Huang T F
Department of Physiology, College of Medicine, National Taiwan University, Taipei, Republic of China.
Chin J Physiol. 1992;35(1):9-19.
A simple model of coronary occlusion and reperfusion in conscious rat was used to test the effects of various drugs on the arrhythmias. Blood pressure and ECG were monitored on a Grass polygraph. Intravenous infusion of test agents started before coronary occlusion and continued through the periods of occlusion and reperfusion. The free radical scavengers (allopurinol 12.3 mg/kg, mannitol 33.0 mg/kg, N-2-mercapto-propionyl glycine 8.6 mg/kg and adenosine 10.0 mg/kg), class 1-4 antiarrhythmic drugs (lidocaine 10.2 mg/kg, quinidine 12.3 mg/kg, propranolol 4.9 mg/kg, amiodarone 5.6 mg/kg and verapamil 1.1 mg/kg), aspirin 24.5 mg/kg and benadryl 3.7 mg/kg reduced the incidence of ventricular fibrillation and shortened the duration of arrhythmias during occlusion and reperfusion. Cimetidine 6.9 mg/kg was ineffective to exert the antiarrhythmic action. These results implicate that multiple factors, such as ionic channels (Na, K and Ca), free radicals, arachidonate metabolites and histamine release may play significant roles in genesis of arrhythmias during myocardial ischemia and reperfusion.
采用清醒大鼠冠状动脉闭塞和再灌注的简单模型来测试各种药物对心律失常的影响。通过Grass多导生理记录仪监测血压和心电图。在冠状动脉闭塞前开始静脉输注受试药物,并在闭塞和再灌注期间持续给药。自由基清除剂(别嘌呤醇12.3mg/kg、甘露醇33.0mg/kg、N-2-巯基丙酰甘氨酸8.6mg/kg和腺苷10.0mg/kg)、1-4类抗心律失常药物(利多卡因10.2mg/kg、奎尼丁12.3mg/kg、普萘洛尔4.9mg/kg、胺碘酮5.6mg/kg和维拉帕米1.1mg/kg)、阿司匹林24.5mg/kg和苯海拉明3.7mg/kg可降低心室颤动的发生率,并缩短闭塞和再灌注期间心律失常的持续时间。西咪替丁6.9mg/kg无抗心律失常作用。这些结果表明,离子通道(钠、钾和钙)、自由基、花生四烯酸代谢产物和组胺释放等多种因素可能在心肌缺血和再灌注期间心律失常的发生中起重要作用。