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High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice

A balanced redox state is critical for proper healing. Although human chronic wounds are characterized by high levels of oxidative stress (OS), whether OS levels are critical for chronic wound development is not known. For these studies, we used our chronic wound model in diabetic mice that has simi...

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Autores principales: Kim, Jane H., Yang, Benjamin, Tedesco, Amanda, Lebig, Elyson Gavin D., Ruegger, Paul M., Xu, Karen, Borneman, James, Martins-Green, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917777/
https://www.ncbi.nlm.nih.gov/pubmed/31848388
http://dx.doi.org/10.1038/s41598-019-55644-3
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author Kim, Jane H.
Yang, Benjamin
Tedesco, Amanda
Lebig, Elyson Gavin D.
Ruegger, Paul M.
Xu, Karen
Borneman, James
Martins-Green, Manuela
author_facet Kim, Jane H.
Yang, Benjamin
Tedesco, Amanda
Lebig, Elyson Gavin D.
Ruegger, Paul M.
Xu, Karen
Borneman, James
Martins-Green, Manuela
author_sort Kim, Jane H.
collection PubMed
description A balanced redox state is critical for proper healing. Although human chronic wounds are characterized by high levels of oxidative stress (OS), whether OS levels are critical for chronic wound development is not known. For these studies, we used our chronic wound model in diabetic mice that has similar characteristics as human chronic wounds, including naturally developed biofilm. We hypothesize that OS levels in wound tissues are critical for chronic wound initiation and development. We show that increased OS levels in the wound correlate with increased chronicity. Moreover, without increased OS levels, biofilm taken from chronic wounds and placed in new excision wounds do not create chronic wounds. Similarly, high OS levels in the wound tissue in the absence of the skin microbiome do not lead to chronic wounds. These findings show that both high OS levels and bacteria are needed for chronic wound initiation and development. In conclusion, OS levels in the wound at time of injury are critical for biofilm formation and chronic wound development and may be a good predictor of the degree of wound chronicity. Treating such wounds might be accomplished by managing OS levels with antioxidants combined with manipulation of the skin microbiome after debridement.
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spelling pubmed-69177772019-12-19 High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice Kim, Jane H. Yang, Benjamin Tedesco, Amanda Lebig, Elyson Gavin D. Ruegger, Paul M. Xu, Karen Borneman, James Martins-Green, Manuela Sci Rep Article A balanced redox state is critical for proper healing. Although human chronic wounds are characterized by high levels of oxidative stress (OS), whether OS levels are critical for chronic wound development is not known. For these studies, we used our chronic wound model in diabetic mice that has similar characteristics as human chronic wounds, including naturally developed biofilm. We hypothesize that OS levels in wound tissues are critical for chronic wound initiation and development. We show that increased OS levels in the wound correlate with increased chronicity. Moreover, without increased OS levels, biofilm taken from chronic wounds and placed in new excision wounds do not create chronic wounds. Similarly, high OS levels in the wound tissue in the absence of the skin microbiome do not lead to chronic wounds. These findings show that both high OS levels and bacteria are needed for chronic wound initiation and development. In conclusion, OS levels in the wound at time of injury are critical for biofilm formation and chronic wound development and may be a good predictor of the degree of wound chronicity. Treating such wounds might be accomplished by managing OS levels with antioxidants combined with manipulation of the skin microbiome after debridement. Nature Publishing Group UK 2019-12-17 /pmc/articles/PMC6917777/ /pubmed/31848388 http://dx.doi.org/10.1038/s41598-019-55644-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Jane H.
Yang, Benjamin
Tedesco, Amanda
Lebig, Elyson Gavin D.
Ruegger, Paul M.
Xu, Karen
Borneman, James
Martins-Green, Manuela
High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice
title High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice
title_full High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice
title_fullStr High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice
title_full_unstemmed High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice
title_short High Levels of Oxidative Stress and Skin Microbiome are Critical for Initiation and Development of Chronic Wounds in Diabetic Mice
title_sort high levels of oxidative stress and skin microbiome are critical for initiation and development of chronic wounds in diabetic mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917777/
https://www.ncbi.nlm.nih.gov/pubmed/31848388
http://dx.doi.org/10.1038/s41598-019-55644-3
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