almokalant has been researched along with Myocardial-Ischemia* in 2 studies
2 other study(ies) available for almokalant and Myocardial-Ischemia
Article | Year |
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Effect of almokalant a specific inhibitor of IKr on myocardial ischaemia-reperfusion induced arrhythmias in rabbits.
The antiarrhythmic effect of almokalant, a new type III antiarrhythmic agent, was examined by occluding and releasing the left circumflex coronary artery for 10 min, respectively, in openchest, pentobarbital-anaesthetized albino rabbits. Almokalant pretreatment increased the number of animals developing no arrythmias (5/9 vs. 1/12 in controls), and decreased the incidence of ventricular fibrillation (1/9 vs. 9/12) during reperfusion. According to our results almokalant can protect the heart against arrhythmias induced by ischaemia and reperfusion. Topics: Animals; Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Electric Conductivity; Female; Male; Myocardial Ischemia; Myocardial Reperfusion Injury; Potassium; Propanolamines; Rabbits | 1996 |
Class III antiarrhythmic action and inotropy: effects of almokalant in acute ischaemic heart failure in dogs.
We studied the haemodynamic and metabolic effects of the novel class III antiarrhythmic agent almokalant (H 234/09) in acute ischaemic heart failure at a dose prolonging ventricular repolarization. In pentobarbital anaesthetized dogs, heart failure was induced by microembolization of the area supplied by the main left coronary artery until a stable left ventricular end-diastolic pressure (LVEDP) of 32 +/- 2 mmHg was achieved. Embolization depressed LV dP/dt(max), LV dP/dt(min), left ventricular systolic pressure (LVSP) and cardiac output. After intravenous infusion of almokalant (0.35 micrograms/kg) LV dP/dt(max) and LV dP/dt(min) were not significantly changed at paced cycle length of 300 msec., whereas LVSP and aortic pressure decreased both at spontaneous and paced cycle length of 300 msec. LVEDP remained unchanged. Heart rate decreased from 185 +/- 7 to 167 +/- 5 beats/min., and corrected QT-time (QTc) increased from 9.5 +/- 0.3 to 10.4 +/- 0.5 msec. Arterial concentration and net myocardial uptake of glucose, lactate and free fatty acids were not significantly influenced by almokalant. In conclusion, almokalant at a dose prolonging ventricular repolarization had no negative inotropic effect in acute ischaemic heart failure. Topics: Acute Disease; Animals; Anti-Arrhythmia Agents; Cardiotonic Agents; Dogs; Electrocardiography; Embolization, Therapeutic; Female; Hemodynamics; Male; Myocardial Ischemia; Myocardium; Oxygen Consumption; Propanolamines | 1992 |