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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6437867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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