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Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice
PURPOSE: The main objective is to investigate the protective effect of camel milk (CM) on radiation-induced intestinal injury. METHODS: The C57BL/6 J mice in 2 experiments were assigned into control group (Con), irradiation group (IR), and CM+irradiation group (CM+IR). After receiving the CM via gav...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020251/ https://www.ncbi.nlm.nih.gov/pubmed/33867894 http://dx.doi.org/10.1177/15593258211003798 |
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author | Chen, Yu-Zhong Li, Chao Gu, Jia Lv, Si-chen Song, Jia-ying Tang, Zhi-bing Duan, Guang-Xin Qin, Li-Qiang Zhao, Lin Xu, Jia-Ying |
author_facet | Chen, Yu-Zhong Li, Chao Gu, Jia Lv, Si-chen Song, Jia-ying Tang, Zhi-bing Duan, Guang-Xin Qin, Li-Qiang Zhao, Lin Xu, Jia-Ying |
author_sort | Chen, Yu-Zhong |
collection | PubMed |
description | PURPOSE: The main objective is to investigate the protective effect of camel milk (CM) on radiation-induced intestinal injury. METHODS: The C57BL/6 J mice in 2 experiments were assigned into control group (Con), irradiation group (IR), and CM+irradiation group (CM+IR). After receiving the CM via gavage for 14 days, the mice in the first experiment were exposed to 6 Gy X-ray whole body irradiation, and survival rate was compared among the groups. Mice in the second experiment were exposed to 4 Gy irradiation and sacrificed at day 7. The small intestines were collected to examine the histopathological changes and to determine the anti-oxidative index and HMGB1/TLR4 inflammatory pathway. Fasting blood was used to measure serum pro-inflammatory factors. RESULTS: Compared with the IR group, the survival time was prolonged, and survival rate was increased in the CM+IR group. CM increased levels of SOD and GSH and decreased MDA in the jejunum. Furthermore, intestinal protein expression of HMGB1/TLR4 pathway (TLR4, NF-κB, and HMGB1) was up-regulated by CM intervention. CM decreased the serum levels of TNF-α and IL-1β and increased IL-10 level. CONCLUSIONS: CM extended the survival time and had a protective effect against radiation-induced jejunum injury by regulation of antioxidant capacity and HMGB1/TLR4/NF-κB/MyD88 inflammatory signaling pathway. |
format | Online Article Text |
id | pubmed-8020251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-80202512021-04-16 Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice Chen, Yu-Zhong Li, Chao Gu, Jia Lv, Si-chen Song, Jia-ying Tang, Zhi-bing Duan, Guang-Xin Qin, Li-Qiang Zhao, Lin Xu, Jia-Ying Dose Response Original Article PURPOSE: The main objective is to investigate the protective effect of camel milk (CM) on radiation-induced intestinal injury. METHODS: The C57BL/6 J mice in 2 experiments were assigned into control group (Con), irradiation group (IR), and CM+irradiation group (CM+IR). After receiving the CM via gavage for 14 days, the mice in the first experiment were exposed to 6 Gy X-ray whole body irradiation, and survival rate was compared among the groups. Mice in the second experiment were exposed to 4 Gy irradiation and sacrificed at day 7. The small intestines were collected to examine the histopathological changes and to determine the anti-oxidative index and HMGB1/TLR4 inflammatory pathway. Fasting blood was used to measure serum pro-inflammatory factors. RESULTS: Compared with the IR group, the survival time was prolonged, and survival rate was increased in the CM+IR group. CM increased levels of SOD and GSH and decreased MDA in the jejunum. Furthermore, intestinal protein expression of HMGB1/TLR4 pathway (TLR4, NF-κB, and HMGB1) was up-regulated by CM intervention. CM decreased the serum levels of TNF-α and IL-1β and increased IL-10 level. CONCLUSIONS: CM extended the survival time and had a protective effect against radiation-induced jejunum injury by regulation of antioxidant capacity and HMGB1/TLR4/NF-κB/MyD88 inflammatory signaling pathway. SAGE Publications 2021-03-30 /pmc/articles/PMC8020251/ /pubmed/33867894 http://dx.doi.org/10.1177/15593258211003798 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Chen, Yu-Zhong Li, Chao Gu, Jia Lv, Si-chen Song, Jia-ying Tang, Zhi-bing Duan, Guang-Xin Qin, Li-Qiang Zhao, Lin Xu, Jia-Ying Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice |
title | Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice |
title_full | Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice |
title_fullStr | Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice |
title_full_unstemmed | Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice |
title_short | Anti-Oxidative and Immuno-Protective Effect of Camel Milk on Radiation-Induced Intestinal Injury in C57BL/6 J Mice |
title_sort | anti-oxidative and immuno-protective effect of camel milk on radiation-induced intestinal injury in c57bl/6 j mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020251/ https://www.ncbi.nlm.nih.gov/pubmed/33867894 http://dx.doi.org/10.1177/15593258211003798 |
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