Evidence map›Paper›PMID 28655609›Full record

ArticleNeuropharmacology2017

Oxytocin in the medial prefrontal cortex attenuates anxiety: Anatomical and receptor specificity and mechanism of action.

Sara Sabihi, Shirley M Dong, Skyler D Maurer, Caitlin Post, Benedetta Leuner

Open access · greenAbstract read
In one paragraph

Article in Neuropharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Neuropeptidergic systems in psychiatric disorders.Frontiers in endocrinology · 2025
    Review
  8. Article
  9. Mechanisms of Social Attachment Between Children and Pet Dogs.Animals : an open access journal from MDPI · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Roles of Oxytocin in Stress Responses, Allostasis and Resilience.International journal of molecular sciences · 2021
    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 1 institution in 1 country.

Sara SabihiThe Ohio State University, Department of Psychology, Columbus, OH 43210, United States.
Shirley M DongThe Ohio State University, Department of Psychology, Columbus, OH 43210, United States.
Skyler D MaurerThe Ohio State University, Department of Psychology, Columbus, OH 43210, United States.
Caitlin PostThe Ohio State University, Department of Psychology, Columbus, OH 43210, United States.
Benedetta LeunerThe Ohio State University, Department of Psychology, Columbus, OH 43210, United States; The Ohio State University, Department of Neuroscience, Columbus, OH 43210, United States; The Ohio State University, Behavioral Neuroendocrinology Group, Columbus, OH 43210, United States. Electronic address: leuner.1@osu.edu.
The Ohio State University · US

Funding

Motherhood, Oxytocin and the Medial Prefrontal CortexR00MH084148 · NIMH · OHIO STATE UNIVERSITY · PI LEUNER, BENEDETTA J · 2011 to 2013
$720k
Gestational Stress and Oxytocin-Dopamine Interactions in New MothersR21HD083791 · NICHD · OHIO STATE UNIVERSITY · PI LEUNER, BENEDETTA J · 2015 to 2016
$403k
NICHD NIH HHS R21 HD083791NIMH NIH HHS R00 MH084148
6 · The paper itself

Abstract

Numerous studies in animals and humans have established that oxytocin (OT) reduces anxiety. In rats, the prelimbic (PL) subregion of the medial prefrontal cortex (mPFC) is among the brain areas implicated in the anxiolytic actions of OT. However, questions remain about the anatomical and receptor specificity of OT and its mechanism of action. Here we assessed whether the regulation of anxiety by mPFC OT is restricted to the PL subregion and evaluated whether oxytocin receptor (OTR) activation is required for OT to have an anxiolytic effect. We also examined whether OT interacts with GABA in the mPFC to reduce anxiety and investigated the extent to which OT in the mPFC affects activation of mPFC GABA neurons as well as neuronal activation in the amygdala, a primary target of the mPFC which is part of the neural network regulating anxiety. We found that OT reduced anxiety-like behavior when delivered to the PL, but not infralimbic or anterior cingulate subregions of the mPFC. The anxiolytic effect of OT in the PL mPFC was blocked by pretreatment with an OTR, but not a vasopressin receptor, antagonist as well as with a GABA

Indexed as

AnimalsAntidiuretic Hormone Receptor AntagonistsAnxietyGABA-A Receptor AntagonistsGABAergic NeuronsGyrus CinguliMaleMotor ActivityOxytocinPrefrontal CortexRats, Sprague-DawleyReceptors, GABA-AReceptors, OxytocinReceptors, VasopressinSynaptic TransmissionAntidiuretic Hormone Receptor AntagonistsGABA-A Receptor AntagonistsOxytocinReceptors, GABA-AReceptors, OxytocinReceptors, VasopressinAmygdalaAnxietyGABAMedial prefrontal cortexOxytocinPrelimbic

Identifiers

PMID28655609
PMCPMC5997257
OpenAlexW2635338433

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.