Evidence map›Paper›PMID 24025838›Full record

ArticleNature2013

Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin.

Gül Dölen, Ayeh Darvishzadeh, Kee Wui Huang, Robert C Malenka

Open access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 643 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
643citing papers in PubMed, 1 pooled it
80.4field-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

643 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,192 citations in OpenAlex.

  1. Pooled it
  2. Oxytocin Amplifies Negative Response to Ambiguity in Adolescent Females With and Without Eating Disorders.European eating disorders review : the journal of the Eating Disorders Association · 2025
    Trial
  3. Trial
  4. Trial
  5. Nucleus accumbens neuron subtype translatome signatures in socially stressed females.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
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  11. Proximity in mice induced by an auditory-conditioned stimulus.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  12. Article
  13. Article
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  15. Article
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  19. Review
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583 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Gül DölenNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, 265 Campus Drive, Stanford, California 94305, USA.
Ayeh Darvishzadeh
Kee Wui Huang
Robert C Malenka
Stanford University · US

Funding

TRANSGENIC COREP01DA008227 · NIDA · YALE UNIVERSITY · PI NESTLER, ERIC J. · 1993 to 2018
$28.1M
VECTOR COREP30NS069375 · NINDS · STANFORD UNIVERSITY · PI STEINBERG, GARY K · 2011 to 2019
$6.3M
Cell type-specific role of Homer proteins in synaptic plasticityR21DA032955 · NIDA · STANFORD UNIVERSITY · PI MALENKA, ROBERT C · 2011 to 2012
$436k
NIDA NIH HHS P01 DA008227NIDA NIH HHS R21 DA032955NINDS NIH HHS NS069375NINDS NIH HHS P30 NS069375
6 · The paper itself

Abstract

Social behaviours in species as diverse as honey bees and humans promote group survival but often come at some cost to the individual. Although reinforcement of adaptive social interactions is ostensibly required for the evolutionary persistence of these behaviours, the neural mechanisms by which social reward is encoded by the brain are largely unknown. Here we demonstrate that in mice oxytocin acts as a social reinforcement signal within the nucleus accumbens core, where it elicits a presynaptically expressed long-term depression of excitatory synaptic transmission in medium spiny neurons. Although the nucleus accumbens receives oxytocin-receptor-containing inputs from several brain regions, genetic deletion of these receptors specifically from dorsal raphe nucleus, which provides serotonergic (5-hydroxytryptamine; 5-HT) innervation to the nucleus accumbens, abolishes the reinforcing properties of social interaction. Furthermore, oxytocin-induced synaptic plasticity requires activation of nucleus accumbens 5-HT1B receptors, the blockade of which prevents social reward. These results demonstrate that the rewarding properties of social interaction in mice require the coordinated activity of oxytocin and 5-HT in the nucleus accumbens, a mechanistic insight with implications for understanding the pathogenesis of social dysfunction in neuropsychiatric disorders such as autism.

Indexed as

RewardSocial BehaviorAnimalsAutistic DisorderConditioning, PsychologicalFemaleGene DeletionLong-Term Synaptic DepressionMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNeuronsNucleus AccumbensOxytocinOxytocinReceptor, Serotonin, 5-HT1BReceptors, OxytocinSerotonin

Identifiers

PMID24025838
PMCPMC4091761
OpenAlexW2099168883

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.