Key result
UP 614-04 was about five times less cardiotoxic and four to eight times less potent as a cardiodepressor than imipramine or clomipramine in guinea pigs and dogs.
Why the study?
Does UP 614-04 have lower cardiotoxicity and cardiodepressor effects compared to tricyclic antidepressants in guinea pigs and dogs?
Does UP 614-04 have lower cardiotoxicity and cardiodepressor effects compared to tricyclic antidepressants in guinea pigs and dogs?
In animal models, the potential antidepressant UP 614-04 exhibits significantly lower cardiotoxicity and cardiodepressor effects compared to standard tricyclic antidepressants.
Answers are grounded in this paper and cite their sources.
Should not yet influence antidepressant selection; leaves open translation of lower cardiotoxicity from animal models to humans.
The cardiotoxic and hemodynamic effects of intravenously administered UP 614‐04, imipramine, clomipramine, and amitriptyline were compared using guinea pigs and dogs. In guinea pigs, determinations of minimal lethal dose and electrocardioraphic changes indicated that UP 614‐04 was much less cardiotoxic than the three tricyclic antidepressants tested. In dogs, both imipramine and clomipramine exerted more pronounced effects than UP 614‐04 on hemodynamic parameters. However, all three agents had qualitatively similar dose–response characteristics in that low doses produced slight increases in systolic blood pressure and heart rate, intermediate doses did not alter haemodynamic parameters, and high doses produced marked cardiodepressor effects. Imipramine and clomipramine were also much more potent than UP 614‐04 in potentiating the pressor action of intravenously administered norepinephrine. Taken together, these results have indicated that UP 614‐04 is about five times less cardiotoxic and about four to eight times less potent as a cardiodepressor than imipramine or clomipramine.
No takes yet. Share an insight, caveat, or question.
Cazes et al. (1983) studied this question. UP 614-04 vs. imipramine, clomipramine, and amitriptyline was evaluated on Minimal lethal dose, electrocardiographic changes, and hemodynamic parameters. UP 614-04 was about five times less cardiotoxic and four to eight times less potent as a cardiodepressor than imipramine or clomipramine in guinea pigs and dogs.
Synapse has enriched 10 related papers. Consider them for comparative context: