Evidence map›Paper›PMID 29852406›Full record

ArticlePsychoneuroendocrinology2018

Role of oxytocin in the ventral tegmental area in social reinforcement.

Johnathan M Borland, Kymberly N Grantham, Lauren M Aiani, Kyle J Frantz, H Elliott Albers

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
5.4field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 53 citations in OpenAlex.

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  4. 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
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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

5 authors at 1 institution in 1 country.

Johnathan M BorlandCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, 30302, USA.
Kymberly N GranthamCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, 30302, USA.
Lauren M AianiCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, 30302, USA.
Kyle J FrantzCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, 30302, USA.
H Elliott AlbersCenter for Behavioral Neuroscience, Neuroscience Institute, Georgia State University, Atlanta, GA, 30302, USA. Electronic address: biohea@gsu.edu.
Georgia State University · US

Funding

Sex Differences in the Social BrainR01MH110212 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, MICHOPOULOS, VASILIKI · 2016 to 2020
$3.3M
Sex differences in oxytocin modulation of social reward in the mesolimbic dopamine systemF31MH113367 · NIMH · GEORGIA STATE UNIVERSITY · PI BORLAND, JOHNATHAN · 2017 to 2018
$76k
NIMH NIH HHS F31 MH113367NIMH NIH HHS R01 MH110212
6 · The paper itself

Abstract

The rewarding properties of social interactions play a critical role in the development and maintenance of social relationships, and deficits in social reward are associated with various psychiatric disorders. In the present study, we used a novel Operant Social Preference (OSP) task to investigate the reinforcing properties of social interactions under conditions of high or low reward value, and high or low behavioral effort in male Syrian hamsters. Further, we investigated the role of oxytocin (OT) in a key structure of the mesolimbic reward system, the ventral tegmental area (VTA), in mediating the reinforcing properties of social interaction. Adult male hamsters were placed in a three-chambered apparatus, and allowed access to either a social chamber containing an unrestrained conspecific or a non-social chamber, by pushing through a one-way entry, vertical-swing door. Increasing the duration of social interaction (reward value) decreased the frequency of entering the social interaction chambers, whereas decreasing the duration of social interaction conversely increased the frequency of entries. Moreover, increasing behavioral effort required to access social interaction decreased the frequency of entries, especially under conditions when the duration of social interaction was only 5 s. OT injected into the VTA decreased the frequency of entering social interaction chambers in a manner similar to that observed when duration was increased, whereas injection of an OT receptor antagonist in the VTA increased the frequency of seeking social interaction. Taken together, these data support the hypothesis that activation of OT receptors in the VTA are critical for the reinforcing properties of social interactions. Furthermore, social interactions may exhibit duration and cost dependent reinforcing effects on behavior similar to those observed with food and drugs of abuse.

Indexed as

Reinforcement, SocialAnimalsConditioning, OperantCricetinaeMaleMesocricetusOxytocinReceptors, OxytocinReinforcement, PsychologyRewardVentral Tegmental AreaOxytocinReceptors, OxytocinDopamineMesolimbic dopamine systemNeuropeptidesOperantSocial behaviorSocial cognitionSocial interactionSocial motivationSocial rewardSocial salienceVasopressin

Identifiers

PMID29852406
PMCPMC6109598
OpenAlexW2804684418

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.