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Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng
BACKGROUND: Korean ginseng is an ethnopharmacologically valuable herbal plant with various biological properties including anticancer, antiatherosclerosis, antidiabetic, and anti-inflammatory activities. Since there is currently no drug or therapeutic remedy derived from Korean ginseng, we developed...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452522/ https://www.ncbi.nlm.nih.gov/pubmed/26045689 http://dx.doi.org/10.1016/j.jgr.2014.10.004 |
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author | Baek, Kwang-Soo Hong, Yong Deog Kim, Yong Sung, Nak Yoon Yang, Sungjae Lee, Kyoung Min Park, Joo Yong Park, Jun Seong Rho, Ho Sik Shin, Song Seok Cho, Jae Youl |
author_facet | Baek, Kwang-Soo Hong, Yong Deog Kim, Yong Sung, Nak Yoon Yang, Sungjae Lee, Kyoung Min Park, Joo Yong Park, Jun Seong Rho, Ho Sik Shin, Song Seok Cho, Jae Youl |
author_sort | Baek, Kwang-Soo |
collection | PubMed |
description | BACKGROUND: Korean ginseng is an ethnopharmacologically valuable herbal plant with various biological properties including anticancer, antiatherosclerosis, antidiabetic, and anti-inflammatory activities. Since there is currently no drug or therapeutic remedy derived from Korean ginseng, we developed a ginsenoside-enriched fraction (AP-SF) for prevention of various inflammatory symptoms. METHODS: The anti-inflammatory efficacy of AP-SF was tested under in vitro inflammatory conditions including nitric oxide (NO) production and inflammatory gene expression. The molecular events of inflammatory responses were explored by immunoblot analysis. RESULTS: AP-SF led to a significant suppression of NO production compared with a conventional Korean ginseng saponin fraction, induced by both lipopolysaccharide and zymosan A. Interestingly, AP-SF strongly downregulated the mRNA levels of genes for inducible NO synthase, tumor necrosis factor-α, and cyclooxygenase) without affecting cell viability. In agreement with these observations, AP-SF blocked the nuclear translocation of c-Jun at 2 h and also reduced phosphorylation of p38, c-Jun N-terminal kinase, and TAK-1, all of which are important for c-Jun translocation. CONCLUSION: Our results suggest that AP-SF inhibits activation of c-Jun-dependent inflammatory events. Thus, AP-SF may be useful as a novel anti-inflammatory remedy. |
format | Online Article Text |
id | pubmed-4452522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-44525222015-06-04 Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng Baek, Kwang-Soo Hong, Yong Deog Kim, Yong Sung, Nak Yoon Yang, Sungjae Lee, Kyoung Min Park, Joo Yong Park, Jun Seong Rho, Ho Sik Shin, Song Seok Cho, Jae Youl J Ginseng Res Research Article BACKGROUND: Korean ginseng is an ethnopharmacologically valuable herbal plant with various biological properties including anticancer, antiatherosclerosis, antidiabetic, and anti-inflammatory activities. Since there is currently no drug or therapeutic remedy derived from Korean ginseng, we developed a ginsenoside-enriched fraction (AP-SF) for prevention of various inflammatory symptoms. METHODS: The anti-inflammatory efficacy of AP-SF was tested under in vitro inflammatory conditions including nitric oxide (NO) production and inflammatory gene expression. The molecular events of inflammatory responses were explored by immunoblot analysis. RESULTS: AP-SF led to a significant suppression of NO production compared with a conventional Korean ginseng saponin fraction, induced by both lipopolysaccharide and zymosan A. Interestingly, AP-SF strongly downregulated the mRNA levels of genes for inducible NO synthase, tumor necrosis factor-α, and cyclooxygenase) without affecting cell viability. In agreement with these observations, AP-SF blocked the nuclear translocation of c-Jun at 2 h and also reduced phosphorylation of p38, c-Jun N-terminal kinase, and TAK-1, all of which are important for c-Jun translocation. CONCLUSION: Our results suggest that AP-SF inhibits activation of c-Jun-dependent inflammatory events. Thus, AP-SF may be useful as a novel anti-inflammatory remedy. Elsevier 2015-04 2014-11-08 /pmc/articles/PMC4452522/ /pubmed/26045689 http://dx.doi.org/10.1016/j.jgr.2014.10.004 Text en Copyright © 2014, The Korean Society of Ginseng, Published by Elsevier. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Research Article Baek, Kwang-Soo Hong, Yong Deog Kim, Yong Sung, Nak Yoon Yang, Sungjae Lee, Kyoung Min Park, Joo Yong Park, Jun Seong Rho, Ho Sik Shin, Song Seok Cho, Jae Youl Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng |
title | Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng |
title_full | Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng |
title_fullStr | Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng |
title_full_unstemmed | Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng |
title_short | Anti-inflammatory activity of AP-SF, a ginsenoside-enriched fraction, from Korean ginseng |
title_sort | anti-inflammatory activity of ap-sf, a ginsenoside-enriched fraction, from korean ginseng |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452522/ https://www.ncbi.nlm.nih.gov/pubmed/26045689 http://dx.doi.org/10.1016/j.jgr.2014.10.004 |
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