Désilets M, Baumgarten C M
Am J Physiol. 1986 Aug;251(2 Pt 1):C197-208. doi: 10.1152/ajpcell.1986.251.2.C197.
Intracellular K+, Na+, and Cl- activities (aiK, aiNa and aiCl) were measured in ventricular myocytes enzymatically isolated from adult rabbit heart. The activities in normal Tyrode solution containing 2.5 mM Ca2+ were the following (in mM): aiK = 100.0 +/- 3.5 (n = 9); aiNa = 8.4 +/- 1.5 (n = 6); and aiCl = 17.9 +/- 1.5 (n = 11) (mean +/- SE). Membrane potential was -81.6 +/- 0.7 mV (n = 26). These values were determined after correction for changes of junction and tip potential at the reference electrode, estimated to be 4.9 +/- 0.6 mV (n = 7) for 0.15 M KCl-filled electrodes; and intracellular interference detected by the Cl- ion-selective electrode, 11.2 +/- 0.6 mM (n = 4). Extended-tip shunting was avoided by fabricating Na+ ion-selective microelectrodes from aluminosilicate rather than borosilicate glass. These results show that isolated cardiac cells can maintain normal intracellular ion activities. Diffusion of electrolyte from the reference electrode can rapidly alter the intracellular milieu, however. After 10 min of impalement with 0.15 M KCl-filled microelectrodes (resistance approximately equal to 25 M omega), aiK increased by 8.7 +/- 2.0 mM and aiCl by 10.3 +/- 3.1 mM. In contrast, aiNa did not significantly change during the double impalement.
在从成年兔心脏酶解分离的心室肌细胞中测量细胞内钾离子(aiK)、钠离子(aiNa)和氯离子(aiCl)的活性。在含有2.5 mM钙离子的正常台氏液中的活性如下(单位:mM):aiK = 100.0 +/- 3.5(n = 9);aiNa = 8.4 +/- 1.5(n = 6);aiCl = 17.9 +/- 1.5(n = 11)(平均值 +/- 标准误)。膜电位为 -81.6 +/- 0.7 mV(n = 26)。这些值是在对参比电极处的液接电位和尖端电位变化进行校正后确定的,对于填充0.15 M KCl的电极,估计液接电位为4.9 +/- 0.6 mV(n = 7);以及通过氯离子选择性电极检测到的细胞内干扰为11.2 +/- 0.6 mM(n = 4)。通过用铝硅酸盐而非硼硅酸盐玻璃制作钠离子选择性微电极来避免尖端扩展分流。这些结果表明,分离的心肌细胞能够维持正常的细胞内离子活性。然而,电解质从参比电极的扩散会迅速改变细胞内环境。在用填充0.15 M KCl的微电极刺入10分钟后(电阻约等于25 MΩ),aiK增加了8.7 +/- 2.0 mM,aiCl增加了10.3 +/- 3.1 mM。相比之下,在双重刺入过程中aiNa没有显著变化。