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Protective action of diazepam and of sympathomimetic amines against amitryptyline-induced toxicity.

Factors that contribute to the lethality of amitriptyline overdosage were studied in cats. Amitriptyline (50 mg/kg) given i.p. to unanesthetized cats produced convulsions in all of the animals and death in five of six animals; pretreatment with diazepam (5 mg/kg) protected against the convulsions and death. Respiratory depression contributed to the mortality when amitriptyline was given i.v. in cats anesthetized with pentobarbital as indicated by the finding that artificial respiration delayed the time of death induced by a continuous i.v. infusion of the drug. The i.v. infusion of amitriptyline in pentobarbitalized cats under artificial respiration produced death due to cardiovascular collapse. The latter was characterized by hypotension, bradycardia, depression of myocardial contractile force, atrioventricular block, intraventricular conduction delay and cardiac arrhythmias. These effects appear to be due to a direct membrane (quindine-like) cardiotoxic action of amitriptyline. Dopamine and dobutamine were effective in protecting the animals against the acute cardiovascular collapse induced by amitriptyline. The protection was associated with a diminution of the hypotension, the negative inotropic and chronotropic actions and the incidence of atrioventricular block produced by the tricyclic antidepressant drug. The results suggest that the positive chronotropic, inotropic and dromotropic actions of the amines may all be contributory factors in their protection action. Isoproterenol and norepinephrine were less effective than the other two amines.

Amitriptyline↗

[Calorigenic action of beta-sympathomimetics].

In experiments on narcotized rats it has been demonstrated that not only isoprenaline and orciprenaline but terbutaline, salbutamol and clenbuterol as well have calorigenic effects. The effectiveness is regressing considerably from isoprenaline over orciprenaline, salbutamol and terbutaline. Clenbuterol, too, has essentially weaker calorigenic effects than isoprenaline. The duration of calorigenic effects rise clearly from isoprenaline over orciprenaline, terbutaline, salbutamol and clenbuterol, while this effect is beginning more hesitatingly in the same order of these substances.

Albuterol↗