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Acrolein, A Reactive Product of Lipid Peroxidation, Induces Oxidative Modification of Cytochrome c

机译:丙烯醛,脂质过氧化的反应产物,诱导细胞色素c的氧化修饰

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Acrolein (ACR) is a well-known carbonyl toxin produced by lipid peroxidation of polyunsaturated fatty acids, which is involved in the pathogenesis of neurodegenerative disorders such as Alzheimer’s disease (AD). In Alzheimer`s brain, ACR was found to be elevated in hippocampus and temporal cortex where oxidative stress is high. In this study, we evaluated oxidative modification of cytochrome c occurring after incubation with ACR. When cytochrome c was incubated with ACR, protein aggregation increased in a dose-dependent manner. The formation of carbonyl compounds and the release of iron were obtained in ACR-treated cytochrome c. Reactive oxygen species scavengers and iron specific chelator inhibited the ACR-mediated cytochrome c modification and carbonyl compound formation. Our data demonstrate that oxidative damage of cytochrome c by ACR might induce disruption of cyotochrome c structure and iron mishandling as a contributing factor to the pathology of AD.
机译:丙烯醛(ACR)是由多不饱和脂肪酸的脂质过氧化作用产生的一种众所周知的羰基毒素,其参与神经退行性疾病(例如阿尔茨海默氏病(AD))的发病机理。在阿尔茨海默氏症的大脑中,发现氧化应激高的海马和颞叶皮质中的ACR升高。在这项研究中,我们评估了与ACR孵育后细胞色素c的氧化修饰。当将细胞色素c与ACR孵育时,蛋白质聚集以剂量依赖性方式增加。在ACR处理的细胞色素c中获得了羰基化合物的形成和铁的释放。活性氧清除剂和铁特异性螯合剂抑制了ACR介导的细胞色素c修饰和羰基化合物的形成。我们的数据表明,ACR对细胞色素c的氧化损伤可能诱导细胞色素c结构的破坏和铁的不当处理,这是导致AD病理的一个因素。

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