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Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats

It has been widely established that serotonin plays important role in the regulation of emotional and social behaviour. Rodents with a genetic deletion of the serotonin reuptake transporter (SERT) are used as a model to study lifelong consequences of increased extracellular 5‐HT levels due to its im...

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Autores principales: Golebiowska, Joanna, Hołuj, Małgorzata, Potasiewicz, Agnieszka, Piotrowska, Diana, Kuziak, Agata, Popik, Piotr, Homberg, Judith R., Nikiforuk, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937290/
https://www.ncbi.nlm.nih.gov/pubmed/31889084
http://dx.doi.org/10.1038/s41598-019-56629-y
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author Golebiowska, Joanna
Hołuj, Małgorzata
Potasiewicz, Agnieszka
Piotrowska, Diana
Kuziak, Agata
Popik, Piotr
Homberg, Judith R.
Nikiforuk, Agnieszka
author_facet Golebiowska, Joanna
Hołuj, Małgorzata
Potasiewicz, Agnieszka
Piotrowska, Diana
Kuziak, Agata
Popik, Piotr
Homberg, Judith R.
Nikiforuk, Agnieszka
author_sort Golebiowska, Joanna
collection PubMed
description It has been widely established that serotonin plays important role in the regulation of emotional and social behaviour. Rodents with a genetic deletion of the serotonin reuptake transporter (SERT) are used as a model to study lifelong consequences of increased extracellular 5‐HT levels due to its impaired reuptake. SERT knock-out (SERT-KO) mice and rats consistently showed anxiety-like symptoms and social deficits. Nevertheless, the impact of SERT deletion on socioemotional ultrasonic communication has not been addressed. Here we investigated the impact of lifelong serotonin abundance on ultrasonic vocalisation accompanying social interactions and open field exploration in rats. SERT-KO rats displayed reduced overall duration of social contacts, but increased time spent on following the conspecific. The altered pattern of social behaviour in SERT-KO rats was accompanied by the structural changes in ultrasonic vocalisations, as they differed from their controls in distribution of call categories. Moreover, SERT deletion resulted in anxiety-like behaviours assessed in the open field test. Their anxious phenotype resulted in a lower tendency to emit appetitive 50-kHz calls during novelty exploration. The present study demonstrates that genetic deletion of SERT not only leads to the deficits in social interaction and increased anxiety but also affects ultrasonic communication.
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spelling pubmed-69372902020-01-06 Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats Golebiowska, Joanna Hołuj, Małgorzata Potasiewicz, Agnieszka Piotrowska, Diana Kuziak, Agata Popik, Piotr Homberg, Judith R. Nikiforuk, Agnieszka Sci Rep Article It has been widely established that serotonin plays important role in the regulation of emotional and social behaviour. Rodents with a genetic deletion of the serotonin reuptake transporter (SERT) are used as a model to study lifelong consequences of increased extracellular 5‐HT levels due to its impaired reuptake. SERT knock-out (SERT-KO) mice and rats consistently showed anxiety-like symptoms and social deficits. Nevertheless, the impact of SERT deletion on socioemotional ultrasonic communication has not been addressed. Here we investigated the impact of lifelong serotonin abundance on ultrasonic vocalisation accompanying social interactions and open field exploration in rats. SERT-KO rats displayed reduced overall duration of social contacts, but increased time spent on following the conspecific. The altered pattern of social behaviour in SERT-KO rats was accompanied by the structural changes in ultrasonic vocalisations, as they differed from their controls in distribution of call categories. Moreover, SERT deletion resulted in anxiety-like behaviours assessed in the open field test. Their anxious phenotype resulted in a lower tendency to emit appetitive 50-kHz calls during novelty exploration. The present study demonstrates that genetic deletion of SERT not only leads to the deficits in social interaction and increased anxiety but also affects ultrasonic communication. Nature Publishing Group UK 2019-12-30 /pmc/articles/PMC6937290/ /pubmed/31889084 http://dx.doi.org/10.1038/s41598-019-56629-y Text en © The Author(s) 2019 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
Golebiowska, Joanna
Hołuj, Małgorzata
Potasiewicz, Agnieszka
Piotrowska, Diana
Kuziak, Agata
Popik, Piotr
Homberg, Judith R.
Nikiforuk, Agnieszka
Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
title Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
title_full Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
title_fullStr Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
title_full_unstemmed Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
title_short Serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
title_sort serotonin transporter deficiency alters socioemotional ultrasonic communication in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937290/
https://www.ncbi.nlm.nih.gov/pubmed/31889084
http://dx.doi.org/10.1038/s41598-019-56629-y
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