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Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring

The etiology of Autism Spectrum Disorders (ASD) includes a strong genetic component and a complicated environmental component. Recent evidence indicates that maternal diabetes, including gestational diabetes, is associated with an increased prevalence of ASD. While previous studies have looked into...

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Autores principales: Aviel-Shekler, Keren, Hamshawi, Yara, Sirhan, Worood, Getselter, Dmitriy, Srikanth, Kolluru D., Malka, Assaf, Piran, Ron, Elliott, Evan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688640/
https://www.ncbi.nlm.nih.gov/pubmed/33239620
http://dx.doi.org/10.1038/s41398-020-01096-7
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author Aviel-Shekler, Keren
Hamshawi, Yara
Sirhan, Worood
Getselter, Dmitriy
Srikanth, Kolluru D.
Malka, Assaf
Piran, Ron
Elliott, Evan
author_facet Aviel-Shekler, Keren
Hamshawi, Yara
Sirhan, Worood
Getselter, Dmitriy
Srikanth, Kolluru D.
Malka, Assaf
Piran, Ron
Elliott, Evan
author_sort Aviel-Shekler, Keren
collection PubMed
description The etiology of Autism Spectrum Disorders (ASD) includes a strong genetic component and a complicated environmental component. Recent evidence indicates that maternal diabetes, including gestational diabetes, is associated with an increased prevalence of ASD. While previous studies have looked into possible roles for maternal diabetes in neurodevelopment, there are few studies into how gestational diabetes, with no previous diabetic or metabolic phenotype, may affect neurodevelopment. In this study, we have specifically induced gestational diabetes in mice, followed by behavioral and molecular phenotyping of the mice offspring. Pregnant mice were injected with STZ a day after initiation of pregnancy. Glucose levels increased to diabetic levels between E7 and E14 in pregnancy in a subset of the pregnant animals. Male offspring of Gestational Diabetic mothers displayed increased repetitive behaviors with no dysregulation in the three-chambered social interaction test. RNA-seq analysis revealed a dysregulation in genes related to forebrain development in the frontal cortex and a dysregulation of a network of neurodevelopment and immune related genes in the striatum. Together, these results give evidence that gestational diabetes can induce changes in adulthood behavior and gene transcription in the brain.
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spelling pubmed-76886402020-12-03 Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring Aviel-Shekler, Keren Hamshawi, Yara Sirhan, Worood Getselter, Dmitriy Srikanth, Kolluru D. Malka, Assaf Piran, Ron Elliott, Evan Transl Psychiatry Article The etiology of Autism Spectrum Disorders (ASD) includes a strong genetic component and a complicated environmental component. Recent evidence indicates that maternal diabetes, including gestational diabetes, is associated with an increased prevalence of ASD. While previous studies have looked into possible roles for maternal diabetes in neurodevelopment, there are few studies into how gestational diabetes, with no previous diabetic or metabolic phenotype, may affect neurodevelopment. In this study, we have specifically induced gestational diabetes in mice, followed by behavioral and molecular phenotyping of the mice offspring. Pregnant mice were injected with STZ a day after initiation of pregnancy. Glucose levels increased to diabetic levels between E7 and E14 in pregnancy in a subset of the pregnant animals. Male offspring of Gestational Diabetic mothers displayed increased repetitive behaviors with no dysregulation in the three-chambered social interaction test. RNA-seq analysis revealed a dysregulation in genes related to forebrain development in the frontal cortex and a dysregulation of a network of neurodevelopment and immune related genes in the striatum. Together, these results give evidence that gestational diabetes can induce changes in adulthood behavior and gene transcription in the brain. Nature Publishing Group UK 2020-11-25 /pmc/articles/PMC7688640/ /pubmed/33239620 http://dx.doi.org/10.1038/s41398-020-01096-7 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
Aviel-Shekler, Keren
Hamshawi, Yara
Sirhan, Worood
Getselter, Dmitriy
Srikanth, Kolluru D.
Malka, Assaf
Piran, Ron
Elliott, Evan
Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
title Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
title_full Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
title_fullStr Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
title_full_unstemmed Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
title_short Gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
title_sort gestational diabetes induces behavioral and brain gene transcription dysregulation in adult offspring
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688640/
https://www.ncbi.nlm.nih.gov/pubmed/33239620
http://dx.doi.org/10.1038/s41398-020-01096-7
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