有效地降解了花生四烯酸,脱氧核糖和质粒DNA。去铁胺(DFO),甘露醇和过氧化氢酶可明显抑制花生四烯酸的过氧化和脱氧核糖的降解。但是,除了游离铁介导的自由基反应外,H2O2与肌红蛋白相互作用期间形成的较高氧化态的铁的作用也可能参与氧化降解过程。 GMbO2使羰基含量的形成(氧化应激的指标)更高。与MbO2相比,GMbO2迅速被自氧化并与硝基蓝四唑共氧化,表明GMbO2中Mb的速率增加和超氧自由基形成。 GMb表现出比Mb更多的过氧化物酶活性,这与存在H2O2时铁肌红蛋白的形成呈正相关。这些发现与糖基化引起的肌红蛋白的修饰和自由基形成增加的机制有关。尽管肌红蛋白的糖基化在肌肉细胞中并不重要,但是循环中游离的肌红蛋白如果被糖化,则可能通过引起氧化应激而构成严重威胁,尤其是在糖尿病患者中。

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