J Korean Soc Biol Psychiatry.  1998 Jun;5(1):83-94.

Association of Schizophrenia with Pathological Aging : A Behavioral and Histological Study Using Animal Model

Abstract


OBJECTIVES
Phencyclidine(PCP) or PCP-like substances such as ketamine have been know to rekindle the cognitive dysfunction in schizophrenia. The aims of this study were to identify whether PCP-like substances can produce cognitive deficit in schizophrenia, to discuss relation with aging process, and finally to speculate underlying neurochemical mecha-nisms by various drug responses.
METHODS
In experiment I, radial maze tests were done in 24 Sprague-Dawley rats for 3 days to get baseline data. Being divided into 4 groups(6 rats respectively) of normal aged, normal adult controls, atropine-treated and ketamine-treated, the radial maze tests were repeated on every week for 6 weeks, and then the rats were sacrificed by intracardiac perfusion with phosphate-buffered 10% formaldehyde solution for histology. The brain specimen was stained with hematoxylin-eosin to count cells in the prefrontal cortex and hippocampus. In experiment II, radial maze tests were done for 48 rats before any drug treatment and only after ketamine administration. Thereafter, haloperidol, bromocriptine, clonidine, nimodipine, tacrine, valproic acid, naloxone and fluoxetine were intramuscularly injected on every other day in addition to ketamine. Radial maze tests were repeated on every week for 6 weeks, and then rats were prepared by the same procedure for histology.
RESULTS
1) Reaction times of radial maze tests of atropine-treated rats were significantly prolonged than those of normal aged(p<0.05) or normal adult controls(p<0.05). Cell numbers of prefrontal cortex & hippocampus in ketamine-treated rats were significantly reduced than those in normal aged(p<0.05) or normal adult controls(p<0.005). 2) Reduced cell numbers by ketamine became significantly raised by tacrine administration in prefrontal cortex $ hippocampus(p<0.05), while there were no significant changes on radial maze test. Cell numbers also tended to be raised by nimodipine, fluoxetine and haloperidol administration.
CONCLUSIONS
In conclusion, the visuospatial memory disorders in ketamine-induced psychotic rats might be partly associated with aging process. Furthermore, the responses to the various drugs suggested cholinergic system might have an important role in the neurochemical mechanism of the cognitive dysfunction in ketamine-induced psychosis. Otherwise, calcium metabolism as well as serotonergic and dopaminergic systems seemed to be possibly related.


MeSH Terms

Acetylcholine
Adult
Aging*
Animals*
Brain
Bromocriptine
Calcium
Cell Count
Clonidine
Fluoxetine
Formaldehyde
Haloperidol
Hippocampus
Humans
Ketamine
Memory Disorders
Metabolism
Models, Animal*
Naloxone
Nimodipine
Perfusion
Prefrontal Cortex
Psychotic Disorders
Rats
Rats, Sprague-Dawley
Reaction Time
Schizophrenia*
Tacrine
Valproic Acid
Acetylcholine
Bromocriptine
Calcium
Clonidine
Fluoxetine
Formaldehyde
Haloperidol
Ketamine
Naloxone
Nimodipine
Tacrine
Valproic Acid
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