Evidence map›Paper›PMID 30467338›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

Sex-dependent regulation of social reward by oxytocin receptors in the ventral tegmental area.

Johnathan M Borland, Lauren M Aiani, Alisa Norvelle, Kymberly N Grantham, Kylie O'Laughlin, Joseph I Terranova, Kyle J Frantz, H Elliott Albers

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
9.4field-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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Kinetics of oxytocin effects on amygdala and striatal reactivity vary between women and men.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Trial
  4. Article
  5. Article
  6. Dichotomous Regulation of Social Behaviors by Nucleus Accumbens Neurons in Female and Male Syrian Hamsters.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. PVN-NAc Shell-VP Circuit OT and OTR Neurons Regulate Pair Bonding via D2R and D1R.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  14. Review
  15. Stress drives a switch in sex preference.Science (New York, N.Y.) · 2025
    Article
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  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

8 authors at 1 institution in 1 country.

Johnathan M BorlandCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
Lauren M AianiCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
Alisa NorvelleCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
Kymberly N GranthamCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
Kylie O'LaughlinCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
Joseph I TerranovaCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
Kyle J FrantzCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA.
H Elliott AlbersCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, USA. biohea@gsu.edu.
Georgia State University · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Sex Differences in the Social BrainR01MH110212 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, MICHOPOULOS, VASILIKI · 2016 to 2020
$3.3M
Advances in the Study of Social NeuroendocrinologyR21MH109302 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, HUHMAN, KIM L · 2016 to 2017
$417k
Sex differences in oxytocin modulation of social reward in the mesolimbic dopamine systemF31MH113367 · NIMH · GEORGIA STATE UNIVERSITY · PI BORLAND, JOHNATHAN · 2017 to 2018
$76k
NIH HHS P51 OD011132NIMH NIH HHS R01 MH110212NIMH NIH HHS R21 MH109302U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) F31MH113367U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH110212
6 · The paper itself

Abstract

Social reward is critical for social relationships, and yet we know little about the characteristics of social interactions that are rewarding or the neural mechanisms underlying that reward. Here, we investigate the sex-dependent role of oxytocin receptors within the ventral tegmental area (VTA) in mediating the magnitude and valence of social reward. Operant and classical conditioning tests were used to measure social reward associated with same-sex social interactions. The effects of oxytocin, selective oxytocin receptor agonists, antagonists, and vehicle injected into the VTA on social reward was determined in male and female Syrian hamsters. The colocalization of FOS and oxytocin in sites that project to the VTA following social interaction was also determined. Females find same-sex social interactions more rewarding than males and activation of oxytocin receptors in the VTA is critical for social reward in females, as well as males. These studies provide support for the hypothesis that there is an inverted U relationship between the duration of social interaction and social reward, mediated by oxytocin; and that in females the dose-response relationship is initiated at lower doses compared with males. Same-sex social interaction is more rewarding in females than in males, and an inverted U relationship mediated by oxytocin may have a critical role in assigning positive and negative valence to social stimuli. Understanding these sex differences in social reward processing may be essential for understanding the sex differences in the prevalence of many psychiatric disorders and the development of gender-specific treatments of neuropsychiatric disorders.

Indexed as

RewardSex CharacteristicsSocial BehaviorAnimalsConditioning, ClassicalConditioning, OperantCricetinaeDose-Response Relationship, DrugFemaleInterpersonal RelationsMaleMicroinjectionsOxytocinReceptors, OxytocinVentral Tegmental AreaOxytocinReceptors, Oxytocin

Identifiers

PMID30467338
PMCPMC6372681
OpenAlexW2899947562

What OpenQuestion holds

Textmetadata
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.