Evidence map›Paper›PMID 24211371›Full record

ArticleBehavioural brain research2014

Repetitive behavior profile and supersensitivity to amphetamine in the C58/J mouse model of autism.

Sheryl S Moy, Natallia V Riddick, Viktoriya D Nikolova, Brian L Teng, Kara L Agster, Randal J Nonneman, Nancy B Young, Lorinda K Baker, Jessica J Nadler, James W Bodfish

Open access · greenAbstract read
In one paragraph

Article in Behavioural brain research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 72 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Sheryl S MoyCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA. Electronic address: ssmoy@med.unc.edu.
Natallia V RiddickCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Viktoriya D NikolovaDepartment of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Brian L TengCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Chemical Biology and Medicinal Chemistry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Kara L AgsterCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Randal J NonnemanCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Nancy B YoungCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Lorinda K BakerCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Jessica J NadlerCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
James W BodfishCarolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA; Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
University of North Carolina at Chapel Hill · US

Funding

UNC MRDD Research CenterP30HD003110 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BELGER, AYSENIL · 1985 to 2012
$28.7M
TREATMENT PROJECTU54MH066418 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PIVEN, JOSEPH · 2002 to 2006
$7.9M
RESTRICTED REPETITIVE BEHAVIOR IN AUTISMR01MH073402 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BODFISH, JAMES WILLIAM, DICHTER, GABRIEL S · 2004 to 2015
$2.9M
Early Intervention in a mouse model of NMDA hypofunctionR01MH080069 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOY, SHERYL S · 2008 to 2012
$1.4M
Characterization of a Novel Mouse Model of Restricted Repetitive BehaviorsR21MH084132 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOY, SHERYL S · 2009 to 2010
$407k
NICHD NIH HHS P30 HD003110NICHD NIH HHS P30 HD03110NIMH NIH HHS MH080069NIMH NIH HHS MH084132NIMH NIH HHS MH73402NIMH NIH HHS R01 MH073402NIMH NIH HHS R01 MH080069NIMH NIH HHS R21 MH084132NIMH NIH HHS U54 MH066418NIMH NIH HHS U54 MH66418
6 · The paper itself

Abstract

Restricted repetitive behaviors are core symptoms of autism spectrum disorders (ASDs). The range of symptoms encompassed by the repetitive behavior domain includes lower-order stereotypy and self-injury, and higher-order indices of circumscribed interests and cognitive rigidity. Heterogeneity in clinical ASD profiles suggests that specific manifestations of repetitive behavior reflect differential neuropathology. The present studies utilized a set of phenotyping tasks to determine a repetitive behavior profile for the C58/J mouse strain, a model of ASD core symptoms. In an observational screen, C58/J demonstrated overt motor stereotypy, but not over-grooming, a commonly-used measure for mouse repetitive behavior. Amphetamine did not exacerbate motor stereotypy, but had enhanced stimulant effects on locomotion and rearing in C58/J, compared to C57BL/6J. Both C58/J and Grin1 knockdown mice, another model of ASD-like behavior, had marked deficits in marble-burying. In a nose poke task for higher-order repetitive behavior, C58/J had reduced holeboard exploration and preference for non-social, versus social, olfactory stimuli, but did not demonstrate cognitive rigidity following familiarization to an appetitive stimulus. Analysis of available high-density genotype data indicated specific regions of divergence between C58/J and two highly-sociable strains with common genetic lineage. Strain genome comparisons identified autism candidate genes, including Cntnap2 and Slc6a4, located within regions divergent in C58/J. However, Grin1, Nlgn1, Sapap3, and Slitrk5, genes linked to repetitive over-grooming, were not in regions of divergence. These studies suggest that specific repetitive phenotypes can be used to distinguish ASD mouse models, with implications for divergent underlying mechanisms for different repetitive behavior profiles.

Indexed as

AmphetamineAnimalsAutistic DisorderDisease Models, AnimalDizocilpine MaleateExcitatory Amino Acid AntagonistsExploratory BehaviorFemaleLocomotionMaleMiceMice, Inbred StrainsMice, KnockoutNerve Tissue ProteinsReceptors, N-Methyl-D-AspartateRecognition, PsychologyAmphetamineDizocilpine MaleateExcitatory Amino Acid AntagonistsGprin1 protein, mouseNerve Tissue ProteinsReceptors, N-Methyl-D-AspartateAutism spectrum disorderCircumscribed interestsHyperactivityNMDA receptorOlfactionSNP analysis

Identifiers

PMID24211371
PMCPMC3883138
OpenAlexW1978960933

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.