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Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation
Abnormal microglia activation causes sever neuroinflammation, contributing to the development of many diseases, yet the mechanism remains incompletely unknown. In current study, we identified that Hydroxysafflor yellow A (HYA), a chalcone glycoside derived from Carthamus tinctorius L effectively att...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517830/ https://www.ncbi.nlm.nih.gov/pubmed/33041785 http://dx.doi.org/10.3389/fphar.2020.01315 |
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author | Qin, Xiude Chen, Juanjuan Zhang, Guowei Li, Chuanpeng Zhu, Jinqiang Xue, Hong Li, Jinfang Guan, Tianxiang Zheng, Haotao Liu, Yu Cai, Haobin |
author_facet | Qin, Xiude Chen, Juanjuan Zhang, Guowei Li, Chuanpeng Zhu, Jinqiang Xue, Hong Li, Jinfang Guan, Tianxiang Zheng, Haotao Liu, Yu Cai, Haobin |
author_sort | Qin, Xiude |
collection | PubMed |
description | Abnormal microglia activation causes sever neuroinflammation, contributing to the development of many diseases, yet the mechanism remains incompletely unknown. In current study, we identified that Hydroxysafflor yellow A (HYA), a chalcone glycoside derived from Carthamus tinctorius L effectively attenuates LPS-induced inflammation response in primary microglia via regulating the expression of inflammatory genes and remodeling the polarization of microglia. We also reported the effects of HYA on improving lipopolysaccharide (LPS)-stimulated mitochondrial dysfunction and oxidative stress for the first time. Interestingly, we found that HYA could serves as an effective SIRT1 activator. Deficiency of SIRT1 abrogates the protective effects of HYA against LPS-induced response. Overall, our data suggest HYA, a novel SIRT1 activator, could serve as an effective approach to treat LPS-induced neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-7517830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75178302020-10-09 Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation Qin, Xiude Chen, Juanjuan Zhang, Guowei Li, Chuanpeng Zhu, Jinqiang Xue, Hong Li, Jinfang Guan, Tianxiang Zheng, Haotao Liu, Yu Cai, Haobin Front Pharmacol Pharmacology Abnormal microglia activation causes sever neuroinflammation, contributing to the development of many diseases, yet the mechanism remains incompletely unknown. In current study, we identified that Hydroxysafflor yellow A (HYA), a chalcone glycoside derived from Carthamus tinctorius L effectively attenuates LPS-induced inflammation response in primary microglia via regulating the expression of inflammatory genes and remodeling the polarization of microglia. We also reported the effects of HYA on improving lipopolysaccharide (LPS)-stimulated mitochondrial dysfunction and oxidative stress for the first time. Interestingly, we found that HYA could serves as an effective SIRT1 activator. Deficiency of SIRT1 abrogates the protective effects of HYA against LPS-induced response. Overall, our data suggest HYA, a novel SIRT1 activator, could serve as an effective approach to treat LPS-induced neurodegenerative diseases. Frontiers Media S.A. 2020-09-11 /pmc/articles/PMC7517830/ /pubmed/33041785 http://dx.doi.org/10.3389/fphar.2020.01315 Text en Copyright © 2020 Qin, Chen, Zhang, Li, Zhu, Xue, Li, Guan, Zheng, Liu and Cai http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Qin, Xiude Chen, Juanjuan Zhang, Guowei Li, Chuanpeng Zhu, Jinqiang Xue, Hong Li, Jinfang Guan, Tianxiang Zheng, Haotao Liu, Yu Cai, Haobin Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation |
title | Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation |
title_full | Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation |
title_fullStr | Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation |
title_full_unstemmed | Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation |
title_short | Hydroxysafflor Yellow A Exerts Anti-Inflammatory Effects Mediated by SIRT1 in Lipopolysaccharide-Induced Microglia Activation |
title_sort | hydroxysafflor yellow a exerts anti-inflammatory effects mediated by sirt1 in lipopolysaccharide-induced microglia activation |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517830/ https://www.ncbi.nlm.nih.gov/pubmed/33041785 http://dx.doi.org/10.3389/fphar.2020.01315 |
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