Zygmunt A C, Robitelle D C, Eddlestone G T
Masonic Medical Research Laboratory, Utica, New York 13501-1787, USA.
Am J Physiol. 1997 Sep;273(3 Pt 2):H1096-106. doi: 10.1152/ajpheart.1997.273.3.H1096.
The contributions of the 4-aminopyridine (4-AP)-sensitive transient outward potassium conductance (Ito1) and the calcium-activated chloride conductance (ICl(Ca)] to cardiac action potentials were investigated in canine ventricular myocytes. Action potentials or currents were recorded at 37 degrees C using standard whole cell or amphotericin B perforated-patch-clamp techniques. Inhibition of Ito1 by 1 mM 4-AP prolonged phase 1 repolarization, elevated the action potential notch, and depressed the plateau. Action potential voltage clamp revealed that 4-AP blocked a rapidly decaying outward current during phase 1 without affecting plateau or diastolic currents. These results suggested that depression of the plateau was not a direct result of Ito1 inhibition but followed from delayed phase 1 repolarization. Calcium current (ICa) at the peak of the action potential dome was reduced 60 +/- 4% when the rate of phase 1 repolarization was reduced. ICl(Ca) measured by action potential clamp reversed over the course of the action potential. Chloride fluxes associated with outward and inward components of the 4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonic acid-sensitive current were +130 +/- 17 and -184 +/- 20 (pA.ms)/pF, respectively. The effects of selective inhibition of ICl(Ca) on the action potential were dependent on the rate of early repolarization and the prominence of the notch. Inhibition of ICl(Ca) elevated the plateau and slightly abbreviated action potential duration when the notch was prominent. When repolarization was prolonged and the notch was shallow, inhibition of ICl(Ca) elevated the notch and the plateau and abbreviated duration. We have shown that Ito1 and ICl(Ca) contribute to canine ventricular action potentials. The extent of overlap between Ito1 and ICl(Ca) during the action potential is largely determined by the amplitude of Ito1 and the depth of the notch. Regional differences in the density of Ito1, or interventions that moderate phase 1 repolarization by reducing this current, will have considerable effect on the time course of ICa and calcium-dependent conductances.
在犬心室肌细胞中研究了4-氨基吡啶(4-AP)敏感的瞬时外向钾电流(Ito1)和钙激活氯电流(ICl(Ca))对心脏动作电位的作用。使用标准全细胞或两性霉素B穿孔膜片钳技术在37℃记录动作电位或电流。1 mM 4-AP抑制Ito1可延长1期复极化,提高动作电位切迹,并压低平台期。动作电位电压钳显示,4-AP在1期阻断快速衰减的外向电流,而不影响平台期或舒张期电流。这些结果表明,平台期压低不是Ito1抑制的直接结果,而是继发于延迟的1期复极化。当1期复极化速率降低时,动作电位圆顶峰值处的钙电流(ICa)降低60±4%。通过动作电位钳测量的ICl(Ca)在动作电位过程中发生反转。与4-乙酰氨基-4'-异硫氰基芪-2,2'-二磺酸敏感电流的外向和内向成分相关的氯通量分别为+130±17和-184±20(pA.ms)/pF。选择性抑制ICl(Ca)对动作电位的影响取决于早期复极化速率和切迹的突出程度。当切迹明显时,抑制ICl(Ca)可提高平台期并略微缩短动作电位持续时间。当复极化延长且切迹较浅时,抑制ICl(Ca)可提高切迹和平台期并缩短持续时间。我们已经表明,Ito1和ICl(Ca)对犬心室动作电位有作用。动作电位期间Ito1和ICl(Ca)的重叠程度在很大程度上由Ito1的幅度和切迹的深度决定。Ito1密度的区域差异或通过降低该电流来调节1期复极化的干预措施,将对ICa和钙依赖性电流的时间进程产生相当大的影响。