Evidence map›Paper›PMID 35140347›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2022

Opioid-blunted cortisol response to stress is associated with increased negative mood and wanting of social reward.

Claudia Massaccesi, Matthaeus Willeit, Boris B Quednow, Urs M Nater, Claus Lamm, Daniel Müller, Giorgia Silani

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.8field-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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Endocannabinoid contributions to the perception of socially relevant, affective touch in humans.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Endocannabinoids and related lipids linked to social exclusion in individuals with chronic non-medical prescription opioid use.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  9. TheFrontiers in psychology · 2024
    Article
  10. Observational
  11. Article
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

7 authors at 4 institutions in 2 countries.

Claudia MassaccesiDepartment of Clinical and Health Psychology, Faculty of Psychology, University of Vienna, Vienna, Austria. claudia.massaccesi@univie.ac.at.ORCID http://orcid.org/0000-0003-0519-6324
Matthaeus WilleitDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
Boris B QuednowExperimental and Clinical Pharmacopsychology, Department of Psychiatry, Psychotherapy and Psychosomatics, Psychiatric Hospital of the University of Zurich, Zurich, Switzerland.
Urs M NaterDepartment of Clinical and Health Psychology, Faculty of Psychology, University of Vienna, Vienna, Austria.
Claus LammDepartment of Cognition, Emotion, and Methods in Psychology, Faculty of Psychology, University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-5422-0653
Daniel MüllerInstitute for Clinical Chemistry, University Hospital Zurich, Zurich, Switzerland.
Giorgia SilaniDepartment of Clinical and Health Psychology, Faculty of Psychology, University of Vienna, Vienna, Austria. giorgia.silani@univie.ac.at.
University of Vienna · ATMedical University of Vienna · ATUniversity Hospital of Zurich · CHUniversity of Zurich · CH

Funding

Austrian Science Fund FWF W 1262EPA EP-C-15-003
6 · The paper itself

Abstract

Animal research suggests a central role of the μ-opioid receptor (MOR) system in regulating affiliative behaviors and in mediating the stress-buffering function of social contact. However, the neurochemistry of stress-related social contact seeking in humans is still poorly understood. In a randomized, double-blind, between-subjects design, healthy female volunteers (N = 80) received either 10 mg of the µ-opioid agonist morphine sulfate, or a placebo. Following a standardized psychosocial stress induction, participants engaged in a social reward task, in which the motivation to obtain skin-to-skin social touch and the hedonic reactions elicited by such touch were assessed. Morphine prevented the increase of salivary cortisol typically observed following acute stress exposure. Notably, this altered HPA axis responsivity was associated with increased negative affect in response to psychosocial stress, and with enhanced subjective wanting of highly rewarding social contact. These findings provide novel evidence on the effect of exogenous opioids administration on the reactions to psychosocial stress and point to a state-dependent regulation of social motivation.

Indexed as

Analgesics, OpioidHydrocortisoneAnimalsFemaleHumansHypothalamo-Hypophyseal SystemMorphinePituitary-Adrenal SystemRewardAnalgesics, OpioidHydrocortisoneMorphine

Identifiers

PMID35140347
PMCPMC9372154
OpenAlexW4210882950

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.