Butz Silvia, Driamov Sergey, Remondino Andrea, Bellahcene Mohamed, Beier Konstantin, Ziegler André, Buser Peter T, Zaugg Christian E
Experimental Cardiology Research Group, Department of Research, University Hospital of Basel, Switzerland.
J Pharm Pharmacol. 2004 Apr;56(4):521-8. doi: 10.1211/0022357023178.
Based on clinical and experimental studies, angiotensin II receptor blockers and angiotensin converting enzyme inhibitors have been proposed to exert acute anti-arrhythmic effects in heart failure patients. Therefore, the goal of this study was to assess acute anti-arrhythmic effects of losartan and enalaprilat in hypertrophied rat hearts during low-flow ischaemia and reperfusion. In dose-finding experiments in non-hypertrophied isolated perfused hearts, we performed dose-response curves of losartan and enalaprilat studying monophasic action potential duration at 90% repolarisation (MAPD(90%)) and ventricular fibrillation (VF) threshold. Subsequently, we determined the effects of losartan and enalaprilat (in therapeutically relevant concentrations) on ventricular tachyarrhythmias induced by low-flow ischaemia/reperfusion in hearts demonstrating left ventricular (LV) hypertrophy 70 days after aortic banding. We found that neither drug significantly affected MAPD(90%) (1 nM-1 mM) or VF threshold (1 microM losartan and 10 microM enalaprilat) in non-hypertrophied hearts. Similarly in hypertrophied hearts, neither drug significantly affected the incidence or the duration of ventricular tachyarrhythmias (ventricular tachycardia and VF) during low-flow ischaemia. However, 1 microM losartan significantly reduced the duration of ventricular tachyarrhythmias during reperfusion. In conclusion, neither losartan nor enalaprilat is acutely anti-arrhythmic in hypertrophied rat hearts during low-flow ischaemia. During reperfusion, however, losartan but not enalaprilat exerts acute anti-arrhythmic effects.
基于临床和实验研究,有人提出血管紧张素II受体阻滞剂和血管紧张素转换酶抑制剂对心力衰竭患者具有急性抗心律失常作用。因此,本研究的目的是评估氯沙坦和依那普利拉在低流量缺血和再灌注期间对肥厚大鼠心脏的急性抗心律失常作用。在非肥厚性离体灌注心脏的剂量探索实验中,我们绘制了氯沙坦和依那普利拉的剂量反应曲线,研究90%复极化时的单相动作电位持续时间(MAPD(90%))和室颤(VF)阈值。随后,我们确定了氯沙坦和依那普利拉(治疗相关浓度)对主动脉缩窄70天后出现左心室(LV)肥厚的心脏中低流量缺血/再灌注诱导的室性快速心律失常的影响。我们发现,在非肥厚性心脏中,两种药物均未显著影响MAPD(90%)(1 nM - 1 mM)或VF阈值(1 μM氯沙坦和10 μM依那普利拉)。同样,在肥厚性心脏中,两种药物均未显著影响低流量缺血期间室性快速心律失常(室性心动过速和VF)的发生率或持续时间。然而,1 μM氯沙坦显著缩短了再灌注期间室性快速心律失常的持续时间。总之,在低流量缺血期间,氯沙坦和依那普利拉对肥厚大鼠心脏均无急性抗心律失常作用。然而,在再灌注期间,氯沙坦具有急性抗心律失常作用,而依那普利拉则没有。