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作 者:朱东亚[1,2,3] 王如斌[1,2,3] 彭元瑜
机构地区:[1]中国药科大学新药研究中心 [2]山东医科大学药学系药物化学教研室 [3]海口市制药厂
出 处:《中国药理学与毒理学杂志》1997年第1期31-34,共4页Chinese Journal of Pharmacology and Toxicology
基 金:江苏省科委应用基础研究基金
摘 要:在大鼠离体Langendorf灌流心脏观察四丙酰关附醇胺(TPGFA)对再灌性心律失常及心肌Na+,K+,Ca2+水平的影响.TPGFA6-12mgL-1显著降低30min缺血+30min复灌和吡那地尔(1.25μmolL-1)+12min缺氧+40min再给氧两种模型的室性心动过速和心室纤颤发生率;TPGFA3-12mgL-1可显著减慢心率,延长心电图的QTc,减少K+从心肌细胞内丢失;12mgL-1时还减少细胞内Ca2+堆积.结果表明TPGFA可保护大鼠离体心脏的再灌性心律失常,其作用机理可能与抑制外向K+电流有关.The effects of tetrapropinyl guan fu alcohol amine(TPGFA) on the incidence of ventricular tachycardia (VT) and ventricular fibrillation (VF) induced by reperfusion and the contents of Na +, K + and Ca 2+ were studied in isolated rat hearts. Ischemia (30 min) followed by 30 min reperfusion, VT and VF occurred in 8/8 and 7/8 hearts respectively; in contrast, those occurred in 3/8 and 1/8 hearts exposed to 6 mg·L 1 TPGFA, and 1/8 and 0 hearts exposed to 12 mg·L 1 TPGFA respectively. All hearts (8/8) subjected to pinacidil (1.25 μmol·L 1 ) plus 12 min hypoxia and 40 min reoxygenation developed VT and VF. However the incidence of VT and VF in hearts reperfused was 3/8 and 2/8 respectively in the presence of 6 mg·L 1 TPGFA, and that was 1/8 and 0 respectively in the presence of 12 mg·L 1 TPGFA. TPGFA at concentrations of 3-12 mg·L 1 significantly protected hearts against K + loss and prolonged QT c of ECG induced by ischemia reperfusion. The results suggest that TPGFA inhibits ischemia reperfusion induced myocardial K + loss and protects the heart against life threaten reperfusion arrhythmias.
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