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Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota

Although radiation therapy is a cornerstone of modern management of malignancies, various side effects are inevitably linked to abdominal and pelvic cancer after radiotherapy. Radiation-mediated gastrointestinal (GI) toxicity impairs the life quality of cancer survivors and even shortens their lifes...

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Autores principales: Xiao, Hui-wen, Li, Yuan, Luo, Dan, Dong, Jia-li, Zhou, Li-xin, Zhao, Shu-yi, Zheng, Qi-sheng, Wang, Hai-chao, Cui, Ming, Fan, Sai-jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799803/
https://www.ncbi.nlm.nih.gov/pubmed/29371696
http://dx.doi.org/10.1038/emm.2017.246
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author Xiao, Hui-wen
Li, Yuan
Luo, Dan
Dong, Jia-li
Zhou, Li-xin
Zhao, Shu-yi
Zheng, Qi-sheng
Wang, Hai-chao
Cui, Ming
Fan, Sai-jun
author_facet Xiao, Hui-wen
Li, Yuan
Luo, Dan
Dong, Jia-li
Zhou, Li-xin
Zhao, Shu-yi
Zheng, Qi-sheng
Wang, Hai-chao
Cui, Ming
Fan, Sai-jun
author_sort Xiao, Hui-wen
collection PubMed
description Although radiation therapy is a cornerstone of modern management of malignancies, various side effects are inevitably linked to abdominal and pelvic cancer after radiotherapy. Radiation-mediated gastrointestinal (GI) toxicity impairs the life quality of cancer survivors and even shortens their lifespan. Hydrogen has been shown to protect against tissue injuries caused by oxidative stress and excessive inflammation, but its effect on radiation-induced intestinal injury was previously unknown. In the present study, we found that oral gavage with hydrogen-water increased the survival rate and body weight of mice exposed to total abdominal irradiation (TAI); oral gavage with hydrogen-water was also associated with an improvement in GI tract function and the epithelial integrity of the small intestine. Mechanistically, microarray analysis revealed that hydrogen-water administration upregulated miR-1968-5p levels, thus resulting in parallel downregulation of MyD88 expression in the small intestine after TAI exposure. Additionally, high-throughput sequencing showed that hydrogen-water oral gavage resulted in retention of the TAI-shifted intestinal bacterial composition in mice. Collectively, our findings suggested that hydrogen-water might be used as a potential therapeutic to alleviate intestinal injury induced by radiotherapy for abdominal and pelvic cancer in preclinical settings.
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spelling pubmed-57998032018-02-21 Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota Xiao, Hui-wen Li, Yuan Luo, Dan Dong, Jia-li Zhou, Li-xin Zhao, Shu-yi Zheng, Qi-sheng Wang, Hai-chao Cui, Ming Fan, Sai-jun Exp Mol Med Original Article Although radiation therapy is a cornerstone of modern management of malignancies, various side effects are inevitably linked to abdominal and pelvic cancer after radiotherapy. Radiation-mediated gastrointestinal (GI) toxicity impairs the life quality of cancer survivors and even shortens their lifespan. Hydrogen has been shown to protect against tissue injuries caused by oxidative stress and excessive inflammation, but its effect on radiation-induced intestinal injury was previously unknown. In the present study, we found that oral gavage with hydrogen-water increased the survival rate and body weight of mice exposed to total abdominal irradiation (TAI); oral gavage with hydrogen-water was also associated with an improvement in GI tract function and the epithelial integrity of the small intestine. Mechanistically, microarray analysis revealed that hydrogen-water administration upregulated miR-1968-5p levels, thus resulting in parallel downregulation of MyD88 expression in the small intestine after TAI exposure. Additionally, high-throughput sequencing showed that hydrogen-water oral gavage resulted in retention of the TAI-shifted intestinal bacterial composition in mice. Collectively, our findings suggested that hydrogen-water might be used as a potential therapeutic to alleviate intestinal injury induced by radiotherapy for abdominal and pelvic cancer in preclinical settings. Nature Publishing Group 2018-01 2018-01-26 /pmc/articles/PMC5799803/ /pubmed/29371696 http://dx.doi.org/10.1038/emm.2017.246 Text en Copyright © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Xiao, Hui-wen
Li, Yuan
Luo, Dan
Dong, Jia-li
Zhou, Li-xin
Zhao, Shu-yi
Zheng, Qi-sheng
Wang, Hai-chao
Cui, Ming
Fan, Sai-jun
Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota
title Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota
title_full Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota
title_fullStr Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota
title_full_unstemmed Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota
title_short Hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via MyD88’s effects on the gut microbiota
title_sort hydrogen-water ameliorates radiation-induced gastrointestinal toxicity via myd88’s effects on the gut microbiota
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799803/
https://www.ncbi.nlm.nih.gov/pubmed/29371696
http://dx.doi.org/10.1038/emm.2017.246
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