Hof R P, Hof A, Neumann P
J Cardiovasc Pharmacol. 1982 May-Jun;4(3):352-62. doi: 10.1097/00005344-198205000-00003.
The hemodynamic effects of PY 108-068 (PY), a new benzoxadiazolyle dihydropyridine derivative with calcium antagonistic effects on vascular smooth muscle, were investigated in chloralose--urethane-anesthetized open-chest cats. Regional blood flow was measured with tracer microspheres. PY lowered blood pressure and increased cardiac output similarly to nifedipine (N). Unlike the latter drug, PY decreased heart rate without showing evidence of cardiodepression. Right atrial pressure increased slightly less than with N. All these effects were dose dependent in the dose range from 1 to 43 micrograms/kg i.v.. PY and N increased myocardial blood flow to the same extent initially, and redistributed it in favor of the outer layer of the left ventricle. The activity of sublingually administered PY was comparable to that of a similar intravenous dose. An approximately three times larger intraduodenal dose was needed for similar effects. Our results provide preliminary in vivo evidence that it is possible to separate the negative chronotropic from the negative inotropic effects of calcium antagonists.
在水合氯醛-乌拉坦麻醉的开胸猫身上,研究了新型苯并恶二唑基二氢吡啶衍生物PY 108-068(PY)对血管平滑肌具有钙拮抗作用的血流动力学效应。用示踪微球测量局部血流量。PY降低血压并增加心输出量,与硝苯地平(N)相似。与后一种药物不同,PY降低心率但未显示出心脏抑制的迹象。右心房压力升高略低于N。所有这些效应在静脉注射剂量为1至43微克/千克的范围内均呈剂量依赖性。PY和N最初使心肌血流量增加的程度相同,并使其重新分布有利于左心室外层。舌下给药的PY活性与相似静脉剂量的活性相当。产生相似效应需要十二指肠内剂量大约大三倍。我们的结果提供了初步的体内证据,表明有可能将钙拮抗剂的负性变时作用与负性变力作用分开。