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Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation

BACKGROUND: Recent literatures indicate that maternal hormone exposure is a risk factor for autism spectrum disorder (ASD). We hypothesize that prenatal progestin exposure may counteract the neuroprotective effect of estrogen and contribute to ASD development, and we aim to develop a method to ameli...

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Autores principales: Xie, Weiguo, Ge, Xiaohu, Li, Ling, Yao, Athena, Wang, Xiaoyan, Li, Min, Gong, Xiang, Chu, Zhigang, Lu, Zhe, Huang, Xiaodong, Jiao, Yun, Wang, Yifei, Xiao, Meifang, Chen, Haijia, Xiang, Wei, Yao, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090838/
https://www.ncbi.nlm.nih.gov/pubmed/30123446
http://dx.doi.org/10.1186/s13229-018-0225-5
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author Xie, Weiguo
Ge, Xiaohu
Li, Ling
Yao, Athena
Wang, Xiaoyan
Li, Min
Gong, Xiang
Chu, Zhigang
Lu, Zhe
Huang, Xiaodong
Jiao, Yun
Wang, Yifei
Xiao, Meifang
Chen, Haijia
Xiang, Wei
Yao, Paul
author_facet Xie, Weiguo
Ge, Xiaohu
Li, Ling
Yao, Athena
Wang, Xiaoyan
Li, Min
Gong, Xiang
Chu, Zhigang
Lu, Zhe
Huang, Xiaodong
Jiao, Yun
Wang, Yifei
Xiao, Meifang
Chen, Haijia
Xiang, Wei
Yao, Paul
author_sort Xie, Weiguo
collection PubMed
description BACKGROUND: Recent literatures indicate that maternal hormone exposure is a risk factor for autism spectrum disorder (ASD). We hypothesize that prenatal progestin exposure may counteract the neuroprotective effect of estrogen and contribute to ASD development, and we aim to develop a method to ameliorate prenatal progestin exposure-induced autism-like behavior. METHODS: Experiment 1: Prenatal progestin exposure-induced offspring are treated with resveratrol (RSV) through either prenatal or postnatal exposure and then used for autism-like behavior testing and other biomedical analyses. Experiment 2: Prenatal norethindrone (NET) exposure-induced offspring are treated with ERβ knockdown lentivirus together with RSV for further testing. Experiment 3: Pregnant dams are treated with prenatal NET exposure together with RSV, and the offspring are used for further testing. RESULTS: Eight kinds of clinically relevant progestins were used for prenatal exposure in pregnant dams, and the offspring showed decreased ERβ expression in the amygdala with autism-like behavior. Oral administration of either postnatal or prenatal RSV treatment significantly reversed this effect with ERβ activation and ameliorated autism-like behavior. Further investigation showed that RSV activates ERβ and its target genes by demethylation of DNA and histone on the ERβ promoter, and then minimizes progestin-induced oxidative stress as well as the dysfunction of mitochondria and lipid metabolism in the brain, subsequently ameliorating autism-like behavior. CONCLUSIONS: We conclude that resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation. Our data suggest that prenatal progestin exposure is a strong risk factor for autism-like behavior. Many potential clinical progestin applications, including oral contraceptive pills, preterm birth drugs, and progestin-contaminated drinking water or seafood, may be risk factors for ASD. In addition, RSV may be a good candidate for clinically rescuing or preventing ASD symptoms in humans, while high doses of resveratrol used in the animals may be a potential limitation for human application. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13229-018-0225-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-60908382018-08-17 Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation Xie, Weiguo Ge, Xiaohu Li, Ling Yao, Athena Wang, Xiaoyan Li, Min Gong, Xiang Chu, Zhigang Lu, Zhe Huang, Xiaodong Jiao, Yun Wang, Yifei Xiao, Meifang Chen, Haijia Xiang, Wei Yao, Paul Mol Autism Research BACKGROUND: Recent literatures indicate that maternal hormone exposure is a risk factor for autism spectrum disorder (ASD). We hypothesize that prenatal progestin exposure may counteract the neuroprotective effect of estrogen and contribute to ASD development, and we aim to develop a method to ameliorate prenatal progestin exposure-induced autism-like behavior. METHODS: Experiment 1: Prenatal progestin exposure-induced offspring are treated with resveratrol (RSV) through either prenatal or postnatal exposure and then used for autism-like behavior testing and other biomedical analyses. Experiment 2: Prenatal norethindrone (NET) exposure-induced offspring are treated with ERβ knockdown lentivirus together with RSV for further testing. Experiment 3: Pregnant dams are treated with prenatal NET exposure together with RSV, and the offspring are used for further testing. RESULTS: Eight kinds of clinically relevant progestins were used for prenatal exposure in pregnant dams, and the offspring showed decreased ERβ expression in the amygdala with autism-like behavior. Oral administration of either postnatal or prenatal RSV treatment significantly reversed this effect with ERβ activation and ameliorated autism-like behavior. Further investigation showed that RSV activates ERβ and its target genes by demethylation of DNA and histone on the ERβ promoter, and then minimizes progestin-induced oxidative stress as well as the dysfunction of mitochondria and lipid metabolism in the brain, subsequently ameliorating autism-like behavior. CONCLUSIONS: We conclude that resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation. Our data suggest that prenatal progestin exposure is a strong risk factor for autism-like behavior. Many potential clinical progestin applications, including oral contraceptive pills, preterm birth drugs, and progestin-contaminated drinking water or seafood, may be risk factors for ASD. In addition, RSV may be a good candidate for clinically rescuing or preventing ASD symptoms in humans, while high doses of resveratrol used in the animals may be a potential limitation for human application. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13229-018-0225-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-02 /pmc/articles/PMC6090838/ /pubmed/30123446 http://dx.doi.org/10.1186/s13229-018-0225-5 Text en © The Author(s). 2018 Open AccessThis article is 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 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Xie, Weiguo
Ge, Xiaohu
Li, Ling
Yao, Athena
Wang, Xiaoyan
Li, Min
Gong, Xiang
Chu, Zhigang
Lu, Zhe
Huang, Xiaodong
Jiao, Yun
Wang, Yifei
Xiao, Meifang
Chen, Haijia
Xiang, Wei
Yao, Paul
Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation
title Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation
title_full Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation
title_fullStr Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation
title_full_unstemmed Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation
title_short Resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through ERβ activation
title_sort resveratrol ameliorates prenatal progestin exposure-induced autism-like behavior through erβ activation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090838/
https://www.ncbi.nlm.nih.gov/pubmed/30123446
http://dx.doi.org/10.1186/s13229-018-0225-5
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