Kirlin P C, Pitt B, Lucchesi B R
J Cardiovasc Pharmacol. 1981 Jul-Aug;3(4):896-905. doi: 10.1097/00005344-198107000-00023.
The hemodynamic effects of the inotropic agents prenalterol and dobutamine were compared in a canine model of acute ischemic heart failure following two-vessel coronary artery constriction. Intravenous infusions of both inotropic agents resulted in improvement of cardiac output, left ventricular maximum dP/dt, and contractile force in the nonischemic zone and in a decrease in systemic vascular resistance. No significant changes occurred in ischemic zone contractile force or left ventricular end-diastolic pressure following either inotropic agent compared to saline controls. Significant differences between the two inotropic agents consisted of prenalterol's markedly longer duration of action (hemodynamic half life of 3 hr after discontinuation compared to a value of 1.7 min after dobutamine discontinuation) and greater augmentation of cardiac output at high-dose dobutamine due to greater increases in heart rate. However, similar hemodynamic effects were noted with prenalterol and dobutamine at doses which increased nonischemic contractile force 50%. Both inotropic agents were associated with ventricular arrhythmias in the acute ischemic state. Implications regarding the use of prenalterol and dobutamine in clinical acute ischemic low-output states are discussed.
在双支冠状动脉缩窄所致的犬急性缺血性心力衰竭模型中,比较了变力性药物普瑞特罗和多巴酚丁胺的血流动力学效应。静脉输注这两种变力性药物均可使心输出量、左心室最大dp/dt以及非缺血区的收缩力得到改善,并使体循环血管阻力降低。与生理盐水对照组相比,使用任何一种变力性药物后,缺血区收缩力或左心室舒张末期压力均无显著变化。这两种变力性药物之间的显著差异在于,普瑞特罗的作用持续时间明显更长(停药后血流动力学半衰期为3小时,而多巴酚丁胺停药后的半衰期为1.7分钟),且在高剂量多巴酚丁胺时,由于心率增加幅度更大,心输出量增加更为显著。然而,在使非缺血性收缩力增加50%的剂量下,普瑞特罗和多巴酚丁胺的血流动力学效应相似。在急性缺血状态下,这两种变力性药物均与室性心律失常有关。文中讨论了普瑞特罗和多巴酚丁胺在临床急性缺血性低输出状态中的应用意义。