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首页> 外文期刊>The biochemical journal >Reoxygenation-dependent decrease in mitochondrial NADH:CoQ reductase (Complex I) activity in the hypoxic/reoxygenated rat heart
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Reoxygenation-dependent decrease in mitochondrial NADH:CoQ reductase (Complex I) activity in the hypoxic/reoxygenated rat heart

机译:缺氧/复氧大鼠心脏线粒体NADH:CoQ还原酶(复合体I)活性的复氧依赖性降低

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pReoxygenation of the hypoxic myocardium results in a number of processes, including an O2-dependent increase in total tissue Ca2+ and cell lysis in which mitochondrial electron transport plays a key role. In the present study we have isolated mitochondria from perfused rat hearts subjected to hypoxia and found no change in their respiratory function relative to controls. In contrast, mitochondria isolated immediately after reoxygenation of hypoxic-perfused hearts exhibited a specific and significant decrease in NADH:CoQ reductase (Complex I; EC 1.6.5.3) activity, as measured both polarographically and spectrophotometrically. Isolated cardiomyocytes subjected to a similar protocol of hypoxia/reoxygenation also exhibited a specific decrease in Complex I activity. Myocardial perfusion with media containing Ruthenium Red protected against the reoxygenation-dependent loss of Complex I activity. These observations taken together suggest that mitochondrial Ca2+ uptake on reoxygenation is implicated in the mechanism of the specific loss of Complex I activity./p
机译:低氧心肌的再氧化导致许多过程,包括O2依赖的总组织Ca2 +的增加和细胞裂解,其中线粒体电子传递起关键作用。在本研究中,我们从经历过缺氧的灌注大鼠心脏中分离出线粒体,发现其呼吸功能相对于对照组没有变化。相比之下,低氧灌注心脏再充氧后立即分离出的线粒体在极谱法和分光光度法下均显示出NADH:CoQ还原酶(复合体I; EC 1.6.5.3)活性的特异性和显着降低。经历了类似的缺氧/复氧方案的分离的心肌细胞也表现出复合物I活性的特异性降低。使用含钌红的培养基进行心肌灌注可防止复氧依赖性复合体I活性丧失。这些观察结果共同表明,线粒体钙离子在复氧过程中的摄取与复合物I活性特异性丧失的机制有关。

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