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Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice
Superovulation procedures and assisted reproductive technologies have been widely used to treat couples who have infertility problems. Although generally safe, the superovulation procedures are associated with a series of complications, such as ovarian hyper-stimulation syndrome, thromboembolism, an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990379/ https://www.ncbi.nlm.nih.gov/pubmed/29787998 http://dx.doi.org/10.18632/aging.101449 |
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author | Zhang, Jinjin Lai, Zhiwen Shi, Liangyan Tian, Yong Luo, Aiyue Xu, Zheyuan Ma, Xiangyi Wang, Shixuan |
author_facet | Zhang, Jinjin Lai, Zhiwen Shi, Liangyan Tian, Yong Luo, Aiyue Xu, Zheyuan Ma, Xiangyi Wang, Shixuan |
author_sort | Zhang, Jinjin |
collection | PubMed |
description | Superovulation procedures and assisted reproductive technologies have been widely used to treat couples who have infertility problems. Although generally safe, the superovulation procedures are associated with a series of complications, such as ovarian hyper-stimulation syndrome, thromboembolism, and adnexal torsion. The role of long-term repeated superovulation in ovarian aging and especially in associated disorders such as osteoporosis and cardiovascular diseases is still unclear. In this study, we sought to determine if repeated superovulation by ten cycles of treatment with pregnant mare serum gonadotropin/human chorionic gonadotropin could affect ovarian reserve, ovarian function, bone density and heart function. Ovarian reserve and function were reflected by the size of the primordial follicle pool, anti-Mullerian hormone expressions, hormone levels and fertility status. Furthermore, we examined bone density and heart function by microCT and cardiovascular ultrasonography, respectively. After repeated superovulation, the size of the primordial follicle pool and the expression of anti-mullerian hormone decreased, along with the concentrations of estrogen and progesterone. Mice exposed to repeated superovulation showed an obvious decrease in fertility and fecundity. Furthermore, both bone density and heart ejection fraction significantly decreased. These results suggest that repeated superovulation may increase the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging. |
format | Online Article Text |
id | pubmed-5990379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-59903792018-06-07 Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice Zhang, Jinjin Lai, Zhiwen Shi, Liangyan Tian, Yong Luo, Aiyue Xu, Zheyuan Ma, Xiangyi Wang, Shixuan Aging (Albany NY) Research Paper Superovulation procedures and assisted reproductive technologies have been widely used to treat couples who have infertility problems. Although generally safe, the superovulation procedures are associated with a series of complications, such as ovarian hyper-stimulation syndrome, thromboembolism, and adnexal torsion. The role of long-term repeated superovulation in ovarian aging and especially in associated disorders such as osteoporosis and cardiovascular diseases is still unclear. In this study, we sought to determine if repeated superovulation by ten cycles of treatment with pregnant mare serum gonadotropin/human chorionic gonadotropin could affect ovarian reserve, ovarian function, bone density and heart function. Ovarian reserve and function were reflected by the size of the primordial follicle pool, anti-Mullerian hormone expressions, hormone levels and fertility status. Furthermore, we examined bone density and heart function by microCT and cardiovascular ultrasonography, respectively. After repeated superovulation, the size of the primordial follicle pool and the expression of anti-mullerian hormone decreased, along with the concentrations of estrogen and progesterone. Mice exposed to repeated superovulation showed an obvious decrease in fertility and fecundity. Furthermore, both bone density and heart ejection fraction significantly decreased. These results suggest that repeated superovulation may increase the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging. Impact Journals 2018-05-22 /pmc/articles/PMC5990379/ /pubmed/29787998 http://dx.doi.org/10.18632/aging.101449 Text en Copyright © 2018 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Zhang, Jinjin Lai, Zhiwen Shi, Liangyan Tian, Yong Luo, Aiyue Xu, Zheyuan Ma, Xiangyi Wang, Shixuan Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
title | Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
title_full | Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
title_fullStr | Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
title_full_unstemmed | Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
title_short | Repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
title_sort | repeated superovulation increases the risk of osteoporosis and cardiovascular diseases by accelerating ovarian aging in mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990379/ https://www.ncbi.nlm.nih.gov/pubmed/29787998 http://dx.doi.org/10.18632/aging.101449 |
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