Evidence map›Paper›PMID 27066536›Full record

ArticleeNeuro

Atypical Social Development in Vasopressin-Deficient Brattleboro Rats.

Matthew J Paul, Nicole V Peters, Mary K Holder, Anastasia M Kim, Jack Whylings, Joseph I Terranova, Geert J de Vries

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.1field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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  14. Neonatal CSF vasopressin concentration predicts later medical record diagnoses of autism spectrum disorder.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  18. Birth delivery mode alters perinatal cell death in the mouse brain.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

7 authors at 2 institutions in 1 country.

Matthew J PaulPsychology Department, University at Buffalo , SUNY, Buffalo, New York 14260.
Nicole V PetersNeuroscience Department, Georgia State University , Atlanta, Georgia 30302.
Mary K HolderNeuroscience Department, Georgia State University , Atlanta, Georgia 30302.
Anastasia M KimNeuroscience Department, Georgia State University , Atlanta, Georgia 30302.
Jack WhylingsNeuroscience Department, Georgia State University , Atlanta, Georgia 30302.
Joseph I TerranovaNeuroscience Department, Georgia State University , Atlanta, Georgia 30302.
Geert J de VriesNeuroscience Department, Georgia State University , Atlanta, Georgia 30302.
Georgia State University · USUniversity at Buffalo, State University of New York · US

Funding

The Neural Basis of Sexually Dimorphic Brain FunctionR01MH047538 · NIMH · UNIVERSITY OF MASSACHUSETTS AMHERST · PI DE VRIES, GEERT J. · 1991 to 2013
$3.2M
NIMH NIH HHS R01 MH047538NIMH NIH HHS R01-MH-047538
6 · The paper itself

Abstract

Over the past 3 decades, a large body of evidence has accumulated demonstrating that the neuropeptide arginine vasopressin (AVP) plays a critical role in regulating social behavior. The overwhelming majority of this evidence comes from adults, leaving a gap in our understanding of the role of AVP during development. Here, we investigated the effect of chronic AVP deficiency on a suite of juvenile social behaviors using Brattleboro rats, which lack AVP due to a mutation in the Avp gene. Social play behavior, huddling, social investigation & allogrooming, and ultrasonic vocalizations (USVs) of male and female rats homozygous for the Brattleboro mutation (Hom) were compared with their wild-type (WT) and heterozygous (Het) littermates during same-sex, same-genotype social interactions. Male and female Hom juveniles exhibited less social play than their Het and WT littermates throughout the rise, peak, and decline of the developmental profile of play. Hom juveniles also emitted fewer prosocial 50 kHz USVs, and spectrotemporal characteristics (call frequency and call duration) of individual call types differed from those of WT and Het juveniles. However, huddling behavior was increased in Hom juveniles, and social investigation and 22 kHz USVs did not differ across genotypes, demonstrating that not all social interactions were affected in the same manner. Collectively, these data suggest that the Avp gene plays a critical role in juvenile social development.

Indexed as

Social BehaviorAge FactorsAnalysis of VarianceAnimalsAnimals, NewbornFemaleGenotypeHeterozygoteHomozygoteMaleMutationRatsRats, BrattleboroRats, Long-EvansSex FactorsSocial Behavior DisordersVasopressinsplay behaviorpostnatal developmentsocial behaviorultrasonic vocalizationsvasopressin

Identifiers

PMID27066536
PMCPMC4822146
OpenAlexW2309764657

What OpenQuestion holds

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LicenceCC BY
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.