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Journal ArticleDOI

Autism-like behavioral phenotypes in BTBR T+tf/J mice

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TLDR
Robust and selective social deficits, repetitive self‐grooming, genetic stability and commercial availability of the BTBR inbred strain encourage its use as a research tool to search for background genes relevant to the etiology of autism, and to explore therapeutics to treat the core symptoms.
Abstract
Autism is a behaviorally defined neurodevelopmental disorder of unknown etiology. Mouse models with face validity to the core symptoms offer an experimental approach to test hypotheses about the causes of autism and translational tools to evaluate potential treatments. We discovered that the inbred mouse strain BTBR T+tf/J (BTBR) incorporates multiple behavioral phenotypes relevant to all three diagnostic symptoms of autism. BTBR displayed selectively reduced social approach, low reciprocal social interactions and impaired juvenile play, as compared with C57BL/6J (B6) controls. Impaired social transmission of food preference in BTBR suggests communication deficits. Repetitive behaviors appeared as high levels of self-grooming by juvenile and adult BTBR mice. Comprehensive analyses of procedural abilities confirmed that social recognition and olfactory abilities were normal in BTBR, with no evidence for high anxiety-like traits or motor impairments, supporting an interpretation of highly specific social deficits. Database comparisons between BTBR and B6 on 124 putative autism candidate genes showed several interesting single nucleotide polymorphisms (SNPs) in the BTBR genetic background, including a nonsynonymous coding region polymorphism in Kmo. The Kmo gene encodes kynurenine 3-hydroxylase, an enzyme-regulating metabolism of kynurenic acid, a glutamate antagonist with neuroprotective actions. Sequencing confirmed this coding SNP in Kmo, supporting further investigation into the contribution of this polymorphism to autism-like behavioral phenotypes. Robust and selective social deficits, repetitive self-grooming, genetic stability and commercial availability of the BTBR inbred strain encourage its use as a research tool to search for background genes relevant to the etiology of autism, and to explore therapeutics to treat the core symptoms.

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Citations
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Journal ArticleDOI

Behavioural phenotyping assays for mouse models of autism

TL;DR: Robust phenotypes in mouse models hold great promise as translational tools for discovering effective treatments for components of autism spectrum disorders.
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Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

TL;DR: In this paper, Shank3 gene deletions were found to lead to repetitive grooming and impaired social interaction in mice with autism spectrum disorders (ASDs) and other non-syndromic ASDs.
Journal ArticleDOI

Kynurenines in the mammalian brain: when physiology meets pathology

TL;DR: With recently developed pharmacological agents, it is now possible to restore metabolic equilibrium and envisage novel therapeutic interventions on the basis of the kynurenine pathway.
Journal ArticleDOI

Common circuit defect of excitatory-inhibitory balance in mouse models of autism

TL;DR: ASD mouse models may share a PV-circuit disruption, providing new insight into circuit development and potential prevention by treatment of autism, and a meta-analysis of PV expression in previously published ASD mouse models is performed.
References
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Journal Article

Autistic disturbances of affective contact

Leo Kanner
- 01 Jan 1943 - 
Journal Article

Autistic disturbances of affective contact.

Leo Kanner
Journal ArticleDOI

A comparison of the social postures of some common laboratory rodents.

TL;DR: A number of general concepts are discussed, for example the relation of convulsions to flight behaviour, the reduction of incoming aggressive stimuli in submissive postures, "Cut-Off", and the inhibition of biting in the more social species.
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