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Nucleic acid oxidation: an early feature of Alzheimer's disease

机译:核酸氧化:阿尔茨海默氏病的早期特征

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摘要

Studies of oxidative damage during the progression of Alzheimer's disease (AD) suggest its central role in disease pathogenesis. To investigate levels of nucleic acid oxidation in both early and late stages of AD, levels of multiple base adducts were quantified in nuclear and mitochondrial DNA from the superior and middle temporal gyri (SMTG), inferior parietal lobule (IPL), and cerebellum (CER) of age-matched normal control subjects, subjects with mild cognitive impairment, preclinical AD, late-stage AD, and non-AD neurological disorders (diseased control; DC) using gas chromatography/mass spectrometry. Median levels of multiple DNA adducts in nuclear and mitochondrial DNA were significantly (p <= 0.05) elevated in the SMTG, IPL, and CER in multiple stages of AD and in DC subjects. Elevated levels of fapyguanine and fapyadenine in mitochondrial DNA suggest a hypoxic environment early in the progression of AD and in DC subjects. Overall, these data suggest that oxidative damage is an early event not only in the pathogenesis of AD but is also present in neurodegenerative diseases in general.
机译:对阿尔茨海默氏病(AD)进展过程中的氧化损伤的研究表明,其在疾病发病机理中的重要作用。为了研究AD早期和晚期的核酸氧化水平,定量分析了颞中上回(SMTG),顶叶小叶(IPL)和小脑(CER)的核和线粒体DNA中的多种碱基加合物的水平。年龄匹配的正常对照受试者,患有轻度认知障碍,临床前AD,晚期AD和非AD神经系统疾病(疾病对照; DC)的受试者,采用气相色谱/质谱法。在ADTG和DC受试者的多个阶段中,SMTG,IPL和CER中核和线粒体DNA中多个DNA加合物的中值水平显着(p <= 0.05)升高。线粒体DNA中Fapyguanine和Fapyadenine的水平升高表明AD和DC受试者早期出现了低氧环境。总的来说,这些数据表明氧化损伤不仅是AD发病的早期事件,而且通常也存在于神经退行性疾病中。

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