Evidence map›Paper›PMID 26911439›Full record

ArticleSocial neuroscience2017

Selective localization of oxytocin receptors and vasopressin 1a receptors in the human brainstem.

Sara M Freeman, Aaron L Smith, Mark M Goodman, Karen L Bales

Open access · greenAbstract readValidation Study
In one paragraph

Article in Social neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
13.2field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Oxytocin Reduces Alcohol Cue-Reactivity in Alcohol-Dependent Rats and Humans.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Trial
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Oxytocin and testosterone administration amplify viewing preferences for sexual images in male rhesus macaques.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  11. Complementary Role of Oxytocin and Vasopressin in Cardiovascular Regulation.International journal of molecular sciences · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
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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

4 authors at 2 institutions in 1 country.

Sara M Freemana California National Primate Research Center , University of California-Davis , Davis , CA , USA.
Aaron L Smithb Center for Translational Social Neuroscience, Yerkes National Primate Research Center , Emory University , Atlanta , GA , USA.
Mark M Goodmanc Department of Radiology and Imaging Sciences, Center for Systems Imaging , Emory University , Atlanta , GA , USA.
Karen L Balesd Department of Psychology , University of California-Davis , Davis , CA , USA.
Emory University · USUniversity of California, Davis · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
CHARACTERIZATION OF OXYTOCIN RECEPTORS IN AUTISM SPECTRUM DISORDERR21MH110014 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BALES, KAREN L. · 2015 to 2016
$417k
NIH HHS P51 OD011107NIMH NIH HHS R21 MH110014
6 · The paper itself

Abstract

Intranasal oxytocin (OT) affects a suite of human social behaviors, including trust, eye contact, and emotion recognition. However, it is unclear where oxytocin receptors (OXTR) and the structurally related vasopressin 1a receptors (AVPR1a) are expressed in the human brain. We have previously described a reliable, pharmacologically informed receptor autoradiography protocol for visualizing these receptors in postmortem primate brain tissue. We used this technique in human brainstem tissue to identify the neural targets of OT and vasopressin. To determine binding selectivity of the OXTR radioligand and AVPR1a radioligand, sections were incubated in four conditions: radioligand alone, radioligand with the selective AVPR1a competitor SR49059, and radioligand with a low or high concentration of the selective OXTR competitor ALS-II-69. We found selective OXTR binding in the spinal trigeminal nucleus, a conserved region of OXTR expression in all primate species investigated to date. We found selective AVPR1a binding in the nucleus prepositus, an area implicated in eye gaze stabilization. The tissue's postmortem interval (PMI) was not correlated with either the specific or nonspecific binding of either radioligand, indicating that it will not likely be a factor in similar postmortem studies. This study provides critical data for future studies of OXTR and AVPR1a in human brain tissue.

Indexed as

AcetylcholinesteraseAdolescentAdultAutoradiographyBrain StemHumansMaleMiddle AgedReceptors, OxytocinReceptors, VasopressinYoung AdultAcetylcholinesteraseAVPR1A protein, humanOXTR protein, humanReceptors, OxytocinReceptors, VasopressinBrainstemneuropeptidesnucleus prepositusreceptor autoradiographyspinal trigeminal nucleus

Identifiers

PMID26911439
PMCPMC5474119
OpenAlexW2290898970

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.