Dumovic P, Burrows G D, Vohra J, Davies B, Scoggins B A
Arch Toxicol. 1976 Aug 18;35(4):255-62. doi: 10.1007/BF00570267.
The effects on the heart rate and ECG of anaesthetised guines-pigs of amitriptyline, doxepin, imipramine and nortiptyline infused at 1.0 mg/kg/min until death were observed. In addition an in vitro study on guinea-pig atria was performed on the chronotropic and inotropic effects of these drugs and of desmethylimipramine and protriptyline at a concentration of 10(-5) M. The effect of sodium bicarbonate (3 mEq/kg i.v.) and propranolol (0.01--0.2 mg/kg i.v.) on amitriptyline and doxepin induced ECG changes was also assessed. A difference in the cardiac effects of the in vivo and in vitro model was observed. Guinea-pigs infused with doxepin survived significantly longer than those infused with amitriptyline, imipramine or nortriptyline. No statistically significant difference was found between the tricyclic drugs with respect to onset of widening of the QRS complex, increased PR and QT intervals. In the spontaneously beating atrial preparation doxepin was the most potent cardio-depressant. Sodium bicarbonate had no effect on arrhythmias induced by tricyclics, while propranolol, apart from the bradycardia induced, was without beneficial effect on the ECG. The guinea-pig provides a good model for studying the arrhythmogenic actions of tricyclic antidepressants.
观察了以1.0毫克/千克/分钟的速度输注阿米替林、多塞平、丙咪嗪和去甲替林直至死亡对麻醉豚鼠心率和心电图的影响。此外,还对豚鼠心房进行了体外研究,观察了这些药物以及去甲丙咪嗪和普罗替林在浓度为10(-5)M时对变时性和变力性的影响。还评估了碳酸氢钠(静脉注射3毫当量/千克)和普萘洛尔(静脉注射0.01 - 0.2毫克/千克)对阿米替林和多塞平所致心电图变化的影响。观察到体内和体外模型在心脏效应方面存在差异。输注多塞平的豚鼠存活时间明显长于输注阿米替林、丙咪嗪或去甲替林的豚鼠。在QRS波群增宽、PR间期和QT间期增加的起始方面,三环类药物之间未发现统计学上的显著差异。在自发搏动的心房标本中,多塞平是最有效的心脏抑制剂。碳酸氢钠对三环类药物诱发的心律失常没有影响,而普萘洛尔除了诱发心动过缓外,对心电图没有有益作用。豚鼠为研究三环类抗抑郁药的致心律失常作用提供了一个良好的模型。