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The heterozygous reeler mouse: behavioural phenotype.
Jana Podhorna1, Michael Didriksen
1Department of Psychopharmacology, Psychosis, H. Lundbeck A/S, Ottiliavej 9, 2500 Copenhagen-Valby, Denmark. jpod@lundbeck.com
Behavioural Brain Research
|June 29, 2004
Summary
Heterozygous reeler mice (+/rl) were evaluated as a potential genetic model for schizophrenia. Comprehensive behavioral testing revealed no significant differences compared to wild-type littermates, suggesting they are not suitable for schizophrenia research.
Area of Science:
- Neuroscience
- Behavioral Genetics
- Psychiatric Research
Background:
- The heterozygous reeler mouse (+/rl) has been proposed as a potential genetic model for schizophrenia.
- Previous studies have yielded conflicting results regarding the suitability of +/rl mice for modeling schizophrenia.
Purpose of the Study:
- To investigate the behavioral phenotype of heterozygous reeler mice (+/rl) across different age groups.
- To determine if +/rl mice exhibit behavioral abnormalities relevant to schizophrenia compared to wild-type (+/+) littermates.
Main Methods:
- A comprehensive battery of behavioral tests was administered to young and adult male and female +/rl mice and their +/+ littermates.
- Tests included the Irwin test, rotarod, spontaneous locomotor activity, social behavior assays, light-dark transition, startle response, prepulse inhibition, and hot-plate test.
Main Results:
- Overall, +/rl mice did not exhibit significant behavioral differences from +/+ littermates across most tests and age groups.
- Adult male +/rl mice showed increased engagement in social investigation.
- Behavioral measures were influenced by sex and age, with younger females more active in the light-dark test and males more aggressive in social interactions; rotarod performance declined with age.
Conclusions:
- The heterozygous reeler mouse (+/rl) displays largely normal behavior across a wide range of tests.
- These findings contradict previous suggestions and indicate that +/rl mice may not be a suitable genetic model for schizophrenia research.