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Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells

BACKGROUND: Oyaksungisan (OY) has been used as a traditional drug in east-Asian countries. However, its effect on inflammation still remains unknown. In this study, to provide insight into the biological effects of OY and OY fermented by Lactobacillus, we investigated their effects on lipopolysaccha...

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Autores principales: Oh, You-Chang, Cho, Won-Kyung, Oh, Jin Hui, Im, Ga Young, Jeong, Yun Hee, Yang, Min Cheol, Ma, Jin Yeul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323419/
https://www.ncbi.nlm.nih.gov/pubmed/22405334
http://dx.doi.org/10.1186/1472-6882-12-17
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author Oh, You-Chang
Cho, Won-Kyung
Oh, Jin Hui
Im, Ga Young
Jeong, Yun Hee
Yang, Min Cheol
Ma, Jin Yeul
author_facet Oh, You-Chang
Cho, Won-Kyung
Oh, Jin Hui
Im, Ga Young
Jeong, Yun Hee
Yang, Min Cheol
Ma, Jin Yeul
author_sort Oh, You-Chang
collection PubMed
description BACKGROUND: Oyaksungisan (OY) has been used as a traditional drug in east-Asian countries. However, its effect on inflammation still remains unknown. In this study, to provide insight into the biological effects of OY and OY fermented by Lactobacillus, we investigated their effects on lipopolysaccharide (LPS)-mediated inflammation in the RAW 264.7 murine macrophage cells. METHODS: The investigation was focused on whether OY and fermented OYs could inhibit the production of pro-inflammatory mediators such as nitric oxide (NO) and prostaglandin (PG) E(2 )as well as the expression of inducible nitric oxide synthase (iNOS), cyclooxygenase (COX)-2, tumor necrosis factor (TNF)-α, interleukin (IL)-6, nuclear factor (NF)-κB and mitogen-activated protein kinases (MAPKs) in LPS-stimulated RAW 264.7 cells. RESULTS: We found that OY inhibits a little LPS-induced NO, PGE(2), TNF-α and IL-6 productions as well as the expressions of iNOS and COX-2. Interestingly, the fermentation significantly increased its inhibitory effect on the expression of all pro-inflammatory mediators. Furthermore, the fermented OYs exhibited elevated inhibition on the translocation of NF-κB p65 through reduced IκBα degradation as well as the phosphorylations of extracellular signal-regulated kinase (ERK), p38 and c-Jun NH(2)-terminal kinase (JNK) MAPKs than untreated control or original OY. CONCLUSIONS: Finally, the fermentation by Lactobacillus potentiates the anti-inflammatory effect of OY by inhibiting NF-κB and MAPK activity in the macrophage cells.
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spelling pubmed-33234192012-04-11 Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells Oh, You-Chang Cho, Won-Kyung Oh, Jin Hui Im, Ga Young Jeong, Yun Hee Yang, Min Cheol Ma, Jin Yeul BMC Complement Altern Med Research Article BACKGROUND: Oyaksungisan (OY) has been used as a traditional drug in east-Asian countries. However, its effect on inflammation still remains unknown. In this study, to provide insight into the biological effects of OY and OY fermented by Lactobacillus, we investigated their effects on lipopolysaccharide (LPS)-mediated inflammation in the RAW 264.7 murine macrophage cells. METHODS: The investigation was focused on whether OY and fermented OYs could inhibit the production of pro-inflammatory mediators such as nitric oxide (NO) and prostaglandin (PG) E(2 )as well as the expression of inducible nitric oxide synthase (iNOS), cyclooxygenase (COX)-2, tumor necrosis factor (TNF)-α, interleukin (IL)-6, nuclear factor (NF)-κB and mitogen-activated protein kinases (MAPKs) in LPS-stimulated RAW 264.7 cells. RESULTS: We found that OY inhibits a little LPS-induced NO, PGE(2), TNF-α and IL-6 productions as well as the expressions of iNOS and COX-2. Interestingly, the fermentation significantly increased its inhibitory effect on the expression of all pro-inflammatory mediators. Furthermore, the fermented OYs exhibited elevated inhibition on the translocation of NF-κB p65 through reduced IκBα degradation as well as the phosphorylations of extracellular signal-regulated kinase (ERK), p38 and c-Jun NH(2)-terminal kinase (JNK) MAPKs than untreated control or original OY. CONCLUSIONS: Finally, the fermentation by Lactobacillus potentiates the anti-inflammatory effect of OY by inhibiting NF-κB and MAPK activity in the macrophage cells. BioMed Central 2012-03-12 /pmc/articles/PMC3323419/ /pubmed/22405334 http://dx.doi.org/10.1186/1472-6882-12-17 Text en Copyright ©2012 Oh et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Oh, You-Chang
Cho, Won-Kyung
Oh, Jin Hui
Im, Ga Young
Jeong, Yun Hee
Yang, Min Cheol
Ma, Jin Yeul
Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells
title Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells
title_full Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells
title_fullStr Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells
title_full_unstemmed Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells
title_short Fermentation by Lactobacillus enhances anti-inflammatory effect of Oyaksungisan on LPS-stimulated RAW 264.7 mouse macrophage cells
title_sort fermentation by lactobacillus enhances anti-inflammatory effect of oyaksungisan on lps-stimulated raw 264.7 mouse macrophage cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323419/
https://www.ncbi.nlm.nih.gov/pubmed/22405334
http://dx.doi.org/10.1186/1472-6882-12-17
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