Nielsen-Kudsk F, Quist S
Acta Pharmacol Toxicol (Copenh). 1980 Apr;46(4):263-9. doi: 10.1111/j.1600-0773.1980.tb02452.x.
The cardiac effects of supratherapeutic concentrations of two tricyclic antidepressants were studied in isolated rabbit hearts, which were perfused with a modified Krebs-Henseleit solution containing 0.25 or 0.50 micrograms ml-1 of amitriptyline or 0.28 micrograms mg-1 of clomipramine. The following parameters were continuously recorded:heart rate, amplitude and rate of contraction, coronary flow rate, myocardial oxygen consumption and ECG. The lowest concentration of amitriptyline caused a time correlated decrease (20%) in the frequency of spontaneous beating and a pronounced decrease in the amplitude (62%) and rate of cardiac contraction (58%). Maximum increases of the PQ-interval of about 46% and of the QRS-complex of about 100% were observed. At the higher amitriptyline concentration these effect further increased. Clomipramine 0.28 micrograms ml-1 also had a very pronounced and time correlated negative inotropic effect, but the effects upon the conduction velocities were substantially lesser than those produced by the equimilar concentration of amitriptyline. The compounds caused only insignificant changes in coronary flow. The oxygen consumption did not decrease in proportion to the decrease in contractility, as an expression of decreased myocardial efficiency. The effects of the drugs are discussed in relation to theri myocardial accumulation pharmacokinetics and influence upon the membraneous sodium and calcium flux and intracellular metabolism.
研究了两种三环类抗抑郁药超治疗浓度对离体兔心脏的影响,这些心脏用含有0.25或0.50微克/毫升阿米替林或0.28微克/毫克氯米帕明的改良Krebs-Henseleit溶液灌注。连续记录以下参数:心率、收缩幅度和速率、冠状动脉血流量、心肌耗氧量和心电图。阿米替林的最低浓度导致自发搏动频率随时间相关下降(20%),心脏收缩幅度(62%)和速率(58%)显著下降。观察到PQ间期最大增加约46%,QRS波群最大增加约100%。在较高的阿米替林浓度下,这些效应进一步增强。0.28微克/毫升的氯米帕明也有非常明显的、与时间相关的负性肌力作用,但对传导速度的影响明显小于同等浓度的阿米替林。这些化合物仅引起冠状动脉血流量的微小变化。耗氧量并未与收缩力的下降成比例下降,这表明心肌效率降低。结合药物在心肌中的蓄积、药代动力学以及对膜钠和钙通量及细胞内代谢的影响,对这些药物的作用进行了讨论。