Evidence map›Paper›PMID 29875448›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

Involvement of dopamine, but not norepinephrine, in the sex-specific regulation of juvenile socially rewarding behavior by vasopressin.

Remco Bredewold, Nara F Nascimento, Grace S Ro, Shannon E Cieslewski, Christina J Reppucci, Alexa H Veenema

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

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  7. Vasopressin regulates social play behavior in sex-specific ways through glutamate modulation in the lateral septum.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
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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

6 authors at 2 institutions in 1 country.

Remco BredewoldDepartment of Psychology, Neurobiology of Social Behavior Laboratory, Michigan State University, East Lansing, MI, USA. bredewol@msu.edu.ORCID http://orcid.org/0000-0001-5715-5837
Nara F NascimentoDepartment of Psychology, Neurobiology of Social Behavior Laboratory, Boston College, Chestnut Hill, MA, USA.
Grace S RoDepartment of Psychology, Neurobiology of Social Behavior Laboratory, Boston College, Chestnut Hill, MA, USA.
Shannon E CieslewskiDepartment of Psychology, Neurobiology of Social Behavior Laboratory, Boston College, Chestnut Hill, MA, USA.
Christina J ReppucciDepartment of Psychology, Neurobiology of Social Behavior Laboratory, Michigan State University, East Lansing, MI, USA.ORCID http://orcid.org/0000-0002-7252-9996
Alexa H VeenemaDepartment of Psychology, Neurobiology of Social Behavior Laboratory, Michigan State University, East Lansing, MI, USA.
Boston College · USMichigan State University · US

Funding

Sex-specific regulation of social playR01MH102456 · NIMH · MICHIGAN STATE UNIVERSITY · PI VEENEMA, ALEXANDRA H. · 2014 to 2018
$1.7M
NIMH NIH HHS R01 MH102456
6 · The paper itself

Abstract

Social play is a highly rewarding behavior displayed mostly during the juvenile period. We recently showed that vasopressin V1a receptor (V1aR) blockade in the lateral septum (LS) enhances social play in male juvenile rats, but reduces it in females. Here, we determined whether the LS-AVP system modulates dopamine (DA) and/or norepinephrine (NE) neurotransmission in the LS to regulate social play behavior in sex-specific ways. Using microdialysis combined with retrodialysis, we demonstrated that both LS-AVP administration and social play exposure increased extracellular LS-DA release in females, but not in males. Pharmacological blockade of LS-DA receptors reduced social play in both sexes, but required a higher dose in females. This suggests that baseline LS-DA release is sufficient for social play in males, while increased LS-DA release is necessary for social play in females. Administration of a V1aR antagonist into the LS inhibited the social play-induced increase in extracellular LS-DA release in females. Furthermore, co-administration of the DA agonist apomorphine prevented the LS-V1aR blockade-induced decrease in social play in females. This suggests that LS-V1aR blockade reduces social play in females by dampening the rise in LS-DA release. Extracellular LS-NE release was enhanced in response to pharmacological manipulations of the LS-AVP system and to social play in males and/or females, but pharmacological blockade or stimulation of LS-NE receptors did not alter social play in either sex. Overall, we define a mechanism by which the LS-AVP system alters LS-DA neurotransmission differently in males than females resulting in the sex-specific regulation of juvenile social play behavior.

Indexed as

RewardSocial BehaviorAnimalsDopamineFemaleMaleMicrodialysisNorepinephrinePlay and PlaythingsRatsRats, WistarReceptors, VasopressinSeptum of BrainSex CharacteristicsVasopressinsDopamineNorepinephrineReceptors, VasopressinVasopressins

Identifiers

PMID29875448
PMCPMC6098123
OpenAlexW2804053821

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.