Cytochrome c Oxidase Inhibition by ATP Decreases Mitochondrial ROS Production

被引:17
|
作者
Ramzan, Rabia [1 ]
Dolga, Amalia M. [2 ]
Michels, Susanne [3 ]
Weber, Petra [1 ]
Culmsee, Carsten [3 ]
Rastan, Ardawan J. [1 ]
Vogt, Sebastian [1 ]
机构
[1] Univ Hosp Giessen & Marburg UKGM, Dept Heart Surg, Mitochondrial Bioenerget Lab, Baldingerstr 1, D-35043 Marburg, Germany
[2] Univ Groningen, Fac Math & Nat Sci, NL-49747 AG Groningen, Netherlands
[3] Philipps Univ Marburg, Inst Pharmacol & Clin Pharm, D-35043 Marburg, Germany
关键词
cytochrome c oxidase; ATP; mitochondrial membrane potential; ROS; OXIDATIVE-PHOSPHORYLATION; RESPIRATORY CONTROL; ELECTRON-TRANSPORT; HEART; STRESS; MECHANISMS; GENERATION; TISSUES; DAMAGE;
D O I
10.3390/cells11060992
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study addresses the eventual consequence of cytochrome c oxidase (CytOx) inhibition by ATP at high ATP/ADP ratio in isolated rat heart mitochondria. Earlier, it has been demonstrated that the mechanism of allosteric ATP inhibition of CytOx is one of the key regulations of mitochondrial functions. It is relevant that aiming to maintain a high ATP/ADP ratio for the measurement of CytOx activity effectuating the enzymatic inhibition as well as mitochondrial respiration, optimal concentration of mitochondria is critically important. Likewise, only at this concentration, were the differences in Delta psi(m) and ROS concentrations measured under various conditions significant. Moreover, when CytOx activity was inhibited in the presence of ATP, mitochondrial respiration and Delta psi(m) both remained static, while the ROS production was markedly decreased. Consubstantial results were found when the electron transport chain was inhibited by antimycin A, letting only CytOx remain functional to support the energy production. This seems to corroborate that the decrease in mitochondrial ROS production is solely the effect of ATP binding to CytOx which results in static respiration as well as membrane potential.
引用
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页数:15
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