Sur I’activité anti-arythmique d’un nouvel agent de blocage beta-adrénergique
- 1 January 1966
- journal article
- research article
- Published by S. Karger AG in JMIR AI
- Vol. 49 (Suppl. 1), 45-58
- https://doi.org/10.1159/000168951
Abstract
Butydrine (2-sec. butylamino-1-(5,6,7,8-tetrahydro-2-naphtyl) ethanol HCL) was studied in normal subjects and in patients suffering from various types of arrhythmias. The drug apparently has no significant metabolic effect. It causes a mild bradycardia with an increase in both systolic and diastolic arterial pressures. It blocks the metabolic, hemodynamic and arrhythmic effects otherwise elicited by an epinephrine infusion. In atrial fibrillation, the drug leads to a decrease in ventricular rate, even in patients previously digitalized. The combination of butydrine and digitalis is more effective than either drug alone. Butydrine is particularly effective in reverting extrasystoles due to digitalis intoxication. It has little effect in paroxysmal atrial fibrillation and in atrial or ventricular paroxysmal tachycardia. It does not influence the tachycardia due to hyperthyroidism.This publication has 4 references indexed in Scilit:
- EFFECT OF ADRENERGIC RECEPTOR BLOCKADE ON THE TACHYCARDIA OF THYROTOXICOSIS AND ANXIETY STATEThe Lancet, 1965
- Reversal of Digitalis Intoxication by Beta-Adrenergic Blockade with PronethalolNew England Journal of Medicine, 1964
- Pharmacodynamic Effects of Beta-Adrenergic Receptor Blockade in Patients with Hyperthyroidism *JCI Insight, 1964
- INFLUENCE OF DICHLOROISOPROTERENOL (DCI) AND RELATED COMPOUNDS UPON OUABAIN AND ACETYLSTROPHANTHIDIN INDUCED CARDIAC ARRHYTHMIAS1961