Satow Y
J Neurobiol. 1978 Jan;9(1):81-91. doi: 10.1002/neu.480090107.
Ca or EGTA was ionophoretically injected into Paramecium tetraurelia to change [Ca]i. Ca decreased the resting membrane resistance and hyperpolarized the membrane. EGTA had the opposite effect. EGTA following TEA, which suppress GK, had little effect on resistance or resting potential. The I-V relation at steady state was studied before and after EGTA injection while the cell bathed in either K- or TEA-solution. The response to inward test pulses after EGTA injection was similar to that after TEA injection. These results show that [Ca]i controls a steady-state K permeability in Paramecium tetraurelia. A prolonged Ca-spike was recorded after EGTA injection. The plateau potentials in various Ca concentrations in a TEA-solution show the Nernst slope (29 mV for tenfold change in [Ca]o). This result suggests that the prolonged depolarization in this condition is due to a Ca current, after suppression of K-permeability and when [Ca]i is low. The difficulty of obtaining quantitative data on the internal Ca, and the difference between the effects of EGTA injection and TEA injection are discussed.
将钙离子(Ca)或乙二醇双四乙酸(EGTA)通过离子电泳注入四膜虫,以改变细胞内钙离子浓度([Ca]i)。Ca降低了静息膜电阻并使膜超极化。EGTA则产生相反的效果。在加入抑制钾通道(GK)的四乙铵(TEA)后再加入EGTA,对电阻或静息电位几乎没有影响。在细胞浸浴于钾溶液或TEA溶液中时,研究了注入EGTA前后的稳态电流-电压(I-V)关系。注入EGTA后对内向测试脉冲的反应与注入TEA后相似。这些结果表明,[Ca]i控制着四膜虫的稳态钾通透性。注入EGTA后记录到一个延长的钙峰。在TEA溶液中不同钙浓度下的平台电位显示能斯特斜率([Ca]o变化10倍时为29 mV)。这一结果表明,在这种情况下延长的去极化是由于在钾通透性被抑制且[Ca]i较低时的钙电流所致。文中还讨论了获取细胞内钙定量数据的困难以及注入EGTA和注入TEA效果之间的差异。