Murata T, Okajima Y, Akaike N
Comp Biochem Physiol A Comp Physiol. 1984;77(2):287-91. doi: 10.1016/0300-9629(84)90062-8.
The origin of the transient asymmetry of intracellular resting potentials between the anterior and posterior lens fibers was investigated in the isolated American bullfrog lens by a conventional microelectrode technique. In high K+, Rb+, Cs+, or NH+4 test solution applied only to the lens anterior or posterior side, anterior fibers depolarized at a slower rate than posterior ones. After a long exposure, however, the transient potential difference disappeared. The magnitude of the depolarizations of the lens fibers was in the order of K+ greater than Rb+ greater than Cs+ greater than NH+4. The resting potentials plotted as a function of external K+ concentrations ([K]0) were in agreement with Nernst equation predictions with a slope of 58 mV/decade ion concentration change. A small Na+ permeability is unmasked at a [K]0 less than 10 mM. It was concluded that the transient difference measured in potentials of anterior and posterior lens fibers on increasing external K+, Rb+, Cs+ or NH+4 depends on the anterior epithelial cell layer, which is a diffusional barrier for ions penetrating into the lens interior.
采用传统微电极技术,在分离出的美国牛蛙晶状体中,研究了晶状体前、后纤维细胞内静息电位短暂不对称性的起源。在仅施加于晶状体前侧或后侧的高钾、铷、铯或铵测试溶液中,前纤维的去极化速率比后纤维慢。然而,长时间暴露后,短暂的电位差消失。晶状体纤维去极化的幅度顺序为:钾>铷>铯>铵。以外部钾离子浓度([K]0)为函数绘制的静息电位与能斯特方程预测结果一致,斜率为每十倍离子浓度变化58 mV。在[K]0小于10 mM时,可揭示出较小的钠离子通透性。得出的结论是,在增加外部钾、铷、铯或铵时,测量到的晶状体前、后纤维电位的短暂差异取决于前上皮细胞层,该细胞层是离子渗透进入晶状体内部的扩散屏障。