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Effect of prenatal methamphetamine administration during gestational days on mice

BACKGROUND: Methamphetamine (MA) is one of most common illicit drugs which were reported that nearly half of MA consumers are women. MA can cross through placenta and affects pregnancy and fetus development. OBJECTIVE: Our aim was to evaluate effects of injected MA on crown-rump length, head and pla...

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Autores principales: Khoradmehr, Arezoo, Danafar, Amirhossein, Halvaei, Iman, Golzadeh, Jalal, Hosseini, Mahya, Mirjalili, Tahereh, Anvari, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Clinical Center for Infertility 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306984/
https://www.ncbi.nlm.nih.gov/pubmed/25653675
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author Khoradmehr, Arezoo
Danafar, Amirhossein
Halvaei, Iman
Golzadeh, Jalal
Hosseini, Mahya
Mirjalili, Tahereh
Anvari, Morteza
author_facet Khoradmehr, Arezoo
Danafar, Amirhossein
Halvaei, Iman
Golzadeh, Jalal
Hosseini, Mahya
Mirjalili, Tahereh
Anvari, Morteza
author_sort Khoradmehr, Arezoo
collection PubMed
description BACKGROUND: Methamphetamine (MA) is one of most common illicit drugs which were reported that nearly half of MA consumers are women. MA can cross through placenta and affects pregnancy and fetus development. OBJECTIVE: Our aim was to evaluate effects of injected MA on crown-rump length, head and placental circumference, body weight, histological changes and apoptosis in fetus. MATERIALS AND METHODS: Twenty-four NMRI pregnant mice were randomly divided into five groups. First, second and third groups were injected intraperitoneally 10 mg/kg/day MA during gestational days (GD): GD1-7, GD8-14, and GD1-14, respectively. Forth group, as sham, was injected saline from GD1-14, and finally control which was received neither MA nor saline. On GD15 cervical dislocated pregnant mice, fetus and placenta were weighed and fetus crown-rump length was measured. Hematoxylin and Eosin staining and TUNEL assay were applied to assess histological changes and apoptosis respectively. RESULTS: Fetus body weight and crown-rump length showed significant decrease in third compared to first and second groups (p≤0.001). There were significant differences in head circumference in control and sham compared to third group (0.5 (0.5-0.6), 0.6 (0.5-0.8), 0.4 (0.4-0.5) cm respectively, p≤0.001). Also fetus that treated with MA showed lower placenta circumference compared to control and sham groups. Histological changes such as exencephaly, hemorrhage and immature fetus were observed in second and third groups. Apoptotic cells in second and third groups were higher than controls, but differences were not significant. CONCLUSION: It seems MA abuse during pregnancy can cause morphological and histological changes in mice fetus but the exact mechanism remains unclear.
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spelling pubmed-43069842015-02-04 Effect of prenatal methamphetamine administration during gestational days on mice Khoradmehr, Arezoo Danafar, Amirhossein Halvaei, Iman Golzadeh, Jalal Hosseini, Mahya Mirjalili, Tahereh Anvari, Morteza Iran J Reprod Med Original Article BACKGROUND: Methamphetamine (MA) is one of most common illicit drugs which were reported that nearly half of MA consumers are women. MA can cross through placenta and affects pregnancy and fetus development. OBJECTIVE: Our aim was to evaluate effects of injected MA on crown-rump length, head and placental circumference, body weight, histological changes and apoptosis in fetus. MATERIALS AND METHODS: Twenty-four NMRI pregnant mice were randomly divided into five groups. First, second and third groups were injected intraperitoneally 10 mg/kg/day MA during gestational days (GD): GD1-7, GD8-14, and GD1-14, respectively. Forth group, as sham, was injected saline from GD1-14, and finally control which was received neither MA nor saline. On GD15 cervical dislocated pregnant mice, fetus and placenta were weighed and fetus crown-rump length was measured. Hematoxylin and Eosin staining and TUNEL assay were applied to assess histological changes and apoptosis respectively. RESULTS: Fetus body weight and crown-rump length showed significant decrease in third compared to first and second groups (p≤0.001). There were significant differences in head circumference in control and sham compared to third group (0.5 (0.5-0.6), 0.6 (0.5-0.8), 0.4 (0.4-0.5) cm respectively, p≤0.001). Also fetus that treated with MA showed lower placenta circumference compared to control and sham groups. Histological changes such as exencephaly, hemorrhage and immature fetus were observed in second and third groups. Apoptotic cells in second and third groups were higher than controls, but differences were not significant. CONCLUSION: It seems MA abuse during pregnancy can cause morphological and histological changes in mice fetus but the exact mechanism remains unclear. Research and Clinical Center for Infertility 2015-01 /pmc/articles/PMC4306984/ /pubmed/25653675 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
Khoradmehr, Arezoo
Danafar, Amirhossein
Halvaei, Iman
Golzadeh, Jalal
Hosseini, Mahya
Mirjalili, Tahereh
Anvari, Morteza
Effect of prenatal methamphetamine administration during gestational days on mice
title Effect of prenatal methamphetamine administration during gestational days on mice
title_full Effect of prenatal methamphetamine administration during gestational days on mice
title_fullStr Effect of prenatal methamphetamine administration during gestational days on mice
title_full_unstemmed Effect of prenatal methamphetamine administration during gestational days on mice
title_short Effect of prenatal methamphetamine administration during gestational days on mice
title_sort effect of prenatal methamphetamine administration during gestational days on mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306984/
https://www.ncbi.nlm.nih.gov/pubmed/25653675
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