Nonaka K, Ueno A
Arzneimittelforschung. 1985;35(10):1499-502.
Cardiovascular effects of cinpropazide (1-(3',4',5'-trimethoxycinnamoyl)-4-(N-isopropylaminocarbonylme th yl)-piperazine maleate) administered i.v. and p.o. were investigated in unanesthetized and unrestrained dogs by means of radiotelemetering system with preceding chronic implantations of an aortic and a venous catheter, Doppler flow probe around circumflex branch in the left coronary artery and subcutaneous ECG electrodes. Intravenous administration of cinpropazide indicated that the drug was much less potent in coronary vasodilating property than newly introduced group of coronary vasodilators. However, the oral administration of this agent efficiently exhibited a remarkable increase in the coronary blood flow, suggesting that this agent has an extremely high bioavailability. It is concluded that cinpropazide is a coronary vasodilator to succeed nifedipine and nicorandil exhibiting an actual increase of coronary blood flow by oral administration in the dog.
通过带有预先长期植入的主动脉和静脉导管、左冠状动脉回旋支周围的多普勒血流探头以及皮下心电图电极的无线电遥测系统,在未麻醉和未约束的犬中研究了静脉注射和口服肉桂哌嗪(1-(3',4',5'-三甲氧基肉桂酰基)-4-(N-异丙基氨基羰基甲基)-哌嗪马来酸盐)的心血管效应。静脉注射肉桂哌嗪表明,该药物在冠状动脉舒张特性方面的效力远低于新引入的一组冠状动脉舒张剂。然而,口服该药物有效地使冠状动脉血流量显著增加,表明该药物具有极高的生物利用度。得出的结论是,肉桂哌嗪是一种继硝苯地平和尼可地尔之后的冠状动脉舒张剂,在犬中口服可使冠状动脉血流量实际增加。