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The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model

This study aimed to examine the impact of BPA exposure on pregnancy and foetuses on cardiac tissues and the expression of cardiac microRNAs (miRNAs) related to heart development and diseases. Pregnancy is known to be the “critical windows” in determining the offspring physical and cells development...

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Autores principales: Rasdi, Zatilfarihiah, Kamaludin, Roziana, Ab. Rahim, Sharaniza, Syed Ahmad Fuad, Syed Baharom, Othman, Mohd Hafiz Dzarfan, Siran, Rosfaiizah, Mohd Nor, Noor Shafina, Abdul Hamid Hasani, Narimah, Sheikh Abdul Kadir, Siti Hamimah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125099/
https://www.ncbi.nlm.nih.gov/pubmed/32246001
http://dx.doi.org/10.1038/s41598-020-62420-1
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author Rasdi, Zatilfarihiah
Kamaludin, Roziana
Ab. Rahim, Sharaniza
Syed Ahmad Fuad, Syed Baharom
Othman, Mohd Hafiz Dzarfan
Siran, Rosfaiizah
Mohd Nor, Noor Shafina
Abdul Hamid Hasani, Narimah
Sheikh Abdul Kadir, Siti Hamimah
author_facet Rasdi, Zatilfarihiah
Kamaludin, Roziana
Ab. Rahim, Sharaniza
Syed Ahmad Fuad, Syed Baharom
Othman, Mohd Hafiz Dzarfan
Siran, Rosfaiizah
Mohd Nor, Noor Shafina
Abdul Hamid Hasani, Narimah
Sheikh Abdul Kadir, Siti Hamimah
author_sort Rasdi, Zatilfarihiah
collection PubMed
description This study aimed to examine the impact of BPA exposure on pregnancy and foetuses on cardiac tissues and the expression of cardiac microRNAs (miRNAs) related to heart development and diseases. Pregnancy is known to be the “critical windows” in determining the offspring physical and cells development in their life after birth. The increment of the risk of cardiovascular disease (CVD) in a later stage of life has been reported by few studies demonstrated from prenatal exposure of BPA. BPA has been shown to alter miRNAs expression profiles for organ development, regeneration and metabolic functions. These alterations have been associated with the risk of CVDs. However, the associations between pregnancy outcomes and miRNAs expression in cardiac of mother- and foetuses-exposed to BPA are still not entirely explored. In BPA-exposed pregnant rat groups, a significant weight gained was observed in comparison to control (p < 0.05). Interestingly, significant changes in systolic and diastolic blood pressure between the first and third trimester of BPA-exposed pregnant rats were also observed (p < 0.05). In BPA-exposed pregnant rats, miR-499-5p was significantly altered in the heart (p < 0.01). Meanwhile, altered miR-17-5p, -208-3p, and -210-3p expressions were observed in all heart of the foetuses from BPA-exposed pregnant rats (p < 0.05). In H&E staining, BPA-exposed foetal hearts showed a sign of fibrosis while BPA-exposed pregnant rats showed muscle remnant. Masson trichrome staining further confirmed the presence of fibrosis observed in BPA-exposed foetal heart and reduced expression of cardiac troponin I (cTnI) was also observed in BPA-exposed foetal heart. In summary, altered cardiac miRNAs with histological changes were observed in both mother- and foetus-exposed BPA These findings put forward the importance of future work to further understand how prenatal BPA exposure affect foetuses in their later stage of life.
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spelling pubmed-71250992020-04-08 The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model Rasdi, Zatilfarihiah Kamaludin, Roziana Ab. Rahim, Sharaniza Syed Ahmad Fuad, Syed Baharom Othman, Mohd Hafiz Dzarfan Siran, Rosfaiizah Mohd Nor, Noor Shafina Abdul Hamid Hasani, Narimah Sheikh Abdul Kadir, Siti Hamimah Sci Rep Article This study aimed to examine the impact of BPA exposure on pregnancy and foetuses on cardiac tissues and the expression of cardiac microRNAs (miRNAs) related to heart development and diseases. Pregnancy is known to be the “critical windows” in determining the offspring physical and cells development in their life after birth. The increment of the risk of cardiovascular disease (CVD) in a later stage of life has been reported by few studies demonstrated from prenatal exposure of BPA. BPA has been shown to alter miRNAs expression profiles for organ development, regeneration and metabolic functions. These alterations have been associated with the risk of CVDs. However, the associations between pregnancy outcomes and miRNAs expression in cardiac of mother- and foetuses-exposed to BPA are still not entirely explored. In BPA-exposed pregnant rat groups, a significant weight gained was observed in comparison to control (p < 0.05). Interestingly, significant changes in systolic and diastolic blood pressure between the first and third trimester of BPA-exposed pregnant rats were also observed (p < 0.05). In BPA-exposed pregnant rats, miR-499-5p was significantly altered in the heart (p < 0.01). Meanwhile, altered miR-17-5p, -208-3p, and -210-3p expressions were observed in all heart of the foetuses from BPA-exposed pregnant rats (p < 0.05). In H&E staining, BPA-exposed foetal hearts showed a sign of fibrosis while BPA-exposed pregnant rats showed muscle remnant. Masson trichrome staining further confirmed the presence of fibrosis observed in BPA-exposed foetal heart and reduced expression of cardiac troponin I (cTnI) was also observed in BPA-exposed foetal heart. In summary, altered cardiac miRNAs with histological changes were observed in both mother- and foetus-exposed BPA These findings put forward the importance of future work to further understand how prenatal BPA exposure affect foetuses in their later stage of life. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125099/ /pubmed/32246001 http://dx.doi.org/10.1038/s41598-020-62420-1 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
Rasdi, Zatilfarihiah
Kamaludin, Roziana
Ab. Rahim, Sharaniza
Syed Ahmad Fuad, Syed Baharom
Othman, Mohd Hafiz Dzarfan
Siran, Rosfaiizah
Mohd Nor, Noor Shafina
Abdul Hamid Hasani, Narimah
Sheikh Abdul Kadir, Siti Hamimah
The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model
title The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model
title_full The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model
title_fullStr The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model
title_full_unstemmed The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model
title_short The impacts of intrauterine Bisphenol A exposure on pregnancy and expression of miRNAs related to heart development and diseases in animal model
title_sort impacts of intrauterine bisphenol a exposure on pregnancy and expression of mirnas related to heart development and diseases in animal model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125099/
https://www.ncbi.nlm.nih.gov/pubmed/32246001
http://dx.doi.org/10.1038/s41598-020-62420-1
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