Elliott S J, Schilling W P
Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030.
Am J Physiol. 1992 Jul;263(1 Pt 2):H96-102. doi: 10.1152/ajpheart.1992.263.1.H96.
We have previously shown that oxidant stress activates Ca(2+)-dependent K+ efflux in pulmonary vascular endothelial cells. The present study was performed to determine the effect of oxidant stress on Na+ and K+ homeostasis using the radiotracers, 22Na+ and 86Rb+. Cellular ion contents at equilibrium were determined after incubation of cells with tert-butyl hydroperoxide (t-BOOH; 0.4 mM) for various durations. Cell content of 86Rb+ was unchanged through incubation periods of 2 h but was significantly decreased at 3 h, whereas cell content of 22Na+ progressively increased with increasing incubation duration. The effect of t-BOOH on Na+ pump and Na(+)-K(+)-Cl- cotransporter activities was examined via measurement of 86Rb+ influx in the absence or presence of ouabain and bumetanide, respectively. Oxidant stress time dependently increased ouabain-sensitive 86Rb+ influx, with little alteration in specific ouabain binding. In contrast, bumetanide-sensitive 86Rb+ influx was decreased by incubation with the oxidant. These findings suggest that the oxidant-induced increase in cellular Na+ content is associated with increased plasmalemmal Na(+)-K(+)-adenosinetriphosphatase activity. Furthermore, inward ion movement via the bumetanide-sensitive pathway is decreased, suggesting that oxidant stress inhibits the Na(+)-K(+)-Cl- cotransporter.
我们之前已经表明,氧化应激可激活肺血管内皮细胞中依赖钙的钾离子外流。本研究旨在使用放射性示踪剂22Na+和86Rb+来确定氧化应激对钠钾稳态的影响。在用叔丁基过氧化氢(t-BOOH;0.4 mM)孵育细胞不同时长后,测定平衡状态下的细胞离子含量。在长达2小时的孵育期内,86Rb+的细胞含量没有变化,但在3小时时显著降低,而22Na+的细胞含量则随着孵育时间的增加而逐渐增加。分别通过在不存在或存在哇巴因和布美他尼的情况下测量86Rb+内流,来检测t-BOOH对钠泵和Na(+)-K(+)-Cl-共转运体活性的影响。氧化应激使哇巴因敏感的86Rb+内流呈时间依赖性增加,而哇巴因特异性结合几乎没有改变。相反,用氧化剂孵育会使布美他尼敏感的86Rb+内流减少。这些发现表明,氧化剂诱导的细胞内钠含量增加与质膜Na(+)-K(+)-三磷酸腺苷酶活性增加有关。此外,通过布美他尼敏感途径的内向离子移动减少,这表明氧化应激会抑制Na(+)-K(+)-Cl-共转运体。