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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Main Authors: Toshiko Umeda, Noriko Takashima, Ryoko Nakagawa, Motoko Maekawa, Shiro Ikegami, Takeo Yoshikawa, Kazuto Kobayashi, Kazuo Okanoya, Kaoru Inokuchi, Noriko Osumi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-12-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3006426?pdf=render
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spelling 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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