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Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure
Serotonergic dysregulation is implicated in numerous psychiatric disorders. Serotonin plays widespread trophic roles during neurodevelopment; thus perturbations to this system during development may increase risk for neurodevelopmental disorders. Epidemiological studies have examined association bet...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071194/ https://www.ncbi.nlm.nih.gov/pubmed/30073191 http://dx.doi.org/10.1523/ENEURO.0120-18.2018 |
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author | Maloney, Susan E. Akula, Shyam Rieger, Michael A. McCullough, Katherine B. Chandler, Krystal Corbett, Adrian M. McGowin, Audrey E. Dougherty, Joseph D. |
author_facet | Maloney, Susan E. Akula, Shyam Rieger, Michael A. McCullough, Katherine B. Chandler, Krystal Corbett, Adrian M. McGowin, Audrey E. Dougherty, Joseph D. |
author_sort | Maloney, Susan E. |
collection | PubMed |
description | Serotonergic dysregulation is implicated in numerous psychiatric disorders. Serotonin plays widespread trophic roles during neurodevelopment; thus perturbations to this system during development may increase risk for neurodevelopmental disorders. Epidemiological studies have examined association between selective serotonin reuptake inhibitor (SSRI) treatment during pregnancy and increased autism spectrum disorder (ASD) risk in offspring. It is unclear from these studies whether ASD susceptibility is purely related to maternal psychiatric diagnosis, or if treatment poses additional risk. We sought to determine whether maternal SSRI treatment alone or in combination with genetically vulnerable background was sufficient to induce offspring behavior disruptions relevant to ASD. We exposed C57BL/6J or Celf6 (+/-) mouse dams to fluoxetine (FLX) during different periods of gestation and lactation and characterized offspring on tasks assessing social communicative interaction and repetitive behavior patterns including sensory sensitivities. We demonstrate robust reductions in pup ultrasonic vocalizations (USVs) and alterations in social hierarchy behaviors, as well as perseverative behaviors and tactile hypersensitivity. Celf6 mutant mice demonstrate social communicative deficits and perseverative behaviors, without further interaction with FLX. FLX re-exposure in adulthood ameliorates the tactile hypersensitivity yet exacerbates the dominance phenotype. This suggests acute deficiencies in serotonin levels likely underlie the abnormal responses to sensory stimuli, while the social alterations are instead due to altered development of social circuits. These findings indicate maternal FLX treatment, independent of maternal stress, can induce behavioral disruptions in mammalian offspring, thus contributing to our understanding of the developmental role of the serotonin system and the possible risks to offspring of SSRI treatment during pregnancy. |
format | Online Article Text |
id | pubmed-6071194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-60711942018-08-02 Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure Maloney, Susan E. Akula, Shyam Rieger, Michael A. McCullough, Katherine B. Chandler, Krystal Corbett, Adrian M. McGowin, Audrey E. Dougherty, Joseph D. eNeuro New Research Serotonergic dysregulation is implicated in numerous psychiatric disorders. Serotonin plays widespread trophic roles during neurodevelopment; thus perturbations to this system during development may increase risk for neurodevelopmental disorders. Epidemiological studies have examined association between selective serotonin reuptake inhibitor (SSRI) treatment during pregnancy and increased autism spectrum disorder (ASD) risk in offspring. It is unclear from these studies whether ASD susceptibility is purely related to maternal psychiatric diagnosis, or if treatment poses additional risk. We sought to determine whether maternal SSRI treatment alone or in combination with genetically vulnerable background was sufficient to induce offspring behavior disruptions relevant to ASD. We exposed C57BL/6J or Celf6 (+/-) mouse dams to fluoxetine (FLX) during different periods of gestation and lactation and characterized offspring on tasks assessing social communicative interaction and repetitive behavior patterns including sensory sensitivities. We demonstrate robust reductions in pup ultrasonic vocalizations (USVs) and alterations in social hierarchy behaviors, as well as perseverative behaviors and tactile hypersensitivity. Celf6 mutant mice demonstrate social communicative deficits and perseverative behaviors, without further interaction with FLX. FLX re-exposure in adulthood ameliorates the tactile hypersensitivity yet exacerbates the dominance phenotype. This suggests acute deficiencies in serotonin levels likely underlie the abnormal responses to sensory stimuli, while the social alterations are instead due to altered development of social circuits. These findings indicate maternal FLX treatment, independent of maternal stress, can induce behavioral disruptions in mammalian offspring, thus contributing to our understanding of the developmental role of the serotonin system and the possible risks to offspring of SSRI treatment during pregnancy. Society for Neuroscience 2018-07-09 /pmc/articles/PMC6071194/ /pubmed/30073191 http://dx.doi.org/10.1523/ENEURO.0120-18.2018 Text en Copyright © 2018 Maloney et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Maloney, Susan E. Akula, Shyam Rieger, Michael A. McCullough, Katherine B. Chandler, Krystal Corbett, Adrian M. McGowin, Audrey E. Dougherty, Joseph D. Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure |
title | Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure |
title_full | Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure |
title_fullStr | Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure |
title_full_unstemmed | Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure |
title_short | Examining the Reversibility of Long-Term Behavioral Disruptions in Progeny of Maternal SSRI Exposure |
title_sort | examining the reversibility of long-term behavioral disruptions in progeny of maternal ssri exposure |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071194/ https://www.ncbi.nlm.nih.gov/pubmed/30073191 http://dx.doi.org/10.1523/ENEURO.0120-18.2018 |
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