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In vitro development of embryos from experimentally Kerack-addicted Mice

BACKGROUND: Prenatal drug exposure, as a common public health concern, is associated with an increased risk of adverse effects on early embryo development. OBJECTIVE: To investigate the in vitro development of - embryo from experimentally Kerack-addicted mice. MATERIALS AND METHODS: Twenty-five fema...

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Autores principales: Mohammadzadeh, Elham, Amjadi, Fatemeh-Sadat, Movahedin, Mansoureh, Zandieh, Zahra, Nazmara, Zohreh, Eslahi, Neda, Shirinbayan, Peymaneh, Asgari, Hamid Reza, Azad, Nahid, Salimi, Maryam, Koruji, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Clinical Center for Infertility 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601932/
https://www.ncbi.nlm.nih.gov/pubmed/29177242
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author Mohammadzadeh, Elham
Amjadi, Fatemeh-Sadat
Movahedin, Mansoureh
Zandieh, Zahra
Nazmara, Zohreh
Eslahi, Neda
Shirinbayan, Peymaneh
Asgari, Hamid Reza
Azad, Nahid
Salimi, Maryam
Koruji, Morteza
author_facet Mohammadzadeh, Elham
Amjadi, Fatemeh-Sadat
Movahedin, Mansoureh
Zandieh, Zahra
Nazmara, Zohreh
Eslahi, Neda
Shirinbayan, Peymaneh
Asgari, Hamid Reza
Azad, Nahid
Salimi, Maryam
Koruji, Morteza
author_sort Mohammadzadeh, Elham
collection PubMed
description BACKGROUND: Prenatal drug exposure, as a common public health concern, is associated with an increased risk of adverse effects on early embryo development. OBJECTIVE: To investigate the in vitro development of - embryo from experimentally Kerack-addicted mice. MATERIALS AND METHODS: Twenty-five female mice were studied in five groups: control, vehicle, and three experimental groups of Kerack-dependent mice (I, II, and III) which received different doses of Kerack for 14 days. After the establishment of addiction model (7 days), experimental groups I, II, and III were given Kerack intraperitoneally at the doses of 5, 35, and 70 mg/kg, twice a day for a period of 7 days, respectively. The vehicle group received normal saline and lemon juice whilst the control group just received water and food. Morulae were obtained through oviduct flashing. The survived embryos were cultured in T6+ 5mg/ml bovine serum albumin. The developmental rates up to hatched stage daily and embryo quality (differential staining and Tunnel staining) were also assessed RESULTS: The developmental potential of embryos obtained from the addicted mother was significantly decreased in comparison with control group. There was a significant reduction in the rate of blastocyst formation in the high dose Kerack dependent group. However, in addicted mice there was reduction in the total cell number (40.92% vs. 65.08% in control) and, inner cell mass percentage (17.17% vs. 26.15% in control) while apoptotic cells numbers were increased (7.17 vs. 1.46 in control) (p<0.05). CONCLUSION: The Kerack addiction during pregnancy retards preimplantation development and induces apoptosis.
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spelling pubmed-56019322017-11-24 In vitro development of embryos from experimentally Kerack-addicted Mice Mohammadzadeh, Elham Amjadi, Fatemeh-Sadat Movahedin, Mansoureh Zandieh, Zahra Nazmara, Zohreh Eslahi, Neda Shirinbayan, Peymaneh Asgari, Hamid Reza Azad, Nahid Salimi, Maryam Koruji, Morteza Int J Reprod Biomed Original Article BACKGROUND: Prenatal drug exposure, as a common public health concern, is associated with an increased risk of adverse effects on early embryo development. OBJECTIVE: To investigate the in vitro development of - embryo from experimentally Kerack-addicted mice. MATERIALS AND METHODS: Twenty-five female mice were studied in five groups: control, vehicle, and three experimental groups of Kerack-dependent mice (I, II, and III) which received different doses of Kerack for 14 days. After the establishment of addiction model (7 days), experimental groups I, II, and III were given Kerack intraperitoneally at the doses of 5, 35, and 70 mg/kg, twice a day for a period of 7 days, respectively. The vehicle group received normal saline and lemon juice whilst the control group just received water and food. Morulae were obtained through oviduct flashing. The survived embryos were cultured in T6+ 5mg/ml bovine serum albumin. The developmental rates up to hatched stage daily and embryo quality (differential staining and Tunnel staining) were also assessed RESULTS: The developmental potential of embryos obtained from the addicted mother was significantly decreased in comparison with control group. There was a significant reduction in the rate of blastocyst formation in the high dose Kerack dependent group. However, in addicted mice there was reduction in the total cell number (40.92% vs. 65.08% in control) and, inner cell mass percentage (17.17% vs. 26.15% in control) while apoptotic cells numbers were increased (7.17 vs. 1.46 in control) (p<0.05). CONCLUSION: The Kerack addiction during pregnancy retards preimplantation development and induces apoptosis. Research and Clinical Center for Infertility 2017-07 /pmc/articles/PMC5601932/ /pubmed/29177242 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mohammadzadeh, Elham
Amjadi, Fatemeh-Sadat
Movahedin, Mansoureh
Zandieh, Zahra
Nazmara, Zohreh
Eslahi, Neda
Shirinbayan, Peymaneh
Asgari, Hamid Reza
Azad, Nahid
Salimi, Maryam
Koruji, Morteza
In vitro development of embryos from experimentally Kerack-addicted Mice
title In vitro development of embryos from experimentally Kerack-addicted Mice
title_full In vitro development of embryos from experimentally Kerack-addicted Mice
title_fullStr In vitro development of embryos from experimentally Kerack-addicted Mice
title_full_unstemmed In vitro development of embryos from experimentally Kerack-addicted Mice
title_short In vitro development of embryos from experimentally Kerack-addicted Mice
title_sort in vitro development of embryos from experimentally kerack-addicted mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601932/
https://www.ncbi.nlm.nih.gov/pubmed/29177242
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