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Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice

We used 3 biological metrics highly relevant to health risks, that is, cell death, inflammation, and global DNA methylation, to determine the late effects of low doses (0.05 or 0.1 Gy) of (137)Cs γ rays on the bone marrow, lung, and testis collected at 6 months post-irradiation from the same exposed...

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Autores principales: Jangiam, Witawat, Udomtanakunchai, Chatchanok, Reungpatthanaphong, Paiboon, Tungjai, Montree, Honikel, Louise, Gordon, Chris R., Rithidech, Kanokporn Noy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302279/
https://www.ncbi.nlm.nih.gov/pubmed/30622448
http://dx.doi.org/10.1177/1559325818815031
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author Jangiam, Witawat
Udomtanakunchai, Chatchanok
Reungpatthanaphong, Paiboon
Tungjai, Montree
Honikel, Louise
Gordon, Chris R.
Rithidech, Kanokporn Noy
author_facet Jangiam, Witawat
Udomtanakunchai, Chatchanok
Reungpatthanaphong, Paiboon
Tungjai, Montree
Honikel, Louise
Gordon, Chris R.
Rithidech, Kanokporn Noy
author_sort Jangiam, Witawat
collection PubMed
description We used 3 biological metrics highly relevant to health risks, that is, cell death, inflammation, and global DNA methylation, to determine the late effects of low doses (0.05 or 0.1 Gy) of (137)Cs γ rays on the bone marrow, lung, and testis collected at 6 months post-irradiation from the same exposed BALB/cJ mouse. This integrative approach has not been used for such a purpose. Mice exposed to 0 or 1 Gy of radiation served as a sham or positive control group, respectively. The results could deliver information for better health risk assessment across tissues, including better scientific basis for radiation protection and clinical application. We found no changes in the levels of all studied biological metrics (except a significant increase in the levels of an anti-inflammatory cytokine, ie, interleukin 10) in tissues of 0.05-Gy exposed mice, when compared to those in sham controls. In contrast, significantly increased levels of cell death and inflammation, including a significant loss of global 5-hydroxymethylcytosine, were found in all tissues of the same mice exposed to 0.1 or 1.0 Gy. Our data demonstrated not only no harm but also hormesis in the 0.05-Gy exposed mice. However, the hormetic effect appears to be dependent on biological metrics and tissue.
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spelling pubmed-63022792019-01-08 Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice Jangiam, Witawat Udomtanakunchai, Chatchanok Reungpatthanaphong, Paiboon Tungjai, Montree Honikel, Louise Gordon, Chris R. Rithidech, Kanokporn Noy Dose Response Original Article We used 3 biological metrics highly relevant to health risks, that is, cell death, inflammation, and global DNA methylation, to determine the late effects of low doses (0.05 or 0.1 Gy) of (137)Cs γ rays on the bone marrow, lung, and testis collected at 6 months post-irradiation from the same exposed BALB/cJ mouse. This integrative approach has not been used for such a purpose. Mice exposed to 0 or 1 Gy of radiation served as a sham or positive control group, respectively. The results could deliver information for better health risk assessment across tissues, including better scientific basis for radiation protection and clinical application. We found no changes in the levels of all studied biological metrics (except a significant increase in the levels of an anti-inflammatory cytokine, ie, interleukin 10) in tissues of 0.05-Gy exposed mice, when compared to those in sham controls. In contrast, significantly increased levels of cell death and inflammation, including a significant loss of global 5-hydroxymethylcytosine, were found in all tissues of the same mice exposed to 0.1 or 1.0 Gy. Our data demonstrated not only no harm but also hormesis in the 0.05-Gy exposed mice. However, the hormetic effect appears to be dependent on biological metrics and tissue. SAGE Publications 2018-12-19 /pmc/articles/PMC6302279/ /pubmed/30622448 http://dx.doi.org/10.1177/1559325818815031 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Jangiam, Witawat
Udomtanakunchai, Chatchanok
Reungpatthanaphong, Paiboon
Tungjai, Montree
Honikel, Louise
Gordon, Chris R.
Rithidech, Kanokporn Noy
Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice
title Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice
title_full Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice
title_fullStr Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice
title_full_unstemmed Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice
title_short Late Effects of Low-Dose Radiation on the Bone Marrow, Lung, and Testis Collected From the Same Exposed BALB/cJ Mice
title_sort late effects of low-dose radiation on the bone marrow, lung, and testis collected from the same exposed balb/cj mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302279/
https://www.ncbi.nlm.nih.gov/pubmed/30622448
http://dx.doi.org/10.1177/1559325818815031
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