Beck F X, Dörge A, Giebisch G, Thurau K
Department of Physiology, University of Munich, Federal Republic of Germany.
Kidney Int. 1990 Jun;37(6):1423-8. doi: 10.1038/ki.1990.132.
To study the short-term uptake of potassium across the basolateral membrane into individual tubule cells, rubidium was used and measured by electron microprobe analysis. Changes of rubidium uptake were interpreted to reflect altered sodium entry and basolateral Na-K-ATPase activity. The effects of hydrochlorothiazide, amiloride and furosemide were determined in saline-loaded animals. Hydrochlorothiazide inhibited rubidium uptake in proximal convoluted and distal convoluted tubule cells. The effect was largest in distal convoluted tubule cells. Amiloride reduced rubidium uptake in principal cells as well as in proximal convoluted, distal convoluted and connecting tubule cells. Furosemide depressed rubidium uptake in distal convoluted tubule cells, but increased uptake in principal cells. Rubidium uptake into intercalated cells was not affected by any of the diuretics used. Hydrochlorothiazide and amiloride altered rubidium uptake also in cells not associated with the main diuretic action. These effects of hydrochlorothiazide and amiloride may be due to interference with cell transport mechanisms of Na-H and anion exchange.
为了研究钾通过基底外侧膜进入单个肾小管细胞的短期摄取情况,采用铷并通过电子微探针分析进行测量。铷摄取的变化被解释为反映钠进入和基底外侧钠钾ATP酶活性的改变。在盐水负荷的动物中测定了氢氯噻嗪、阿米洛利和呋塞米的作用。氢氯噻嗪抑制近端曲管和远端曲管细胞中的铷摄取。在远端曲管细胞中作用最大。阿米洛利减少主细胞以及近端曲管、远端曲管和连接管细胞中的铷摄取。呋塞米降低远端曲管细胞中的铷摄取,但增加主细胞中的摄取。闰细胞中的铷摄取不受所用任何利尿剂的影响。氢氯噻嗪和阿米洛利在与主要利尿作用无关的细胞中也改变了铷摄取。氢氯噻嗪和阿米洛利的这些作用可能是由于干扰了钠氢和阴离子交换的细胞转运机制。