Schettino T, Köhler M, Frömter E
Pflugers Arch. 1985 Sep;405(1):58-65. doi: 10.1007/BF00591098.
Individual glands of rabbit gastric mucosa were prepared for measurements of cell membrane potentials. In the first experiments a collagenase isolation technique was used which produced gland fragments that were fixed on agarose. In later experiments a microdissection technique was used which allowed whole glands to be isolated that were held in suction pipettes. Individual parietal or chief cells could be recognized and impaled with microelectrodes, however, the yield of reliable recordings was small and the distinction from artifacts sometimes difficult. In acceptable recordings the membrane potentials of both cell types varied between around -20 and -35 mV or exceptionally -50 mV in both preparations, with mean values being around -26 mV. The significance of the recordings was tested by ion substitution experiments. Substitution of all chloride by sulfate increased the membrane potential to values ranging up to -60 and -80 mV that are commonly observed in other cells.
制备兔胃黏膜的单个腺体用于测量细胞膜电位。在最初的实验中,使用了胶原酶分离技术,该技术产生固定在琼脂糖上的腺体片段。在后来的实验中,使用了显微解剖技术,该技术可以分离出保存在吸管中的完整腺体。可以识别单个壁细胞或主细胞并用微电极刺入,然而,可靠记录的产量很低,并且有时很难与伪迹区分开来。在可接受的记录中,两种细胞类型的膜电位在两种制剂中均在约-20至-35 mV之间变化,或异常情况下为-50 mV,平均值约为-26 mV。通过离子替代实验测试了记录的意义。用硫酸盐替代所有氯离子可将膜电位提高到其他细胞中常见的-60至-80 mV的值。