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Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum
OBJECTIVE: Extensive research has been done to assess the efficacy of herbs for treating different disorders. Dorema ammoniacum (D. ammoniacum) is used in folk medicines for various goals. The application of herbs in medicine is accompanied by harmful effects. Chick embryo is considered a suitable m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103434/ https://www.ncbi.nlm.nih.gov/pubmed/32257887 |
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author | Tavakkoli, Hadi Derakhshanfar, Amin Moayedi, Javad Poostforoosh Fard, Ali |
author_facet | Tavakkoli, Hadi Derakhshanfar, Amin Moayedi, Javad Poostforoosh Fard, Ali |
author_sort | Tavakkoli, Hadi |
collection | PubMed |
description | OBJECTIVE: Extensive research has been done to assess the efficacy of herbs for treating different disorders. Dorema ammoniacum (D. ammoniacum) is used in folk medicines for various goals. The application of herbs in medicine is accompanied by harmful effects. Chick embryo is considered a suitable model for assessing drugs toxicity. The present study aimed to evaluate the changes in vasculature in chick’s extra-embryonic membrane following D. ammoniacum treatment. Alterations in molecular pathways associated with early embryonic angiogenesis such as vascular endothelial growth factor A (VEGF-A) were also evaluated. MATERIALS AND METHODS: Fertile chicken (Ross 308) eggs were allocated into three similar groups; sham, control and D. ammoniacum groups; in D. ammoniacum group, eggs were inoculated with plant’s extract at doses of 50 or 100 mg per kg egg-weight. RESULTS: Analysis of the extra-embryonic membrane vasculature revealed that D. ammoniacum extract decreases some vascular parameters such as vessels area, total vessels length, vascular branch and increases lacunarity. This herb’s vascular toxicity was in a dose-dependent manner. Down-regulation of the expression of VEGF-A was also seen in the extract-treated extra-embryonic membrane. CONCLUSION: Vascular toxicity of D. ammoniacum was confirmed by data presented in this paper. We conclude that alteration of vascular parameters and gene expression might finally lead to embryo malformation due to D. ammoniacum consumption. Therefore, the use of this herb must be limited during the fetal growth period especially at doses higher than 50 mg per kg. |
format | Online Article Text |
id | pubmed-7103434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-71034342020-04-03 Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum Tavakkoli, Hadi Derakhshanfar, Amin Moayedi, Javad Poostforoosh Fard, Ali Avicenna J Phytomed Original Research Article OBJECTIVE: Extensive research has been done to assess the efficacy of herbs for treating different disorders. Dorema ammoniacum (D. ammoniacum) is used in folk medicines for various goals. The application of herbs in medicine is accompanied by harmful effects. Chick embryo is considered a suitable model for assessing drugs toxicity. The present study aimed to evaluate the changes in vasculature in chick’s extra-embryonic membrane following D. ammoniacum treatment. Alterations in molecular pathways associated with early embryonic angiogenesis such as vascular endothelial growth factor A (VEGF-A) were also evaluated. MATERIALS AND METHODS: Fertile chicken (Ross 308) eggs were allocated into three similar groups; sham, control and D. ammoniacum groups; in D. ammoniacum group, eggs were inoculated with plant’s extract at doses of 50 or 100 mg per kg egg-weight. RESULTS: Analysis of the extra-embryonic membrane vasculature revealed that D. ammoniacum extract decreases some vascular parameters such as vessels area, total vessels length, vascular branch and increases lacunarity. This herb’s vascular toxicity was in a dose-dependent manner. Down-regulation of the expression of VEGF-A was also seen in the extract-treated extra-embryonic membrane. CONCLUSION: Vascular toxicity of D. ammoniacum was confirmed by data presented in this paper. We conclude that alteration of vascular parameters and gene expression might finally lead to embryo malformation due to D. ammoniacum consumption. Therefore, the use of this herb must be limited during the fetal growth period especially at doses higher than 50 mg per kg. Mashhad University of Medical Sciences 2020 /pmc/articles/PMC7103434/ /pubmed/32257887 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 Research Article Tavakkoli, Hadi Derakhshanfar, Amin Moayedi, Javad Poostforoosh Fard, Ali Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum |
title | Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum |
title_full | Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum |
title_fullStr | Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum |
title_full_unstemmed | Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum |
title_short | Utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of Dorema ammoniacum |
title_sort | utilization of a chicken embryo membrane model for evaluation of embryonic vascular toxicity of dorema ammoniacum |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7103434/ https://www.ncbi.nlm.nih.gov/pubmed/32257887 |
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