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Moricizine is a class I antiarrhythmic agent.1 It induces both tonic and phasic blocks of sodium currents in isolated guinea pig atrial myocytes when used at a concentration of 30 µM and induces a tonic block of sodium currents in isolated guinea pig ventricular myocytes at 1 and 10 µM. Moricizine (1-3 mg/kg) reduces spontaneous arrhythmias occurring 24 hours after ligation of the left anterior descending (LAD) coronary artery in dogs as a model of myocardial infarction.2 It also reduces arrhythmias occurring 2-5 days after LAD coronary ligation in the same model. Formulations containing moricizine have previously been used in the treatment of ventricular arrhythmias.
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1. Analysis of moricizine block of sodium current in isolated guinea-
2. Effects of the phenothiazine analog, EN-