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丙吡胺对未麻醉犬心电图及心室功能的影响。

Effects of disopyramide on the electrocardiogram and ventricular function in the unanesthetized dog.

作者信息

Crosby H H, Hamlin R L, Strauch S M

出版信息

J Vet Pharmacol Ther. 1984 Sep;7(3):167-75. doi: 10.1111/j.1365-2885.1984.tb00896.x.

Abstract

The antiarrhythmic compound disopyramide has been shown to possess negative inotropic effects. The present study was conducted to establish the effects of graded doses of disopyramide on ventricular function and electrocardiograms from healthy, awake dogs. Electrocardiograms and echocardiograms were obtained during a control period, and during an experimental period in which the six dogs on test received 7.5, 15 or 30 mg disopyramide per kg body weight orally three times per day. Six other dogs served as vehicle controls. No changes of statistical significance occurred in heart rate. The PQ interval was prolonged at all doses, the QRS complex was prolonged only at the highest dose, and the QT interval was prolonged at the intermediate and high doses. Left ventricular pre-ejection period (PEP) was prolonged in a dose-dependent relationship, and the left ventricular ejection time (ET) was shortened only at the highest dose. The percent shortening fraction of the left ventricle (% delta D) decreased significantly at intermediate and high doses, while the ratio of pre-ejection period to ejection time increased in a dose-dependent relationship. Conclusions are that even in therapeutic levels disopyramide produces significant reduction in left ventricular function, and that ratio of PEP/ET correlates better with the dose of disopyramide than did % delta D. This study demonstrates the feasibility of evaluating cardiac effects of compounds by non-invasive means.

摘要

抗心律失常化合物丙吡胺已被证明具有负性肌力作用。本研究旨在确定不同剂量的丙吡胺对健康清醒犬的心室功能和心电图的影响。在对照期以及实验期获取心电图和超声心动图,实验期内,六只受试犬每天口服三次每千克体重7.5、15或30毫克丙吡胺。另外六只犬作为溶剂对照。心率未发生具有统计学意义的变化。所有剂量下PQ间期均延长,仅最高剂量时QRS波群延长,中高剂量时QT间期延长。左心室射血前期(PEP)呈剂量依赖性延长,仅最高剂量时左心室射血时间(ET)缩短。左心室缩短分数百分比(%ΔD)在中高剂量时显著降低,而射血前期与射血时间的比值呈剂量依赖性增加。结论是,即使在治疗水平,丙吡胺也会使左心室功能显著降低,并且PEP/ET比值与丙吡胺剂量的相关性优于%ΔD。本研究证明了通过非侵入性手段评估化合物心脏效应的可行性。

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