Nelson D J, Ehrenfeld J, Lindemann B
J Membr Biol. 1978;40 Spec No:91-119. doi: 10.1007/BF02026000.
Cells of isolated frog skin epithelium were observed microscopically during impalement with standard microelectrodes of 5 to 20 Momega resistance, filled with 3 m KCl. Impaled cells, as well as some neighboring cells, were seen to swell 10 to 100 sec after impalement, while the negative potential recorded by the microelectrode depolarized (open circuit conditions). Apparently, osmotic swelling of small epithelial cells may be caused by diffusion of KCl from such electrodes. This conclusion is supported by calculations quoted from the literature of KCl loss from microelectrodes. Intracellular recordings from epithelia with destructed cellular membranes gave negative "pre-tip potentials" of up to mV. The potentials could be altered by electrode movement, by decreasing the ambient pH or the tip-pH and by modifying the fixed charges of the tissue chemically. It is shown that even a moderate loss of KCl, which will not result in appreciable swelling, can produce negative potentials in front of the electrode tip if the protoplasm has a high density of negative fixed charges. We suggest the use of 3 m KCl electrodes with resistances above 30 Momega if after impalement compression of intracellular material by the tip can be avoided. Where such compression cannot be avoided, it is best to fill the microelectrode with an isotonic solution which mimics the electrolyte composition of the cytosol.
在用电阻为5至20兆欧的标准微电极刺入分离的蛙皮上皮细胞时,用显微镜进行观察,微电极内充有3摩尔氯化钾。刺入的细胞以及一些相邻细胞在刺入后10至100秒会出现肿胀,同时微电极记录的负电位会去极化(开路条件)。显然,小上皮细胞的渗透性肿胀可能是由氯化钾从这类电极扩散所致。文献中引用的关于微电极氯化钾损失的计算结果支持了这一结论。对细胞膜已破坏的上皮进行细胞内记录时,会产生高达毫伏的负“尖端前电位”。这些电位可因电极移动、降低周围环境pH值或尖端pH值以及通过化学方法改变组织的固定电荷而改变。结果表明,如果原生质具有高密度的负固定电荷,即使氯化钾有适度损失(这不会导致明显肿胀),也会在电极尖端前方产生负电位。我们建议,如果刺入后能避免尖端对细胞内物质的挤压,可使用电阻高于30兆欧的3摩尔氯化钾电极。若无法避免这种挤压,最好用模拟细胞质电解质成分的等渗溶液填充微电极。