Wiley J S, Cooper R A
J Clin Invest. 1974 Mar;53(3):745-55. doi: 10.1172/JCI107613.
The influxes of Na(+) and K(+) into the human red cell appear to be interrelated. This relationship was investigated under conditions in which either Na(+) or K(+) concentration outside the cell was varied or one cation was replaced by Mg(2+), choline(+), or Li(+). The effects of furosemide on Na(+) and K(+) movements were studied in the presence of ouabain. When ouabain was present, Na(+) influx was higher with K(+) ions externally than with other cations externally. Furosemide inhibited this K(+)-stimulated Na(+) influx, but it had little effect when K(+) was absent. Ouabain-insensitive K(+) influx was stimulated two-fold by external Na(+) compared with other cations. Furosemide also inhibited this stimulation, but it had little effect when Mg(2+) or choline(+) replaced external Na(+). Thus it was confirmed that synergism exists between the ouabain-insensitive influxes of Na(+) and K(+) and it was demostrated that furosemide inhibits this cooperative effect. The ouabain-insensitive influx of both K(+) and Na(+) showed a hyperbolic "saturating" dependence on the external concentration of the transported cation. Furosemide therefore eliminates a saturable component of influx of each cation. The net uptake of Na(+) in the presence of ouabain was stimulated by K(+) ions. A similar effect was observed with red cells, in which Li(+) replaced nearly all the internal Na(+) plus K(+) ions. In these cells, net Na(+) uptake was stimulated by external K(+), and net K(+) uptake was stimulated by external Na(+). Furosemide inhibited this mutual stimulation of net cation entries. The inhibitory action of furosemide was not limited to inward flux and net movement of Na(+) and K(+). Furosemide also inhibited the efflux of Na(+) into Na(+)-free media and the efflux of K(+) into K(+)-free media. It appeared, therefore, that the action of furosemide was not explained by inhibition of exchange diffusion. These data are consistent with an ouabain-insensitive transport process that facilitates the inward cotransport of Na(+) plus K(+)-ions, and that can produce a net movement of both ions. Although this process under some conditions mediates an equal bidirectional flux of both Na(+) and K(+), it cannot be defined as exchange diffusion. The contransport process is inhibited by furosemide.
钠离子(Na⁺)和钾离子(K⁺)流入人体红细胞的过程似乎是相互关联的。在细胞外Na⁺或K⁺浓度发生变化,或者一种阳离子被镁离子(Mg²⁺)、胆碱离子(choline⁺)或锂离子(Li⁺)取代的条件下,对这种关系进行了研究。在哇巴因存在的情况下,研究了呋塞米对Na⁺和K⁺转运的影响。当存在哇巴因时,细胞外为K⁺离子时的Na⁺流入量高于细胞外为其他阳离子时的情况。呋塞米抑制了这种K⁺刺激的Na⁺流入,但在没有K⁺时其作用很小。与其他阳离子相比,细胞外Na⁺使哇巴因不敏感的K⁺流入增加了两倍。呋塞米也抑制了这种刺激,但当Mg²⁺或choline⁺取代细胞外Na⁺时,其作用很小。因此证实了Na⁺和K⁺的哇巴因不敏感流入之间存在协同作用,并且证明呋塞米抑制了这种协同效应。K⁺和Na⁺的哇巴因不敏感流入对转运阳离子的细胞外浓度均呈现双曲线型的“饱和”依赖性。因此,呋塞米消除了每种阳离子流入的可饱和成分。在哇巴因存在的情况下,K⁺离子刺激了Na⁺的净摄取。在用Li⁺取代几乎所有细胞内Na⁺加K⁺离子的红细胞中也观察到了类似的效应。在这些细胞中,细胞外K⁺刺激了Na⁺的净摄取,细胞外Na⁺刺激了K⁺的净摄取。呋塞米抑制了这种阳离子净进入的相互刺激。呋塞米的抑制作用并不局限于Na⁺和K⁺的内向通量和净移动。呋塞米还抑制了Na⁺向无Na⁺培养基的外流以及K⁺向无K⁺培养基的外流。因此,似乎呋塞米的作用不能用抑制交换扩散来解释。这些数据与一种哇巴因不敏感的转运过程一致,该过程促进Na⁺和K⁺离子的同向内向转运,并且可以使两种离子产生净移动。尽管在某些条件下该过程介导了Na⁺和K⁺的等量双向通量,但它不能被定义为交换扩散。同向转运过程被呋塞米抑制。