Effect of the sarcolemmal KATP channel blocker HMR1098 on arrhythmias induced by programmed electrical stimulation in canine old myocardial infarction model:: Comparison with glibenclamide

被引:9
作者
Zhu, BM
Miyamoto, S
Nagasawa, Y [1 ]
Wajima, T
Hashimoto, K
机构
[1] Yamanashi Univ, Interdisciplinary Grad Sch Med & Engn, Dept Pharmacol, Tamaho, Yamanashi 4093898, Japan
[2] Aventis Pharma Ltd, Pharmacol, Kawagoe, Saitama 3501165, Japan
关键词
sarcolemmal K-ATP channel; HMR1098; ischemic arrhythmia; programmed electrical stimulation; old myocardial infarction;
D O I
10.1254/jphs.93.106
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The blockade of myocardial K-ATP channels may be antiarrhythmic for ischemic arrhythmias. A new sulfonylthiourea, HMR1098 (1-{5-[2-(5-chloro-o-anisamido)ethyl]-2-methoxyphenylsulfonyl}-3-methylthiourea, sodium salt), was demonstrated to be a cardioselective K-ATP-channel antagonist and to suppress arrhythmias during acute ischemia. We investigated effects of HMR1098 on the arrhythmias induced by programmed electrical stimulation (PES) in a canine old myocardial infarction model. HMR1098 (3 mg/kg, i.v.) significantly improved the scores of PES-induced ventricular arrhythmias, without changing the blood glucose concentrations. A classical sulfonylurea, glibenclamide (1 mg/kg, i.v.), had no significant effects on these arrhythmias, but reduced the blood glucose and increased the plasma insulin concentrations.
引用
收藏
页码:106 / 113
页数:8
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