细胞外Ba^2＋对内向整流钾通道的阻断作用

实验采用双微电极电压箝（ＴＥＶ）法研究Ｂａ＾２＋对非洲爪蟾卵母细胞表达的内向整流钾通道（ＩＲＫ１）的阻断作用。细胞外Ｂａ＾２＋浓度分别为０,１,３,１０和１００μｍｏｌ／Ｌ,Ｋ＾＋浓度分别为１０和９０ｍｍｏｌ／Ｌ,可见快速开通道阻断剂Ｂａ＾２＋对ＩＲＫ１的瞬间电流（施加电压后１ｍｓ）的阻断作用依赖Ｂａ＾２＋、Ｋ＾＋、时间和电压;但对ＩＲＫ１的开关特性几乎无影响,ＩＲＫ１对之不通透。三级指数拟合的结

Blocking effects of extracellular Ba(2+) on the inward rectifier potassium channel

Two-microelectrode voltage clamp (TEV) method was used to study the blocking effects of extracellular Ba(2+) on the inward rectifier potassium channel (IRK1) expressed in Xenopus oocytes. Blockage of Ba(2+) on IRK1 (1 ms after voltage applied) is Ba(2+) concentration (0,1,3,10 or 100 micromol/L) dependent with 10 or 90 mmol/L potassium and also voltage-dependent. Ba(2+) almost has no effect on the open/close of IRK1. IRK1 is not permeable to Ba(2+). Three exponential fitting analysis indicates that Ba(2+) and K(+) compete the same binding site in IRK1 when external Ba(2+) concentration is lower (1 or 3 micromol/L). The time constant of IRK1 does not increase, but the concentration dependency of the weights of the fittings increases with the increase of external Ba(2+) concentration. As a result, the inactivation becomes faster and faster as the external Ba(2+) concentration increases. Moreover, since the time constant of the channel decreases and the weights of the fittings concentration dependently increase with the increase of external Ba(2+) concentration (10 or 100 micromol/L), the inactivation becomes faster and faster. It is demonstrated that Ba(2+) can contact with deeper binding sites in IRK1 as external Ba(2+) concentration increases. It is suggested that two different mechanisms may underlie the external Ba(2+) blocking effect. External Mn(2+) or Mg(2+) can compete with external Ba(2+) at the IRK1 binding site at an external Ba(2+) concentration of 30 mol/L and K(+) concentration of 90 mmol/L. Inactivation becomes slower and slower and Ba(2+) is repelled from the IRK1 binding site when Mg(2+) or Mn(2+) con-centration is further increased. Mg(2+), but not Mn(2+), can contact with deeper binding sites of IRK1 to block the channel, suggesting that multiple-ion blockage may exist in IRK1.