Gibala P, Knezl V, Sotníková R
Ustav experimentálnej farmakológie Centra fyziologických vied Slovenskej akadémie vied, Bratislava.
Cesk Farm. 1990 Feb;39(1):15-7.
In acute experiments on anaesthetized dogs, the haemodynamic effect of etacizine (0.5 and 1.0 mg.kg-1 i.v.) and lidocaine (2.5 and 10 mg.kg-1 i.v.) were compared. Etacizine produced a decrease in heart rate and a temporary decrease in myocardial contractility. After the dose of 1 mg.kg-1 there occurred a temporary increase in peripheral vascular resistance. It did not affect aortal blood pressure, systolic and minute output volume of the heart. Lidocaine produced a decrease in heart rate, aortal blood pressure, systolic and minute output cardiac volume with a rapid return to the original values. Besides this negative effect it was possible to observe an increase in the minute output volume and peripheral vascular resistance with larger doses, which gives evidence of the central effect of the drug.
在对麻醉犬进行的急性实验中,比较了乙卡嗪(静脉注射0.5和1.0毫克/千克)和利多卡因(静脉注射2.5和10毫克/千克)的血流动力学效应。乙卡嗪使心率降低,心肌收缩力暂时下降。在剂量为1毫克/千克后,外周血管阻力出现暂时增加。它不影响主动脉血压、心脏的收缩和每分钟输出量。利多卡因使心率、主动脉血压、心脏收缩和每分钟输出量降低,并迅速恢复到原始值。除了这种负面影响外,还可以观察到较大剂量时每分钟输出量和外周血管阻力增加,这证明了该药物的中枢作用。