Evidence map›Paper›PMID 39302438›Full record

ArticlePsychopharmacology2025

Exploring the role of orexins in the modulation of social reward.

Inês M Amaral, Sara Ouaidat, Laura Scheffauer, Anna E Granza, Diogo G Monteiro, Ahmad Salti, Alex Hofer, Rana El Rawas

Abstract read
In one paragraph

Article in Psychopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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No citing paper in PubMed yet.

4 · The record

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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

8 authors.

Inês M Amaral *Division of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria.
Sara Ouaidat *Division of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria.
Laura Scheffauer *Division of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria.
Anna E GranzaDivision of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria.
Diogo G MonteiroDivision of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria.
Ahmad SaltiUniversity Clinic of Ophthalmology and Optometry, Kepler University Hospital, Johannes Kepler University Linz, Linz, 4020, Austria.
Alex HoferDivision of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria.
Rana El RawasDivision of Psychiatry I, Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology, Medical University Innsbruck, Innsbruck, 6020, Austria. rana.el-rawas@i-med.ac.at.

Funding

Medizinischer Forschungsfonds Tirol (MFF) [Project number: 329]
6 · The paper itself

Abstract

rationalepositive social interactions are essential for mental health, by offering emotional support, reducing stress levels, and promoting resilience against drugs of abuse effects. However, not all individuals perceive social interaction as rewarding.

objectivesthe goal of this study was to investigate whether the modulation of the orexin system can shift passive coping and non-social behavior (vulnerable) to active coping and social behavior (resilient). This knowledge is primordial for stress- and addiction-related disorders, and for other psychiatric disorders involving impairment in social interaction.

methodsmale C57/BL6N mice categorized into social and non-social groups, received injections of SB334867, a selective orexin 1 receptor (OX1R) antagonist, before the conditioning sessions with a male conspecific of the same weight and age.

resultsour results from the conditioned place preference test (CPP) show that SB334867 has no effect on social preference in non-social mice, but it reduces their stress levels and depression-like behavior. These effects appear to be due to a higher OX1R expression in the basolateral amygdala (BLA), a stress-related brain area, of non-social mice compared to their social counterparts.

conclusionsthese data suggest that the orexin system may be a target to alleviate stress and depression-like behavior in non-social individuals rather than to promote social reward.

Indexed as

OrexinsRewardSocial BehaviorSocial InteractionAdaptation, PsychologicalAnimalsBehavior, AnimalBenzoxazolesMaleMiceMice, Inbred C57BLNaphthyridinesOrexin Receptor AntagonistsOrexin ReceptorsUrea1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl ureaBenzoxazolesNaphthyridinesOrexin Receptor AntagonistsOrexin ReceptorsOrexinsUreaConditioned place preferenceDepressionOrexinOrexin 1 receptorRewardSB334867Social impairmentsSocial interactionSocial preferenceStress

Identifiers

PMID39302438
PMCPMC11775052

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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.