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E-4031和替地沙米对大鼠体内再灌注诱导的心律失常和QT间期的作用及相互作用。

Actions and interactions of E-4031 and tedisamil on reperfusion-induced arrhythmias and QT interval in rat in vivo.

作者信息

Bril A, Landais L, Gout B

机构信息

SmithKline Beecham Laboratoires Pharmaceutiques, Unité de Recherche, Saint Grégoire, France.

出版信息

Cardiovasc Drugs Ther. 1993 Apr;7(2):233-40. doi: 10.1007/BF00878513.

DOI:10.1007/BF00878513
PMID:8357777
Abstract

The effects of the Ito blocker, tedisamil (0.1, 1.0, and 3.0 mg/kg, IV), and the IK blocker, E-4031 (0.1, 1.0, and 3.0 mg/kg, IV), on the incidence and duration of reperfusion-induced arrhythmias were compared in the anesthetized rat (n = 12 per group). Reperfusion arrhythmias were evaluated after a 5 minute occlusion period of the left main coronary artery. In the absence of any pronounced effect on blood pressure, tedisamil and E-4031 reduced heart rate in a dose-dependent manner. During the preischemic period, QTc interval was increased by tedisamil but was not changed by E-4031. Both compounds increased the QTc interval during the ischemic period and also during the reperfusion. E-4031 was unable to reduce the incidence and duration of reperfusion-induced ventricular arrhythmias after 5 minutes of coronary artery occlusion. Tedisamil dose-dependently reduced the duration of reperfusion arrhythmias and their incidence. In a second set of experiments, the combination of tedisamil (1.0 mg/kg) with E-4031 (1.0 mg/kg) was administered. The electrocardiographic action of this combination was similar to that observed with tedisamil given alone. However, with the combination the incidence of fibrillation was reduced from 83% in the control group to 8% in the treated group (p < 0.001), and the mortality was reduced from 67% to 0% (p < 0.001), that is, to a greater extent than with tedisamil (1.0 mg/kg) alone. The results show that the blockade of Ito by tedisamil allows a reduction of reperfusion-induced mortality and that a specific IK blocker (E-4031) is devoid of antifibrillatory action in the anesthetized rat.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在麻醉大鼠中(每组n = 12),比较了Ito阻滞剂替地沙米(静脉注射0.1、1.0和3.0 mg/kg)和IK阻滞剂E-4031(静脉注射0.1、1.0和3.0 mg/kg)对再灌注诱导的心律失常的发生率和持续时间的影响。在左主冠状动脉闭塞5分钟后评估再灌注心律失常。在对血压无明显影响的情况下,替地沙米和E-4031以剂量依赖的方式降低心率。在缺血前期,替地沙米使QTc间期延长,但E-4031对其无影响。两种化合物在缺血期和再灌注期均使QTc间期延长。冠状动脉闭塞5分钟后,E-4031不能降低再灌注诱导的室性心律失常的发生率和持续时间。替地沙米剂量依赖性地降低再灌注心律失常的持续时间及其发生率。在第二组实验中,给予替地沙米(1.0 mg/kg)与E-4031(1.0 mg/kg)的组合。该组合的心电图作用与单独给予替地沙米时观察到的相似。然而,使用该组合时,颤动发生率从对照组的83%降至治疗组的8%(p < 0.001),死亡率从67%降至0%(p < 0.001),即降低程度比单独使用替地沙米(1.0 mg/kg)更大。结果表明,替地沙米对Ito的阻滞可降低再灌注诱导的死亡率,并且特定的IK阻滞剂(E-4031)在麻醉大鼠中没有抗颤动作用。(摘要截短至250字)

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