Mitochondrial transmembrane potential and pH gradient during anoxia

寡霉素 洋地黄素 膜电位 生物化学 胞浆 线粒体 化学 ATP合酶 腺嘌呤核苷酸 线粒体载体 糖酵解 生物物理学 跨膜蛋白 缬霉素 化学渗透 电化学梯度 抗霉素A 细胞外 生物 ATP酶 核苷酸 新陈代谢 细菌外膜 受体 大肠杆菌 基因
作者
Börje S. Andersson,Tak Yee Aw,Dean P. Jones
出处
期刊:American Journal of Physiology-cell Physiology [American Physical Society]
卷期号:252 (4): C349-C355 被引量:192
标识
DOI:10.1152/ajpcell.1987.252.4.c349
摘要

The effect of anoxia on the mitochondrial transmembrane potential and pH gradient was studied in a preparation of isolated hepatocytes. Transmembrane potential (delta psi) was calculated from the distribution of triphenylmethylphosphonium between the mitochondrial, cytosolic, and extracellular compartments, which were separated by digitonin fractionation and centrifugation. Mitochondrial and cytosolic pH values were calculated from the distribution of the weak acid, dimethadione, which was determined similarly. After 30 min anoxia, the magnitude of mitochondrial delta psi was decreased from -163 to -133 mV and the delta pH (mitochondria vs. cytoplasm) was essentially unchanged (aerobic, 0.78 +/- 0.08; anaerobic, 0.76 +/- 0.11). Thus the protonmotive force (delta p = delta psi-Z delta pH), is largely retained even in the absence of electron flow and ATP synthesis. Inhibitors of the ATP synthase (oligomycin), mitochondrial adenine nucleotide carrier (atractyloside), and glycolytic pathway (2-deoxy-D-glucose) do not affect the ability of the cell to maintain delta psi during anoxia. Therefore, the results indicate that retention of the protonmotive force is not due to utilization of ATP produced by glycolysis and suggest that mechanisms exist to preserve ion distribution during anoxia.

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