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A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells
The beneficial health promoting effects of ginseng from vitalizing the body to enhancing long life have been well explored very rapidly in the past few years. Up till now many ginsenosides have been discovered for their marvelous therapeutic effects. However during past three years, a novel ginseng...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633694/ https://www.ncbi.nlm.nih.gov/pubmed/26579204 http://dx.doi.org/10.1155/2015/624132 |
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author | Saba, Evelyn Jeon, Bo Ra Jeong, Da-Hye Lee, Kija Goo, Youn-Kyoung Kwak, Dongmi Kim, Suk Roh, Seong-Soo Kim, Sung Dae Nah, Seung-Yeol Rhee, Man Hee |
author_facet | Saba, Evelyn Jeon, Bo Ra Jeong, Da-Hye Lee, Kija Goo, Youn-Kyoung Kwak, Dongmi Kim, Suk Roh, Seong-Soo Kim, Sung Dae Nah, Seung-Yeol Rhee, Man Hee |
author_sort | Saba, Evelyn |
collection | PubMed |
description | The beneficial health promoting effects of ginseng from vitalizing the body to enhancing long life have been well explored very rapidly in the past few years. Up till now many ginsenosides have been discovered for their marvelous therapeutic effects. However during past three years, a novel ginseng compound has been discovered, called gintonin, that differs from other ginsenosides on the basis of its signal transduction and chemical nature. Gintonin has been widely studied for its anti-Alzheimer's disease activities and other neuropathies. However, its anti-inflammatory activity remained unexplored. In our study we have reported for the first time the anti-inflammatory activity of gintonin on RAW 264.7 cells. We found that gintonin potently suppresses the nitric oxide production without any cytotoxicity at given doses and also efficiently suppressed the levels of proinflammatory cytokines. Moreover, it mediaes its signal transduction via MAPK and NF-κB pathways and revives the levels of mir-34a and mir-93. These findings are valuable for the anti-inflammatory effects of this new compound with particular reference to microRNA involvement in the ginseng family. |
format | Online Article Text |
id | pubmed-4633694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-46336942015-11-17 A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells Saba, Evelyn Jeon, Bo Ra Jeong, Da-Hye Lee, Kija Goo, Youn-Kyoung Kwak, Dongmi Kim, Suk Roh, Seong-Soo Kim, Sung Dae Nah, Seung-Yeol Rhee, Man Hee Evid Based Complement Alternat Med Research Article The beneficial health promoting effects of ginseng from vitalizing the body to enhancing long life have been well explored very rapidly in the past few years. Up till now many ginsenosides have been discovered for their marvelous therapeutic effects. However during past three years, a novel ginseng compound has been discovered, called gintonin, that differs from other ginsenosides on the basis of its signal transduction and chemical nature. Gintonin has been widely studied for its anti-Alzheimer's disease activities and other neuropathies. However, its anti-inflammatory activity remained unexplored. In our study we have reported for the first time the anti-inflammatory activity of gintonin on RAW 264.7 cells. We found that gintonin potently suppresses the nitric oxide production without any cytotoxicity at given doses and also efficiently suppressed the levels of proinflammatory cytokines. Moreover, it mediaes its signal transduction via MAPK and NF-κB pathways and revives the levels of mir-34a and mir-93. These findings are valuable for the anti-inflammatory effects of this new compound with particular reference to microRNA involvement in the ginseng family. Hindawi Publishing Corporation 2015 2015-10-12 /pmc/articles/PMC4633694/ /pubmed/26579204 http://dx.doi.org/10.1155/2015/624132 Text en Copyright © 2015 Evelyn Saba et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Saba, Evelyn Jeon, Bo Ra Jeong, Da-Hye Lee, Kija Goo, Youn-Kyoung Kwak, Dongmi Kim, Suk Roh, Seong-Soo Kim, Sung Dae Nah, Seung-Yeol Rhee, Man Hee A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells |
title | A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells |
title_full | A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells |
title_fullStr | A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells |
title_full_unstemmed | A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells |
title_short | A Novel Korean Red Ginseng Compound Gintonin Inhibited Inflammation by MAPK and NF-κB Pathways and Recovered the Levels of mir-34a and mir-93 in RAW 264.7 Cells |
title_sort | novel korean red ginseng compound gintonin inhibited inflammation by mapk and nf-κb pathways and recovered the levels of mir-34a and mir-93 in raw 264.7 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633694/ https://www.ncbi.nlm.nih.gov/pubmed/26579204 http://dx.doi.org/10.1155/2015/624132 |
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