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作 者:王培德[1,2] 马学民[1,2] 张慧灵[1,2] 杨玉梅[1,2] 杨煜荣[1,2] 王洪诚[1,2] 劳爱娜[1,2]
机构地区:[1]包头医学院药理教研室 [2]中国科学院上海药物研究所
出 处:《中国药理学通报》1997年第3期263-265,共3页Chinese Pharmacological Bulletin
摘 要:目的与方法:给麻醉大鼠恒速iv刺乌头碱观察ECG变化及ip小剂量刺乌头碱对动物实验性心律失常的影响。结果:iv剂量至2.54±0.06mg·kg-1时,HR显著减慢,P-R间期显著延长,当剂量增至4.12~8.19mg·kg-1时,可分别引起VP、VT、VF及CA等;经ip0.5mg·kg-1时,则能对抗乌头碱、氯化钡诱发的大鼠心律失常,显著提高哇巴因诱发豚鼠心律失常的剂量。结论:小剂量刺乌头碱具有抗心律失常作用,而大剂量又可诱发心律失常。AIM & METHODS:The effects of lappaconitine (LA) on ECG infused in a constant rate in anesthetized rats and the effects of a low dose of LA(ip) on experimental arrhythmia were studied. RESULTS:LA decreased significantly the heart rates and increased markedly the P R intervals at iv dose of 2 54±0 06 mg·kg -1 . Up to 4 12 ̄8 19 mg·kg -1 , LA caused ventricular premature beats (VP), ventricular tachycardia (VT), ventricular fibrillation (VF) and cardiac arrest (CA), respectively. LA (0 5 mg·kg -1 , ip) prevented the arrhythmias induced by aconitine and BaCl 2 in rats and increased significantly the doses of ouabain to induce arrhythmias in guinea pigs. CONCLUSIONS:A low dose of LA can prevent the arrhythmias, whereas the high dose of LA can induce the arrhythmia and their relationship seems to be the therapeutic action and the toxic reaction in heart of some anti arrhythmic drugs.
分 类 号:R972.2[医药卫生—药品] R282.710.5[医药卫生—药学]
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