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In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells

Intermediate frequency magnetic fields (IF-MFs) at ~85 kHz are one of the components of wireless power transfer (WPT) systems. However, the available data needed for the assessment of the safety of organisms from IF-MF exposure are scarce. Thus, there is an imminent need to accumulate evidence-based...

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Autores principales: Ohtani, Shin, Ushiyama, Akira, Wada, Keiji, Suzuki, Yukihisa, Hattori, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036096/
https://www.ncbi.nlm.nih.gov/pubmed/36579461
http://dx.doi.org/10.1093/jrr/rrac081
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author Ohtani, Shin
Ushiyama, Akira
Wada, Keiji
Suzuki, Yukihisa
Hattori, Kenji
author_facet Ohtani, Shin
Ushiyama, Akira
Wada, Keiji
Suzuki, Yukihisa
Hattori, Kenji
author_sort Ohtani, Shin
collection PubMed
description Intermediate frequency magnetic fields (IF-MFs) at ~85 kHz are one of the components of wireless power transfer (WPT) systems. However, the available data needed for the assessment of the safety of organisms from IF-MF exposure are scarce. Thus, there is an imminent need to accumulate evidence-based assessment data. In particular, if humans are exposed to IF-MF due to an accident or trouble, they are at increased risk of being exposed to high-intensity IF-MF within a short period. The already existing exposure system was improved to a system that could intermittently expose animals at 3 s intervals. This system allows the exposure of a mouse to high-intensity IF-MF (frequency: 82.3 kHz; induced electric field: 87 V/m, which was 3.8 times the basic restriction level for occupational exposure in the ICNIRP guideline), while regulating the heat generated by the coil. In vivo genotoxicity after IF-MF exposure was assessed using micronucleus (MN) test, Pig-a assay, and gpt assay. The results of MN test and Pig-a assay in hematopoietic cells revealed that neither the reticulocytes nor the mature erythrocytes exhibited significant increases in the IF-MF-exposed group compared with that in the sham-exposed group. In germ cells, MN test and gpt assay outcomes showed that IF-MF exposure did not cause any genetic or chromosomal abnormality. Based on these data, there was no genotoxic effect of our set IF-MF exposure on somatic and germ cells. These findings can contribute to the widespread use of WPT systems as effective data of IF-MF safety assessment.
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spelling pubmed-100360962023-03-24 In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells Ohtani, Shin Ushiyama, Akira Wada, Keiji Suzuki, Yukihisa Hattori, Kenji J Radiat Res Regular Paper Intermediate frequency magnetic fields (IF-MFs) at ~85 kHz are one of the components of wireless power transfer (WPT) systems. However, the available data needed for the assessment of the safety of organisms from IF-MF exposure are scarce. Thus, there is an imminent need to accumulate evidence-based assessment data. In particular, if humans are exposed to IF-MF due to an accident or trouble, they are at increased risk of being exposed to high-intensity IF-MF within a short period. The already existing exposure system was improved to a system that could intermittently expose animals at 3 s intervals. This system allows the exposure of a mouse to high-intensity IF-MF (frequency: 82.3 kHz; induced electric field: 87 V/m, which was 3.8 times the basic restriction level for occupational exposure in the ICNIRP guideline), while regulating the heat generated by the coil. In vivo genotoxicity after IF-MF exposure was assessed using micronucleus (MN) test, Pig-a assay, and gpt assay. The results of MN test and Pig-a assay in hematopoietic cells revealed that neither the reticulocytes nor the mature erythrocytes exhibited significant increases in the IF-MF-exposed group compared with that in the sham-exposed group. In germ cells, MN test and gpt assay outcomes showed that IF-MF exposure did not cause any genetic or chromosomal abnormality. Based on these data, there was no genotoxic effect of our set IF-MF exposure on somatic and germ cells. These findings can contribute to the widespread use of WPT systems as effective data of IF-MF safety assessment. Oxford University Press 2022-12-29 /pmc/articles/PMC10036096/ /pubmed/36579461 http://dx.doi.org/10.1093/jrr/rrac081 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Paper
Ohtani, Shin
Ushiyama, Akira
Wada, Keiji
Suzuki, Yukihisa
Hattori, Kenji
In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
title In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
title_full In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
title_fullStr In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
title_full_unstemmed In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
title_short In vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
title_sort in vivo genotoxicity of high-intensity intermediate frequency magnetic fields in somatic cells and germ cells
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036096/
https://www.ncbi.nlm.nih.gov/pubmed/36579461
http://dx.doi.org/10.1093/jrr/rrac081
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