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Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy

OBJECTIVE: To determine the relationship between maternal bone resorption and bone development in fetuses. METHODS: Female SD rats were injected with either fluorescent calcium indicator calcein alone or together with tetracycline 1 week before pregnancy, followed by fluorescence detection in fetal...

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Autores principales: Jia, Huanhuan, Rao, Li, Miu, Kai Kei, Tang, Shuangjie, Chen, Wei, Yang, Guozhu, Li, Yuying, Li, Qingnan, Chen, Jun, Lu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042177/
https://www.ncbi.nlm.nih.gov/pubmed/32140467
http://dx.doi.org/10.3389/fcell.2020.00083
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author Jia, Huanhuan
Rao, Li
Miu, Kai Kei
Tang, Shuangjie
Chen, Wei
Yang, Guozhu
Li, Yuying
Li, Qingnan
Chen, Jun
Lu, Li
author_facet Jia, Huanhuan
Rao, Li
Miu, Kai Kei
Tang, Shuangjie
Chen, Wei
Yang, Guozhu
Li, Yuying
Li, Qingnan
Chen, Jun
Lu, Li
author_sort Jia, Huanhuan
collection PubMed
description OBJECTIVE: To determine the relationship between maternal bone resorption and bone development in fetuses. METHODS: Female SD rats were injected with either fluorescent calcium indicator calcein alone or together with tetracycline 1 week before pregnancy, followed by fluorescence detection in fetal tibias 21 days post-treatment. Alendronate was subsequently administered to pregnant rats to inhibit maternal bone resorption, while maternal bone turnover and fetal bone development were both examined. RESULTS: The maternal fluorescent labeled calcium before pregnancy was found in the fetal tibia. This indicated that the calcium of maternal bones may be released into the maternal circulation through high bone resorption during pregnancy, thereby participating in the fetal bone development. Bone histomorphometry and serum biomarker results showed that Alendronate significantly inhibited maternal bone resorption in pregnant rats when compared to normal pregnant rats. Moreover, the body weight, bone mass, and bone length of the fetuses in the Alendronate group were significantly decreased; while no apparent abnormality in placental morphology was observed. The above results implied that when maternal bone resorption is suppressed, the development of the fetal bone shall also be suppressed. CONCLUSION: Calcium in the maternal bone is released into the maternal circulation through bone resorption during pregnancy which represents an important material source in fetal bone development. Therefore, high bone turnover during pregnancy is essential for mammalian embryonic bone development.
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spelling pubmed-70421772020-03-05 Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy Jia, Huanhuan Rao, Li Miu, Kai Kei Tang, Shuangjie Chen, Wei Yang, Guozhu Li, Yuying Li, Qingnan Chen, Jun Lu, Li Front Cell Dev Biol Cell and Developmental Biology OBJECTIVE: To determine the relationship between maternal bone resorption and bone development in fetuses. METHODS: Female SD rats were injected with either fluorescent calcium indicator calcein alone or together with tetracycline 1 week before pregnancy, followed by fluorescence detection in fetal tibias 21 days post-treatment. Alendronate was subsequently administered to pregnant rats to inhibit maternal bone resorption, while maternal bone turnover and fetal bone development were both examined. RESULTS: The maternal fluorescent labeled calcium before pregnancy was found in the fetal tibia. This indicated that the calcium of maternal bones may be released into the maternal circulation through high bone resorption during pregnancy, thereby participating in the fetal bone development. Bone histomorphometry and serum biomarker results showed that Alendronate significantly inhibited maternal bone resorption in pregnant rats when compared to normal pregnant rats. Moreover, the body weight, bone mass, and bone length of the fetuses in the Alendronate group were significantly decreased; while no apparent abnormality in placental morphology was observed. The above results implied that when maternal bone resorption is suppressed, the development of the fetal bone shall also be suppressed. CONCLUSION: Calcium in the maternal bone is released into the maternal circulation through bone resorption during pregnancy which represents an important material source in fetal bone development. Therefore, high bone turnover during pregnancy is essential for mammalian embryonic bone development. Frontiers Media S.A. 2020-02-19 /pmc/articles/PMC7042177/ /pubmed/32140467 http://dx.doi.org/10.3389/fcell.2020.00083 Text en Copyright © 2020 Jia, Rao, Miu, Tang, Chen, Yang, Li, Li, Chen and Lu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Jia, Huanhuan
Rao, Li
Miu, Kai Kei
Tang, Shuangjie
Chen, Wei
Yang, Guozhu
Li, Yuying
Li, Qingnan
Chen, Jun
Lu, Li
Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy
title Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy
title_full Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy
title_fullStr Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy
title_full_unstemmed Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy
title_short Inhibited Maternal Bone Resorption Suppress Fetal Rat Bone Development During Pregnancy
title_sort inhibited maternal bone resorption suppress fetal rat bone development during pregnancy
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042177/
https://www.ncbi.nlm.nih.gov/pubmed/32140467
http://dx.doi.org/10.3389/fcell.2020.00083
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