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卡维地洛抗实验性心律失常作用
引用本文:吕艳青,周际安,曾繁典.卡维地洛抗实验性心律失常作用[J].中国药理学通报,1999,15(5):428-431.
作者姓名:吕艳青  周际安  曾繁典
作者单位:同济医科大学临床药理研究所!武汉430030暨南大学医学院药理学教研室,广州510630,同济医科大学临床药理研究所!武汉430030,同济医科大学临床药理研究所!武汉430030
摘    要:目的 评价卡维地洛(CVD)抗实验性心律失常作用,并与β受体阻断剂普萘洛尔(PRO) 进行比较。方法 采用氯仿致小鼠室颤(VF) , 哇巴因、乌头碱致豚鼠、大鼠心律失常,肾上腺素致豚鼠心律失常, 以及结扎大鼠冠状动脉诱发心律失常等5 种模型。结果 与溶媒对照组相比, CVD1 mg·kg-1 显著降低氯仿诱发的小鼠VF 发生率〔18-75 %(3/16) vs81-25% (13/16),P< 0-01〕,此作用与PRO 相似。1 mg·kg-1 CVD 和PRO 均显著提高致室早(VE) , 室速(VT), VF, 心搏停止(CA) 所需哇巴因和乌头碱用量( P<0-01 vs 溶剂对照组) ;CVD 对抗哇巴因的致心律失常作用较等剂量PRO 显著( P< 0-01 ,CVD vs PRO)。CVD 剂量依赖性地显著缩短iv 肾上腺素40 μg·kg- 1 所致心律失常持续时间,有效减少结扎冠脉诱发的缺血性心律失常VT,VF,CA 的发生率并缩短VT 的持续时间。结论 CVD 具有抗多种实验性心律失常作用,该作用在等剂量时至少与PRO 相近,或强于PRO。CVD的这种作用最终将有益于接受其治疗的原发性高血压、冠心病、充血性心力衰竭患者

关 键 词:卡维地洛  肾上腺素  乌头碱  哇巴因  氯仿  心律失常  心肌缺血

Protective effects of carvedilol on experimental arrhythmias
L Yan Qing,ZHOU Ji An,ZENG Fan Dian.Protective effects of carvedilol on experimental arrhythmias[J].Chinese Pharmacological Bulletin,1999,15(5):428-431.
Authors:L Yan Qing  ZHOU Ji An  ZENG Fan Dian
Abstract:AIM The aim was to evaluate the antiarrhythmic effects provided by carvedilol, and compared with propranolol in several arrhythmia animal models. METHODS Experiments were performed in 5 arrhythmic animal models, inhalation of chloroform to induce ventricular fibrillation (VF) in mice, ouabain induced or aconitine induced arrhythmia in guinea pigs or rats, adrenaline induced arrhythmia in guinea pigs and ligation of coronary artery of rats to induce arrhythmia. RESULTS Carvedilol 1 mg·kg -1 significantly reduced the chloroform induced VF incidence in mice18 75% (3/16) vs 81 25%(13/16), carvedilol vs vehicle]. The effects were similar to which of propranolol. The doses of ouabain and aconitine to produce ventricular extrasystole (VE), ventricular tachycardia (VT), VF, cardiac arrest (CA) were significantly increased in 1 mg·kg -1 of carvedilol and of propranolol groups respectively ( P <0 01 vs vehicle). At the same dose, the effects of carvedilol on ouabain induced arrhythmia were greater than those of propranolol (P <0 01 vs vehicle, P< 0 01 vs propranolol). The duration of arrhythmia induced by 40 μg·kg -1 adrenaline were significantly reduced by carvedilol, in a dose dependent manner. Besides these, carvedilol also effectively reduced VT, VF, CA incidences and duration of VT in animals subjected to coronary artery ligation. CONCLUSIONS Carvedilol has antiarrhythmic effects in various animal models. At the same dose, 1 mg·kg -1 , its antiarrhythmic effects were at least equal to which of propranolol, or more potent. The antiarrhythmic effects provided by carvedilol may ultimately be beneficial to patients subjected to essential hypertension, coronary artery disease or congestive heart failure.
Keywords:carvedilol  adrenaline  aconitine  ouabain  chloroform  arrhythmia  myocardia  ischemic
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