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Clinical Chemistry and Laboratory Medicine (CCLM)

Published in Association with the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM)

Editor-in-Chief: Plebani, Mario

Ed. by Gillery, Philippe / Greaves, Ronda / Lackner, Karl J. / Lippi, Giuseppe / Melichar, Bohuslav / Payne, Deborah A. / Schlattmann, Peter


IMPACT FACTOR 2018: 3.638

CiteScore 2018: 2.44

SCImago Journal Rank (SJR) 2018: 1.191
Source Normalized Impact per Paper (SNIP) 2018: 1.205

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1437-4331
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Volume 41, Issue 10

Issues

Mitochondrial Oxidative Stress and Mitochondrial DNA

Dongchon Kang / Naotaka Hamasaki
Published Online: 2005-06-01 | DOI: https://doi.org/10.1515/CCLM.2003.195

Abstract

Mitochondria produce reactive oxygen species (ROS) under physiological conditions in association with activity of the respiratory chain in aerobic ATP production. The production of ROS is essentially a function of O2 consumption. Hence, increased mitochondrial activity per se can be an oxidative stress to cells. Furthermore, production of ROS is markedly enhanced in many pathological conditions in which the respiratory chain is impaired. Because mitochondrial DNA, which is essential for execution of normal oxidative phosphorylation, is located in proximity to the ROS-generating respiratory chain, it is more oxidatively damaged than is nuclear DNA. Cumulative damage of mitochondrial DNA is implicated in the aging process and in the progression of such common diseases as diabetes, cancer, and heart failure. Clin Chem Lab Med 2003; 41(10):12811288

About the article

Published Online: 2005-06-01

Published in Print: 2003-09-19


Citation Information: Clinical Chemistry and Laboratory Medicine, Volume 41, Issue 10, Pages 1281–1288, ISSN (Print) 1434-6621, DOI: https://doi.org/10.1515/CCLM.2003.195.

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