Kinard T A, Liu X Y, Liu S, Stimers J R
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock 72205.
Am J Physiol. 1994 Jan;266(1 Pt 1):C37-41. doi: 10.1152/ajpcell.1994.266.1.C37.
To determine if environmental factors influence the external K (K0) dependence of Na-K pump current (Ip), we systematically varied internal (pipette) Na (Napip) and Na-K pump activity while measuring the K0 dependence in adult rat cardiac myocytes. For each Napip, reactivation of Ip by K0 was dose dependent. The maximal Ip (Ipmax) and apparent affinity for K0 binding to the Na-K pump (K0.5) increased as Napip increased. The results of making an equimolar substitution of tetramethylammonium for K and Cs, and partial Ip inhibition with ouabain, also showed that Ipmax and K0.5 increased as Napip increased. We simulated pump activity as a function of intracellular Na (Nai) and K0 using a cyclic model of the Na-K pump and found that the model predicts K0.5 for K0 binding increases as Na increases, even when the conditions are adjusted by removing pipette K and partial pump inhibition with ouabain.
为了确定环境因素是否会影响钠钾泵电流(Ip)对胞外钾(K0)的依赖性,我们在测量成年大鼠心肌细胞中K0依赖性的同时,系统地改变了胞内(移液管)钠(Napip)和钠钾泵活性。对于每个Napip,K0对Ip的重新激活呈剂量依赖性。随着Napip增加,最大Ip(Ipmax)以及K0与钠钾泵结合的表观亲和力(K0.5)也增加。用四甲基铵等摩尔替代钾和铯,以及用哇巴因部分抑制Ip的结果,也表明随着Napip增加,Ipmax和K0.5增加。我们使用钠钾泵的循环模型模拟了作为细胞内钠(Nai)和K0函数的泵活性,发现该模型预测,即使通过去除移液管钾并用哇巴因部分抑制泵来调整条件,K0与K0结合的K0.5也会随着钠的增加而增加。