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Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development
OBJECTIVE(S): This study investigated the possible effects of low (3 mg/kg) and high (6 mg/kg) doses of nicotine on the skeletal development of rat fetuses by the double staining method and the protective role of melatonin (10 mg/kg) against these effects. MATERIALS AND METHODS: Eighteen adult femal...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118089/ https://www.ncbi.nlm.nih.gov/pubmed/30186564 http://dx.doi.org/10.22038/IJBMS.2018.26705.6539 |
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author | Yılmaz, Halil Ertekin, Tolga Atay, Emre Nisari, Mehtap Susar Güler, Hatice Al, Özge Payas, Ahmet Yılmaz, Seher |
author_facet | Yılmaz, Halil Ertekin, Tolga Atay, Emre Nisari, Mehtap Susar Güler, Hatice Al, Özge Payas, Ahmet Yılmaz, Seher |
author_sort | Yılmaz, Halil |
collection | PubMed |
description | OBJECTIVE(S): This study investigated the possible effects of low (3 mg/kg) and high (6 mg/kg) doses of nicotine on the skeletal development of rat fetuses by the double staining method and the protective role of melatonin (10 mg/kg) against these effects. MATERIALS AND METHODS: Eighteen adult female Wistar-Albino rats were divided into six groups (n=3, each) as control, low-dose nicotine, high-dose nicotine, low-dose nicotine+melatonin, high-dose nicotine + melatonin and melatonin. While nicotine was given to the experimental groups on gestation days 1–20, nicotine and melatonin were administered together to the treatment groups. The fetuses were delivered by cesarean section on the 20(th) day of pregnancy. The skeletal systems of the fetuses were stained using the double staining method. The forelimbs and hindlimbs of the fetuses were firstly investigated under a stereomicroscope, and then their photos were taken. The total bone length, the length of the ossified part and the ossification rate were calculated using the ImageJ program. RESULTS: The degree of ossification in the bones of the feet and the hands was determined. When the total bone length and the length of the ossified part were evaluated, they were significantly decreased in the nicotine groups (P<0.05), but were close to each other in the treatment and the control groups (P<0.05). CONCLUSION: It has been found that the use of nicotine during pregnancy delays skeletal ossification and that melatonin, a powerful antioxidant, eliminates the teratogenic effects of nicotine. |
format | Online Article Text |
id | pubmed-6118089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-61180892018-09-05 Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development Yılmaz, Halil Ertekin, Tolga Atay, Emre Nisari, Mehtap Susar Güler, Hatice Al, Özge Payas, Ahmet Yılmaz, Seher Iran J Basic Med Sci Original Article OBJECTIVE(S): This study investigated the possible effects of low (3 mg/kg) and high (6 mg/kg) doses of nicotine on the skeletal development of rat fetuses by the double staining method and the protective role of melatonin (10 mg/kg) against these effects. MATERIALS AND METHODS: Eighteen adult female Wistar-Albino rats were divided into six groups (n=3, each) as control, low-dose nicotine, high-dose nicotine, low-dose nicotine+melatonin, high-dose nicotine + melatonin and melatonin. While nicotine was given to the experimental groups on gestation days 1–20, nicotine and melatonin were administered together to the treatment groups. The fetuses were delivered by cesarean section on the 20(th) day of pregnancy. The skeletal systems of the fetuses were stained using the double staining method. The forelimbs and hindlimbs of the fetuses were firstly investigated under a stereomicroscope, and then their photos were taken. The total bone length, the length of the ossified part and the ossification rate were calculated using the ImageJ program. RESULTS: The degree of ossification in the bones of the feet and the hands was determined. When the total bone length and the length of the ossified part were evaluated, they were significantly decreased in the nicotine groups (P<0.05), but were close to each other in the treatment and the control groups (P<0.05). CONCLUSION: It has been found that the use of nicotine during pregnancy delays skeletal ossification and that melatonin, a powerful antioxidant, eliminates the teratogenic effects of nicotine. Mashhad University of Medical Sciences 2018-08 /pmc/articles/PMC6118089/ /pubmed/30186564 http://dx.doi.org/10.22038/IJBMS.2018.26705.6539 Text en © Iranian Journal of Basic Medical Sciences 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 Yılmaz, Halil Ertekin, Tolga Atay, Emre Nisari, Mehtap Susar Güler, Hatice Al, Özge Payas, Ahmet Yılmaz, Seher Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
title | Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
title_full | Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
title_fullStr | Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
title_full_unstemmed | Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
title_short | Antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
title_sort | antioxidant role of melatonin against nicotine’s teratogenic effects on embryonic bone development |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118089/ https://www.ncbi.nlm.nih.gov/pubmed/30186564 http://dx.doi.org/10.22038/IJBMS.2018.26705.6539 |
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