Hillyard S D, Zeiske W, Van Driessche W
Biochim Biophys Acta. 1982 Nov 22;692(3):455-61. doi: 10.1016/0005-2736(82)90397-2.
In the presence of the Na+ -channel blocker amiloride, the short-circuit current across the skins of bullfrog tadpoles in metamorphic stages XIX-XXIV was subjected to fluctuation analysis. The resulting power spectra contained a Lorentzian component of which the plateau value (S0) decreased while the corner frequency (fc) increased as the mucosal amiloride concentration was increased from 0.5 to 24 microM. From the linear relationship between the fc values and the amiloride concentrations it was possible to determine the binding (k'01) and unbinding (k10) constants for amiloride to its receptor on the Na+ channel. With these parameters as well as short-circuit current and S0 values, the current through the individual Na+ channels (i) was calculated (average 0.58 pA). It did not increase significantly during late metamorphosis. The density of Na+ channels (M) in the apical membrane, on the other hand, increased significantly. It would appear that the increase in short-circuit current which occurs at this time is due primarily to an increase in amiloride-blockable Na+ channels. Unexpectedly, a Lorentzian component could be fitted to power spectra in amiloride-treated skins (stages XIX-XXI) which showed no amiloride-sensitive short-circuit current. Moreover, the typical increase in fc with the amiloride concentration did not occur in these animals.
在存在钠离子通道阻滞剂氨氯吡咪的情况下,对处于变态发育阶段XIX - XXIV的牛蛙蝌蚪皮肤的短路电流进行了波动分析。所得功率谱包含一个洛伦兹分量,当黏膜氨氯吡咪浓度从0.5微摩尔增加到24微摩尔时,该分量的平台值(S0)降低,而转折频率(fc)增加。根据fc值与氨氯吡咪浓度之间的线性关系,可以确定氨氯吡咪与其在钠离子通道上的受体的结合常数(k'01)和解离常数(k10)。利用这些参数以及短路电流和S0值,计算出通过单个钠离子通道的电流(i)(平均0.58皮安)。在变态发育后期,该电流没有显著增加。另一方面,顶端膜中钠离子通道的密度(M)显著增加。看来此时发生的短路电流增加主要是由于对氨氯吡咪可阻断的钠离子通道增加所致。出乎意料的是,在氨氯吡咪处理的皮肤(阶段XIX - XXI)的功率谱中可以拟合出一个洛伦兹分量,而这些皮肤并没有对氨氯吡咪敏感的短路电流。此外,在这些动物中,fc并没有随着氨氯吡咪浓度的增加而出现典型的增加。