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Diminished Superoxide Generation Is Associated With Respiratory Chain Dysfunction and Changes in the Mitochondrial Proteome of Sensory Neurons From Diabetic Rats

机译:超氧化物生成的减少与糖尿病大鼠的呼吸链功能障碍和感觉神经元线粒体蛋白质组的变化有关。

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摘要

Objective-impairments in mitochondrial function have been proposed to play a role in the etiology of diabetic sensory neuropathy. We tested the hypothesis that mitochondrial dysfunction in axons of sensory neurons in type 1 diabetes is due to abnormal activity of the respiratory chain and an altered mitochondrial proteome. Research design and methods-proteomic analysis using stable isotope labeling with amino acids in cell culture (silac) determined expression of proteins in mitochondria from dorsal root ganglia (drg) of control, 22-week-old streptozotocin (stz)-diabetic rats, and diabetic rats treated with insulin. Rates of oxygen consumption and complex activities in mitochondria from drg were measured. Fluorescence imaging of axons of cultured sensory neurons determined the effect of diabetes on mitochondrial polarization status, oxidative stress, and mitochondrial matrix-specific reactive oxygen species (ros). Results-proteins associated with mitochondrial dysfunction, oxidative phosphorylation, ubiquinone biosynthesis, and the citric acid cycle were downregulated in diabetic samples. For example, cytochrome c oxidase subunit iv (cox iv; a complex fv protein) and nadh dehydrogenase fe-s protein 3 (ndufs3; a complex i protein) were reduced by 29 and 36% (p < 0.05), respectively, in diabetes and confirmed previous western blot studies. Respiration and mitochondrial complex activity was significantly decreased by 15 to 32% compared with control. The axons of diabetic neurons exhibited oxidative stress and depolarized mitochondria, an aberrant adaption to oligomycin-in-duced mitochondrial membrane hyperpolarization, but reduced levels of intramitochondrial superoxide compared with control. Conclusions-abnormal mitochondrial function correlated with a downregulation of mitochondrial proteins, with components of the respiratory chain targeted in lumbar drg in diabetes. The reduced activity of the respiratory chain was associated with diminished superoxide generation within the mitochondrial matrix and did not contribute to oxidative stress in axons of diabetic neurons. Alternative pathways involving polyol pathway activity appear to contribute to raised ros in axons of diabetic neurons under high glucose concentration. Diabetes 60:288-297,2011
机译:已经提出线粒体功能的客观障碍在糖尿病感觉神经病的病因学中起作用。我们测试了一种假设,即1型糖尿病患者感觉神经元轴突中的线粒体功能障碍是由于呼吸链的异常活动和线粒体蛋白质组的改变所致。研究设计和方法-在细胞培养物中使用氨基酸进行稳定同位素标记的蛋白质组学分析(silac)确定了对照组,22周龄链脲佐菌素(stz)-糖尿病大鼠的背根神经节(drg)线粒体中蛋白质的表达糖尿病大鼠用胰岛素治疗。测量了来自drg的线粒体中的耗氧率和复杂活动。培养的感觉神经元轴突的荧光成像确定了糖尿病对线粒体极化状态,氧化应激和线粒体基质特异性活性氧(ros)的影响。结果与糖尿病患者血浆中与线粒体功能异常,氧化磷酸化,泛醌生物合成和柠檬酸循环有关的蛋白质被下调。例如,在糖尿病中,细胞色素C氧化酶亚基iv(cox iv;复合fv蛋白)和nadh脱氢酶fe-s蛋白3(ndufs3;复合i蛋白)分别降低了29%和36%(p <0.05)。并确认了先前的蛋白质印迹研究。与对照相比,呼吸和线粒体复合物活性显着降低了15%至32%。糖尿病神经元的轴突表现出氧化应激和去极化的线粒体,异常适应寡聚霉素诱导的线粒体膜超极化,但与对照相比线粒体内超氧化物水平降低。结论线粒体功能异常与线粒体蛋白的下调有关,并与糖尿病腰椎中呼吸道的成分有关。呼吸链活性的降低与线粒体基质内超氧化物生成的减少有关,并且对糖尿病神经元轴突的氧化应激没有贡献。在高葡萄糖浓度下,涉及多元醇途径活性的替代途径似乎有助于增加糖尿病神经元轴突中的ros。糖尿病60:288-297,2011

著录项

  • 来源
    《Diabetes》 |2011年第1期|p.288-297|共10页
  • 作者单位

    St. Boniface Hospital Research Centre, Winnipeg, Manitoba,Canada,Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Manitoba, Canada;

    St. Boniface Hospital Research Centre, Winnipeg, Manitoba,Canada;

    St. Boniface Hospital Research Centre, Winnipeg, Manitoba,Canada;

    St. Boniface Hospital Research Centre, Winnipeg, Manitoba,Canada,Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Manitoba, Canada;

    Department of Pharmacology and Toxicology, University of Kansas, Lawrence, Kansas;

    St. Boniface Hospital Research Centre, Winnipeg, Manitoba,Canada,Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Manitoba, Canada;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:46:32

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