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Maternal immune activation affects socio-communicative behavior in adult rats

A wide body of evidence suggests a relationship between maternal immune activation (MIA) and neurodevelopmental disorders such as autism spectrum disorder (ASD). Since social and communicative deficits are included in the first diagnostic criterion of ASD, we aimed to characterize socio-communicativ...

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Autores principales: Gzieło, Kinga, Piotrowska, Diana, Litwa, Ewa, Popik, Piotr, Nikiforuk, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894913/
https://www.ncbi.nlm.nih.gov/pubmed/36732579
http://dx.doi.org/10.1038/s41598-023-28919-z
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author Gzieło, Kinga
Piotrowska, Diana
Litwa, Ewa
Popik, Piotr
Nikiforuk, Agnieszka
author_facet Gzieło, Kinga
Piotrowska, Diana
Litwa, Ewa
Popik, Piotr
Nikiforuk, Agnieszka
author_sort Gzieło, Kinga
collection PubMed
description A wide body of evidence suggests a relationship between maternal immune activation (MIA) and neurodevelopmental disorders such as autism spectrum disorder (ASD). Since social and communicative deficits are included in the first diagnostic criterion of ASD, we aimed to characterize socio-communicative behaviors in the MIA model based on prenatal exposure to poly(I:C). Our previous studies demonstrated impaired socio-communicative functioning in poly(I:C)-exposed adolescent rats. Therefore, the current study sought to clarify whether these changes would persist beyond adolescence. For this purpose, we analyzed behavior during the social interaction test and recorded ultrasonic vocalizations (USVs) accompanying interactions between adult poly(I:C) rats. The results demonstrated that the altered pattern of social behavior in poly(I:C) males was accompanied by the changes in acoustic parameters of emitted USVs. Poly(I:C) males also demonstrated an impaired olfactory preference for social stimuli. While poly(I:C) females did not differ from controls in socio-positive behaviors, they displayed aggression during the social encounter and were more reactive to somatosensory stimulation. Furthermore, the locomotor pattern of poly(I:C) animals were characterized by repetitive behaviors. Finally, poly(I:C) reduced parvalbumin and GAD67 expression in the cerebellum. The results showed that prenatal poly(I:C) exposure altered the pattern of socio-communicative behaviors of adult rats in a sex-specific manner.
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spelling pubmed-98949132023-02-04 Maternal immune activation affects socio-communicative behavior in adult rats Gzieło, Kinga Piotrowska, Diana Litwa, Ewa Popik, Piotr Nikiforuk, Agnieszka Sci Rep Article A wide body of evidence suggests a relationship between maternal immune activation (MIA) and neurodevelopmental disorders such as autism spectrum disorder (ASD). Since social and communicative deficits are included in the first diagnostic criterion of ASD, we aimed to characterize socio-communicative behaviors in the MIA model based on prenatal exposure to poly(I:C). Our previous studies demonstrated impaired socio-communicative functioning in poly(I:C)-exposed adolescent rats. Therefore, the current study sought to clarify whether these changes would persist beyond adolescence. For this purpose, we analyzed behavior during the social interaction test and recorded ultrasonic vocalizations (USVs) accompanying interactions between adult poly(I:C) rats. The results demonstrated that the altered pattern of social behavior in poly(I:C) males was accompanied by the changes in acoustic parameters of emitted USVs. Poly(I:C) males also demonstrated an impaired olfactory preference for social stimuli. While poly(I:C) females did not differ from controls in socio-positive behaviors, they displayed aggression during the social encounter and were more reactive to somatosensory stimulation. Furthermore, the locomotor pattern of poly(I:C) animals were characterized by repetitive behaviors. Finally, poly(I:C) reduced parvalbumin and GAD67 expression in the cerebellum. The results showed that prenatal poly(I:C) exposure altered the pattern of socio-communicative behaviors of adult rats in a sex-specific manner. Nature Publishing Group UK 2023-02-02 /pmc/articles/PMC9894913/ /pubmed/36732579 http://dx.doi.org/10.1038/s41598-023-28919-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gzieło, Kinga
Piotrowska, Diana
Litwa, Ewa
Popik, Piotr
Nikiforuk, Agnieszka
Maternal immune activation affects socio-communicative behavior in adult rats
title Maternal immune activation affects socio-communicative behavior in adult rats
title_full Maternal immune activation affects socio-communicative behavior in adult rats
title_fullStr Maternal immune activation affects socio-communicative behavior in adult rats
title_full_unstemmed Maternal immune activation affects socio-communicative behavior in adult rats
title_short Maternal immune activation affects socio-communicative behavior in adult rats
title_sort maternal immune activation affects socio-communicative behavior in adult rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9894913/
https://www.ncbi.nlm.nih.gov/pubmed/36732579
http://dx.doi.org/10.1038/s41598-023-28919-z
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