Imanishi S, Arita M, Kiyosue T, Aomine M
J Pharmacol Exp Ther. 1983 Apr;225(1):198-205.
The effects of various concentrations (1-1000 microM) of SG-75 nitrate or nicorandil) were investigated in action potentials of canine Purkinje fibers with microelectrodes. In normal fibers stimulated at the standard cycle length of 1500 msec, the drug (1-100 microM) produced dose-dependent shortening in action potential duration without changes in the resting potential, the maximum rate of rise of phase 0 and the slope of phase 4 depolarization. The drug-induced percentage of shortening in the action potential duration was more pronounced at lower rates of stimulation and lower external K+ concentrations, but the shortening was unchanged in lower external Na+ concentrations. Depolarizations produced by Ba++ (0.04 mM) and low K+ (less than or equal to 1.35 mM) solution were partially reversed by the drug, whereas there were no effects on the high K+ (5.4-24.7 mM)-induced depolarizations. Stretch-induced depolarization was also partially recovered in the presence of the drug. SG-75 shortened the duration of the slow response produced by isoproterenol (1 microM) in the presence of 24.7 mM K+, with little change in the maximum rate of rise. We concluded that SG-75 increases membrane K+ conductance in cardiac Purkinje fibers probably by modifying ix1 and iK1 channels without changing the slow inward currents and that the effects are not mediated by muscarinic receptors. The computed action potentials indicated that this view was reasonable.
采用微电极研究了不同浓度(1 - 1000微摩尔)的SG - 75硝酸盐或尼可地尔对犬浦肯野纤维动作电位的影响。在以1500毫秒标准周期长度刺激的正常纤维中,该药物(1 - 100微摩尔)可使动作电位时程呈剂量依赖性缩短,而静息电位、0期最大上升速率和4期去极化斜率均无变化。在较低刺激频率和较低细胞外钾离子浓度时,药物引起的动作电位时程缩短百分比更为明显,但在较低细胞外钠离子浓度时,缩短程度不变。由钡离子(0.04毫摩尔)和低钾(小于或等于1.35毫摩尔)溶液引起的去极化可被该药物部分逆转,而对高钾(5.4 - 24.7毫摩尔)诱导的去极化则无影响。在药物存在的情况下,牵张诱导的去极化也部分恢复。在24.7毫摩尔钾离子存在时,SG - 75可缩短异丙肾上腺素(1微摩尔)产生的慢反应时程,最大上升速率变化不大。我们得出结论,SG - 75可能通过改变内向整流钾电流(ix1)和内向整流钾电流(iK1)通道增加心脏浦肯野纤维的膜钾离子电导,而不改变缓慢内向电流,且这些作用不是由毒蕈碱受体介导的。计算得到的动作电位表明这一观点是合理的。