线粒体功能障碍及其抗氧化剂管理

K. Koteeswaran, N. Keerthana
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摘要

对于正常的细胞功能来说,ATP的产生是非常重要的,它是由线粒体产生的,它们也是一个重要的细胞器。当线粒体功能障碍发生时,有时会产生高能量需求,这对神经元细胞之间的信号传递等细胞至关重要,也影响心肌细胞。线粒体作为细胞的动力源,通过活性氧在分子间传递信号,并决定细胞的命运。但有时活性氧产生的时间更多,为了维持线粒体正常的稳态功能,线粒体电子传递需要快速激活抗氧化防御系统。但是当抗氧化防御系统没有做出正确的反应或缺失导致线粒体功能障碍时,它们会在人类神经系统中产生退行性疾病,它们会显著地导致心脏病理因为线粒体在心脏组织中更丰富由于线粒体功能障碍,它们还与肺相关疾病有关,如石棉,肺癌,慢性气道疾病和肺纤维化。与核DNA相比,线粒体DNA对氧化剂更敏感,因为它们编码线粒体蛋白质。当线粒体DNA受到损伤时,会发生电子传递链损伤和线粒体膜的潜在损失。本文总结了氧化应激诱导线粒体功能障碍产生肺相关、心脏相关和神经相关疾病的途径之一是通过抗氧化诱导线粒体生物发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial Dysfunction and Their Management by Antioxidants
For normal cell functioning generation of ATP is very important, and it is produced by mitochondria, and they also an important organelle. When sometimes mitochondrial dysfunction occur produces high energy will be demanded, and it is critical for cells such as signal transmission between neuronal cells and also affects cardiomyocytes. Mitochondria and their role to act as power house of the cell and through reactive oxygen species they transmit signaling between molecule and also determination of cellular fate. But sometimes the reactive oxygen species generated more that time, for maintaining normal homeostatic mitochondrial function rapid activation of antioxidant defense system that is required by mitochondrial electron transport. But that time antioxidant defense system is not responded properly or absent that cause mitochondrial dysfunction is occurred at that time they produce degenerative diseases in human beings that is nervous system, and they significantly contribute to produce a cardiac pathology because mitochondria are more abundant in cardiac tissues due to mitochondrial dysfunction, and also they are involved in lung related diseases that is asbestos, lung cancer, chronic airway disease and lung fibrosis. When compared to nuclear DNA the mitochondrial DNA is more sensitive to oxidants because they encode the mitochondrial proteins. When damages to mitochondrial DNA, that case impairment occurs in electron transport chain and potential loss in mitochondrial membrane.  In this review I concluded that by, oxidative stress induced mitochondrial dysfunction produced lung related heart related and neurological related disease and their one of the way of  prevention is by antioxidant induced mitochondrial biogenesis.
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