Visuospatial working memory is impaired in an animal model of schizophrenia induced by acute MK-801: an effect of pretraining
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23558085
DOI
10.1016/j.pbb.2013.03.014
PII: S0091-3057(13)00080-4
Knihovny.cz E-resources
- MeSH
- Excitatory Amino Acid Antagonists toxicity MeSH
- Dizocilpine Maleate toxicity MeSH
- Rats MeSH
- Disease Models, Animal * MeSH
- Rats, Long-Evans MeSH
- Schizophrenia chemically induced physiopathology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Excitatory Amino Acid Antagonists MeSH
- Dizocilpine Maleate MeSH
Deficient working memory was proposed as an endophenotype of schizophrenia. Such deficits are also commonly found in animal models of schizophrenia-like behavior of various origins. An allothetic place avoidance alternation task was proposed as a behavioral test of visuospatial working memory. This study tested the hypothesis that working memory in this test would be impaired by acute pre-test treatment with MK-801 (dizocilpine) in an animal model possessing high phenomenological and predictive validity. Furthermore, the study sought to determine the effect of pretraining to the task prior to treatment on the subsequent learning in the animal model. The results show that both doses of MK-801 (0.12 mg/kg and 0.15 mg/kg) significantly impaired working memory in the alternation paradigm, and both doses also increased locomotor activity. Notably, in previously pretrained animals, the significant effect of MK-801 on working memory was absent, despite persistent hyperlocomotion. These results showed that a deficit in working memory was detectable in this animal model of schizophrenia-like behavior, but its occurrence depended on the previous experience of animals with familiarization in the task.
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