A COMPARISON IN RABBIT ISOLATED HEARTS OF THE DYSRHYTHMOGENIC POTENTIAL OF AMITRIPTYLINE, MAPROTILINE AND MIANSERIN IN RELATION TO THEIR ABILITY TO BLOCK NORADRENALINE UPTAKE
- 1 April 1977
- journal article
- research article
- Published by Wiley in British Journal of Pharmacology
- Vol. 59 (4) , 651-660
- https://doi.org/10.1111/j.1476-5381.1977.tb07734.x
Abstract
1. In isolated hearts of rabbits, perfusion with (-)-noradrenaline (0.0059 to 5.9 micronM) resulted in chronotropic and inotropic responses and a shortening of the interval between peak atrial and peak ventricular tensions (the A-V contraction interval). No dysrhythmias developed but at higher concentrations (590 micronM) 2 out of 7 hearts developed dysrhythmias (extrasystoles). 2. Perfusion with the antidepressants amitriptyline or maprotiline (4.8 micronM) or mianserin (28.8 micronM) reduced ventricular force, did not change heart rate and only amitriptyline reduced atrial force and lengthened the A-V contraction interval. At 4.8 micronM mianserin produced only a marginal shortening of the A-V contraction interval. 3. At these concentrations no dysrhythmias developed but at higher concentrations (amitriptyline 8 micronM, maprotiline 8 micronM, mianserin 60 micronM) all the agents produced dysrhythmias involving an interference with atrio-ventricular synchronization. 4. In the presence of mianserin (4.8 micronM) perfusion with noradrenaline (0.0059 to 5.9 micronM) shortened the A-V contraction interval and did not produce dysrhythmias. In the presence of amitriptyline or maprotiline (4.8 micronM) or mianserin (28.8 micronM) the A-V contraction interval generally lengthened and most hearts developed dysrhythmias (usually involving interference with atrio-ventricular synchronization). 5. [3H]-(-)-Noradrenaline uptake in perfused rabbit hearts and in mouse isolated atria or vasa deferentia was inhibited by the antidepressants to a similar extent, amitriptyline being marginally most potent (molar potency taken as 1.0), maprotiline being less potent (1.5) and mianserin least potent (2.0)). 6. It is concluded that of these three antidepressants, mianserin is least cardiotoxic in this preparation and that the ability of these antidepressants to predispose to noradrenaline-induced dysrhythmias is not related to blockade of noradrenaline uptake.Keywords
This publication has 19 references indexed in Scilit:
- Comparative study of the effects of mianserin, a tetracyclic antidepressant, and of imipramine on uptake and release of neurotransmitters in synaptosomesJournal of Pharmacy and Pharmacology, 1976
- Cardiovascular effects of amitriptyline, nortriptyline, protriptyline and doxepin in conscious rabbitsEuropean Journal of Pharmacology, 1974
- Interactions between Sympathomimetic Amines and Antidepressant Agents in ManBMJ, 1973
- Propranolol in the treatment of cardiacarrhythmias associated with amitriptyline intoxicationThe Journal of Pediatrics, 1973
- A specific gas-chromatographic method for the measurement of “steady-state” plasma levels of amitriptyline and nortriptyline in patientsClinica Chimica Acta; International Journal of Clinical Chemistry, 1971
- Correlation of Subjective Side Effects with Plasma Concentrations of NortriptylineBMJ, 1970
- Plasma protein binding of tricyclic anti-depressants in manBiochemical Pharmacology, 1969
- Cardiac Abnormalities in Poisoning with Tricyclic AntidepressantsBMJ, 1969
- CARDIAC COMPLICATIONS DURING TREATMENT WITH IMIPRAMIN (TOFRANIL)Acta Psychiatrica Scandinavica, 1961