Antiarrhythmic effects of MS-551, a new class III antiarrhythmic agent, on canine models of ventricular arrhythmia.
Antiarrhythmic effects of MS-551, a new class III antiarrhythmic agent, on canine models of ventricular arrhythmia.
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MS-551(一种新型 III 类抗心律失常药物)对犬室性心律失常模型的抗心律失常作用。
DOI:
10.1254/jjp.58.107
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发表时间:
1992
期刊:
影响因子:
--
通讯作者:
T. Katakami
中科院分区:
文献类型:
--
作者:
J. Kamiya;M. Ishii;T. Katakami
The antiarrhythmic effects of MS-551, which prolongs cardiac action potential duration without affecting the maximum upstroke velocity of the action potential, were assessed in three different canine ventricular arrhythmia models: 1) ventricular tachycardia (VT) induced by electrical stimuli 3-5 days after myocardial infarction, 2) spontaneous ventricular tachyarrhythmias 24-48 hr after two-stage coronary ligation and 3) ventricular tachyarrhythmias induced by digitalis. Intravenous administration of MS-551 (0.1-1 mg/kg) decreased the susceptibility in 10 dogs out of 13 to VT or ventricular fibrillation evoked by programmed electrical stimulation (PES) delivered to the ventricular septum 3-5 days after myocardial infarction. Oral administration of MS-551 (3 mg/kg) also decreased the susceptibility to VT evoked by PES in 7 out of 10 conscious postinfarction dogs. Concurrently, intravenous (0.1-1 mg/kg) or oral (3 mg/kg) administration of MS-551 produced increases in the ventricular effective refractory periods (ERP) by 7 +/- 1% - 17 +/- 3% or 13 +/- 2%, respectively. Similarly, d-sotalol (0.3-3 mg/kg, i.v. and 10 mg/kg, p.o.) decreased the susceptibility to VT with increased ERP. However, MS-551 (1 and 10 mg/kg, i.v.) failed to inhibit both canine two-stage coronary ligation arrhythmia and digitalis arrhythmia. These results suggest that MS-551 is a pure class III antiarrhythmic drug which may be effective in the treatment of life-threatening reentrant tachyarrhythmias, but not in automaticity arrhythmias.
DOI:
--
发表时间:
1981
期刊:
The Journal of pharmacology and experimental therapeutics
影响因子:
--
作者:
Patterson,E;Gibson,JK;Lucchesi,BR
通讯作者:
Lucchesi,BR
影响因子:
5
作者:
Kopia,GA;Eller,BT;Patterson,E;Shea,MJ;Lucchesi,BR
通讯作者:
Lucchesi,BR
影响因子:
3
作者:
Lynch,JJ;Wilber,DJ;Montgomery,DG;Hsieh,TM;Patterson,E;Lucchesi,BR
通讯作者:
Lucchesi,BR