Fujisawa S, Ono K, Iijima T
Department of Pharmacology, Akita University School of Medicine, Hondoh 1-1-1, Akita 010-8543, Japan.
Br J Pharmacol. 2000 Mar;129(5):1007-13. doi: 10.1038/sj.bjp.0703126.
The slowly activating delayed rectifier K(+) current (I(Ks)) was recorded in single myocytes dissociated from guinea-pig ventricles and the mechanism underlying the block of I(Ks) by a chromanol derivative, 293B, was investigated. In the presence of 1 - 100 microM 293B, activation phase of I(Ks) was followed by a slower decay during 10 s depolarizing pulses. Both the rate and extent of the decay were increased in a concentration-dependent manner. The relationship between the concentration of 293B and the block showed a Hill's coefficient of approximately 1. The half-inhibitory concentration was approximately 3.0 microM and did not differ significantly at various membrane potentials from +20 to +80 mV. A mathematical model for the 293B block was constructed on the basis of multiple closed and open states for the I(Ks) channels, and the blocking rate was calculated by fitting the model to the original current traces. The blocking rate constant showed a linear function with the 293B concentration, indicating 1 : 1 binding stoichiometry. At +80 mV the blocking rate was 4x10(4) M(-1) s(-1) and the unblocking rate was 0.2 s(-1). The results indicate that 293B is an open channel blocker with relatively smaller blocking rate than those reported so far for time-dependent blockade of various ionic channels.
在从豚鼠心室分离的单个心肌细胞中记录缓慢激活的延迟整流钾电流(I(Ks)),并研究了苯并二氢吡喃衍生物293B对I(Ks)的阻断机制。在存在1 - 100微摩尔293B的情况下,在10秒的去极化脉冲期间,I(Ks)的激活阶段之后是较慢的衰减。衰减的速率和程度均以浓度依赖性方式增加。293B浓度与阻断之间的关系显示希尔系数约为1。半抑制浓度约为3.0微摩尔,在从+20到+80毫伏的各种膜电位下无显著差异。基于I(Ks)通道的多个关闭和开放状态构建了293B阻断的数学模型,并通过将该模型拟合到原始电流迹线来计算阻断速率。阻断速率常数与293B浓度呈线性函数关系,表明结合化学计量比为1:1。在+80毫伏时,阻断速率为4×10(4) M(-1) s(-1),解阻断速率为0.2 s(-1)。结果表明,293B是一种开放通道阻断剂,其阻断速率相对较小,低于迄今为止报道的各种离子通道时间依赖性阻断的速率。