Wang W H
Department of Pharmacology, New York Medical College, Valhalla 10595.
Am J Physiol. 1994 Oct;267(4 Pt 2):F599-605. doi: 10.1152/ajprenal.1994.267.4.F599.
We have used the patch-clamp technique to study the apical K+ channels in the thick ascending limb (TAL) of the rat kidney. Two types of K+ channels, a low-conductance and an intermediate-conductance K+ channel, were identified in both cell-attached and inside-out patches. We confirmed the previously reported intermediate-conductance K+ channel (72 pS), which is inhibited by millimolar cell ATP, acidic pH, Ba2+, and quinidine (4). We now report a second K+ channel in apical membrane of the TAL. The slope conductance of this low-conductance K+ channel is 30 pS, and its open probability is 0.80 in cell-attached patches. This channel is not voltage dependent, and application of 2 mM ATP in the bath inhibits channel activity in inside-out patches. In addition, 250 microM glyburide, an ATP-sensitive K+ channel inhibitor, blocks channel activity, whereas the same concentration of glyburide has no inhibitory effect on the 72-pS K+ channel. Channel activity of the 30-pS K+ channel decreases rapidly upon excision of patches (channel run down). Application of 0.1 mM ATP and the catalytic subunit of adenosine 3',5'-cyclic monophosphate (cAMP)-dependent protein kinase A (PKA) restores channel activity. Furthermore, addition of 0.1 mM 8-(4-chlorophenylthio)-cAMP or 50-100 pM vasopressin in the cell-attached patches increases channel activity. In conclusion, two types of K+ channels are present in the apical membrane of TAL of rat kidney, and PKA plays an important role in modulation of the low-conductance K+ channel activity.
我们运用膜片钳技术研究了大鼠肾脏髓袢升支粗段(TAL)顶端的钾离子通道。在细胞贴附式和内面向外式膜片中均鉴定出两种类型的钾离子通道,即低电导钾离子通道和中等电导钾离子通道。我们证实了先前报道的中等电导钾离子通道(72 pS),它受到毫摩尔浓度的细胞内ATP、酸性pH值、钡离子和奎尼丁的抑制(4)。我们现在报道TAL顶端膜中的第二种钾离子通道。这种低电导钾离子通道的斜率电导为30 pS,在细胞贴附式膜片中其开放概率为0.80。该通道不依赖电压,浴槽中加入2 mM ATP会抑制内面向外式膜片中的通道活性。此外,250 microM格列本脲(一种ATP敏感性钾离子通道抑制剂)可阻断通道活性,而相同浓度的格列本脲对72 - pS钾离子通道没有抑制作用。30 - pS钾离子通道的活性在膜片切除后迅速下降(通道耗竭)。加入0.1 mM ATP和3',5'-环磷酸腺苷(cAMP)依赖性蛋白激酶A(PKA)的催化亚基可恢复通道活性。此外,在细胞贴附式膜片中加入0.1 mM 8 -(4 - 氯苯硫基)- cAMP或50 - 100 pM血管加压素可增加通道活性。总之,大鼠肾脏TAL顶端膜中存在两种类型的钾离子通道,PKA在调节低电导钾离子通道活性中起重要作用。