Mortensen E, Yang T, Refsum H
Department of Medical Physiology, University of Tromsø, Norway.
Pharmacol Toxicol. 1992 Jun;70(6 Pt 1):443-7. doi: 10.1111/j.1600-0773.1992.tb00505.x.
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.
我们研究了新型III类抗心律失常药物阿尔莫卡兰(H 234/09)在急性缺血性心力衰竭中以延长心室复极的剂量时的血流动力学和代谢效应。在戊巴比妥麻醉的犬中,通过微栓塞左冠状动脉主要供血区域诱导心力衰竭,直至达到稳定的左心室舒张末期压力(LVEDP)为32±2 mmHg。栓塞降低了左心室dp/dt(最大值)、左心室dp/dt(最小值)、左心室收缩压(LVSP)和心输出量。静脉输注阿尔莫卡兰(0.35微克/千克)后,在300毫秒的起搏周期长度下,左心室dp/dt(最大值)和左心室dp/dt(最小值)无显著变化,而在300毫秒的自发和起搏周期长度下,LVSP和主动脉压力均降低。LVEDP保持不变。心率从185±7次/分钟降至167±5次/分钟,校正QT间期(QTc)从9.5±0.3毫秒增加至10.4±0.5毫秒。阿尔莫卡兰对动脉血中葡萄糖、乳酸和游离脂肪酸的浓度及心肌净摄取量无显著影响。总之,在急性缺血性心力衰竭中,以延长心室复极的剂量使用阿尔莫卡兰无负性肌力作用。