behavior/neurological
• mice show increased sensitivity to psychotomimetic drugs, MK801 and PCP
• antipsychotic drugs, haloperidol, clozapine, and risperidone, reduce locomotor activity to a greater extent than in wild-type mice, indicating increased sensitivity to antipsychotic drugs
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• cued fear memory is impaired, with increased freezing compared to wild-type mice
• pre-exposure to cue without shock does not reduce the cued fear memory as in wild-type mice
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• latent inhibition is impaired
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• in an object recognition test, mice do not show a greater preference for the new object as seen in wild-type mice indicating impaired object recognition memory
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• in the Morris water maze, mutants do not show a decline in the latency in finding the platform within the four trials as in wild-type mice, indicating impaired spatial working memory
• in the Y-maze, adult mice exhibit more total arm entries than wild-type mice, and less spontaneous alternation but more alternate arm returns, indicating impaired working memory
• young mice exhibit more total arm entries, less spontaneous alternation and more alternate arm returns in the Y-maze, indicating impaired working memory at an early age
• the GABAergic antagonist PTX improves working memory in mutants
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• mice spend more time in the proximity of two new objects than wild-type mice, indicating exaggerated responses to novel objects
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• adult and young (4-5 weeks of age) mice show higher locomotor activity in the open field test than wild-type mice
• adult mice show locomotor hyperactivity in both short-term and long-term habituation tests
• antipsychotic drugs, haloperidol, clozapine, and risperidone, reduce locomotor activity to a greater extent than in wild-type mice, indicating increased sensitivity to antipsychotic drugs
• the GABAergic antagonist PTX reduces locomotor activity in mutants
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• young mice show abnormal social behaviors, showing a larger number of scattered cotton particles in the cages than wild-type mice
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nervous system
N |
• mice show normal striatal dopamine levels
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• percent prepulse inhibition is lower than in wild-type mice, indicating impaired sensorimotor gating
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• the GABA antagonist PTX induces a tonic current in mutant prefrontal cortex unlike in wild-type mice in which PTX fails to induce any tonic current, and amplitudes of sIPSCs are smaller in mutants but the decay time is prolonged, indicating enhanced tonic GABA currents in prefrontal cortex
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• percent prepulse inhibition is lower than in wild-type mice
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
schizophrenia | DOID:5419 |
OMIM:181500 |
J:204368 |