Weld F M, Bigger J T
Circ Res. 1976 Mar;38(3):203-8. doi: 10.1161/01.res.38.3.203.
We studied the effects of lidocaine (1-5 mg/liter) on the diastolic currents of sheep Purkinje fibers by the two-microelectrode voltage clamp technique to obtain additional information on how lidocaine decreases the slope of spontaneous diastolic depolarization of mammalian Purkinje fibers. During voltage clamps we measured both the magnitude and time course of activation and deactivation of the time- and voltage-dependent potassium "pacemaker current" (iK2), and also the steady state current-voltage relationship throughout the pacemaker voltage range. At a concentration of 1 mg/liter lidocaine had no effect on the amplitude of iK2. In contrast, at 5 mg/liter, lidocaine diminished the magnitude of iK2 throughout the voltage range of pacemaker depolarization. Lidocaine (1-5 mg/liter) had no effect on either (1) the transmembrane voltage at which iK2 is half-activated, (2) the reversal voltage for iK2, or (3) the kinetics of iK2. Lidocaine (1-5 mg/liter) increased the steady state outward transmembrane current. This effect of lidocaine can be attributed to a variable contribution from both an increase in time-independent outward potassium current (iK1) and a decrease in background inward current.
我们采用双微电极电压钳技术研究了利多卡因(1 - 5毫克/升)对绵羊浦肯野纤维舒张期电流的影响,以获取关于利多卡因如何降低哺乳动物浦肯野纤维自发性舒张期去极化斜率的更多信息。在电压钳实验过程中,我们测量了时间和电压依赖性钾“起搏电流”(iK2)激活和失活的幅度及时间进程,以及整个起搏电压范围内的稳态电流 - 电压关系。浓度为1毫克/升时,利多卡因对iK2的幅度没有影响。相反,在5毫克/升时,利多卡因在起搏去极化的整个电压范围内减小了iK2的幅度。利多卡因(1 - 5毫克/升)对以下方面均无影响:(1)iK2半激活时的跨膜电压;(2)iK2的反转电压;(3)iK2的动力学。利多卡因(1 - 5毫克/升)增加了稳态外向跨膜电流。利多卡因的这种作用可归因于非时间依赖性外向钾电流(iK1)增加和背景内向电流减少的不同程度的贡献。