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Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation
Therapy using hot springs, including the high-level radioactive gas “radon”, is traditionally conducted as an alternative treatment for various diseases. Oxidative-stress-related diseases are inhibited by the enhancement of antioxidative functions following radon inhalation. We have reported that ra...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9518353/ https://www.ncbi.nlm.nih.gov/pubmed/36078464 http://dx.doi.org/10.3390/ijerph191710750 |
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author | Kanzaki, Norie Sakoda, Akihiro Kataoka, Takahiro Sun, Lue Tanaka, Hiroshi Ohtsu, Iwao Yamaoka, Kiyonori |
author_facet | Kanzaki, Norie Sakoda, Akihiro Kataoka, Takahiro Sun, Lue Tanaka, Hiroshi Ohtsu, Iwao Yamaoka, Kiyonori |
author_sort | Kanzaki, Norie |
collection | PubMed |
description | Therapy using hot springs, including the high-level radioactive gas “radon”, is traditionally conducted as an alternative treatment for various diseases. Oxidative-stress-related diseases are inhibited by the enhancement of antioxidative functions following radon inhalation. We have reported that radon inhalation increased the level of anti-oxidants, such as glutathione (G-SH), in the brain and had a protective antioxidative effect against transient global cerebral ischemic injury. However, no studies have yet revealed the changes in G-SH associated substances after radon inhalation. In this study, we comprehensively analyzed several metabolites, focusing on G-SH. Mice were exposed to radon at concentrations of 200, 2000, or 20,000 Bq/m(3) for 1, 3, or 10 days. We detected 27 metabolites in the mouse brains. The result showed that the L-methionine levels increased, whereas the levels of urea, glutathione, and sulfite ion decreased under any condition. Although the ratio of G-SH to oxidized glutathione (GS-SG) decreased, glutathione monosulfide (G-S-SH) and cysteine monosulfide (Cys-S-SH) increased after radon inhalation. G-S-SH and Cys-S-SH can produce a biological defense against the imbalance of the redox state at very low-dose irradiation following radon inhalation because they are strong scavengers of reactive oxygen species. Additionally, we performed an overall assessment of high-dimensional data and showed some specific characteristics. We showed the changes in metabolites after radon inhalation using partial least squares-discriminant analysis and self-organizing maps. The results showed the health effects of radon, especially the state of sulfur-related metabolites in mouse brains under the exposure conditions for radon therapy. |
format | Online Article Text |
id | pubmed-9518353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95183532022-09-29 Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation Kanzaki, Norie Sakoda, Akihiro Kataoka, Takahiro Sun, Lue Tanaka, Hiroshi Ohtsu, Iwao Yamaoka, Kiyonori Int J Environ Res Public Health Article Therapy using hot springs, including the high-level radioactive gas “radon”, is traditionally conducted as an alternative treatment for various diseases. Oxidative-stress-related diseases are inhibited by the enhancement of antioxidative functions following radon inhalation. We have reported that radon inhalation increased the level of anti-oxidants, such as glutathione (G-SH), in the brain and had a protective antioxidative effect against transient global cerebral ischemic injury. However, no studies have yet revealed the changes in G-SH associated substances after radon inhalation. In this study, we comprehensively analyzed several metabolites, focusing on G-SH. Mice were exposed to radon at concentrations of 200, 2000, or 20,000 Bq/m(3) for 1, 3, or 10 days. We detected 27 metabolites in the mouse brains. The result showed that the L-methionine levels increased, whereas the levels of urea, glutathione, and sulfite ion decreased under any condition. Although the ratio of G-SH to oxidized glutathione (GS-SG) decreased, glutathione monosulfide (G-S-SH) and cysteine monosulfide (Cys-S-SH) increased after radon inhalation. G-S-SH and Cys-S-SH can produce a biological defense against the imbalance of the redox state at very low-dose irradiation following radon inhalation because they are strong scavengers of reactive oxygen species. Additionally, we performed an overall assessment of high-dimensional data and showed some specific characteristics. We showed the changes in metabolites after radon inhalation using partial least squares-discriminant analysis and self-organizing maps. The results showed the health effects of radon, especially the state of sulfur-related metabolites in mouse brains under the exposure conditions for radon therapy. MDPI 2022-08-29 /pmc/articles/PMC9518353/ /pubmed/36078464 http://dx.doi.org/10.3390/ijerph191710750 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kanzaki, Norie Sakoda, Akihiro Kataoka, Takahiro Sun, Lue Tanaka, Hiroshi Ohtsu, Iwao Yamaoka, Kiyonori Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation |
title | Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation |
title_full | Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation |
title_fullStr | Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation |
title_full_unstemmed | Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation |
title_short | Changes in Sulfur Metabolism in Mouse Brains following Radon Inhalation |
title_sort | changes in sulfur metabolism in mouse brains following radon inhalation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9518353/ https://www.ncbi.nlm.nih.gov/pubmed/36078464 http://dx.doi.org/10.3390/ijerph191710750 |
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