Dong J, Delamere N A, Coca-Prados M
Department of Ophthalmology, University of Louisville School of Medicine, Kentucky 40292.
Am J Physiol. 1994 Jan;266(1 Pt 1):C198-205. doi: 10.1152/ajpcell.1994.266.1.C198.
Inhibition of Na(+)-K(+)-ATPase activates Na(+)-K(+)-2Cl- cotransporter activity in cultured ciliary epithelium. Am. J. Physiol. 266 (Cell Physiol. 35): C198-C205, 1994.--86Rb uptake experiments were conducted to measure Na(+)-K(+)-ATPase activity and Na(+)-K(+)-2Cl- cotransporter activity in a cell line derived from rabbit nonpigmented ciliary epithelium. The presence of a Na(+)-K(+)-2Cl- cotransporter was supported by the observation of a bumetanide-sensitive 86Rb uptake component that was dependent on the extracellular concentration of both sodium and chloride. Potassium influx mediated by the Na(+)-K(+)-2Cl- cotransporter and Na(+)-K(+)-ATPase accounted for approximately 46 and 33% of total potassium uptake, respectively, whereas both ouabain- and bumetanide-resistant uptake accounted for 9%. Inhibition of the Na(+)-K(+)-ATPase had a stimulatory effect on Na(+)-K(+)-2Cl- cotransporter activity, which was dependent on the extent and duration of Na(+)-K(+)-ATPase inhibition. Ouabain treatment stimulated the potassium (86Rb) efflux rate and reduced intracellular potassium ([K]i). Potassium channel blockers suppressed the ouabain-activated potassium efflux and inhibited the ouabain-induced activation of the Na(+)-K(+)-2Cl- cotransporter. We conclude that Na(+)-K(+)-ATPase inhibition leads to the opening of potassium channels, which exacerbates the depletion of cellular potassium; Na(+)-K(+)-2Cl- cotransporter stimulation caused by the fall of [K]i overrides the tendency of increased cellular sodium to inhibit the cotransporter.
抑制钠钾ATP酶可激活培养的睫状体上皮细胞中的钠钾2氯协同转运蛋白活性。《美国生理学杂志》266卷(细胞生理学35):C198 - C205,1994年。——进行了⁸⁶Rb摄取实验,以测量源自兔非色素睫状体上皮细胞系中的钠钾ATP酶活性和钠钾2氯协同转运蛋白活性。观察到布美他尼敏感的⁸⁶Rb摄取成分依赖于细胞外钠和氯的浓度,这支持了钠钾2氯协同转运蛋白的存在。由钠钾2氯协同转运蛋白和钠钾ATP酶介导的钾内流分别约占总钾摄取的46%和33%,而哇巴因和布美他尼抗性摄取占9%。抑制钠钾ATP酶对钠钾2氯协同转运蛋白活性有刺激作用,这取决于钠钾ATP酶抑制的程度和持续时间。哇巴因处理刺激了钾(⁸⁶Rb)外流速率并降低了细胞内钾浓度([K]i)。钾通道阻滞剂抑制了哇巴因激活的钾外流,并抑制了哇巴因诱导的钠钾2氯协同转运蛋白激活。我们得出结论,抑制钠钾ATP酶会导致钾通道开放,这加剧了细胞内钾的消耗;[K]i下降引起的钠钾2氯协同转运蛋白刺激克服了细胞内钠增加抑制协同转运蛋白的趋势。