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7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling

Macrophages play a critical role in a variety of inflammatory diseases. Activation of Keap1/Nrf2/HO-1 signaling results in inactivation of macrophages and amelioration of inflammatory and autoimmune conditions. Hence, discovery for the activators of Keap1/Nrf2/HO-1 signaling has become a promising s...

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Autores principales: Chen, Jian-Yu, Zhu, Guo-Yuan, Su, Xiao-Hui, Wang, Rui, Liu, Juan, Liao, Kangsheng, Ren, Rutong, Li, Ting, Liu, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589640/
https://www.ncbi.nlm.nih.gov/pubmed/28903401
http://dx.doi.org/10.18632/oncotarget.19017
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author Chen, Jian-Yu
Zhu, Guo-Yuan
Su, Xiao-Hui
Wang, Rui
Liu, Juan
Liao, Kangsheng
Ren, Rutong
Li, Ting
Liu, Liang
author_facet Chen, Jian-Yu
Zhu, Guo-Yuan
Su, Xiao-Hui
Wang, Rui
Liu, Juan
Liao, Kangsheng
Ren, Rutong
Li, Ting
Liu, Liang
author_sort Chen, Jian-Yu
collection PubMed
description Macrophages play a critical role in a variety of inflammatory diseases. Activation of Keap1/Nrf2/HO-1 signaling results in inactivation of macrophages and amelioration of inflammatory and autoimmune conditions. Hence, discovery for the activators of Keap1/Nrf2/HO-1 signaling has become a promising strategy for treatment inflammatory diseases. In the current study, the anti-inflammatory potential of 7-deacetylgedunin (7-DGD), a limonin chemical isolated from the fruits of Toona sinensis (A. Juss.) Roem, was intensively examined in vivo and in vitro for the first time. Results showed that 7-DGD alleviated mice mortality induced by LPS. Mechanistic study showed that 7-DGD suppressed macrophage proliferation via induction of cell arrest at the G0/G1 phase. Furthermore, 7-DGD inhibited iNOS expression, which is correlated with the increases of NQO1, HO-1 and UGT1A1 mRNA expression as well as HO-1 protein expression level in the cells. More importantly, 7-DGD markedly decreased Keap1 expression, promoted p62 expression, and facilitated Nrf2 translocation and localization in the nucleus of macrophages, and in turn up-regulates these anti-oxidant enzymes expression, eventually mediated anti-inflammatory effect. Collectively, 7-DGD suppresses inflammation in vivo and in vitro, indicating that the compound is valuable for further investigation as an anti-inflammatory agent in future.
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spelling pubmed-55896402017-09-12 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling Chen, Jian-Yu Zhu, Guo-Yuan Su, Xiao-Hui Wang, Rui Liu, Juan Liao, Kangsheng Ren, Rutong Li, Ting Liu, Liang Oncotarget Research Paper Macrophages play a critical role in a variety of inflammatory diseases. Activation of Keap1/Nrf2/HO-1 signaling results in inactivation of macrophages and amelioration of inflammatory and autoimmune conditions. Hence, discovery for the activators of Keap1/Nrf2/HO-1 signaling has become a promising strategy for treatment inflammatory diseases. In the current study, the anti-inflammatory potential of 7-deacetylgedunin (7-DGD), a limonin chemical isolated from the fruits of Toona sinensis (A. Juss.) Roem, was intensively examined in vivo and in vitro for the first time. Results showed that 7-DGD alleviated mice mortality induced by LPS. Mechanistic study showed that 7-DGD suppressed macrophage proliferation via induction of cell arrest at the G0/G1 phase. Furthermore, 7-DGD inhibited iNOS expression, which is correlated with the increases of NQO1, HO-1 and UGT1A1 mRNA expression as well as HO-1 protein expression level in the cells. More importantly, 7-DGD markedly decreased Keap1 expression, promoted p62 expression, and facilitated Nrf2 translocation and localization in the nucleus of macrophages, and in turn up-regulates these anti-oxidant enzymes expression, eventually mediated anti-inflammatory effect. Collectively, 7-DGD suppresses inflammation in vivo and in vitro, indicating that the compound is valuable for further investigation as an anti-inflammatory agent in future. Impact Journals LLC 2017-07-05 /pmc/articles/PMC5589640/ /pubmed/28903401 http://dx.doi.org/10.18632/oncotarget.19017 Text en Copyright: © 2017 Chen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Jian-Yu
Zhu, Guo-Yuan
Su, Xiao-Hui
Wang, Rui
Liu, Juan
Liao, Kangsheng
Ren, Rutong
Li, Ting
Liu, Liang
7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling
title 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling
title_full 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling
title_fullStr 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling
title_full_unstemmed 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling
title_short 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling
title_sort 7-deacetylgedunin suppresses inflammatory responses through activation of keap1/nrf2/ho-1 signaling
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589640/
https://www.ncbi.nlm.nih.gov/pubmed/28903401
http://dx.doi.org/10.18632/oncotarget.19017
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