Yamada Y, Tohse N, Nagashima M, Yabu H
Department of Physiology, Sapporo Medical University School of Medicine, Sapporo 060-0061, Japan.
J Membr Biol. 1999 Jan 15;167(2):141-9. doi: 10.1007/s002329900478.
Although outward current through inward-rectifier K+ channels has been observed in the whole-cell mode of the patch-clamp technique, no outward unitary current in single-channel studies has been recorded with the physiological ionic conditions. Hence, the relationship between single-channel activities and the inward rectification of the whole-cell current has been poorly understood. Therefore, characteristics of inward-rectifier K+ channels in guinea-pig ventricular myocytes were assessed by the noise analysis of the K+ current using the whole-cell patch clamp method. Partial blockade of the inward-rectifier K+ current by Ba2+ was used to obtain different levels of mean current and current fluctuation as needed for variance-to-mean analysis. The plot of variance of current fluctuation against mean currents was well fitted by theoretical parabolic curves, and the unitary conductance, the open probability, and the density of functional channels were deduced. The unitary conductance of the inward-rectifier K+ channel exhibited an inward-rectification, although the channel open probability and the density of functional channels were not much different at various holding potentials used. The unitary conductance was not changed when the intrapipette concentration of Mg2+ was reduced, but tended to be smaller when the pipette contained high Mg2+ concentration. Spermine also tended to reduce the outward unitary conductances, although the reduction was not statistically significant. These results suggest that the inward rectification in the whole-cell current was due to the inward-rectifying property of the unitary conductance of the K+ channels. Inward rectification of the unitary conductance may be caused by blocking of the channels by both Mg2+ and polyamines.
尽管在膜片钳技术的全细胞模式下已观察到通过内向整流钾通道的外向电流,但在生理离子条件下的单通道研究中尚未记录到外向单位电流。因此,单通道活动与全细胞电流内向整流之间的关系一直未得到很好的理解。因此,采用全细胞膜片钳方法,通过对钾电流的噪声分析来评估豚鼠心室肌细胞中内向整流钾通道的特性。利用Ba2+对内向整流钾电流进行部分阻断,以根据方差-均值分析的需要获得不同水平的平均电流和电流波动。电流波动方差与平均电流的关系图与理论抛物线曲线拟合良好,并推导了单位电导、开放概率和功能性通道密度。内向整流钾通道的单位电导表现出内向整流特性,尽管在使用的不同钳制电位下通道开放概率和功能性通道密度差异不大。当移液管内Mg2+浓度降低时,单位电导不变,但当移液管中Mg2+浓度较高时,单位电导往往较小。精胺也倾向于降低外向单位电导,尽管这种降低在统计学上不显著。这些结果表明,全细胞电流的内向整流是由于钾通道单位电导的内向整流特性。单位电导的内向整流可能是由Mg2+和多胺对通道的阻断引起的。