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Journal of Pharmacology And Experimental Therapeutics, Vol. 164, Issue 2, 317-325, 1968
Copyright © 1968 by American Society for Pharmacology and Experimental Therapeutics


ANTIARRUYTHMIC ACTIVITY OF THE DEXTRO- AND LEVO-ROTATORY ISOMERS OF 4-(2-ISOPROPYLAMINO-1-HYDROXYETHYL) METHANESULFONANILIDE (MJ 1999)

P. SOMANI 1 and D. L. WATSON 1

1 Department of Pharmacology, Marquette School of Medicine, Milwaukee, Wisconsin

The antiarrhythmic activity of levo- and dextro-rotatory isomers of 4-(2-isopropylamino-1-hydroxyethyl) methanesulfonanilide (MJ 1999), a beta adrenergic receptor blocking agent, was investigated in the present work. levo-MJ 1999, which is the active isomer in terms of blockade of the beta receptors, antagonized adrenergically induced ventricular tachycardia and ventricular fibrillation in 0.5 to 1 mg/kg dose but was ineffective against the arrhythmias produced by toxic dose of ouabain or by two-stage coronary artery ligation in cumulative doses of 25 to 35 mg/kg. In the case of dextro-MJ 1999, 10 to 20 mg/kg dose was needed to suppress adrenergically induced arrhythmias. It is concluded that the antiarrhythmic effects of MJ 1999 are a reflection of the specific beta receptor blocking action of the drug and that MJ 1999 is devoid of the nonspecific antiarrhythmic actions seen with some other beta adrenergic blocking agents.

Submitted on June 4, 1968
Accepted on September 16, 1968




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Copyright © 1968 by the American Society for Pharmacology and Experimental Therapeutics.