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新型抗心绞痛药物尼可地尔对兔房室结动作电位和膜电流的电生理效应

Electrophysiologic effects of nicorandil, a new antianginal agent, on action potentials and membrane currents of rabbit atrioventricular node.

作者信息

Habuchi Y, Nishimura M, Watanabe Y

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1987 May;335(5):567-74. doi: 10.1007/BF00169126.

DOI:10.1007/BF00169126
PMID:2956524
Abstract

Electrophysiologic effects of nicorandil, a newly developed coronary vasodilator, on the atrioventricular (AV) node were studied using space-clamped small preparations of the rabbit AV node. At the concentrations of 10(-6), 10(-5) and 10(-4) mol/l, this drug did not cause significant changes in the action potential characteristics including the spontaneous firing frequency, overshoot, maximum diastolic potential, maximum rate of depolarization and action potential duration. When the resting membrane potential of the AV node was obtained by a superfusion with verapamil and then nicorandil was added to the perfusate, no hyperpolarization was observed. This was in sharp contrast to the reported hyperpolarizing action of this drug on the atrial muscle, Purkinje fibres and vascular smooth muscle where the resting potential is much more negative. On the other hand, voltage clamp experiments using double microelectrode techniques revealed that 10(-5) to 10(-4) mol/l nicorandil increased the steady-state outward current at potentials positive to -40 mV and the steady-state inward current at potentials negative to -40 mV. Such a nicorandil-sensitive component of the steady-state current had an average reversal potential of -41.8 mV (n = 5). This component was considered to reflect changes in the time-independent background current, although, at more negative potential levels, it may partially reflect an increase in the hyperpolarization activated inward current (ih). Nicorandil, at the concentrations of 10(-5) and 10(-4) mol/l, increased the slow inward current (isi) by 10.8% (n = 5, p less than 0.01).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用家兔房室结的空间钳制小标本,研究了新开发的冠状动脉扩张剂尼可地尔对房室(AV)结的电生理作用。在10^(-6)、10^(-5)和10^(-4) mol/l的浓度下,该药物未引起动作电位特征的显著变化,包括自发放电频率、超射、最大舒张电位、最大去极化速率和动作电位持续时间。当通过用维拉帕米灌流获得房室结的静息膜电位,然后将尼可地尔添加到灌流液中时,未观察到超极化。这与该药物对心房肌、浦肯野纤维和血管平滑肌的超极化作用形成鲜明对比,在这些组织中静息电位更负。另一方面,使用双微电极技术的电压钳实验表明,10^(-5)至10^(-4) mol/l的尼可地尔在电位高于-40 mV时增加了稳态外向电流,在电位低于-40 mV时增加了稳态内向电流。这种稳态电流的尼可地尔敏感成分的平均反转电位为-41.8 mV(n = 5)。该成分被认为反映了与时间无关的背景电流的变化,尽管在更负的电位水平下,它可能部分反映了超极化激活内向电流(ih)的增加。在10^(-5)和10^(-4) mol/l的浓度下,尼可地尔使慢内向电流(isi)增加了10.8%(n = 5,p < 0.01)。(摘要截断于250字)

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1
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引用本文的文献

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Nicorandil safety in the long-term treatment of coronary heart disease.尼可地尔在冠心病长期治疗中的安全性。
Cardiovasc Drugs Ther. 1995 Mar;9 Suppl 2:237-43. doi: 10.1007/BF00878471.
2
K+ channel openers activate brain sulfonylurea-sensitive K+ channels and block neurosecretion.钾离子通道开放剂可激活大脑中磺酰脲类敏感的钾离子通道,并阻断神经分泌。
Proc Natl Acad Sci U S A. 1990 May;87(9):3489-92. doi: 10.1073/pnas.87.9.3489.
3
Pharmacology and therapeutic effects of nicorandil.尼可地尔的药理学与治疗作用。

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Kinetics and rectification of the slow inward current in the rabbit sinoatrial node cell.家兔窦房结细胞缓慢内向电流的动力学与整流
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Effects of 2-nicotinamidoethyl nitrate on smooth muscle cells and on adrenergic transmission in the guinea-pig and porcine mesenteric arteries.2-烟酰胺基乙基硝酸盐对豚鼠和猪肠系膜动脉平滑肌细胞及肾上腺素能传递的影响。
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Effects of 2-nicotinamidethyl nitrate (SG-75), a new antianginal drug, on the cyclic AMP phosphodiesterase activity.新型抗心绞痛药物2-烟酰胺基乙基硝酸盐(SG-75)对环磷酸腺苷磷酸二酯酶活性的影响。
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Relaxing effect of nicorandil (N-2-(hydroxyethyl)-nicotinamide nitrate), a new anti-angina agent, on the isolated vascular smooth muscle.
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