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Radioprotective properties of tocopherol succinate against ionizing radiation in mice

Threats of nuclear and other radiologic exposures have been increasing but no countermeasure for acute radiation syndrome has been approved by regulatory authorities. In prior publications we have demonstrated the efficacy of tocopherol succinate (TS) as a promising radiation countermeasure with the...

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Autores principales: Singh, Vijay K., Singh, Pankaj K., Wise, Stephen Y., Posarac, Ana, Fatanmi, Oluseyi O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589926/
https://www.ncbi.nlm.nih.gov/pubmed/23038797
http://dx.doi.org/10.1093/jrr/rrs088
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author Singh, Vijay K.
Singh, Pankaj K.
Wise, Stephen Y.
Posarac, Ana
Fatanmi, Oluseyi O.
author_facet Singh, Vijay K.
Singh, Pankaj K.
Wise, Stephen Y.
Posarac, Ana
Fatanmi, Oluseyi O.
author_sort Singh, Vijay K.
collection PubMed
description Threats of nuclear and other radiologic exposures have been increasing but no countermeasure for acute radiation syndrome has been approved by regulatory authorities. In prior publications we have demonstrated the efficacy of tocopherol succinate (TS) as a promising radiation countermeasure with the potential to protect against lethal doses of ionizing radiation exposure. The aim of this study was to gain further insight regarding how TS protects mice against a lethal dose of radiation. CD2F1 mice were injected subcutaneously with 400 mg/kg of TS, and 24 h later exposed to (60)Co γ–radiation. Intestinal tissues or spleen/thymus were harvested after irradiation and analyzed for CD68-positive inflammatory cells and apoptotic cells by immunostaining of jejunal cross-sections. Comet assay was used to analyze DNA damage in various tissues. Phospho-histone H3(pH3) and the proliferating cell nuclear antigen (PCNA) were used as mitotic markers for immunostaining jejunal cross-sections. We observed that injecting TS significantly decreased the number of CD68-positive cells, DNA damage and apoptotic cells (BAX, caspase 3 and cleaved poly(ADP-ribose) polymerase-positive cells) as judged by various apoptotic pathway markers. TS treatment also increased proliferating cells in irradiated mice. Results of this study further support our contention that TS protects mice against lethal doses of ionizing radiation by inhibiting radiation-induced apoptosis and DNA damage while enhancing cell proliferation.
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spelling pubmed-35899262013-03-06 Radioprotective properties of tocopherol succinate against ionizing radiation in mice Singh, Vijay K. Singh, Pankaj K. Wise, Stephen Y. Posarac, Ana Fatanmi, Oluseyi O. J Radiat Res Biology Threats of nuclear and other radiologic exposures have been increasing but no countermeasure for acute radiation syndrome has been approved by regulatory authorities. In prior publications we have demonstrated the efficacy of tocopherol succinate (TS) as a promising radiation countermeasure with the potential to protect against lethal doses of ionizing radiation exposure. The aim of this study was to gain further insight regarding how TS protects mice against a lethal dose of radiation. CD2F1 mice were injected subcutaneously with 400 mg/kg of TS, and 24 h later exposed to (60)Co γ–radiation. Intestinal tissues or spleen/thymus were harvested after irradiation and analyzed for CD68-positive inflammatory cells and apoptotic cells by immunostaining of jejunal cross-sections. Comet assay was used to analyze DNA damage in various tissues. Phospho-histone H3(pH3) and the proliferating cell nuclear antigen (PCNA) were used as mitotic markers for immunostaining jejunal cross-sections. We observed that injecting TS significantly decreased the number of CD68-positive cells, DNA damage and apoptotic cells (BAX, caspase 3 and cleaved poly(ADP-ribose) polymerase-positive cells) as judged by various apoptotic pathway markers. TS treatment also increased proliferating cells in irradiated mice. Results of this study further support our contention that TS protects mice against lethal doses of ionizing radiation by inhibiting radiation-induced apoptosis and DNA damage while enhancing cell proliferation. Oxford University Press 2013-03 2012-10-03 /pmc/articles/PMC3589926/ /pubmed/23038797 http://dx.doi.org/10.1093/jrr/rrs088 Text en Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology 2012. For commercial re-use, please contact journals.permissions@oup.com http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited
spellingShingle Biology
Singh, Vijay K.
Singh, Pankaj K.
Wise, Stephen Y.
Posarac, Ana
Fatanmi, Oluseyi O.
Radioprotective properties of tocopherol succinate against ionizing radiation in mice
title Radioprotective properties of tocopherol succinate against ionizing radiation in mice
title_full Radioprotective properties of tocopherol succinate against ionizing radiation in mice
title_fullStr Radioprotective properties of tocopherol succinate against ionizing radiation in mice
title_full_unstemmed Radioprotective properties of tocopherol succinate against ionizing radiation in mice
title_short Radioprotective properties of tocopherol succinate against ionizing radiation in mice
title_sort radioprotective properties of tocopherol succinate against ionizing radiation in mice
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589926/
https://www.ncbi.nlm.nih.gov/pubmed/23038797
http://dx.doi.org/10.1093/jrr/rrs088
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