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Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage

Until today, it remains controversial whether long-term exposure to extremely low-frequency magnetic fields (ELF-MF) below the legislative exposure limits could result in adverse human health effects. In the present study, the effects of long-term in vitro MF exposure on three different study endpoi...

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Autores principales: Nguyen, Ha, Segers, Seppe, Ledent, Maryse, Anthonissen, Roel, Verschaeve, Luc, Hinsenkamp, Maurice, Collard, Jean-Francois, Feipel, Veronique, Mertens, Birgit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008985/
https://www.ncbi.nlm.nih.gov/pubmed/36923833
http://dx.doi.org/10.1016/j.heliyon.2023.e14097
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author Nguyen, Ha
Segers, Seppe
Ledent, Maryse
Anthonissen, Roel
Verschaeve, Luc
Hinsenkamp, Maurice
Collard, Jean-Francois
Feipel, Veronique
Mertens, Birgit
author_facet Nguyen, Ha
Segers, Seppe
Ledent, Maryse
Anthonissen, Roel
Verschaeve, Luc
Hinsenkamp, Maurice
Collard, Jean-Francois
Feipel, Veronique
Mertens, Birgit
author_sort Nguyen, Ha
collection PubMed
description Until today, it remains controversial whether long-term exposure to extremely low-frequency magnetic fields (ELF-MF) below the legislative exposure limits could result in adverse human health effects. In the present study, the effects of long-term in vitro MF exposure on three different study endpoints (cell viability, genetic damage, and sensitivity to damage induced by known mutagens) were investigated in the human B lymphoblastoid (TK6) cell line. Cells were exposed to 50 Hz MF at three selected magnetic flux densities (i.e., 10, 100, and 500 μT) for different exposure periods ranging from 96h up to 6 weeks. Cell viability following MF exposure was assessed using the ATP-based cell viability assay. Effects of MF exposure on cell genetic damage and cell sensitivity to mutagen-induced damage were evaluated using the in vitro alkaline comet assay and the in vitro cytokinesis block micronucleus assay. The results showed that long-term exposure up to 96h to 50 Hz MF at all tested flux densities could significantly increase TK6 cell viability. In contrast, long-term MF exposure did not affect cell genetic damage, and long-term pre-exposure to MF did not change cell sensitivity to damage induced by known mutagens. At certain time points, statistically significant difference in genotoxicity test results were observed between the MF-exposed cells and the control cells. However, these observations could not be confirmed in the repeat experiments, indicating that they are probably not biologically significant.
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spelling pubmed-100089852023-03-14 Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage Nguyen, Ha Segers, Seppe Ledent, Maryse Anthonissen, Roel Verschaeve, Luc Hinsenkamp, Maurice Collard, Jean-Francois Feipel, Veronique Mertens, Birgit Heliyon Research Article Until today, it remains controversial whether long-term exposure to extremely low-frequency magnetic fields (ELF-MF) below the legislative exposure limits could result in adverse human health effects. In the present study, the effects of long-term in vitro MF exposure on three different study endpoints (cell viability, genetic damage, and sensitivity to damage induced by known mutagens) were investigated in the human B lymphoblastoid (TK6) cell line. Cells were exposed to 50 Hz MF at three selected magnetic flux densities (i.e., 10, 100, and 500 μT) for different exposure periods ranging from 96h up to 6 weeks. Cell viability following MF exposure was assessed using the ATP-based cell viability assay. Effects of MF exposure on cell genetic damage and cell sensitivity to mutagen-induced damage were evaluated using the in vitro alkaline comet assay and the in vitro cytokinesis block micronucleus assay. The results showed that long-term exposure up to 96h to 50 Hz MF at all tested flux densities could significantly increase TK6 cell viability. In contrast, long-term MF exposure did not affect cell genetic damage, and long-term pre-exposure to MF did not change cell sensitivity to damage induced by known mutagens. At certain time points, statistically significant difference in genotoxicity test results were observed between the MF-exposed cells and the control cells. However, these observations could not be confirmed in the repeat experiments, indicating that they are probably not biologically significant. Elsevier 2023-02-27 /pmc/articles/PMC10008985/ /pubmed/36923833 http://dx.doi.org/10.1016/j.heliyon.2023.e14097 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Nguyen, Ha
Segers, Seppe
Ledent, Maryse
Anthonissen, Roel
Verschaeve, Luc
Hinsenkamp, Maurice
Collard, Jean-Francois
Feipel, Veronique
Mertens, Birgit
Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
title Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
title_full Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
title_fullStr Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
title_full_unstemmed Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
title_short Effects of long-term exposure to 50 Hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
title_sort effects of long-term exposure to 50 hz magnetic fields on cell viability, genetic damage, and sensitivity to mutagen-induced damage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008985/
https://www.ncbi.nlm.nih.gov/pubmed/36923833
http://dx.doi.org/10.1016/j.heliyon.2023.e14097
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