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In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events
BACKGROUND: With socio-economic changes, dentists and maxillofacial surgeons are more and more faced with medically compromised patients. Especially, the admission of antirheumatic drugs has increased remarkably. So dentists and maxillofacial surgeons should be aware of related adverse reactions tha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033494/ https://www.ncbi.nlm.nih.gov/pubmed/24884884 http://dx.doi.org/10.1186/1746-160X-10-19 |
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author | Annussek, Tobias Szuwart, Thomas Kleinheinz, Johannes Koiky, Cathrin Wermker, Kai |
author_facet | Annussek, Tobias Szuwart, Thomas Kleinheinz, Johannes Koiky, Cathrin Wermker, Kai |
author_sort | Annussek, Tobias |
collection | PubMed |
description | BACKGROUND: With socio-economic changes, dentists and maxillofacial surgeons are more and more faced with medically compromised patients. Especially, the admission of antirheumatic drugs has increased remarkably. So dentists and maxillofacial surgeons should be aware of related adverse reactions that affect the craniofacial region. To identify possible cellular effects of disease modifying antirheumatic drugs (DMARDs) we investigated the influence of methotrexate (MTX) on human umbilical vein endothelial cells (HUVECs). METHODS: HUVECs were incubated with various concentrations of MTX, corresponding to serum concentrations found in rheumatoid arthritis (RA) patients. The effect of MTX on cell proliferation, differentiation as well as mitochondrial activity was measured by use of immunostaining, cell counting and 3-(4, 5-dimethylthiazol-2-yl)- 2, 5-diphenyltetrazolium bromide (MTT) assay. RESULTS: All samples incubated with MTX (1-1000 nM) showed significantly decreased cell viability when compared to controls. Cells were less proliferating, but did not lose their ability to synthesize endothelial proteins. A slight dose dependency of inhibiting effects was demonstrated. The observed differences between control and sample groups were rising with longer duration. CONCLUSION: Because of the crucial role of endothelial cells and their precursor cells in wound healing, a negative influence of MTX on oral health has to be supposed, correlating to clinical observations of adverse reactions in the oral cavity, such as ulcerative or erosive lesions. |
format | Online Article Text |
id | pubmed-4033494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40334942014-05-27 In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events Annussek, Tobias Szuwart, Thomas Kleinheinz, Johannes Koiky, Cathrin Wermker, Kai Head Face Med Research BACKGROUND: With socio-economic changes, dentists and maxillofacial surgeons are more and more faced with medically compromised patients. Especially, the admission of antirheumatic drugs has increased remarkably. So dentists and maxillofacial surgeons should be aware of related adverse reactions that affect the craniofacial region. To identify possible cellular effects of disease modifying antirheumatic drugs (DMARDs) we investigated the influence of methotrexate (MTX) on human umbilical vein endothelial cells (HUVECs). METHODS: HUVECs were incubated with various concentrations of MTX, corresponding to serum concentrations found in rheumatoid arthritis (RA) patients. The effect of MTX on cell proliferation, differentiation as well as mitochondrial activity was measured by use of immunostaining, cell counting and 3-(4, 5-dimethylthiazol-2-yl)- 2, 5-diphenyltetrazolium bromide (MTT) assay. RESULTS: All samples incubated with MTX (1-1000 nM) showed significantly decreased cell viability when compared to controls. Cells were less proliferating, but did not lose their ability to synthesize endothelial proteins. A slight dose dependency of inhibiting effects was demonstrated. The observed differences between control and sample groups were rising with longer duration. CONCLUSION: Because of the crucial role of endothelial cells and their precursor cells in wound healing, a negative influence of MTX on oral health has to be supposed, correlating to clinical observations of adverse reactions in the oral cavity, such as ulcerative or erosive lesions. BioMed Central 2014-05-22 /pmc/articles/PMC4033494/ /pubmed/24884884 http://dx.doi.org/10.1186/1746-160X-10-19 Text en Copyright © 2014 Annussek et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Annussek, Tobias Szuwart, Thomas Kleinheinz, Johannes Koiky, Cathrin Wermker, Kai In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events |
title | In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events |
title_full | In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events |
title_fullStr | In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events |
title_full_unstemmed | In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events |
title_short | In vitro inhibition of HUVECs by low dose methotrexate – insights into oral adverse events |
title_sort | in vitro inhibition of huvecs by low dose methotrexate – insights into oral adverse events |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033494/ https://www.ncbi.nlm.nih.gov/pubmed/24884884 http://dx.doi.org/10.1186/1746-160X-10-19 |
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