Paradies G, Petrosillo G, Pistolese M, Ruggiero F M
Department of Biochemistry and Molecular Biology and CNR Unit for the Study of Mitochondria and Bioenergetics, University of Bari, Italy.
FEBS Lett. 2000 Jan 28;466(2-3):323-6. doi: 10.1016/s0014-5793(00)01082-6.
The effect of reactive oxygen species (ROS), produced by the mitochondrial respiratory chain, on the activity of cytochrome c oxidase and on the cardiolipin content in bovine heart submitochondrial particles (SMP) was studied. ROS were produced by treatment of succinate-respiring SMP with antimycin A. This treatment resulted in a large production of superoxide anion, measured by epinephrine method, which was blocked by superoxide dismutase (SOD). Exposure of SMP to mitochondrial mediated ROS generation, led to a marked loss of cytochrome c oxidase activity and to a parallel loss of cardiolipin content. Both these effects were completely abolished by SOD+catalase. Added cardiolipin was able to almost completely restore the ROS-induced loss of cytochrome c oxidase activity. No restoration was obtained with peroxidized cardiolipin. These results demonstrate that mitochondrial mediated ROS generation affects the activity of cytochrome c oxidase via peroxidation of cardiolipin which is needed for the optimal functioning of this enzyme complex. These results may prove useful in probing molecular mechanism of ROS-induced peroxidative damage to mitochondria which have been proposed to contribute to aging, ischemia/reperfusion and chronic degenerative diseases.
研究了线粒体呼吸链产生的活性氧(ROS)对牛心亚线粒体颗粒(SMP)中细胞色素c氧化酶活性和心磷脂含量的影响。通过用抗霉素A处理琥珀酸呼吸的SMP来产生ROS。该处理导致通过肾上腺素法测定的超氧阴离子大量产生,超氧化物歧化酶(SOD)可阻断这种产生。将SMP暴露于线粒体介导的ROS生成中,导致细胞色素c氧化酶活性显著丧失,同时心磷脂含量平行下降。超氧化物歧化酶+过氧化氢酶可完全消除这两种效应。添加的心磷脂能够几乎完全恢复ROS诱导的细胞色素c氧化酶活性丧失。过氧化的心磷脂则无法恢复活性。这些结果表明,线粒体介导的ROS生成通过心磷脂过氧化影响细胞色素c氧化酶的活性,而心磷脂过氧化是该酶复合物最佳功能所必需的。这些结果可能有助于探究ROS诱导的线粒体过氧化损伤的分子机制,线粒体过氧化损伤被认为与衰老、缺血/再灌注和慢性退行性疾病有关。