Evidence map›Paper›PMID 26771946›Full record

Trial reportPsychoneuroendocrinology2016

Oxytocin modulates behavioral and physiological responses to a stressor in marmoset monkeys.

Jon Cavanaugh, Sarah B Carp, Chelsea M Rock, Jeffrey A French

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Psychoneuroendocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
8.5field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  11. Intrahypothalamic effects of oxytocin on PVN CRH neurons in response to acute stress.Current opinion in endocrine and metabolic research · 2022
    Article
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  16. Roles of Oxytocin in Stress Responses, Allostasis and Resilience.International journal of molecular sciences · 2021
    Review
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  18. Review
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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 1 institution in 1 country.

Jon CavanaughCallitrichid Research Center, Department of Psychology, University of Nebraska at Omaha, United States. Electronic address: jonryancavanaug@unomaha.edu.
Sarah B CarpCallitrichid Research Center, Department of Psychology, University of Nebraska at Omaha, United States.
Chelsea M RockCallitrichid Research Center, Department of Psychology, University of Nebraska at Omaha, United States.
Jeffrey A FrenchCallitrichid Research Center, Department of Psychology, University of Nebraska at Omaha, United States; Department of Biology, University of Nebraska at Omaha, United States.
University of Nebraska at Omaha · US

Funding

Parenting, Sibling-Support, and Infant DevelopmentR01HD042882 · NICHD · UNIVERSITY OF NEBRASKA OMAHA · PI FRENCH, JEFFREY A · 2002 to 2014
$1.7M
Parenting, Sibling-Support, and Infant DevelopmentR56HD042882 · NICHD · UNIVERSITY OF NEBRASKA OMAHA · PI FRENCH, JEFFREY A · 2008 to 2008
$175k
NICHD NIH HHS HD 042882NICHD NIH HHS R01 HD042882NICHD NIH HHS R56 HD042882
6 · The paper itself

Abstract

Social isolation is a major source of stress and can lead to activation of the hypothalamic-pituitary-adrenal (HPA) axis. The presence of a close social partner can reduce the magnitude of the HPA-axis response during a stressor, a phenomenon known as social buffering. The oxytocin (OXT) system has been identified as one candidate for mediating social buffering due to its role in the facilitation of social bonding and the expression of prosocial behavior. The goal of the present study was to determine whether the OXT system contributes to social buffering of HPA-axis activity in response to stressor exposure in marmoset monkeys (Callithrix jacchus). Male and female marmosets experienced a standardized psychogenic stressor with and without their long-term mate under OXT-treatments (Pro(8)-OXT, Leu(8)-OXT, OXT antagonist, and saline); we assessed HPA-axis activity by measuring urinary cortisol across the stressor. We found that blocking, but not augmenting, the OXT system altered patterns of cortisol and proximity behavior in response to a stressor. We demonstrated that (1) the presence of a mate during a stressor significantly attenuated HPA-axis activity in female, but not male, marmosets; (2) male, but not female, marmosets treated with an OXT antagonist had significantly higher HPA-axis activity across the stressor than when they were treated with saline, suggesting that the OXT system may reduce the stressor-induced rise in cortisol levels; (3) male and female marmosets treated with an OXT antagonist spent significantly less time in close proximity to their mate during the first 30 min of the stressor than when they were treated with saline, suggesting that the OXT system may be important for the expression of partner-seeking behavior during a stressor. Thus, the OXT system and social context differentially influenced how the HPA-axis responded to a stressor in male and female marmosets, and may modulate HPA-axis activity by promoting the expression of proximity behavior with a close social partner.

Indexed as

Adaptation, PhysiologicalAnimalsBehavior, AnimalCallithrixFemaleHormone AntagonistsHydrocortisoneHypothalamo-Hypophyseal SystemMaleOxytocinPituitary-Adrenal SystemSocial BehaviorSocial IsolationStress, PsychologicalHormone AntagonistsHydrocortisoneOxytocinCortisolHPA-axisPro(8)-OXTProximitySocial bufferingStress

Identifiers

PMID26771946
PMCPMC6007987
OpenAlexW2204722956

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.