Wound trauma alters ionizing radiation dose assessment
<p>Abstract</p> <p>Background</p> <p>Wounding following whole-body γ-irradiation (radiation combined injury, RCI) increases mortality. Wounding-induced increases in radiation mortality are triggered by sustained activation of inducible nitric oxide synthase pathways, pe...
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doaj-bf2d1954520b40d799daaa47ccfecde82020-11-24T22:23:51ZengBMCCell & Bioscience2045-37012012-06-01212010.1186/2045-3701-2-20Wound trauma alters ionizing radiation dose assessmentKiang Juliann GGarrison Bradley RBurns True MZhai MinDews Ian CNey Patrick HCary Lynnette HFukumoto RisakuElliott Thomas BLedney G<p>Abstract</p> <p>Background</p> <p>Wounding following whole-body γ-irradiation (radiation combined injury, RCI) increases mortality. Wounding-induced increases in radiation mortality are triggered by sustained activation of inducible nitric oxide synthase pathways, persistent alteration of cytokine homeostasis, and increased susceptibility to bacterial infection. Among these factors, cytokines along with other biomarkers have been adopted for biodosimetric evaluation and assessment of radiation dose and injury. Therefore, wounding could complicate biodosimetric assessments.</p> <p>Results</p> <p>In this report, such confounding effects were addressed. Mice were given <sup>60</sup>Co γ-photon radiation followed by skin wounding. Wound trauma exacerbated radiation-induced mortality, body-weight loss, and wound healing. Analyses of DNA damage in bone-marrow cells and peripheral blood mononuclear cells (PBMCs), changes in hematology and cytokine profiles, and fundamental clinical signs were evaluated. Early biomarkers (1 d after RCI) vs. irradiation alone included significant decreases in survivin expression in bone marrow cells, enhanced increases in γ-H2AX formation in Lin<sup>+</sup> bone marrow cells, enhanced increases in IL-1β, IL-6, IL-8, and G-CSF concentrations in blood, and concomitant decreases in γ-H2AX formation in PBMCs and decreases in numbers of splenocytes, lymphocytes, and neutrophils. Intermediate biomarkers (7 – 10 d after RCI) included continuously decreased γ-H2AX formation in PBMC and enhanced increases in IL-1β, IL-6, IL-8, and G-CSF concentrations in blood. The clinical signs evaluated after RCI were increased water consumption, decreased body weight, and decreased wound healing rate and survival rate. Late clinical signs (30 d after RCI) included poor survival and wound healing.</p> <p>Conclusion</p> <p>Results suggest that confounding factors such as wounding alters ionizing radiation dose assessment and agents inhibiting these responses may prove therapeutic for radiation combined injury and reduce related mortality.</p> http://www.cellandbioscience.com/content/2/1/20RadiationWoundCombined injuryLymphocyteNeutrophilPlateletSplenocyteγ-H2AXCytokineDNA damageSurvivin |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kiang Juliann G Garrison Bradley R Burns True M Zhai Min Dews Ian C Ney Patrick H Cary Lynnette H Fukumoto Risaku Elliott Thomas B Ledney G |
spellingShingle |
Kiang Juliann G Garrison Bradley R Burns True M Zhai Min Dews Ian C Ney Patrick H Cary Lynnette H Fukumoto Risaku Elliott Thomas B Ledney G Wound trauma alters ionizing radiation dose assessment Cell & Bioscience Radiation Wound Combined injury Lymphocyte Neutrophil Platelet Splenocyte γ-H2AX Cytokine DNA damage Survivin |
author_facet |
Kiang Juliann G Garrison Bradley R Burns True M Zhai Min Dews Ian C Ney Patrick H Cary Lynnette H Fukumoto Risaku Elliott Thomas B Ledney G |
author_sort |
Kiang Juliann G |
title |
Wound trauma alters ionizing radiation dose assessment |
title_short |
Wound trauma alters ionizing radiation dose assessment |
title_full |
Wound trauma alters ionizing radiation dose assessment |
title_fullStr |
Wound trauma alters ionizing radiation dose assessment |
title_full_unstemmed |
Wound trauma alters ionizing radiation dose assessment |
title_sort |
wound trauma alters ionizing radiation dose assessment |
publisher |
BMC |
series |
Cell & Bioscience |
issn |
2045-3701 |
publishDate |
2012-06-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Wounding following whole-body γ-irradiation (radiation combined injury, RCI) increases mortality. Wounding-induced increases in radiation mortality are triggered by sustained activation of inducible nitric oxide synthase pathways, persistent alteration of cytokine homeostasis, and increased susceptibility to bacterial infection. Among these factors, cytokines along with other biomarkers have been adopted for biodosimetric evaluation and assessment of radiation dose and injury. Therefore, wounding could complicate biodosimetric assessments.</p> <p>Results</p> <p>In this report, such confounding effects were addressed. Mice were given <sup>60</sup>Co γ-photon radiation followed by skin wounding. Wound trauma exacerbated radiation-induced mortality, body-weight loss, and wound healing. Analyses of DNA damage in bone-marrow cells and peripheral blood mononuclear cells (PBMCs), changes in hematology and cytokine profiles, and fundamental clinical signs were evaluated. Early biomarkers (1 d after RCI) vs. irradiation alone included significant decreases in survivin expression in bone marrow cells, enhanced increases in γ-H2AX formation in Lin<sup>+</sup> bone marrow cells, enhanced increases in IL-1β, IL-6, IL-8, and G-CSF concentrations in blood, and concomitant decreases in γ-H2AX formation in PBMCs and decreases in numbers of splenocytes, lymphocytes, and neutrophils. Intermediate biomarkers (7 – 10 d after RCI) included continuously decreased γ-H2AX formation in PBMC and enhanced increases in IL-1β, IL-6, IL-8, and G-CSF concentrations in blood. The clinical signs evaluated after RCI were increased water consumption, decreased body weight, and decreased wound healing rate and survival rate. Late clinical signs (30 d after RCI) included poor survival and wound healing.</p> <p>Conclusion</p> <p>Results suggest that confounding factors such as wounding alters ionizing radiation dose assessment and agents inhibiting these responses may prove therapeutic for radiation combined injury and reduce related mortality.</p> |
topic |
Radiation Wound Combined injury Lymphocyte Neutrophil Platelet Splenocyte γ-H2AX Cytokine DNA damage Survivin |
url |
http://www.cellandbioscience.com/content/2/1/20 |
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