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细胞呼吸的氧顺应性。线粒体生理学的一个视角。

Oxygen conformance of cellular respiration. A perspective of mitochondrial physiology.

作者信息

Gnaiger Erich

机构信息

Department of Transplant Surgery, University Hospital Innsbruck, Austria.

出版信息

Adv Exp Med Biol. 2003;543:39-55. doi: 10.1007/978-1-4419-8997-0_4.

Abstract

Oxygen pressure declines from normoxic air-level to the microenvironment of mitochondria where cytochrome c oxidase (COX) reduces oxygen to water at oxygen levels as low as 0.3 kPa (2 Torr; 3 microM; 1.5 % air saturation). Intracellular hypoxia is defined as (1) local oxygen pressure below normoxic reference states, or (2) limitation of mitochondrial respiration by oxygen levels below kinetic saturation, resulting in oxyconformance. High-resolution respirometry provides the methodology to measure mitochondrial and cellular oxygen kinetics in the relevant low oxygen range < 1 kPa (7.5 mmHg; 9-10 microM; 5% air saturation). Respiration of isolated heart mitochondria follows hyperbolic oxygen kinetics with half-saturating oxygen pressure, p50, of 0.04 kPa (0.3 Torr; 0.4 microM) in ADP-stimulated state 3. Thus mitochondrial respiration proceeds at 90% of its hyperbolic maximum at the p50 of myoglobin, suggesting the possibility of a small but significant oxygen limitation even under normoxia in active muscle. Any impairment of oxygen delivery, therefore, induces oxyconformance. In addition, a shift of mitochondrial oxygen kinetics to the right, particularly by competitive inhibition of COX by NO, causes a further depression of respiration and a compensatory increase of local oxygen pressure. Above 1 kPa, mitochondrial oxygen uptake increases above hyperbolic saturation, which is probably due to oxygen radical production rather than the kinetics of COX. In cultured cells, the pronounced oxygen uptake above mitochondrial saturation at air-level oxygen pressure cannot be inhibited by rotenone and antimycin A, amounting to > 20 % of routine respiration in fibroblasts. Biochemical models of oxyconformance of COX are evaluated relative to patterns of intracellular oxygen distribution in the tissue and enzyme turnover in vivo, considering the kinetic effects of COX excess capacity on flux through the mitochondrial electron transport chain.

摘要

氧分压从常氧空气水平下降到线粒体的微环境,在那里细胞色素c氧化酶(COX)在低至0.3 kPa(2 Torr;3 microM;1.5%空气饱和度)的氧水平下将氧还原为水。细胞内缺氧定义为:(1)局部氧分压低于常氧参考状态,或(2)氧水平低于动力学饱和时线粒体呼吸的限制,导致氧顺应性。高分辨率呼吸测定法提供了在相关低氧范围<1 kPa(7.5 mmHg;9 - 10 microM;5%空气饱和度)测量线粒体和细胞氧动力学的方法。在ADP刺激的状态3下,分离的心脏线粒体呼吸遵循双曲线氧动力学,半饱和氧分压p50为0.04 kPa(0.3 Torr;0.4 microM)。因此,线粒体呼吸在肌红蛋白的p50时达到其双曲线最大值的90%,这表明即使在活跃肌肉的常氧条件下也可能存在轻微但显著的氧限制。因此,任何氧输送的损害都会诱导氧顺应性。此外,线粒体氧动力学向右移动,特别是通过一氧化氮对COX的竞争性抑制,会导致呼吸进一步降低和局部氧分压的代偿性增加。高于1 kPa时,线粒体氧摄取增加超过双曲线饱和,这可能是由于氧自由基产生而不是COX的动力学。在培养细胞中,在空气水平氧压下高于线粒体饱和的明显氧摄取不能被鱼藤酮和抗霉素A抑制,在成纤维细胞中占常规呼吸的>20%。考虑到COX过量容量对通过线粒体电子传递链通量的动力学影响,相对于组织中细胞内氧分布模式和体内酶周转情况,评估了COX氧顺应性的生化模型。

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