Cargando…

Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture

Enamel matrix derivative Emdogain (EMD) is widely used in periodontal treatment in spite of the fact that its effect on the developing embryo has not been elucidated. The aim of this study was to investigate the teratogenic effect of EMD on the rat embryo neural crest cells. The neural crest is a un...

Descripción completa

Detalles Bibliográficos
Autores principales: Mamashli, Maliheh, Ramezani, Mina, Parsa, Maliheh, Ostad, Seyyed Nasser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813064/
https://www.ncbi.nlm.nih.gov/pubmed/24250425
_version_ 1782289040687497216
author Mamashli, Maliheh
Ramezani, Mina
Parsa, Maliheh
Ostad, Seyyed Nasser
author_facet Mamashli, Maliheh
Ramezani, Mina
Parsa, Maliheh
Ostad, Seyyed Nasser
author_sort Mamashli, Maliheh
collection PubMed
description Enamel matrix derivative Emdogain (EMD) is widely used in periodontal treatment in spite of the fact that its effect on the developing embryo has not been elucidated. The aim of this study was to investigate the teratogenic effect of EMD on the rat embryo neural crest cells. The neural crest is a unique population of cells that migrates from the dorsal neural tube along defined pathways and produces various cell types including the melanocytes, neuronal and glial cells of the sensory, autonomic and enteric nervous system as well as the chromaffin cells of the adrenal gland. These cells have been used extensively for in-vitro studies of neurogenesis. Cultured cells by micromass culture method derived from midbrain of six embryos (13 day postcoitum; 34-36 smites) and exposed to various concentrations of EMD for 5 days at 37°C and differentiated foci were counted. Retinoic Acid (20 μg/mL) was used as standard positive control. These cells were stained using Mayer’s hematoxylin which is specific for staining differentiated cell nucleus. Neutral red staining determines cell viability rather than related cell differentiation but is used for normalization of Mayer’s hematoxylin results. At the concentration as low as 8 μg/mL of EMD, no toxic effect on fetal cells was observed and it is suggested that EMD has no teratogenic effect at studied concentrations.
format Online
Article
Text
id pubmed-3813064
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Shaheed Beheshti University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-38130642013-11-18 Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture Mamashli, Maliheh Ramezani, Mina Parsa, Maliheh Ostad, Seyyed Nasser Iran J Pharm Res Original Article Enamel matrix derivative Emdogain (EMD) is widely used in periodontal treatment in spite of the fact that its effect on the developing embryo has not been elucidated. The aim of this study was to investigate the teratogenic effect of EMD on the rat embryo neural crest cells. The neural crest is a unique population of cells that migrates from the dorsal neural tube along defined pathways and produces various cell types including the melanocytes, neuronal and glial cells of the sensory, autonomic and enteric nervous system as well as the chromaffin cells of the adrenal gland. These cells have been used extensively for in-vitro studies of neurogenesis. Cultured cells by micromass culture method derived from midbrain of six embryos (13 day postcoitum; 34-36 smites) and exposed to various concentrations of EMD for 5 days at 37°C and differentiated foci were counted. Retinoic Acid (20 μg/mL) was used as standard positive control. These cells were stained using Mayer’s hematoxylin which is specific for staining differentiated cell nucleus. Neutral red staining determines cell viability rather than related cell differentiation but is used for normalization of Mayer’s hematoxylin results. At the concentration as low as 8 μg/mL of EMD, no toxic effect on fetal cells was observed and it is suggested that EMD has no teratogenic effect at studied concentrations. Shaheed Beheshti University of Medical Sciences 2011 /pmc/articles/PMC3813064/ /pubmed/24250425 Text en © 2011 by School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services 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
Mamashli, Maliheh
Ramezani, Mina
Parsa, Maliheh
Ostad, Seyyed Nasser
Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture
title Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture
title_full Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture
title_fullStr Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture
title_full_unstemmed Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture
title_short Evaluation of Enamel Matrix Derivative (EMD) Teratogenicity on the Rat Embryo Neural Crest Culture
title_sort evaluation of enamel matrix derivative (emd) teratogenicity on the rat embryo neural crest culture
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813064/
https://www.ncbi.nlm.nih.gov/pubmed/24250425
work_keys_str_mv AT mamashlimaliheh evaluationofenamelmatrixderivativeemdteratogenicityontheratembryoneuralcrestculture
AT ramezanimina evaluationofenamelmatrixderivativeemdteratogenicityontheratembryoneuralcrestculture
AT parsamaliheh evaluationofenamelmatrixderivativeemdteratogenicityontheratembryoneuralcrestculture
AT ostadseyyednasser evaluationofenamelmatrixderivativeemdteratogenicityontheratembryoneuralcrestculture