Kuromaru O, Sakai K
Clin Exp Pharmacol Physiol. 1986 Aug;13(8):619-28. doi: 10.1111/j.1440-1681.1986.tb00947.x.
The cardiohaemodynamic response and the development of tolerance to isosorbide dinitrate (ISDN) were examined in anaesthetized, open-chest dogs. ISDN, infused intravenously (i.v.) for 2 h at a rate of 10 or 30 micrograms/kg per min, decreased systemic blood pressure (systolic, mean and diastolic; SBP), left ventricular (LV) systolic and end-diastolic pressure, LVdP/dt max, pressure-rate product and coronary blood flow. No significant changes in heart rate (HR) and coronary vascular resistance were observed. Intravenous ISDN significantly attenuated the vasodilator effect of bolus intracoronary (i.a.) glyceryl trinitrate (GTN, 1 micrograms), and ISDN (30 micrograms), whereas that of bolus i.a. nicorandil (mononitrate, 20 micrograms) remained unaffected. Just after acute tolerance towards i.a. ISDN was provoked 1 h after starting ISDN infusion (30 micrograms/kg per min, i.v.), the combined infusion of ISDN (i.v.) and nicorandil (30 micrograms/kg per min) was instigated for a further hour. Also, 1 h after the onset of vehicle infusion (i.v.), the combined infusion of vehicle and nicorandil (30 micrograms/kg per min, i.v.) was started. There were essentially no significant differences between the corresponding values concerning the coronary vascular responses obtained from the two combined infusion groups.
在麻醉开胸犬中研究了心血管血液动力学反应以及对硝酸异山梨酯(ISDN)耐受性的发展情况。以每分钟10或30微克/千克的速率静脉输注(i.v.)ISDN 2小时,可降低体循环血压(收缩压、平均压和舒张压;SBP)、左心室(LV)收缩压和舒张末期压力、LVdP/dt max、压力-心率乘积以及冠状动脉血流量。未观察到心率(HR)和冠状动脉血管阻力有显著变化。静脉注射ISDN可显著减弱冠状动脉内(i.a.)推注硝酸甘油(GTN,1微克)和ISDN(30微克)的血管舒张作用,而冠状动脉内推注尼可地尔(单硝酸酯,20微克)的血管舒张作用则不受影响。在开始静脉输注ISDN(每分钟30微克/千克)1小时后引发对冠状动脉内ISDN的急性耐受性后,立即开始联合静脉输注ISDN和尼可地尔(每分钟30微克/千克),持续1小时。此外,在开始静脉输注赋形剂1小时后,开始联合输注赋形剂和尼可地尔(每分钟30微克/千克,i.v.)。从两个联合输注组获得的关于冠状动脉血管反应的相应值之间基本上没有显著差异。