Evidence map›Paper›PMID 32214126›Full record

ArticleScientific reports2020

Oxytocin Receptors Regulate Social Preference in Zebrafish.

Jenny Landin, Daniel Hovey, Bo Xu, David Lagman, Anna Zettergren, Dan Larhammar, Petronella Kettunen, Lars Westberg

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Social Preference Tests in Zebrafish: A Systematic Review.Frontiers in veterinary science · 2020
    Pooled it
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  7. Review
  8. Article
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  10. Article
  11. Article
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  15. Arginine Vasotocin Directly Regulates Spermatogenesis in Adult Zebrafish (International journal of molecular sciences · 2024
    Article
  16. Article
  17. Multiple faces of stress in the zebrafish (Frontiers in physiology · 2024
    Article
  18. Article
  19. 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

8 authors at 2 institutions in 1 country.

Jenny LandinDepartment of Pharmacology, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Daniel HoveyDepartment of Pharmacology, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Bo XuDepartment of Neuroscience, Unit of Pharmacology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
David LagmanDepartment of Neuroscience, Unit of Pharmacology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Anna ZettergrenDepartment of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.
Dan LarhammarDepartment of Neuroscience, Unit of Pharmacology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Petronella Kettunen *Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.ORCID http://orcid.org/0000-0002-2510-3423
Lars Westberg *Department of Pharmacology, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden. lars.westberg@pharm.gu.se.
University of Gothenburg · SEUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With a strong tendency to socialise, the zebrafish is a useful model to study social behaviour, with implications for better treatments of social impairments, for instance in autism spectrum disorders. Although oxytocin is crucial for social behaviour in mammals, the importance of the fish orthologue - isotocin or zebrafish oxytocin (zOT) - for social behaviour in zebrafish is unclear. The aims of this study were firstly, to elucidate the receptor specificity of zOT and the related vasotocin or zebrafish vasopressin (zVP; the orthologue of mammalian vasopressin) and the nonpeptidergic oxytocin receptor antagonist L-368,899, and secondly to investigate if L-368,899 inhibits social preference in zebrafish. The potencies of ligands were evaluated for zOT/zVP family receptors in HEK293 cells. Adult and larval zebrafish were treated with L-368,899 or vehicle and subsequently assessed for social behaviour and anxiety (adults only). The antagonist L-368,899 specifically inhibited the two zOT receptors, but not the two zVP-1 receptors. The antagonist decreased social preference in adult and larval zebrafish. It did not affect anxiety in adults. These results indicate that endogenous zOT, and possibly zVP, is involved in social behaviour in zebrafish via either or both of the two zOT receptors, and show promise for future explorations of the anatomy and evolution of networks underlying social behaviour.

Indexed as

Social BehaviorAnimalsCamphanesHEK293 CellsHumansModels, AnimalModels, PsychologicalOxytocinPiperazinesReceptors, OxytocinVasotocinZebrafishCamphanesL 368899OxytocinPiperazinesReceptors, OxytocinVasotocin

Identifiers

PMID32214126
PMCPMC7096398
OpenAlexW3013321543

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.