Application of a novel Active Allothetic Place Avoidance task (AAPA) in testing a pharmacological model of psychosis in rats: comparison with the Morris Water Maze
Language English Country Ireland Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
15276239
DOI
10.1016/j.neulet.2004.05.037
PII: S0304394004006123
Knihovny.cz E-resources
- MeSH
- Maze Learning drug effects MeSH
- Dizocilpine Maleate pharmacology MeSH
- Rats MeSH
- Disease Models, Animal MeSH
- Rats, Long-Evans MeSH
- Psychotic Disorders psychology MeSH
- Receptors, N-Methyl-D-Aspartate antagonists & inhibitors physiology MeSH
- Avoidance Learning drug effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Dizocilpine Maleate MeSH
- Receptors, N-Methyl-D-Aspartate MeSH
Administration of a non-competitive NMDA antagonist dizocilpine (MK-801) was proposed to be an animal model of psychosis. NMDA-receptor blockade is accompanied by increased locomotion, behavioral deficits, and other changes resembling psychotic symptoms. However, the role of NMDA-receptors in organizing brain representations is not understood yet. We tested the effect of NMDA-receptor blockade by systemic administration of dizocilpine at two different doses (0.1 or 0.2 mg/kg) in a recently designed Active Allothetic Place Avoidance (AAPA), a task which requires rats to separate spatial stimuli from two continuously dissociated subsets. The effect of dizocilpine on learning in the AAPA task was compared with its effect on acquisition of the reference memory version of the Morris Water Maze task. Both doses impaired performance in the Morris Water Maze task, whereas only the higher dose impaired performance in the AAPA task. The Morris Water Maze appears to be more sensitive to dizocilpine-induced behavioral deficit than the AAPA task. These findings support the notion that these two tasks are differentially dependent on the NMDA-receptor function.
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