Hames T K, Burgess C D, George C F
Clin Pharmacol Ther. 1982 Oct;32(4):497-502. doi: 10.1038/clpt.1982.194.
The hemodynamic effects of trazodone (150 mg) and imipramine (75 mg) were examined in eight healthy subjects. Trazodone significantly increased left ventricular ejection time 1 (LVETI), but decreased both preejection period (PEP) and PEP/LVET ratio. It also decreased heart rate and systolic and diastolic blood pressure at 90 min after dosing. Imipramine initially increased total electromechanical systole I (QS2I) and PEP (30 min, P less than 0.01), but at 150 and 180 min after dosing QS2I was significantly lower. Imipramine increased diastolic blood pressure at 30 min (P less than 0.05) and increased systolic blood pressure between 90 and 180 min (P less than 0.05). At 30 and 60 min heart rate was significantly depressed by imipramine. There were no significant changes in the values of stroke volume and cardiac output. These results suggest that trazodone has its major effect on the circulation through its alpha-receptor blocking activity, whereas the effects of imipramine are probably mediated through its ability to block reuptake of norepinephrine.
在8名健康受试者中研究了曲唑酮(150毫克)和丙咪嗪(75毫克)的血流动力学效应。曲唑酮显著增加左心室射血时间1(LVETI),但缩短射血前期(PEP)和PEP/LVET比值。给药后90分钟时,它还降低心率以及收缩压和舒张压。丙咪嗪最初增加总电机械收缩期1(QS2I)和PEP(30分钟时,P<0.01),但给药后150和180分钟时QS2I显著降低。丙咪嗪在30分钟时增加舒张压(P<0.05),并在90至180分钟之间增加收缩压(P<0.05)。在30和60分钟时,丙咪嗪显著降低心率。每搏量和心输出量的值无显著变化。这些结果表明,曲唑酮主要通过其α受体阻断活性对循环产生作用,而丙咪嗪的作用可能是通过其阻断去甲肾上腺素再摄取的能力介导的。