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Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage
Ionizing radiation (IR)‐induced intestinal damage is the major and common injury of patients receiving radiotherapy. Urolithin A (UroA) is a metabolite of the intestinal flora of ellagitannin, a compound found in fruits and nuts such as pomegranates, strawberries and walnuts. UroA shows the immunomo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572803/ https://www.ncbi.nlm.nih.gov/pubmed/34595829 http://dx.doi.org/10.1111/jcmm.16951 |
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author | Zhang, Yuanyang Dong, Yinping Lu, Ping Wang, Xinyue Li, Wenxuan Dong, Hui Fan, Saijun Li, Deguan |
author_facet | Zhang, Yuanyang Dong, Yinping Lu, Ping Wang, Xinyue Li, Wenxuan Dong, Hui Fan, Saijun Li, Deguan |
author_sort | Zhang, Yuanyang |
collection | PubMed |
description | Ionizing radiation (IR)‐induced intestinal damage is the major and common injury of patients receiving radiotherapy. Urolithin A (UroA) is a metabolite of the intestinal flora of ellagitannin, a compound found in fruits and nuts such as pomegranates, strawberries and walnuts. UroA shows the immunomodulatory and anti‐inflammatory capacity in various metabolic diseases. To evaluate the radioprotective effects, UroA(0.4, 2 and 10 mg/kg) were intraperitoneally injected to C57BL/6 male mice 48, 24, 1 h prior to and 24 h after 9.0Gy TBI. The results showed that UroA markedly upregulated the survival of irradiated mice, especially at concentration of 2 mg/kg. UroA improved the intestine morphology architecture and the regeneration ability of enterocytes in irradiated mice. Then, UroA significantly decreased the apoptosis of enterocytes induced by radiation. Additionally, 16S rRNA sequencing analysis showed the effect of UroA is associated with the recovery of the IR‐induced intestinal microbacteria profile changes in mice. Therefore, our results determinated UroA could be developed as a potential candidate for radiomitigators in radiotherapy and accidental nuclear exposure. And the beneficial functions of UroA might be associated with the inhibition of p53‐mediated apoptosis and remodelling of the gut microbes. |
format | Online Article Text |
id | pubmed-8572803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85728032021-11-10 Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage Zhang, Yuanyang Dong, Yinping Lu, Ping Wang, Xinyue Li, Wenxuan Dong, Hui Fan, Saijun Li, Deguan J Cell Mol Med Short Communications Ionizing radiation (IR)‐induced intestinal damage is the major and common injury of patients receiving radiotherapy. Urolithin A (UroA) is a metabolite of the intestinal flora of ellagitannin, a compound found in fruits and nuts such as pomegranates, strawberries and walnuts. UroA shows the immunomodulatory and anti‐inflammatory capacity in various metabolic diseases. To evaluate the radioprotective effects, UroA(0.4, 2 and 10 mg/kg) were intraperitoneally injected to C57BL/6 male mice 48, 24, 1 h prior to and 24 h after 9.0Gy TBI. The results showed that UroA markedly upregulated the survival of irradiated mice, especially at concentration of 2 mg/kg. UroA improved the intestine morphology architecture and the regeneration ability of enterocytes in irradiated mice. Then, UroA significantly decreased the apoptosis of enterocytes induced by radiation. Additionally, 16S rRNA sequencing analysis showed the effect of UroA is associated with the recovery of the IR‐induced intestinal microbacteria profile changes in mice. Therefore, our results determinated UroA could be developed as a potential candidate for radiomitigators in radiotherapy and accidental nuclear exposure. And the beneficial functions of UroA might be associated with the inhibition of p53‐mediated apoptosis and remodelling of the gut microbes. John Wiley and Sons Inc. 2021-10-01 2021-11 /pmc/articles/PMC8572803/ /pubmed/34595829 http://dx.doi.org/10.1111/jcmm.16951 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communications Zhang, Yuanyang Dong, Yinping Lu, Ping Wang, Xinyue Li, Wenxuan Dong, Hui Fan, Saijun Li, Deguan Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage |
title | Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage |
title_full | Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage |
title_fullStr | Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage |
title_full_unstemmed | Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage |
title_short | Gut metabolite Urolithin A mitigates ionizing radiation‐induced intestinal damage |
title_sort | gut metabolite urolithin a mitigates ionizing radiation‐induced intestinal damage |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572803/ https://www.ncbi.nlm.nih.gov/pubmed/34595829 http://dx.doi.org/10.1111/jcmm.16951 |
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