Evidence map›Paper›PMID 34035071›Full record

ArticleeNeuro

Intranasal Administration of Oxytocin Attenuates Social Recognition Deficits and Increases Prefrontal Cortex Inhibitory Postsynaptic Currents following Traumatic Brain Injury.

Avery Runyan, Dana Lengel, Jimmy W Huh, Jessica R Barson, Ramesh Raghupathi

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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.2field-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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Article
  5. Neuropeptidergic systems in psychiatric disorders.Frontiers in endocrinology · 2025
    Review
  6. Article
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  8. Article
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Oxytocin in Women's Health and Disease.Frontiers in endocrinology · 2022
    Review
  16. Review
  17. Review
  18. Review
  19. Review
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

5 authors at 2 institutions in 1 country.

Avery RunyanProgram in Neuroscience, Graduate School of Biomedical Science and Professional Studies, Drexel University College of Medicine, Philadelphia, PA 19129.
Dana LengelProgram in Neuroscience, Graduate School of Biomedical Science and Professional Studies, Drexel University College of Medicine, Philadelphia, PA 19129.
Jimmy W HuhDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Jessica R BarsonProgram in Neuroscience, Graduate School of Biomedical Science and Professional Studies, Drexel University College of Medicine, Philadelphia, PA 19129.ORCID 0000-0001-7227-5730
Ramesh RaghupathiProgram in Neuroscience, Graduate School of Biomedical Science and Professional Studies, Drexel University College of Medicine, Philadelphia, PA 19129 rr79@drexel.edu.
Drexel University · USChildren's Hospital of Philadelphia · US

Funding

Dopaminergic Mechanisms Underlying Behavioral Deficits Following Mild TBIR01NS110898 · NINDS · DREXEL UNIVERSITY · PI RAGHUPATHI, RAMESH · 2020 to 2024
$2.0M
Pathology-directed combination therapy for pediatric TBIR01HD061963 · NICHD · DREXEL UNIVERSITY · PI RAGHUPATHI, RAMESH · 2009 to 2013
$1.4M
NICHD NIH HHS R01 HD061963NINDS NIH HHS R01 NS110898
6 · The paper itself

Abstract

Pediatric traumatic brain injury (TBI) results in heightened risk for social deficits that can emerge during adolescence and adulthood. A moderate TBI in male and female rats on postnatal day 11 (equivalent to children below the age of 4) resulted in impairments in social novelty recognition, defined as the preference for interacting with a novel rat compared with a familiar rat, but not sociability, defined as the preference for interacting with a rat compared with an object in the three-chamber test when tested at four weeks (adolescence) and eight weeks (adulthood) postinjury. The deficits in social recognition were not accompanied by deficits in novel object recognition memory and were associated with a decrease in the frequency of spontaneous inhibitory postsynaptic currents (IPSCs) recorded from pyramidal neurons within Layer II/III of the medial prefrontal cortex (mPFC). Whereas TBI did not affect the expression of oxytocin (OXT) or the OXT receptor (OXTR) mRNAs in the hypothalamus and mPFC, respectively, intranasal administration of OXT before behavioral testing was found to reduce impairments in social novelty recognition and increase IPSC frequency in the mPFC in brain-injured animals. These results suggest that TBI-induced deficits in social behavior may be linked to increased excitability of neurons in the mPFC and suggests that the regulation of GABAergic neurotransmission in this region as a potential mechanism underlying these deficits.

Indexed as

Brain Injuries, TraumaticOxytocinAdministration, IntranasalAdultAnimalsChildFemaleHumansInhibitory Postsynaptic PotentialsMalePrefrontal CortexRatsSocial BehaviorOxytocinexcitabilityGABAergic neurotransmissionintranasal administrationoxytocinpediatric TBIsocial behavior

Identifiers

PMID34035071
PMCPMC8205495
OpenAlexW3165522776

What OpenQuestion holds

Textmetadata
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.