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Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice

Indirubin, a traditional Chinese medicine formulation from the Muricidae family, has been reported to exhibit abroad anti-cancer and anti-inflammation activities and mediate nuclear factor-κB (NF-κB) signal. Thus, this study aimed to investigate the protective effects of indirubin on LPS-induced acu...

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Autores principales: Qi, Tianjie, Li, Haitao, Li, Shuai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5482685/
https://www.ncbi.nlm.nih.gov/pubmed/28525368
http://dx.doi.org/10.18632/oncotarget.17560
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author Qi, Tianjie
Li, Haitao
Li, Shuai
author_facet Qi, Tianjie
Li, Haitao
Li, Shuai
author_sort Qi, Tianjie
collection PubMed
description Indirubin, a traditional Chinese medicine formulation from the Muricidae family, has been reported to exhibit abroad anti-cancer and anti-inflammation activities and mediate nuclear factor-κB (NF-κB) signal. Thus, this study aimed to investigate the protective effects of indirubin on LPS-induced acute lung injury and the potential mechanism in mice. The results showed that LPS treatment caused oxidative stress and inflammation in mice. Indirubin alleviated LPS-caused oxidative stress and inflammation via reducing MDA abundance and IL-1β and TNF-α expressions in mice. Meanwhile, indirubin improved lung NO production and inhibited NF-κB activation caused by LPS exposure. In conclusion, indirubin alleviated LPS-induced acute lung injury via improving antioxidant and anti-inflammatory functions, which might be associated with the NO and NF-κB signals.
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spelling pubmed-54826852017-06-27 Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice Qi, Tianjie Li, Haitao Li, Shuai Oncotarget Research Paper Indirubin, a traditional Chinese medicine formulation from the Muricidae family, has been reported to exhibit abroad anti-cancer and anti-inflammation activities and mediate nuclear factor-κB (NF-κB) signal. Thus, this study aimed to investigate the protective effects of indirubin on LPS-induced acute lung injury and the potential mechanism in mice. The results showed that LPS treatment caused oxidative stress and inflammation in mice. Indirubin alleviated LPS-caused oxidative stress and inflammation via reducing MDA abundance and IL-1β and TNF-α expressions in mice. Meanwhile, indirubin improved lung NO production and inhibited NF-κB activation caused by LPS exposure. In conclusion, indirubin alleviated LPS-induced acute lung injury via improving antioxidant and anti-inflammatory functions, which might be associated with the NO and NF-κB signals. Impact Journals LLC 2017-05-02 /pmc/articles/PMC5482685/ /pubmed/28525368 http://dx.doi.org/10.18632/oncotarget.17560 Text en Copyright: © 2017 Qi et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Qi, Tianjie
Li, Haitao
Li, Shuai
Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
title Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
title_full Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
title_fullStr Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
title_full_unstemmed Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
title_short Indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
title_sort indirubin improves antioxidant and anti-inflammatory functions in lipopolysaccharide-challenged mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5482685/
https://www.ncbi.nlm.nih.gov/pubmed/28525368
http://dx.doi.org/10.18632/oncotarget.17560
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