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线粒体在氧化应激和衰老中的作用。

Role of mitochondria in oxidative stress and ageing.

作者信息

Lenaz G

机构信息

Dipartimento di Biochimica, Università di Bologna, Via Irnerio 48, 40126 Bologna, Italy.

出版信息

Biochim Biophys Acta. 1998 Aug 10;1366(1-2):53-67. doi: 10.1016/s0005-2728(98)00120-0.

Abstract

Mitochondria are deeply involved in the production of reactive oxygen species through one-electron carriers in the respiratory chain; mitochondrial structures are also very susceptible to oxidative stress as evidenced by massive information on lipid peroxidation, protein oxidation, and mitochondrial DNA (mtDNA) mutations. Oxidative stress can induce apoptotic death, and mitochondria have a central role in this and other types of apoptosis, since cytochrome c release in the cytoplasm and opening of the permeability transition pore are important events in the apoptotic cascade. The discovery that mtDNA mutations are at the basis of a number of human pathologies has profound implications: maternal inheritance of mtDNA is the basis of hereditary mitochondrial cytopathies; accumulation of somatic mutations of mtDNA with age has represented the basis of the mitochondrial theory of ageing, by which a vicious circle is established of mtDNA damage, altered oxidative phosphorylation and overproduction of reactive oxygen species. Experimental evidence of respiratory chain defects and of accumulation of multiple mtDNA deletions with ageing is in accordance with the mitochondrial theory, although some other experimental findings are not directly ascribable to its postulates.

摘要

线粒体通过呼吸链中的单电子载体深度参与活性氧的产生;线粒体结构也极易受到氧化应激的影响,大量关于脂质过氧化、蛋白质氧化和线粒体DNA(mtDNA)突变的信息证明了这一点。氧化应激可诱导凋亡性死亡,线粒体在这种及其他类型的凋亡中起核心作用,因为细胞质中细胞色素c的释放和通透性转换孔的开放是凋亡级联反应中的重要事件。mtDNA突变是多种人类疾病基础这一发现具有深远意义:mtDNA的母系遗传是遗传性线粒体细胞病的基础;随着年龄增长,mtDNA体细胞突变的积累是线粒体衰老理论的基础,据此建立了一个恶性循环,即mtDNA损伤、氧化磷酸化改变和活性氧过度产生。呼吸链缺陷以及随着年龄增长多个mtDNA缺失积累的实验证据与线粒体理论相符,尽管其他一些实验结果不能直接归因于该理论的假设。

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