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Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study

BACKGROUND: Benzo(a)pyrene (BaP) as an environmental pollutant is ubiquitous in the environment and it has destructive effects on human health. So far, various studies have demonstrated that BaP can cause adverse effects on the female reproductive system, but the existing information is limited abou...

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Autores principales: Mardanshahi, Zeinab, Karimpour Malekshah, Abbasali, Talebpour Amiri, Fereshteh, Valadan, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Knowledge E 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600280/
https://www.ncbi.nlm.nih.gov/pubmed/31417980
http://dx.doi.org/10.18502/ijrm.v16i12.3680
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author Mardanshahi, Zeinab
Karimpour Malekshah, Abbasali
Talebpour Amiri, Fereshteh
Valadan, Reza
author_facet Mardanshahi, Zeinab
Karimpour Malekshah, Abbasali
Talebpour Amiri, Fereshteh
Valadan, Reza
author_sort Mardanshahi, Zeinab
collection PubMed
description BACKGROUND: Benzo(a)pyrene (BaP) as an environmental pollutant is ubiquitous in the environment and it has destructive effects on human health. So far, various studies have demonstrated that BaP can cause adverse effects on the female reproductive system, but the existing information is limited about the effects of BaP on the endometrial receptivity and embryo implantation. OBJECTIVE: The aim of this study was to investigate the effects of BaP on the endometrial receptivity and implantation in mice. MATERIALS AND METHODS: In this experimental study, 40 pregnant BALB/c mice were divided into 5 groups (n = 8/each) as follows: experimental groups received the doses of 100 µg/kg, 200 µg/kg, and 500 µg/kg BaP dissolved in corn oil, the control group received normal saline and sham group received corn oil. Pregnant mice administered these solutions from Day 1 to Day 5 of gestation by gavage. On Day 6, the mice were sacrificed. Then their embryos were counted and the hormonal, histomorphological and molecular analyses were performed on the mocusa of uterine tube. RESULTS: The data revealed that BaP reduces estrogen and progesterone levels, decreases the number of implantation site, endometrium thickness, uterine lumen diameter, stromal cells and endometrial glands, and blood vessels in the endometrium. However, the expression of Activin receptor-like kinase 5 and E-cadherin genes was not changed by BaP with different doses. CONCLUSION: The finding of this study showed that BaP can change estrogen and progesterone levels, and endometrial morphology leads to impairing the endometrial receptivity and decreasing the number of implantation site.
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spelling pubmed-66002802019-08-15 Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study Mardanshahi, Zeinab Karimpour Malekshah, Abbasali Talebpour Amiri, Fereshteh Valadan, Reza Int J Reprod Biomed Research Article BACKGROUND: Benzo(a)pyrene (BaP) as an environmental pollutant is ubiquitous in the environment and it has destructive effects on human health. So far, various studies have demonstrated that BaP can cause adverse effects on the female reproductive system, but the existing information is limited about the effects of BaP on the endometrial receptivity and embryo implantation. OBJECTIVE: The aim of this study was to investigate the effects of BaP on the endometrial receptivity and implantation in mice. MATERIALS AND METHODS: In this experimental study, 40 pregnant BALB/c mice were divided into 5 groups (n = 8/each) as follows: experimental groups received the doses of 100 µg/kg, 200 µg/kg, and 500 µg/kg BaP dissolved in corn oil, the control group received normal saline and sham group received corn oil. Pregnant mice administered these solutions from Day 1 to Day 5 of gestation by gavage. On Day 6, the mice were sacrificed. Then their embryos were counted and the hormonal, histomorphological and molecular analyses were performed on the mocusa of uterine tube. RESULTS: The data revealed that BaP reduces estrogen and progesterone levels, decreases the number of implantation site, endometrium thickness, uterine lumen diameter, stromal cells and endometrial glands, and blood vessels in the endometrium. However, the expression of Activin receptor-like kinase 5 and E-cadherin genes was not changed by BaP with different doses. CONCLUSION: The finding of this study showed that BaP can change estrogen and progesterone levels, and endometrial morphology leads to impairing the endometrial receptivity and decreasing the number of implantation site. Knowledge E 2019-01-28 /pmc/articles/PMC6600280/ /pubmed/31417980 http://dx.doi.org/10.18502/ijrm.v16i12.3680 Text en Copyright © 2018 Zeinab Mardanshahi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mardanshahi, Zeinab
Karimpour Malekshah, Abbasali
Talebpour Amiri, Fereshteh
Valadan, Reza
Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study
title Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study
title_full Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study
title_fullStr Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study
title_full_unstemmed Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study
title_short Effects of Benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: An experimental study
title_sort effects of benzo(a)pyrene on the endometrial receptivity and embryo implantation in mice: an experimental study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600280/
https://www.ncbi.nlm.nih.gov/pubmed/31417980
http://dx.doi.org/10.18502/ijrm.v16i12.3680
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