Evaluation of Pax6 mutant rat as a model for autism.
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,...
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2010-12-01
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doaj-c4efb8f90d4a459bbf897c6c747b41b92020-11-25T00:44:18ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-12-01512e1550010.1371/journal.pone.0015500Evaluation of Pax6 mutant rat as a model for autism.Toshiko UmedaNoriko TakashimaRyoko NakagawaMotoko MaekawaShiro IkegamiTakeo YoshikawaKazuto KobayashiKazuo OkanoyaKaoru InokuchiNoriko OsumiAutism 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.http://europepmc.org/articles/PMC3006426?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Toshiko Umeda Noriko Takashima Ryoko Nakagawa Motoko Maekawa Shiro Ikegami Takeo Yoshikawa Kazuto Kobayashi Kazuo Okanoya Kaoru Inokuchi Noriko Osumi |
spellingShingle |
Toshiko Umeda Noriko Takashima Ryoko Nakagawa Motoko Maekawa Shiro Ikegami Takeo Yoshikawa Kazuto Kobayashi Kazuo Okanoya Kaoru Inokuchi Noriko Osumi Evaluation of Pax6 mutant rat as a model for autism. PLoS ONE |
author_facet |
Toshiko Umeda Noriko Takashima Ryoko Nakagawa Motoko Maekawa Shiro Ikegami Takeo Yoshikawa Kazuto Kobayashi Kazuo Okanoya Kaoru Inokuchi Noriko Osumi |
author_sort |
Toshiko Umeda |
title |
Evaluation of Pax6 mutant rat as a model for autism. |
title_short |
Evaluation of Pax6 mutant rat as a model for autism. |
title_full |
Evaluation of Pax6 mutant rat as a model for autism. |
title_fullStr |
Evaluation of Pax6 mutant rat as a model for autism. |
title_full_unstemmed |
Evaluation of Pax6 mutant rat as a model for autism. |
title_sort |
evaluation of pax6 mutant rat as a model for autism. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2010-12-01 |
description |
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. |
url |
http://europepmc.org/articles/PMC3006426?pdf=render |
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