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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Losartan but not enalaprilat acutely reduces reperfusion ventricular tachyarrhythmias in hypertrophied rat hearts after low-flow ischaemia.
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Losartan but not enalaprilat acutely reduces reperfusion ventricular tachyarrhythmias in hypertrophied rat hearts after low-flow ischaemia.

机译:氯沙坦但非依那普利拉不降低急性低流量缺血后肥厚大鼠心脏的再灌注室速。

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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.
机译:基于临床和实验研究,已提出血管紧张素II受体阻滞剂和血管紧张素转化酶抑制剂对心力衰竭患者具有急性抗心律不齐的作用。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。在非肥大的离体灌注心脏的剂量查找实验中,我们绘制了氯沙坦和依那普利拉的剂量反应曲线,研究了90%复极(MAPD(90%))和心室纤颤(VF)阈值时的单相动作电位持续时间。随后,我们确定了氯沙坦和依那普利拉(在治疗上相关的浓度)对心脏低流量缺血/再灌注所致的室速性心律失常的影响,证实了主动脉束扎70天后左室肥大。我们发现,两种药物均未显着影响非肥厚性心脏的MAPD(90%)(1 nM-1 mM)或VF阈值(1 microM氯沙坦和10 microM依那普利拉)。同样,在肥厚的心脏中,在低流量缺血期间,两种药物均不会显着影响室性心律失常的发生率或持续时间(室性心动过速和VF)。然而,1 microM氯沙坦可显着减少再灌注期间室性心律失常的持续时间。总之,在低流量缺血时,肥大大鼠心脏中氯沙坦和依那普利拉均无急性抗心律失常作用。然而,在再灌注过程中,氯沙坦但非依那普利拉没有,但起着急性抗心律不齐的作用。

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