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Environmental enrichment modulates affiliative and aggressive social behaviour in the neuroligin-3 R451C mouse model of autism spectrum disorder.

Abstract
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterised by impairments in social communication and the presence of restrictive and repetitive behaviours. A mouse model expressing an autism-associated R451C mutation in the gene encoding the synaptic adhesion protein neuroligin-3 (NL3) has been extensively characterised and shows altered behaviour relevant to core traits observed in ASD. Reported impairments in social behaviours in NL3R451C mice however remain controversial due to inconsistent findings in various assays across different laboratories. Such inconsistencies could plausibly be explained by an increased susceptibility of the NL3R451C mouse social phenotype to environmental modulation. To address this, NL3R451C mice were housed in standard or enriched housing from 4 weeks of age prior to behavioural testing. Enrichment rearing enhanced direct interactions with the stranger mouse in all mice in the three-chamber social interaction test however, NL3R451C mice did not show impairment in social interaction in the three-chamber test, in contrast with previous reports. Environmental enrichment enhanced aggressive behaviour in all mice, and did not specifically alter the heightened aggressive phenotype previously described in NL3R451C mice. Specific genotype effects of enrichment included reduced anxiety-like behaviour in WT mice, and lower locomotor activity levels in NL3 mice. While genotype-specific effects of enrichment were not seen on social behaviour, the general increase in affiliative social interaction and aggression seen in all mice, indicates that these behaviours, are vulnerable to change based on housing condition. Mouse models expressing ASD-associated mutations have great utility in elucidating the neurobiology underling development of core traits and it is crucial that efforts are focussed on those models exhibiting robust phenotypes. In light of the findings in the present study, we suggest approaches to improve replicability and reproducibility in mouse models of ASD.
AuthorsE L Burrows, L Koyama, C May, E L Hill-Yardin, A J Hannan
JournalPharmacology, biochemistry, and behavior (Pharmacol Biochem Behav) Vol. 195 Pg. 172955 (08 2020) ISSN: 1873-5177 [Electronic] United States
PMID32474162 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2020 Elsevier Inc. All rights reserved.
Chemical References
  • Cell Adhesion Molecules, Neuronal
  • Membrane Proteins
  • Nerve Tissue Proteins
  • neuroligin 3
Topics
  • Aggression (psychology)
  • Animals
  • Anxiety
  • Autism Spectrum Disorder (psychology)
  • Behavior, Animal
  • Body Weight
  • Cell Adhesion Molecules, Neuronal (genetics)
  • Disease Models, Animal
  • Female
  • Housing, Animal
  • Locomotion
  • Male
  • Maze Learning
  • Membrane Proteins (genetics)
  • Mice
  • Mice, Inbred C57BL
  • Mutation
  • Nerve Tissue Proteins (genetics)
  • Physical Conditioning, Animal (psychology)
  • Social Interaction

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