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Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity

BACKGROUND: Mutations of the SCN2A gene encoding a voltage-gated sodium channel alpha-II subunit Nav1.2 are associated with neurological disorders such as epilepsy, autism spectrum disorders, intellectual disability, and schizophrenia. However, causal relationships and pathogenic mechanisms underlyi...

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Autores principales: Tatsukawa, Tetsuya, Raveau, Matthieu, Ogiwara, Ikuo, Hattori, Satoko, Miyamoto, Hiroyuki, Mazaki, Emi, Itohara, Shigeyoshi, Miyakawa, Tsuyoshi, Montal, Mauricio, Yamakawa, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437867/
https://www.ncbi.nlm.nih.gov/pubmed/30962870
http://dx.doi.org/10.1186/s13229-019-0265-5
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author Tatsukawa, Tetsuya
Raveau, Matthieu
Ogiwara, Ikuo
Hattori, Satoko
Miyamoto, Hiroyuki
Mazaki, Emi
Itohara, Shigeyoshi
Miyakawa, Tsuyoshi
Montal, Mauricio
Yamakawa, Kazuhiro
author_facet Tatsukawa, Tetsuya
Raveau, Matthieu
Ogiwara, Ikuo
Hattori, Satoko
Miyamoto, Hiroyuki
Mazaki, Emi
Itohara, Shigeyoshi
Miyakawa, Tsuyoshi
Montal, Mauricio
Yamakawa, Kazuhiro
author_sort Tatsukawa, Tetsuya
collection PubMed
description BACKGROUND: Mutations of the SCN2A gene encoding a voltage-gated sodium channel alpha-II subunit Nav1.2 are associated with neurological disorders such as epilepsy, autism spectrum disorders, intellectual disability, and schizophrenia. However, causal relationships and pathogenic mechanisms underlying these neurological defects, especially social and psychiatric features, remain to be elucidated. METHODS: We investigated the behavior of mice with a conventional or conditional deletion of Scn2a in a comprehensive test battery including open field, elevated plus maze, light-dark box, three chambers, social dominance tube, resident-intruder, ultrasonic vocalization, and fear conditioning tests. We further monitored the effects of the positive allosteric modulator of AMPA receptors CX516 on these model mice. RESULTS: Conventional heterozygous Scn2a knockout mice (Scn2a(KO/+)) displayed novelty-induced exploratory hyperactivity and increased rearing. The increased vertical activity was reproduced by heterozygous inactivation of Scn2a in dorsal-telencephalic excitatory neurons but not in inhibitory neurons. Moreover, these phenotypes were rescued by treating Scn2a(KO/+) mice with CX516. Additionally, Scn2a(KO/+) mice displayed mild social behavior impairment, enhanced fear conditioning, and deficient fear extinction. Neuronal activity was intensified in the medial prefrontal cortex of Scn2a(KO/+) mice, with an increase in the gamma band. CONCLUSIONS: Scn2a(KO/+) mice exhibit a spectrum of phenotypes commonly observed in models of schizophrenia and autism spectrum disorder. Treatment with the CX516 ampakine, which ameliorates hyperactivity in these mice, could be a potential therapeutic strategy to rescue some of the disease phenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13229-019-0265-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-64378672019-04-08 Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity Tatsukawa, Tetsuya Raveau, Matthieu Ogiwara, Ikuo Hattori, Satoko Miyamoto, Hiroyuki Mazaki, Emi Itohara, Shigeyoshi Miyakawa, Tsuyoshi Montal, Mauricio Yamakawa, Kazuhiro Mol Autism Research BACKGROUND: Mutations of the SCN2A gene encoding a voltage-gated sodium channel alpha-II subunit Nav1.2 are associated with neurological disorders such as epilepsy, autism spectrum disorders, intellectual disability, and schizophrenia. However, causal relationships and pathogenic mechanisms underlying these neurological defects, especially social and psychiatric features, remain to be elucidated. METHODS: We investigated the behavior of mice with a conventional or conditional deletion of Scn2a in a comprehensive test battery including open field, elevated plus maze, light-dark box, three chambers, social dominance tube, resident-intruder, ultrasonic vocalization, and fear conditioning tests. We further monitored the effects of the positive allosteric modulator of AMPA receptors CX516 on these model mice. RESULTS: Conventional heterozygous Scn2a knockout mice (Scn2a(KO/+)) displayed novelty-induced exploratory hyperactivity and increased rearing. The increased vertical activity was reproduced by heterozygous inactivation of Scn2a in dorsal-telencephalic excitatory neurons but not in inhibitory neurons. Moreover, these phenotypes were rescued by treating Scn2a(KO/+) mice with CX516. Additionally, Scn2a(KO/+) mice displayed mild social behavior impairment, enhanced fear conditioning, and deficient fear extinction. Neuronal activity was intensified in the medial prefrontal cortex of Scn2a(KO/+) mice, with an increase in the gamma band. CONCLUSIONS: Scn2a(KO/+) mice exhibit a spectrum of phenotypes commonly observed in models of schizophrenia and autism spectrum disorder. Treatment with the CX516 ampakine, which ameliorates hyperactivity in these mice, could be a potential therapeutic strategy to rescue some of the disease phenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13229-019-0265-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-28 /pmc/articles/PMC6437867/ /pubmed/30962870 http://dx.doi.org/10.1186/s13229-019-0265-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Tatsukawa, Tetsuya
Raveau, Matthieu
Ogiwara, Ikuo
Hattori, Satoko
Miyamoto, Hiroyuki
Mazaki, Emi
Itohara, Shigeyoshi
Miyakawa, Tsuyoshi
Montal, Mauricio
Yamakawa, Kazuhiro
Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
title Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
title_full Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
title_fullStr Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
title_full_unstemmed Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
title_short Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
title_sort scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine cx516 rescues their hyperactivity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437867/
https://www.ncbi.nlm.nih.gov/pubmed/30962870
http://dx.doi.org/10.1186/s13229-019-0265-5
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