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胺碘酮预先口服负荷剂量在犬体内冠状动脉结扎/再灌注诱导的心律失常模型中的抗心律失常特性:与其他Ⅲ类抗心律失常药物的比较。

Antiarrhythmic properties of a prior oral loading of amiodarone in in vivo canine coronary ligation/reperfusion-induced arrhythmia model: comparison with other class III antiarrhythmic drugs.

作者信息

Nagasawa Yoshinobu, Chen Jianguang, Hashimoto Keitaro

机构信息

Department of Pharmacology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi.

出版信息

J Pharmacol Sci. 2005 Mar;97(3):393-9. doi: 10.1254/jphs.fp0040512. Epub 2005 Mar 12.

Abstract

Amiodarone, which is generally classified as class III antiarrhythmic drug in the Vaughan Williams classification, is widely used for the treatments of refractory arrhythmias. However, we previously reported that intravenous infusion of amiodarone (6.67 mg/kg per hour) did not suppress arrhythmias induced by coronary ligation/reperfusion in dogs. In this study, we examined effects of a prior oral loading of amiodarone on arrhythmias induced by coronary ligation/reperfusion. Sixteen female beagle dogs (8.5 - 12.5 kg) were divided into two groups; one group was given amiodarone (40 mg/kg, orally, n = 8), and the other was given empty gelatin capsules (n = 8) 2 h before the operation. Dogs were anesthetized with pentobarbital and artificially ventilated. The left chest was opened, and the left anterior descending coronary artery was ligated for 30 min and then reperfused. The mean plasma concentration of amiodarone was over 1.3 mug/ml. Although the prior oral loading of amiodarone did not change the QT interval, amiodarone suppressed the number of ectopic beats during coronary ligation and the incidence of ventricular fibrillation during coronary ligation and reperfusion periods (P<0.05 vs control group). In conclusion, a prior oral loading of amiodarone suppressed arrhythmias induced by coronary ligation/reperfusion with a dose that did not prolong the QT interval. This antiarrhythmic property of amiodarone is different from those of the other class III drugs in that antiarrhythmic effects were accompanied by QT prolongation in our all previous studies.

摘要

胺碘酮在 Vaughan Williams 分类中通常被归类为 III 类抗心律失常药物,广泛用于治疗难治性心律失常。然而,我们之前报道过,静脉输注胺碘酮(每小时 6.67 毫克/千克)并不能抑制犬冠状动脉结扎/再灌注诱导的心律失常。在本研究中,我们检查了胺碘酮预先口服负荷对冠状动脉结扎/再灌注诱导的心律失常的影响。将 16 只雌性比格犬(8.5 - 12.5 千克)分为两组;一组在手术前 2 小时给予胺碘酮(40 毫克/千克,口服,n = 8),另一组给予空明胶胶囊(n = 8)。犬用戊巴比妥麻醉并进行人工通气。打开左胸,结扎左前降支冠状动脉 30 分钟,然后再灌注。胺碘酮的平均血浆浓度超过 1.3 微克/毫升。虽然胺碘酮预先口服负荷并未改变 QT 间期,但胺碘酮抑制了冠状动脉结扎期间的异位搏动数量以及冠状动脉结扎和再灌注期间的室颤发生率(与对照组相比,P<0.05)。总之,胺碘酮预先口服负荷以不延长 QT 间期的剂量抑制了冠状动脉结扎/再灌注诱导的心律失常。胺碘酮的这种抗心律失常特性与其他 III 类药物不同,因为我们之前所有的研究中,其他 III 类药物的抗心律失常作用都伴随着 QT 间期延长。

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