Suppr超能文献

人红细胞中对呋塞米敏感的钠钾协同转运。

A furosemide-sensitive cotransport of sodium plus potassium in the human red cell.

作者信息

Wiley J S, Cooper R A

出版信息

J Clin Invest. 1974 Mar;53(3):745-55. doi: 10.1172/JCI107613.

Abstract

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.

摘要

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。

相似文献

1
A furosemide-sensitive cotransport of sodium plus potassium in the human red cell.
J Clin Invest. 1974 Mar;53(3):745-55. doi: 10.1172/JCI107613.
3
Lithium transport pathways in human red blood cells.
J Gen Physiol. 1978 Aug;72(2):233-47. doi: 10.1085/jgp.72.2.233.
4
Sodium and potassium transport in trout (Salmo gairdneri) erythrocytes.
J Physiol. 1984 Feb;347:361-75. doi: 10.1113/jphysiol.1984.sp015070.
5
Thallium and the sodium pump in human red cells.
J Physiol. 1974 Nov;243(1):243-66. doi: 10.1113/jphysiol.1974.sp010752.
8
The ouabain-sensitive fluxes of sodium and potassium in squid giant axons.
J Physiol. 1969 Feb;200(2):459-96. doi: 10.1113/jphysiol.1969.sp008703.
10
Cotransport of lithium and potassium in human red cells.
J Gen Physiol. 1982 Jul;80(1):149-68. doi: 10.1085/jgp.80.1.149.

引用本文的文献

1
SLC transporters as therapeutic targets: emerging opportunities.
Nat Rev Drug Discov. 2015 Aug;14(8):543-60. doi: 10.1038/nrd4626. Epub 2015 Jun 26.
2
Controlled trial of frusemide as an antiepileptic drug in focal epilepsy.
Br J Clin Pharmacol. 1976 Aug;3(4):621-5. doi: 10.1111/j.1365-2125.1976.tb04885.x.
4
The Na-K-Cl cotransporters.
J Bioenerg Biomembr. 1998 Apr;30(2):161-72. doi: 10.1023/a:1020521308985.
5
Alterations in sodium metabolism as an etiological model for hypertension.
Cardiovasc Drugs Ther. 1995 Jun;9(3):377-99. doi: 10.1007/BF00879027.
6
Outward sodium and potassium cotransport in human red cells.
J Membr Biol. 1981;62(3):169-74. doi: 10.1007/BF01998162.
8
Increased erythrocyte cation permeability in thalassemia and conditions of marrow stress.
J Clin Invest. 1981 Apr;67(4):917-22. doi: 10.1172/jci110140.
9
The effect of diuretics on extrarenal potassium tolerance.
Yale J Biol Med. 1982 Sep-Dec;55(5-6):421-8.

本文引用的文献

1
Transport of ions across cellular membranes.
Physiol Rev. 1949 Apr;29(2):127-55. doi: 10.1152/physrev.1949.29.2.127.
2
The connexion between active cation transport and metabolism in erythrocytes.
Biochem J. 1965 Oct;97(1):214-27. doi: 10.1042/bj0970214.
3
5
The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes.
Arch Biochem Biophys. 1963 Jan;100:119-30. doi: 10.1016/0003-9861(63)90042-0.
6
Adenosinetriphosphatase activity and the active movements of alkali metal ions.
J Physiol. 1961 Apr;156(2):274-93. doi: 10.1113/jphysiol.1961.sp006675.
7
The action of cardiac glycosides on sodium and potassium movements in human red cells.
J Physiol. 1957 Apr 3;136(1):148-73. doi: 10.1113/jphysiol.1957.sp005749.
8
Sodium and potassium movements in human red cells.
J Physiol. 1956 Nov 28;134(2):278-310. doi: 10.1113/jphysiol.1956.sp005643.
10
The sensitivity of the sodium pump to external sodium.
J Physiol. 1967 Sep;192(1):175-88. doi: 10.1113/jphysiol.1967.sp008295.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验