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用包埋的偶氮胂III测定人红细胞血影中的被动钙转运。

Passive Ca transport in human red blood cell ghosts measured with entrapped arsenazo III.

作者信息

Yingst D R, Hoffman J F

出版信息

J Gen Physiol. 1984 Jan;83(1):1-17. doi: 10.1085/jgp.83.1.1.

Abstract

The rate of Ca influx into ghosts containing arsenazo III changes with time, being most rapid during the first 5 min after Ca is added to the outside and declining thereafter. The rate of Ca influx is a nonlinear function of extracellular Ca and plateaus as the latter is increased above 1 mM. The rate of Ca influx was measured as a function of the transmembrane gradients of Na and K and changes in the permeability of the membrane to K and Cl produced by valinomycin and SITS (4-acetamido-4'-isothiocyano-stilbene-2-2'-disulfonic acid), respectively. Changes in the rate of Ca influx are consistent with expected effects of these treatments on the membrane potential. Oligomycin (10 micrograms/ml) and quinidine (1 mM) inhibit the rate of Ca uptake by inhibiting Ca-induced changes in the K permeability. At constant membrane potential, furosemide produced a slight (15%) consistent increase in Ca uptake. Other experiments show that resealed ghosts are heterogeneous in their passive permeability to Ca and that A23187 can be used to effectively eliminate such differences. The results of this paper show that resealed human red cell ghosts containing arsenazo III can be used to continuously monitor intracellular free Ca and to study the factors that influence the permeability of the red cell membrane to Ca.

摘要

含有偶氮胂III的血影中钙离子内流速率随时间变化,在向外部添加钙离子后的最初5分钟内最为迅速,此后下降。钙离子内流速率是细胞外钙离子的非线性函数,当细胞外钙离子浓度增加到1 mM以上时达到平台期。测量了钙离子内流速率作为钠和钾跨膜梯度以及缬氨霉素和SITS(4-乙酰氨基-4'-异硫氰基芪-2,2'-二磺酸)分别引起的膜对钾和氯通透性变化的函数。钙离子内流速率的变化与这些处理对膜电位的预期影响一致。寡霉素(10微克/毫升)和奎尼丁(1 mM)通过抑制钙离子诱导的钾通透性变化来抑制钙离子摄取速率。在恒定膜电位下,呋塞米使钙离子摄取量略有(15%)持续增加。其他实验表明,重新封闭的血影对钙离子的被动通透性是异质的,并且A23187可用于有效消除这种差异。本文结果表明,含有偶氮胂III的重新封闭的人红细胞血影可用于连续监测细胞内游离钙离子,并研究影响红细胞膜对钙离子通透性的因素。

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本文引用的文献

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The calcium content of human erythrocytes.人体红细胞的钙含量。
J Physiol. 1968 Dec;199(2):367-81. doi: 10.1113/jphysiol.1968.sp008658.

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