Lisciani R, Baldini A, Benedetti D, Campana A, Barcellona P S
Toxicology. 1978 Jun;10(2):151-8. doi: 10.1016/0300-483x(78)90065-3.
The cardiovascular effects of trazodone, a broad-spectrum antidepressant and its analogue etoperidone, were compared with imipramine, following intravenous infusion in rats. Their effects on electrocardiogram and blood pressure were simultaneously recorded until cardiac arrest. Hypotension was the primary effect of trazodone and etoperidone. ECG changes, i.e. lengthening of the PR interval, were observed only when the blood pressure reached very low values. On the other hand, imipramine produced first the well known ECG changes and then a drop in blood pressure. As far as mortality was concerned, trazodone was the least toxic drug, followed by etoperidone, whereas imipramine was most toxic; these differences being in agreement with the LD50 values reported in rats by the i.v. route. It is concluded that trazodone and etoperidone produce in rats cardiovascular effects, which are different from those of imipramine. Moreover these differences are consistent with their pharmacological properties, particularly their interaction with catecholamines, which are inhibited by trazodone or etoperidone and potentiated by imipramine.
在大鼠静脉注射后,将广谱抗抑郁药曲唑酮及其类似物乙哌立酮的心血管效应与丙咪嗪进行了比较。同时记录它们对心电图和血压的影响,直至心脏停搏。低血压是曲唑酮和乙哌立酮的主要作用。仅当血压降至极低值时才观察到心电图变化,即PR间期延长。另一方面,丙咪嗪首先产生众所周知的心电图变化,然后血压下降。就死亡率而言,曲唑酮是毒性最小的药物,其次是乙哌立酮,而丙咪嗪毒性最大;这些差异与静脉注射途径在大鼠中报道的半数致死量值一致。结论是曲唑酮和乙哌立酮在大鼠中产生的心血管效应与丙咪嗪不同。此外,这些差异与其药理特性一致,特别是它们与儿茶酚胺的相互作用,曲唑酮或乙哌立酮可抑制这种相互作用,而丙咪嗪则可增强这种相互作用。