Marcus N Y, Marcus D C
Washington University Medical School, Department of Ophthalmology, St. Louis, Missouri.
Hear Res. 1990 Feb;44(1):13-23. doi: 10.1016/0378-5955(90)90018-k.
Sheets of utricular epithelium from gerbil were mounted in a micro-Ussing chamber. Step changes in [Na] and [K] on each side of the epithelium led to changes in transepithelial potential difference (Vt) and resistance (Rt) which were consistent with the presence of ionic conductances for these two ions. Responses of Vt to 20 mM Rb steps were similar to those to 20 mM K steps. Several common Na and K channel blockers were applied: No evidence for the presence of amiloride-sensitive Na channels was found. At 10(-6) M, amiloride caused no significant changes in Vt but at 10(-3) M it initially decreased or increased Vt when applied from the apical or the basolateral side, respectively. Ba and quinidine each reduced Vt, quinidine more strongly from the basolateral than from the apical side. Tetraethylammonium, another K channel blocker, had no significant effect from either side. These data suggest that in spite of the low value of Rt, the cellular pathway contributes significantly to the voltage response to cation concentration steps in this epithelium. The mode of action of 10(-3) M amiloride and the K channel blockers remains uncertain.
将沙鼠的椭圆囊上皮薄片安装在微型尤斯灌流小室中。上皮两侧[Na]和[K]的阶跃变化导致跨上皮电位差(Vt)和电阻(Rt)发生变化,这与这两种离子存在离子电导相一致。Vt对20 mM Rb阶跃的反应与对20 mM K阶跃的反应相似。应用了几种常见的Na和K通道阻滞剂:未发现存在amiloride敏感Na通道的证据。在10^(-6) M时,amiloride对Vt无显著影响,但在10^(-3) M时,从顶端或基底外侧施加时,分别最初降低或升高Vt。Ba和奎尼丁均降低Vt,奎尼丁从基底外侧比从顶端更强烈地降低Vt。另一种K通道阻滞剂四乙铵从两侧施加均无显著影响。这些数据表明,尽管Rt值较低,但细胞途径对该上皮中阳离子浓度阶跃的电压反应有显著贡献。10^(-3) M amiloride和K通道阻滞剂的作用方式仍不确定。