Green S T, Petersen O H
Pflugers Arch. 1981 Aug;391(2):119-24. doi: 10.1007/BF00657001.
Intracellular recordings of membrane potentials, input resistance and time constant have been made in vitro from the follicular cells of the rat, rabbit and guinea-pig thyroid glands using glass microelectrodes. The passive permeability properties of these cells have been investigated by altering the concentration of one or more ions in the superfusing fluid. Investigations into the intercellular coupling characteristics of the thyroid gland were made by inserting two microelectrodes into neighbouring communicating cells. The mean transmembrane potentials were between - 60 and - 70 mV in all three species studied. The magnitude of the membrane potential in the rat was found to be dependent mainly upon the gradient for potassium (K+) across the membrane. Current-voltage relationships were investigated in all three species by injecting rectangular de- or hyperpolarizing current pulses through the recording microelectrode. Within a relatively wide range (- 20 to - 80 mV), there was an approximately linear relationship between injected current and change in membrane potential. The input resistance was about 11 Momega in all three species, while the time constant (tau) varied from 5-35 ms. Readmitting K to K-deprived rat thyroids during intracellular microelectrode recording caused a transient hyperpolarization which was unaccompanied by any change in input resistance. The transient hyperpolarization was abolished by ouabain. Addition of 10(-3) M ouabain to the resting cell caused an immediate depolarization of approximately 2 mV. Electrical coupling between neighbouring cells could only be observed if the distance between the tips of the two exploring microelectrodes was less than 15 micrometer. The coupling coefficient (V2/V1) was close to 1. Assuming uniform current spread within one follicle and electrical isolation of individual follicles from each other the specific membrane resistance of the rat thyroid follicular cells was calculated to be 4.9 komegacm2.
使用玻璃微电极在体外对大鼠、兔和豚鼠甲状腺滤泡细胞进行了膜电位、输入电阻和时间常数的细胞内记录。通过改变灌流液中一种或多种离子的浓度,研究了这些细胞的被动通透性特性。通过将两个微电极插入相邻的连通细胞来研究甲状腺的细胞间耦合特性。在所研究的所有三个物种中,平均跨膜电位在 -60 至 -70 mV 之间。发现大鼠的膜电位大小主要取决于跨膜钾(K +)梯度。通过记录微电极注入矩形去极化或超极化电流脉冲,研究了所有三个物种的电流 - 电压关系。在相对较宽的范围内(-20 至 -80 mV),注入电流与膜电位变化之间存在近似线性关系。所有三个物种的输入电阻约为 11 MΩ,而时间常数(τ)在 5 - 35 ms 之间变化。在细胞内微电极记录期间,向缺钾的大鼠甲状腺重新引入钾会引起短暂的超极化,且输入电阻没有任何变化。哇巴因消除了这种短暂的超极化。向静息细胞中加入 10^(-3) M 哇巴因会立即引起约 2 mV 的去极化。仅当两个探测微电极尖端之间的距离小于 15 微米时,才能观察到相邻细胞之间的电耦合。耦合系数(V2/V1)接近 1。假设电流在一个滤泡内均匀分布且各个滤泡相互电隔离,计算出大鼠甲状腺滤泡细胞的比膜电阻为 4.9 kΩ·cm²。