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Ketamine disrupted storage but not retrieval of information in male rats and apomorphine counteracted its impairing effect

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Auteur
Pitsikas N., Carli M.
Date
2020
Language
en
DOI
10.1016/j.neulet.2020.135321
Sujet
apomorphine
ketamine
n methyl dextro aspartic acid receptor
amino acid receptor blocking agent
apomorphine
dopamine receptor stimulating agent
ketamine
animal experiment
animal model
Article
cognition
cognitive defect
controlled study
information retrieval
locomotion
long term memory
low drug dose
male
memory consolidation
neuromodulation
nonhuman
novel object recognition test
passive avoidance test
post hoc analysis
priority journal
rat
animal
drug effect
memory
recall
Wistar rat
Animals
Apomorphine
Dopamine Agonists
Excitatory Amino Acid Antagonists
Ketamine
Male
Memory
Mental Recall
Rats
Rats, Wistar
Recognition, Psychology
Elsevier Ireland Ltd
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Résumé
Ketamine, a non-competitive NMDA receptor antagonist, has been reported to mimic the cognitive symptoms of schizophrenia in animals. It has been reported to produce learning and memory deficits in rodents. However, there have limited number of reports that investigated the specific components of memory process that are affected with ketamine. In the present study, we investigated the effects of ketamine [8 and 20 mg/kg, intraperitoneally, (i.p.)] on storage and retrieval of information in rats using an object recognition test. We examined also whether a low dose range of the D1/D2 dopamine receptor agonist apomorphine (0.05 and 0.1 mg/kg, i.p.) would counteract the effects of ketamine. The results show that ketamine dose-dependently impaired storage of information while it did not affect rats’ retrieval abilities. Administration of apomorphine reversed the ketamine-induced performance deficits in the ORT. The current findings show a differential modulation of post-training memory components (storage and retrieval of information) by ketamine and suggest a functional interaction between dopamine and NMDA receptors in the control of memory storage which may be of relevance to cognitive deficits a core feature of schizophrenia. © 2020 Elsevier B.V.
URI
http://hdl.handle.net/11615/78248
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