Piracetam counteracts the effects of amitriptyline on inhibitory avoidance in CD1 mice

• Published in: Behavioural brain research 2005-04, Vol.159 (2), p.235-242
• Main Authors: Everss, Estrella, Arenas, M. Carmen, Vinader-Caerols, Concepción, Monleón, Santiago, Parra, Andrés
• Format: Article
• Language: English
• Subjects: Amitriptyline; Amitriptyline - antagonists & inhibitors; Analysis of Variance; Animal ethology; Animals; Antidepressants; Antidepressive Agents, Tricyclic - antagonists & inhibitors; Avoidance Learning - drug effects; Biological and medical sciences; Drug Administration Schedule; Drug Interactions; Elevated plus-maze; Female; Fundamental and applied biological sciences. Psychology; Inhibitory avoidance; Male; Mammalia; Medical sciences; Memory - drug effects; Mice; Neuropharmacology; Nootropic Agents - pharmacology; Nootropics; Pharmacology. Drug treatments; Piracetam; Piracetam - pharmacology; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease); Psychology. Psychoanalysis. Psychiatry; Psychopharmacology; Reactive Inhibition; Sex differences; Sex Factors; Statistics, Nonparametric; Vertebrata
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2004.11.004

The purpose of the present work was to study the effects of amitriptyline on animal cognition in relation to some characteristics of its therapeutic effects. The modulation of acute and chronic effects of amitriptyline on inhibitory avoidance in male and female mice by piracetam was investigated. In Experiment 1, mice were subjected to the training phase of inhibitory avoidance conditioning 60 min after acute piracetam (100 mg/kg) or physiological saline administration. Immediately after the behavioural task, they received a single injection of the tricyclic antidepressant amitriptyline (30 mg/kg) or physiological saline. Twenty-four hours later, subjects were tested for avoidance. In Experiment 2, the same doses of amitriptyline and piracetam were chronically administered. Mice were subjected to the training phase of inhibitory avoidance on the 22nd day, and to the test phase 24 h later. Forty-five minutes after test, subjects explored the elevated plus-maze for 5 min in order to assess whether the effects of amitriptyline on avoidance performance may reflect general behavioural changes. Results obtained were that: (a) acute and chronic amitriptyline impaired inhibitory avoidance of male and female mice, (b) piracetam counteracted the effect of acutely administered amitriptyline on inhibitory avoidance, and (c) piracetam counteracted the effects of chronically administered amitriptyline in males but not females in the same learning task. These effects do not seem to be mediated by non-specific drug effects on spontaneous motor activity or anxiety.