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7
Blocking action of chromanol 293B on the slow component of delayed rectifier K(+) current in guinea-pig sino-atrial node cells.色满醇293B对豚鼠窦房结细胞延迟整流钾电流慢成分的阻断作用。
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本文引用的文献

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Effects of the chromanol 293B, a selective blocker of the slow, component of the delayed rectifier K+ current, on repolarization in human and guinea pig ventricular myocytes.色满醇293B(一种延迟整流钾电流慢成分的选择性阻滞剂)对人和豚鼠心室肌细胞复极化的影响。
Cardiovasc Res. 1998 May;38(2):441-50. doi: 10.1016/s0008-6363(98)00021-2.
2
KvLQT1 potassium channel but not IsK is the molecular target for trans-6-cyano-4-(N-ethylsulfonyl-N-methylamino)-3-hydroxy-2,2-dimethyl- chromane.反式-6-氰基-4-(N-乙基磺酰基-N-甲基氨基)-3-羟基-2,2-二甲基苯并二氢吡喃的分子靶点是KvLQT1钾通道而非IsK。
Mol Pharmacol. 1997 Dec;52(6):1131-6. doi: 10.1124/mol.52.6.1131.
3
Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity.MinK对KvLQT1通道活性调控的分子机制及功能意义。
J Biol Chem. 1997 Jul 4;272(27):16713-6. doi: 10.1074/jbc.272.27.16713.
4
Potentiation by nitric oxide of the ATP-sensitive K+ current induced by K+ channel openers in guinea-pig ventricular cells.一氧化氮对豚鼠心室细胞中钾通道开放剂诱导的ATP敏感性钾电流的增强作用。
Br J Pharmacol. 1997 Apr;120(8):1568-74. doi: 10.1038/sj.bjp.0701069.
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Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.K(V)LQT1和minK(IsK)蛋白共同组装形成心脏I(Ks)钾通道。
Nature. 1996 Nov 7;384(6604):80-3. doi: 10.1038/384080a0.
6
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current.K(V)LQT1蛋白和lsK(minK)蛋白相互结合形成心脏钾离子电流I(Ks)。
Nature. 1996 Nov 7;384(6604):78-80. doi: 10.1038/384078a0.
7
Inhibition of IKs in guinea pig cardiac myocytes and guinea pig IsK channels by the chromanol 293B.色满醇293B对豚鼠心肌细胞中IKs及豚鼠IsK通道的抑制作用。
Pflugers Arch. 1996 Oct;432(6):1094-6. doi: 10.1007/s004240050240.
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Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides.III类抗心律失常药物可阻断HERG,一种人类心脏延迟整流钾通道。甲磺酰苯胺类药物对该通道的开放状态进行阻断。
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Current status of class III antiarrhythmic drug therapy.
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在豚鼠心室肌细胞中,293B色满醇对缓慢激活延迟整流钾电流的时间依赖性阻断作用

Time-dependent block of the slowly activating delayed rectifier K(+) current by chromanol 293B in guinea-pig ventricular cells.

作者信息

Fujisawa S, Ono K, Iijima T

机构信息

Department of Pharmacology, Akita University School of Medicine, Hondoh 1-1-1, Akita 010-8543, Japan.

出版信息

Br J Pharmacol. 2000 Mar;129(5):1007-13. doi: 10.1038/sj.bjp.0703126.

DOI:10.1038/sj.bjp.0703126
PMID:10696102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1571911/
Abstract

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.

摘要

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。