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Hyperresponsiveness to phencyclidine in animals lesioned in the amygdala on day 7 of life. Implications for an animal model of schizophrenia.

E W P M Daenen, G Wolterink, J M Van Ree

European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology August 1, 2003 DOI: 10.1016/s0924-977x(03)00029-4 via PubMed

Summary

AI-generated from the abstract

Rats that received ibotenic acid lesions in the amygdala on day 7 of life, a proposed animal model of schizophrenia, showed a stronger behavioral response to phencyclidine (PCP) than sham-operated rats. PCP dose-dependently caused hyperactivity, stereotyped behavior, and social isolation in all rats, but the lesioned animals were hyperresponsive to the drug. This hyperresponsiveness supports the validity of the neonatal amygdala lesion model for studying schizophrenia-like symptoms.

Study at a glance

Characteristics Controlled laboratory experiment Peer reviewed
Population Rats with ibotenic acid lesions in the amygdala on day 7 of life and sham-operated rats
Intervention Phencyclidine (PCP)
Dose graded doses
Key finding Rats lesioned in the amygdala on day 7 of life were hyperresponsive to PCP compared to sham-operated animals.

Abstract

Phencyclidine (PCP) has been described to exacerbate psychotic symptoms in patients suffering from schizophrenia. In rats, PCP, dose-dependently, induces hyperactivity, stereotyped behaviour and social isolation, postulated to represent the positive (hyperactivity, stereotypy) and negative (social isolation) symptoms of schizophrenia. Based on previous studies, ibotenic acid lesions in the amygdala on day 7 of life have been proposed as an animal model of psychiatric neurodevelopmental disorders like schizophrenia. The purpose of the present study was to determine whether the responsiveness to PCP on locomotor activity in animals lesioned in the amygdala on day 7 of life is different from the response to this drug in sham-operated animals. The effect of graded doses of PCP on behaviour was assessed in a small open field. Animals lesioned in the amygdala on day 7 of life appeared to be hyperresponsive to PCP compared to sham-operated animals. The hyperresponsiveness to PCP in rats lesioned in the amygdala on day 7 of life further contributes to the validation of this putative animal model of schizophrenia.

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