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Oxytocin Receptors Regulate Social Preference in Zebrafish

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 orthologu...

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Autores principales: Landin, Jenny, Hovey, Daniel, Xu, Bo, Lagman, David, Zettergren, Anna, Larhammar, Dan, Kettunen, Petronella, Westberg, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096398/
https://www.ncbi.nlm.nih.gov/pubmed/32214126
http://dx.doi.org/10.1038/s41598-020-61073-4
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author Landin, Jenny
Hovey, Daniel
Xu, Bo
Lagman, David
Zettergren, Anna
Larhammar, Dan
Kettunen, Petronella
Westberg, Lars
author_facet Landin, Jenny
Hovey, Daniel
Xu, Bo
Lagman, David
Zettergren, Anna
Larhammar, Dan
Kettunen, Petronella
Westberg, Lars
author_sort Landin, Jenny
collection PubMed
description 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.
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spelling pubmed-70963982020-03-30 Oxytocin Receptors Regulate Social Preference in Zebrafish Landin, Jenny Hovey, Daniel Xu, Bo Lagman, David Zettergren, Anna Larhammar, Dan Kettunen, Petronella Westberg, Lars Sci Rep Article 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. Nature Publishing Group UK 2020-03-25 /pmc/articles/PMC7096398/ /pubmed/32214126 http://dx.doi.org/10.1038/s41598-020-61073-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Landin, Jenny
Hovey, Daniel
Xu, Bo
Lagman, David
Zettergren, Anna
Larhammar, Dan
Kettunen, Petronella
Westberg, Lars
Oxytocin Receptors Regulate Social Preference in Zebrafish
title Oxytocin Receptors Regulate Social Preference in Zebrafish
title_full Oxytocin Receptors Regulate Social Preference in Zebrafish
title_fullStr Oxytocin Receptors Regulate Social Preference in Zebrafish
title_full_unstemmed Oxytocin Receptors Regulate Social Preference in Zebrafish
title_short Oxytocin Receptors Regulate Social Preference in Zebrafish
title_sort oxytocin receptors regulate social preference in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096398/
https://www.ncbi.nlm.nih.gov/pubmed/32214126
http://dx.doi.org/10.1038/s41598-020-61073-4
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