PLoS ONE · 2010 · 71 citations · 60 references
Life SciencesGeneticsNeuroscienceAutism Spectrum DisordersDevelopmental NeurobiologyDevelopmental NeuroscienceAutism Spectrum Disorder GeneticsBrain DevelopmentDevelopmental Behavioral NeurobiologyDevelopmental Behavioral NeuroscienceNeurodevelopmental DisordersNeurodevelopmental GeneticsAggression In Autism Spectrum DisorderAutism Spectrum Disorder ModelsMutationNeurodevelopmental Disorder MutationsNeurological PhenotypingPax6 Gene FunctionPrepulse InhibitionSensorimotor Gating
Autism is a highly variable brain developmental disorder and has a strong genetic basis. Pax6 is a pivotal player in brain development and maintenance. It is expressed in embryonic and adult neural stem cells, in astrocytes in the entire central nervous system, and in neurons in the olfactory bulb, amygdala, thalamus, and cerebellum, functioning in highly context-dependent manners. We have recently reported that Pax6 heterozygous mutant (rSey(2)/+) rats with a spontaneous mutation in the Pax6 gene, show impaired prepulse inhibition (PPI). In the present study, we further examined behaviors of rSey(2)/+ rats and revealed that they exhibited abnormality in social interaction (more aggression and withdrawal) in addition to impairment in rearing activity and in fear-conditioned memory. Ultrasonic vocalization (USV) in rSey(2)+ rat pups was normal in male but abnormal in female. Moreover, treatment with clozapine successfully recovered the defects in sensorimotor gating function, but not in fear-conditioned memory. Taken together with our prior human genetic data and results in other literatures, rSey(2)/+ rats likely have some phenotypic components of autism.
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Behavioural despair in rats: A new model sensitive to antidepressant treatments
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Life Sciences, Genetics, Psychiatry +14