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Antibiotic Alleviates Radiation-Induced Intestinal Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting Fibrosis
[Image: see text] Radiation-induced intestinal injury is a common complication of abdominal radiation therapy. However, the pathological features of radiation-induced intestinal injury and its therapeutic regimen are not very clear. The aim of this study was to investigate the effects of antibiotic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033964/ https://www.ncbi.nlm.nih.gov/pubmed/32095719 http://dx.doi.org/10.1021/acsomega.9b03906 |
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author | Zhao, Zhenguo Cheng, Wei Qu, Wei Shao, Guoyi Liu, Shuanghai |
author_facet | Zhao, Zhenguo Cheng, Wei Qu, Wei Shao, Guoyi Liu, Shuanghai |
author_sort | Zhao, Zhenguo |
collection | PubMed |
description | [Image: see text] Radiation-induced intestinal injury is a common complication of abdominal radiation therapy. However, the pathological features of radiation-induced intestinal injury and its therapeutic regimen are not very clear. The aim of this study was to investigate the effects of antibiotic pretreatment on radiation-induced intestinal injury. Abdominal radiation disrupted the intestinal microbiota balance and significantly reduced bacterial diversity in mice. Antibiotic cocktail (Abx) pretreatment effectively removed the intestinal microbiota of mice, and metronidazole also reduced the diversity of intestinal bacteria to some extent. Two antibiotic pretreatment regimens improved the reconstitution ability of the gut microbiota in mice after radiation. Further experiments showed that Abx pretreatment effectively reduced the content of lipopolysaccharide (LPS) and inhibited the TLR4/MyD88/NF-κB signaling pathway in the ileum. In addition, Abx pretreatment regulated macrophage cell polarization in the ileum, downregulated TGF-β1, phosphorylated Smad-3 and α-SMA protein levels, and upregulated E-cadherin protein expression. Eventually, Abx pretreatment significantly improved the survival rate and attenuated intestinal injury of mice after radiation by reducing inflammation and preventing intestinal fibrosis. These results revealed that antibiotic pretreatment can effectively alleviate gut microbiota turbulence and intestinal damage caused by abdominal radiation in mice. Collectively, these findings add to our understanding of the pathogenesis of radiation enteritis. |
format | Online Article Text |
id | pubmed-7033964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70339642020-02-24 Antibiotic Alleviates Radiation-Induced Intestinal Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting Fibrosis Zhao, Zhenguo Cheng, Wei Qu, Wei Shao, Guoyi Liu, Shuanghai ACS Omega [Image: see text] Radiation-induced intestinal injury is a common complication of abdominal radiation therapy. However, the pathological features of radiation-induced intestinal injury and its therapeutic regimen are not very clear. The aim of this study was to investigate the effects of antibiotic pretreatment on radiation-induced intestinal injury. Abdominal radiation disrupted the intestinal microbiota balance and significantly reduced bacterial diversity in mice. Antibiotic cocktail (Abx) pretreatment effectively removed the intestinal microbiota of mice, and metronidazole also reduced the diversity of intestinal bacteria to some extent. Two antibiotic pretreatment regimens improved the reconstitution ability of the gut microbiota in mice after radiation. Further experiments showed that Abx pretreatment effectively reduced the content of lipopolysaccharide (LPS) and inhibited the TLR4/MyD88/NF-κB signaling pathway in the ileum. In addition, Abx pretreatment regulated macrophage cell polarization in the ileum, downregulated TGF-β1, phosphorylated Smad-3 and α-SMA protein levels, and upregulated E-cadherin protein expression. Eventually, Abx pretreatment significantly improved the survival rate and attenuated intestinal injury of mice after radiation by reducing inflammation and preventing intestinal fibrosis. These results revealed that antibiotic pretreatment can effectively alleviate gut microbiota turbulence and intestinal damage caused by abdominal radiation in mice. Collectively, these findings add to our understanding of the pathogenesis of radiation enteritis. American Chemical Society 2020-02-05 /pmc/articles/PMC7033964/ /pubmed/32095719 http://dx.doi.org/10.1021/acsomega.9b03906 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Zhao, Zhenguo Cheng, Wei Qu, Wei Shao, Guoyi Liu, Shuanghai Antibiotic Alleviates Radiation-Induced Intestinal Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting Fibrosis |
title | Antibiotic Alleviates Radiation-Induced Intestinal
Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting
Fibrosis |
title_full | Antibiotic Alleviates Radiation-Induced Intestinal
Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting
Fibrosis |
title_fullStr | Antibiotic Alleviates Radiation-Induced Intestinal
Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting
Fibrosis |
title_full_unstemmed | Antibiotic Alleviates Radiation-Induced Intestinal
Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting
Fibrosis |
title_short | Antibiotic Alleviates Radiation-Induced Intestinal
Injury by Remodeling Microbiota, Reducing Inflammation, and Inhibiting
Fibrosis |
title_sort | antibiotic alleviates radiation-induced intestinal
injury by remodeling microbiota, reducing inflammation, and inhibiting
fibrosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033964/ https://www.ncbi.nlm.nih.gov/pubmed/32095719 http://dx.doi.org/10.1021/acsomega.9b03906 |
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