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The Effects of Zileuton and Montelukast in Reperfusion-Induced Arrhythmias in Anesthetized Rats

机译:齐留通和孟鲁司特对麻醉大鼠再灌注性心律不齐的影响

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Background: 5-Lipoxygenase is an enzyme involved in the synthesis of leukotriene eicosanoids from arachidonic acid. The therapeutic potential of zileuton, an inhibitor of 5-lipoxygenase, and montelukast, a cysteinyl leukotriene receptor antagonist, for the treatment of ischemia/reperfusion (I/R) injury of the heart has been proposed in a few studies. However, the effects of zileuton and montelukast on 1/R- induced arrhythmias have not been determined. Objective: We assessed the possible protective effects of zileuton and montelukast against I/R-induced arrhythmias. Methods: Forty-five male Wistar albino rats were divided into 5 groups, each containing 9 rats. Group 1: control, Groups 2 and 3: rats treated with montelukast (10 and 30 mg/kg IP); and Groups 4 and 5: rats treated with zileuton (1 and 3 mg/kg IV) 15 minutes before the induction of ischemia. Ischemia and reperfusion were induced by occluding the left main coronary artery of anesthetized rats for 6 minutes followed by reopening the artery for 6 minutes. Results: Both doses of zileuton decreased the mean [SE] arrhythmia score (zileuton 1 mg/kg: 1.4 |0.8]; zileuton 3 mg/kg: 1.3 [0.5] vs control: 2.9 [0.3]; P < 0.05), the duration of ventricular tachycardia, and the total length of arrhythmias, but montelukast was not effective to decrease the ventricular arrhythmias during the 6 minutes of reperfusion. Conclusions: The results indicate for the first time that zileuton exerts an antiarrhythmic effect at different doses and that montelukast is not effective against I/R-induced arrhythmias. These results indicate that zileuton may be a candidate for drug treatment of I/R-induced arrhythmias.
机译:背景:5-脂氧合酶是一种涉及从花生四烯酸合成白三烯类二十烷酸的酶。在一些研究中已经提出了5-脂氧合酶抑制剂齐留通和半胱氨酰白三烯受体拮抗剂孟鲁司特治疗心脏缺血/再灌注(I / R)损伤的治疗潜力。然而,齐留通和孟鲁司特对1 / R诱导的心律不齐的作用尚未确定。目的:我们评估了齐留通和孟鲁司特对I / R引起的心律失常的可能的保护作用。方法:将四十五只雄性Wistar白化病大鼠分为5组,每组9只。第1组:对照组,第2和第3组:用孟鲁司特(10和30 mg / kg IP)治疗的大鼠;以及第4组和第5组:诱导缺血前15分钟接受齐留通(1和3 mg / kg IV)治疗的大鼠。通过将麻醉大鼠的左主冠状动脉闭塞6分钟,然后再将其重新张开6分钟,诱导缺血和再灌注。结果:两种剂量的齐留通均降低了平均[SE]心律失常评分(齐留通1 mg / kg:1.4 | 0.8];齐留通3 mg / kg:1.3 [0.5] vs对照:2.9 [0.3]; P <0.05),室性心动过速的持续时间和心律失常的总长度,但孟鲁司特在再灌注6分钟内不能有效地减少室性心律失常。结论:结果首次表明齐留通在不同剂量下具有抗心律不齐的作用,孟鲁司特对I / R引起的心律不齐无效。这些结果表明齐留通可能是I / R引起的心律失常药物治疗的候选药物。

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