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Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue
Adipose tissue inflammation plays an important role in the regulation of glucose and lipids metabolism. It is unknown whether Ursolic acid (UA) could regulate adipose tissue inflammation, though it can regulate inflammation in many other tissues. In this study, 3T3-L1 adipocytes, DIO mice and lean m...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714451/ https://www.ncbi.nlm.nih.gov/pubmed/32876525 http://dx.doi.org/10.1080/21623945.2020.1814545 |
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author | Feng, Bin Zhu, Yingguo Yan, Lijun Yan, Hui Huang, Xiaohua Jiang, Dandan Li, Zhen Hua, Lun Zhuo, Yong Fang, Zhengfeng Che, Lianqiang Lin, Yan Xu, Shengyu Huang, Chao Zou, Yuanfeng Li, Lixia Wu, De |
author_facet | Feng, Bin Zhu, Yingguo Yan, Lijun Yan, Hui Huang, Xiaohua Jiang, Dandan Li, Zhen Hua, Lun Zhuo, Yong Fang, Zhengfeng Che, Lianqiang Lin, Yan Xu, Shengyu Huang, Chao Zou, Yuanfeng Li, Lixia Wu, De |
author_sort | Feng, Bin |
collection | PubMed |
description | Adipose tissue inflammation plays an important role in the regulation of glucose and lipids metabolism. It is unknown whether Ursolic acid (UA) could regulate adipose tissue inflammation, though it can regulate inflammation in many other tissues. In this study, 3T3-L1 adipocytes, DIO mice and lean mice were treated with UA or vehicle. Gene expression of inflammatory factors, chemokines and immune markers in adipocytes and adipose tissue, cytokines in cell culture medium and serum, and inflammation regulatory pathways in adipocytes were detected. Results showed that UA increased the expression of interleukins and chemokines, but not TNFα, in both adipocytes and adipose tissue. IL6 and MCP1 levels in the cell culture medium and mouse serum were induced by UA treatment. Cd14 expression level and number of CD14+ monocytes were higher in UA treated adipose tissue than those in the control group. Glucose tolerance test was impaired by UA treatment in DIO mice. Mechanistically, UA induced the expression of Tlr4 and the phosphorylation levels of ERK and NFκB in adipocytes. In conclusion, our study indicated that short-term UA administration could induce CD14+ monocytes infiltration by increasing the production of interleukins and chemokines in mouse adipose tissue, which might further impair glucose tolerance test. |
format | Online Article Text |
id | pubmed-7714451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-77144512020-12-08 Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue Feng, Bin Zhu, Yingguo Yan, Lijun Yan, Hui Huang, Xiaohua Jiang, Dandan Li, Zhen Hua, Lun Zhuo, Yong Fang, Zhengfeng Che, Lianqiang Lin, Yan Xu, Shengyu Huang, Chao Zou, Yuanfeng Li, Lixia Wu, De Adipocyte Research Article Adipose tissue inflammation plays an important role in the regulation of glucose and lipids metabolism. It is unknown whether Ursolic acid (UA) could regulate adipose tissue inflammation, though it can regulate inflammation in many other tissues. In this study, 3T3-L1 adipocytes, DIO mice and lean mice were treated with UA or vehicle. Gene expression of inflammatory factors, chemokines and immune markers in adipocytes and adipose tissue, cytokines in cell culture medium and serum, and inflammation regulatory pathways in adipocytes were detected. Results showed that UA increased the expression of interleukins and chemokines, but not TNFα, in both adipocytes and adipose tissue. IL6 and MCP1 levels in the cell culture medium and mouse serum were induced by UA treatment. Cd14 expression level and number of CD14+ monocytes were higher in UA treated adipose tissue than those in the control group. Glucose tolerance test was impaired by UA treatment in DIO mice. Mechanistically, UA induced the expression of Tlr4 and the phosphorylation levels of ERK and NFκB in adipocytes. In conclusion, our study indicated that short-term UA administration could induce CD14+ monocytes infiltration by increasing the production of interleukins and chemokines in mouse adipose tissue, which might further impair glucose tolerance test. Taylor & Francis 2020-09-02 /pmc/articles/PMC7714451/ /pubmed/32876525 http://dx.doi.org/10.1080/21623945.2020.1814545 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Feng, Bin Zhu, Yingguo Yan, Lijun Yan, Hui Huang, Xiaohua Jiang, Dandan Li, Zhen Hua, Lun Zhuo, Yong Fang, Zhengfeng Che, Lianqiang Lin, Yan Xu, Shengyu Huang, Chao Zou, Yuanfeng Li, Lixia Wu, De Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue |
title | Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue |
title_full | Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue |
title_fullStr | Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue |
title_full_unstemmed | Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue |
title_short | Ursolic acid induces the production of IL6 and chemokines in both adipocytes and adipose tissue |
title_sort | ursolic acid induces the production of il6 and chemokines in both adipocytes and adipose tissue |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714451/ https://www.ncbi.nlm.nih.gov/pubmed/32876525 http://dx.doi.org/10.1080/21623945.2020.1814545 |
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