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Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders

Mice emit ultrasonic vocalizations (USVs) in different social conditions: pups maternal separation, juveniles play, adults mating and social investigation. The USVs measurement has become an important instrument for behavioural phenotyping in neurodevelopmental disorders (NDDs). Recently, we have de...

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Autores principales: Premoli, Marika, Bonini, Sara Anna, Mastinu, Andrea, Maccarinelli, Giuseppina, Aria, Francesca, Paiardi, Giulia, Memo, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828716/
https://www.ncbi.nlm.nih.gov/pubmed/31685905
http://dx.doi.org/10.1038/s41598-019-52378-0
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author Premoli, Marika
Bonini, Sara Anna
Mastinu, Andrea
Maccarinelli, Giuseppina
Aria, Francesca
Paiardi, Giulia
Memo, Maurizio
author_facet Premoli, Marika
Bonini, Sara Anna
Mastinu, Andrea
Maccarinelli, Giuseppina
Aria, Francesca
Paiardi, Giulia
Memo, Maurizio
author_sort Premoli, Marika
collection PubMed
description Mice emit ultrasonic vocalizations (USVs) in different social conditions: pups maternal separation, juveniles play, adults mating and social investigation. The USVs measurement has become an important instrument for behavioural phenotyping in neurodevelopmental disorders (NDDs). Recently, we have demonstrated that the deletion of the NFκB1 gene, which encodes the p50 NF-κB subunit, causes NDDs phenotype in mice. In this study, we investigated the ultrasonic communication and the effects of an early social enrichment in mice lacking the NF-κB p50 subunit (p50 KO). In particular, USVs of wild-type (WT), p50 KO and KO exposed to early social enrichment (KO enriched) were recorded using an ultrasound sensitive microphone and analysed by Avisoft software. USVs analysis showed that p50 KO pups emit more and longer vocalizations compared to WT pups. On the contrary, in adulthood, p50 KO mice emit less USVs than WT mice. We also found significant qualitative differences in p50 KO mice USVs compared to WT mice; the changes specifically involved two USVs categories. Early social enrichment had no effect on USVs number, duration and type in p50 KO mice. Together, these data revealed social communication alterations in a mouse model of NDDs; these deficits were not recovered by early social enrichment, strengthening the fact that genetic background prevails on environmental enrichment.
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spelling pubmed-68287162019-11-12 Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders Premoli, Marika Bonini, Sara Anna Mastinu, Andrea Maccarinelli, Giuseppina Aria, Francesca Paiardi, Giulia Memo, Maurizio Sci Rep Article Mice emit ultrasonic vocalizations (USVs) in different social conditions: pups maternal separation, juveniles play, adults mating and social investigation. The USVs measurement has become an important instrument for behavioural phenotyping in neurodevelopmental disorders (NDDs). Recently, we have demonstrated that the deletion of the NFκB1 gene, which encodes the p50 NF-κB subunit, causes NDDs phenotype in mice. In this study, we investigated the ultrasonic communication and the effects of an early social enrichment in mice lacking the NF-κB p50 subunit (p50 KO). In particular, USVs of wild-type (WT), p50 KO and KO exposed to early social enrichment (KO enriched) were recorded using an ultrasound sensitive microphone and analysed by Avisoft software. USVs analysis showed that p50 KO pups emit more and longer vocalizations compared to WT pups. On the contrary, in adulthood, p50 KO mice emit less USVs than WT mice. We also found significant qualitative differences in p50 KO mice USVs compared to WT mice; the changes specifically involved two USVs categories. Early social enrichment had no effect on USVs number, duration and type in p50 KO mice. Together, these data revealed social communication alterations in a mouse model of NDDs; these deficits were not recovered by early social enrichment, strengthening the fact that genetic background prevails on environmental enrichment. Nature Publishing Group UK 2019-11-04 /pmc/articles/PMC6828716/ /pubmed/31685905 http://dx.doi.org/10.1038/s41598-019-52378-0 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
Premoli, Marika
Bonini, Sara Anna
Mastinu, Andrea
Maccarinelli, Giuseppina
Aria, Francesca
Paiardi, Giulia
Memo, Maurizio
Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
title Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
title_full Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
title_fullStr Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
title_full_unstemmed Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
title_short Specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
title_sort specific profile of ultrasonic communication in a mouse model of neurodevelopmental disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828716/
https://www.ncbi.nlm.nih.gov/pubmed/31685905
http://dx.doi.org/10.1038/s41598-019-52378-0
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