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细胞内质子抑制豚鼠心室细胞膜内向整流钾通道。

Intracellular protons inhibit inward rectifier K+ channel of guinea-pig ventricular cell membrane.

作者信息

Ito H, Vereecke J, Carmeliet E

机构信息

Laboratorium voor Fysiologie, Katholieke Universiteit Leuven, Belgium.

出版信息

Pflugers Arch. 1992 Dec;422(3):280-6. doi: 10.1007/BF00376214.

Abstract

The effect of intracellular protons (Hi+) on the inward rectifier K+ channel of the guinea-pig ventricular cell membrane was examined, using the patch-clamp technique. The inward single-channel current was recorded in "inside-out" and "outside-out" patch configurations, while the pH of the solution perfusing the intra- and extracellular side, respectively, was varied. Low intracellular pH (pHi), but not low extracellular pH, inhibited the channel. Low pHi reduced the unit amplitude, which was about 20% smaller at pHi 6.0 than that at pHi 7.4 at every voltage tested. The slope conductance decreased from 41.7 pS at pHi 7.4 to 35.1 pS at pHi 6.0. Low pHi also reduced the channel activity without apparent voltage dependence. The concentration/response curve indicated the half-maximum inhibition at pHi 6.11 and a Hill coefficient of 2.52. Lowering the pHi from 7.4 to 6.0 did not affect the distributions of the open times and the closed times below 50 ms, while the time constant of the histogram constructed from closings longer than 50 ms was approximately doubled. These results indicate that the inward rectifier K+ channel in ventricular myocytes is inhibited by H+ from the intracellular side. This might contribute to the depolarization of the resting membrane potential induced by intracellular acidosis during myocardial ischaemia.

摘要

采用膜片钳技术研究了细胞内质子(Hi+)对豚鼠心室细胞膜内向整流钾通道的影响。分别在“内面向外”和“外面向外”的膜片配置下记录内向单通道电流,同时改变分别灌流细胞内和细胞外侧溶液的pH值。低细胞内pH值(pHi)而非低细胞外pH值会抑制该通道。低pHi降低了单位电流幅度,在每个测试电压下,pHi 6.0时的单位电流幅度比pHi 7.4时小约20%。斜率电导从pHi 7.4时的41.7 pS降至pHi 6.0时的35.1 pS。低pHi还降低了通道活性,且无明显电压依赖性。浓度/反应曲线表明在pHi 6.11时出现半数最大抑制,希尔系数为2.52。将pHi从7.4降至6.0对50 ms以下的开放时间和关闭时间分布没有影响,而由长于50 ms的关闭时间构建的直方图的时间常数大约增加了一倍。这些结果表明,心室肌细胞中的内向整流钾通道受到细胞内侧H+的抑制。这可能有助于心肌缺血期间细胞内酸中毒诱导的静息膜电位去极化。

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