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Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice

The normal intrauterine fluid environment is essential for embryo implantation. In hydrosalpinx patients, the implantation and pregnancy rates are markedly decreased after IVF–embryo transfer, while salpingectomy could significantly improve the pregnancy rates. The leakage of hydrosalpinx fluid into...

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Autores principales: Lu, Shan, Peng, Hongying, Zhang, He, Zhang, Li, Cao, Qichen, Li, Rong, Zhang, Ying, Yan, Liying, Duan, Enkui, Qiao, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806840/
https://www.ncbi.nlm.nih.gov/pubmed/24194934
http://dx.doi.org/10.1371/journal.pone.0078446
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author Lu, Shan
Peng, Hongying
Zhang, He
Zhang, Li
Cao, Qichen
Li, Rong
Zhang, Ying
Yan, Liying
Duan, Enkui
Qiao, Jie
author_facet Lu, Shan
Peng, Hongying
Zhang, He
Zhang, Li
Cao, Qichen
Li, Rong
Zhang, Ying
Yan, Liying
Duan, Enkui
Qiao, Jie
author_sort Lu, Shan
collection PubMed
description The normal intrauterine fluid environment is essential for embryo implantation. In hydrosalpinx patients, the implantation and pregnancy rates are markedly decreased after IVF–embryo transfer, while salpingectomy could significantly improve the pregnancy rates. The leakage of hydrosalpinx fluid into the endometrial cavity was supposed to be the major cause for impaired fertility. However, the underlying mechanisms of hydrosalpinx fluids on implantation and ongoing pregnancy were not fully understood and remain controversial regarding its toxicity. In present study, by infusing different volume of non-toxic fluid (0.9% saline) into uterine lumen before embryo implantation in mice (Day4 08:30), we found that while the embryos were not “flushed out” from the uteri, the timing of implantation was deferred and normal intrauterine distribution (embryo spacing) was disrupted. The abnormal implantation at early pregnancy further lead to embryo growth retardation, miscarriage and increased pregnancy loss, which is similar to the adverse effects observed in hydrosalpinx patients undergoing IVF-ET. We further examined uterine receptivity related gene expression reported to be involved in human hydrosalpinx (Lif, Hoxa10, Integrin α(v) and β(3)). The results showed that expression of integrin α(v) and β(3) were increased in the fluid infused mouse uteri, implicating a compensatory effect to cope with the excessive fluid environment. Our data suggested that the adverse effects of excessive non-toxic luminal fluid on pregnancy are primarily due to the mechanical interference for normal timing and location of embryo apposition, which might be the major cause of decreased implantation rate in IVF-ET patients with hydrosalpinx.
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spelling pubmed-38068402013-11-05 Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice Lu, Shan Peng, Hongying Zhang, He Zhang, Li Cao, Qichen Li, Rong Zhang, Ying Yan, Liying Duan, Enkui Qiao, Jie PLoS One Research Article The normal intrauterine fluid environment is essential for embryo implantation. In hydrosalpinx patients, the implantation and pregnancy rates are markedly decreased after IVF–embryo transfer, while salpingectomy could significantly improve the pregnancy rates. The leakage of hydrosalpinx fluid into the endometrial cavity was supposed to be the major cause for impaired fertility. However, the underlying mechanisms of hydrosalpinx fluids on implantation and ongoing pregnancy were not fully understood and remain controversial regarding its toxicity. In present study, by infusing different volume of non-toxic fluid (0.9% saline) into uterine lumen before embryo implantation in mice (Day4 08:30), we found that while the embryos were not “flushed out” from the uteri, the timing of implantation was deferred and normal intrauterine distribution (embryo spacing) was disrupted. The abnormal implantation at early pregnancy further lead to embryo growth retardation, miscarriage and increased pregnancy loss, which is similar to the adverse effects observed in hydrosalpinx patients undergoing IVF-ET. We further examined uterine receptivity related gene expression reported to be involved in human hydrosalpinx (Lif, Hoxa10, Integrin α(v) and β(3)). The results showed that expression of integrin α(v) and β(3) were increased in the fluid infused mouse uteri, implicating a compensatory effect to cope with the excessive fluid environment. Our data suggested that the adverse effects of excessive non-toxic luminal fluid on pregnancy are primarily due to the mechanical interference for normal timing and location of embryo apposition, which might be the major cause of decreased implantation rate in IVF-ET patients with hydrosalpinx. Public Library of Science 2013-10-23 /pmc/articles/PMC3806840/ /pubmed/24194934 http://dx.doi.org/10.1371/journal.pone.0078446 Text en © 2013 Lu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lu, Shan
Peng, Hongying
Zhang, He
Zhang, Li
Cao, Qichen
Li, Rong
Zhang, Ying
Yan, Liying
Duan, Enkui
Qiao, Jie
Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice
title Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice
title_full Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice
title_fullStr Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice
title_full_unstemmed Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice
title_short Excessive Intrauterine Fluid Cause Aberrant Implantation and Pregnancy Outcome in Mice
title_sort excessive intrauterine fluid cause aberrant implantation and pregnancy outcome in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806840/
https://www.ncbi.nlm.nih.gov/pubmed/24194934
http://dx.doi.org/10.1371/journal.pone.0078446
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