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A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice

BACKGROUND: Aggression is common in patients with autism spectrum disorders (ASD) along with the core symptoms of impairments in social communication and repetitive behavior. Risperidone, an atypical antipsychotic, is widely used to treat aggression in ASD. In order to understand the neurobiological...

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Autores principales: Burrows, Emma L., Laskaris, Liliana, Koyama, Lynn, Churilov, Leonid, Bornstein, Joel C., Hill-Yardin, Elisa L., Hannan, Anthony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650404/
https://www.ncbi.nlm.nih.gov/pubmed/26583067
http://dx.doi.org/10.1186/s13229-015-0055-7
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author Burrows, Emma L.
Laskaris, Liliana
Koyama, Lynn
Churilov, Leonid
Bornstein, Joel C.
Hill-Yardin, Elisa L.
Hannan, Anthony J.
author_facet Burrows, Emma L.
Laskaris, Liliana
Koyama, Lynn
Churilov, Leonid
Bornstein, Joel C.
Hill-Yardin, Elisa L.
Hannan, Anthony J.
author_sort Burrows, Emma L.
collection PubMed
description BACKGROUND: Aggression is common in patients with autism spectrum disorders (ASD) along with the core symptoms of impairments in social communication and repetitive behavior. Risperidone, an atypical antipsychotic, is widely used to treat aggression in ASD. In order to understand the neurobiological underpinnings of these challenging behaviors, a thorough characterisation of behavioral endophenotypes in animal models is required. METHODS: We investigated aggression in mice containing the ASD-associated R451C (arginine to cysteine residue 451 substitution) mutation in neuroligin-3 (NL3). Furthermore, we sought to verify social interaction impairments and assess olfaction, anxiety, and repetitive and restrictive behavior in NL3(R451C) mutant mice. RESULTS: We show a pronounced elevation in aggressive behavior in NL3(R451C) mutant mice. Treatment with risperidone reduced this aggression to wild-type (WT) levels. Juvenile and adult social interactions were also investigated, and subtle differences in initiation of interaction were seen in juvenile NL3(R451C) mice. No genotype differences in olfactory discrimination or anxiety were observed indicating that aggression was not dependent on altered olfaction, stress response, or social preference. We also describe repetitive behavior in NL3(R451C) mice as assessed by a clinically relevant object exploration task. CONCLUSIONS: The presence of aberrant aggression and other behavioral phenotypes in NL3(R451C) mice consistent with clinical traits strengthen face validity of this model of ASD. Furthermore, we demonstrate predictive validity in this model through the reversal of the aggressive phenotype with risperidone. This is the first demonstration that risperidone can ameliorate aggression in an animal model of ASD and will inform mechanistic and therapeutic research into the neurobiology underlying abnormal behaviors in ASD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13229-015-0055-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-46504042015-11-19 A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice Burrows, Emma L. Laskaris, Liliana Koyama, Lynn Churilov, Leonid Bornstein, Joel C. Hill-Yardin, Elisa L. Hannan, Anthony J. Mol Autism Research BACKGROUND: Aggression is common in patients with autism spectrum disorders (ASD) along with the core symptoms of impairments in social communication and repetitive behavior. Risperidone, an atypical antipsychotic, is widely used to treat aggression in ASD. In order to understand the neurobiological underpinnings of these challenging behaviors, a thorough characterisation of behavioral endophenotypes in animal models is required. METHODS: We investigated aggression in mice containing the ASD-associated R451C (arginine to cysteine residue 451 substitution) mutation in neuroligin-3 (NL3). Furthermore, we sought to verify social interaction impairments and assess olfaction, anxiety, and repetitive and restrictive behavior in NL3(R451C) mutant mice. RESULTS: We show a pronounced elevation in aggressive behavior in NL3(R451C) mutant mice. Treatment with risperidone reduced this aggression to wild-type (WT) levels. Juvenile and adult social interactions were also investigated, and subtle differences in initiation of interaction were seen in juvenile NL3(R451C) mice. No genotype differences in olfactory discrimination or anxiety were observed indicating that aggression was not dependent on altered olfaction, stress response, or social preference. We also describe repetitive behavior in NL3(R451C) mice as assessed by a clinically relevant object exploration task. CONCLUSIONS: The presence of aberrant aggression and other behavioral phenotypes in NL3(R451C) mice consistent with clinical traits strengthen face validity of this model of ASD. Furthermore, we demonstrate predictive validity in this model through the reversal of the aggressive phenotype with risperidone. This is the first demonstration that risperidone can ameliorate aggression in an animal model of ASD and will inform mechanistic and therapeutic research into the neurobiology underlying abnormal behaviors in ASD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13229-015-0055-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-14 /pmc/articles/PMC4650404/ /pubmed/26583067 http://dx.doi.org/10.1186/s13229-015-0055-7 Text en © Burrows et al. 2015 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
Burrows, Emma L.
Laskaris, Liliana
Koyama, Lynn
Churilov, Leonid
Bornstein, Joel C.
Hill-Yardin, Elisa L.
Hannan, Anthony J.
A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
title A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
title_full A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
title_fullStr A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
title_full_unstemmed A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
title_short A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
title_sort neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650404/
https://www.ncbi.nlm.nih.gov/pubmed/26583067
http://dx.doi.org/10.1186/s13229-015-0055-7
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