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Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation

Launaea sarmentosa has been extensively used as a nutrient herb in traditional Vietnamese remedies for the treatment of various diseases, especially inflammatory diseases. However, no detailed research has been conducted examining the molecular mechanisms involved in the suppression of inflammatory...

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Autores principales: Nguyen, Thanh Q. C., Binh, Tran Duy, Kusunoki, Ryo, Pham, Tuan L. A., Nguyen, Yen D. H., Nguyen, Trong Tuan, Kanaori, Kenji, Kamei, Kaeko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551017/
https://www.ncbi.nlm.nih.gov/pubmed/32858855
http://dx.doi.org/10.3390/nu12092586
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author Nguyen, Thanh Q. C.
Binh, Tran Duy
Kusunoki, Ryo
Pham, Tuan L. A.
Nguyen, Yen D. H.
Nguyen, Trong Tuan
Kanaori, Kenji
Kamei, Kaeko
author_facet Nguyen, Thanh Q. C.
Binh, Tran Duy
Kusunoki, Ryo
Pham, Tuan L. A.
Nguyen, Yen D. H.
Nguyen, Trong Tuan
Kanaori, Kenji
Kamei, Kaeko
author_sort Nguyen, Thanh Q. C.
collection PubMed
description Launaea sarmentosa has been extensively used as a nutrient herb in traditional Vietnamese remedies for the treatment of various diseases, especially inflammatory diseases. However, no detailed research has been conducted examining the molecular mechanisms involved in the suppression of inflammatory response. Here, we studied the effects of L. sarmentosa methanol extract on lipopolysaccharide (LPS)-induced inflammation using RAW 264.7 macrophages. The extract demonstrated potent antioxidant activity owing to the presence of polyphenolic and flavonoid components. Pretreatment with the extract inhibited LPS-mediated secretion of nitric oxide, reactive oxygen species, and tumor necrosis factor-α as well as the expression of inflammatory cytokines. Furthermore, the activation of the nuclear factor-kappa B pathway and phosphoinositide-3-kinase/protein kinase B pathways was blocked by the extract by inhibiting Akt phosphorylation. Additionally, the mitogen-activated protein kinase pathway was suppressed, and endoplasmic reticulum stress was attenuated. Furthermore, the extract promoted the activity of nuclear factor erythroid-2-related factor 2 resulting in the up-regulation of heme oxygenase-1 pathway, leading to the suppression of oxidative stress and inflammatory response. Taken together, the results indicate that L. sarmentosa exhibits anti-inflammatory effects, and hence, can be further developed as a novel drug for the treatment of diseases associated with excessive inflammation.
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spelling pubmed-75510172020-10-16 Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation Nguyen, Thanh Q. C. Binh, Tran Duy Kusunoki, Ryo Pham, Tuan L. A. Nguyen, Yen D. H. Nguyen, Trong Tuan Kanaori, Kenji Kamei, Kaeko Nutrients Article Launaea sarmentosa has been extensively used as a nutrient herb in traditional Vietnamese remedies for the treatment of various diseases, especially inflammatory diseases. However, no detailed research has been conducted examining the molecular mechanisms involved in the suppression of inflammatory response. Here, we studied the effects of L. sarmentosa methanol extract on lipopolysaccharide (LPS)-induced inflammation using RAW 264.7 macrophages. The extract demonstrated potent antioxidant activity owing to the presence of polyphenolic and flavonoid components. Pretreatment with the extract inhibited LPS-mediated secretion of nitric oxide, reactive oxygen species, and tumor necrosis factor-α as well as the expression of inflammatory cytokines. Furthermore, the activation of the nuclear factor-kappa B pathway and phosphoinositide-3-kinase/protein kinase B pathways was blocked by the extract by inhibiting Akt phosphorylation. Additionally, the mitogen-activated protein kinase pathway was suppressed, and endoplasmic reticulum stress was attenuated. Furthermore, the extract promoted the activity of nuclear factor erythroid-2-related factor 2 resulting in the up-regulation of heme oxygenase-1 pathway, leading to the suppression of oxidative stress and inflammatory response. Taken together, the results indicate that L. sarmentosa exhibits anti-inflammatory effects, and hence, can be further developed as a novel drug for the treatment of diseases associated with excessive inflammation. MDPI 2020-08-26 /pmc/articles/PMC7551017/ /pubmed/32858855 http://dx.doi.org/10.3390/nu12092586 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nguyen, Thanh Q. C.
Binh, Tran Duy
Kusunoki, Ryo
Pham, Tuan L. A.
Nguyen, Yen D. H.
Nguyen, Trong Tuan
Kanaori, Kenji
Kamei, Kaeko
Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation
title Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation
title_full Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation
title_fullStr Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation
title_full_unstemmed Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation
title_short Effects of Launaea sarmentosa Extract on Lipopolysaccharide-Induced Inflammation via Suppression of NF-κB/MAPK Signaling and Nrf2 Activation
title_sort effects of launaea sarmentosa extract on lipopolysaccharide-induced inflammation via suppression of nf-κb/mapk signaling and nrf2 activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551017/
https://www.ncbi.nlm.nih.gov/pubmed/32858855
http://dx.doi.org/10.3390/nu12092586
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