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Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway
BACKGROUND: Korean ginseng (Panax ginseng C.A. Meyer) has been used as a botanical medicine throughout the history of Asian traditional Oriental medicine. Formulated red ginseng (one form of Korean ginseng) has been shown to have antioxidant and chemopreventive effects. METHODS: This study investiga...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635924/ https://www.ncbi.nlm.nih.gov/pubmed/23506615 http://dx.doi.org/10.1186/1472-6882-13-64 |
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author | Dong, Guang-Zhi Jang, Eun Jeong Kang, Seung Ho Cho, Il Je Park, Sun-Dong Kim, Sang Chan Kim, Young Woo |
author_facet | Dong, Guang-Zhi Jang, Eun Jeong Kang, Seung Ho Cho, Il Je Park, Sun-Dong Kim, Sang Chan Kim, Young Woo |
author_sort | Dong, Guang-Zhi |
collection | PubMed |
description | BACKGROUND: Korean ginseng (Panax ginseng C.A. Meyer) has been used as a botanical medicine throughout the history of Asian traditional Oriental medicine. Formulated red ginseng (one form of Korean ginseng) has been shown to have antioxidant and chemopreventive effects. METHODS: This study investigated the cytoprotective effects and mechanism of action of Korean red ginseng extract (RGE) against severe ROS production and mitochondrial impairment in a cytotoxic cell model induced by AA + iron. RESULTS: RGE protected HepG2 cells from AA + iron-induced cytotoxicity by preventing the induction of mitochondrial dysfunction and apoptosis. Moreover, AA + iron-induced production of ROS and reduction of cellular GSH content (an important cellular defense mechanism) were remarkably attenuated by treatment with RGE. At the molecular level, treatment with RGE activated LKB1-dependent AMP-activated protein kinase (AMPK), which in turn led to increased cell survival. The AMPK pathway was confirmed to play an essential role as the effects of RGE on mitochondrial membrane potential were reversed upon treatment with compound C, an AMPK inhibitor. CONCLUSIONS: Our results demonstrate that RGE has the ability to protect cells from AA + iron-induced ROS production and mitochondrial impairment through AMPK activation. |
format | Online Article Text |
id | pubmed-3635924 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36359242013-04-26 Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway Dong, Guang-Zhi Jang, Eun Jeong Kang, Seung Ho Cho, Il Je Park, Sun-Dong Kim, Sang Chan Kim, Young Woo BMC Complement Altern Med Research Article BACKGROUND: Korean ginseng (Panax ginseng C.A. Meyer) has been used as a botanical medicine throughout the history of Asian traditional Oriental medicine. Formulated red ginseng (one form of Korean ginseng) has been shown to have antioxidant and chemopreventive effects. METHODS: This study investigated the cytoprotective effects and mechanism of action of Korean red ginseng extract (RGE) against severe ROS production and mitochondrial impairment in a cytotoxic cell model induced by AA + iron. RESULTS: RGE protected HepG2 cells from AA + iron-induced cytotoxicity by preventing the induction of mitochondrial dysfunction and apoptosis. Moreover, AA + iron-induced production of ROS and reduction of cellular GSH content (an important cellular defense mechanism) were remarkably attenuated by treatment with RGE. At the molecular level, treatment with RGE activated LKB1-dependent AMP-activated protein kinase (AMPK), which in turn led to increased cell survival. The AMPK pathway was confirmed to play an essential role as the effects of RGE on mitochondrial membrane potential were reversed upon treatment with compound C, an AMPK inhibitor. CONCLUSIONS: Our results demonstrate that RGE has the ability to protect cells from AA + iron-induced ROS production and mitochondrial impairment through AMPK activation. BioMed Central 2013-03-18 /pmc/articles/PMC3635924/ /pubmed/23506615 http://dx.doi.org/10.1186/1472-6882-13-64 Text en Copyright © 2013 Dong 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 Dong, Guang-Zhi Jang, Eun Jeong Kang, Seung Ho Cho, Il Je Park, Sun-Dong Kim, Sang Chan Kim, Young Woo Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway |
title | Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway |
title_full | Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway |
title_fullStr | Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway |
title_full_unstemmed | Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway |
title_short | Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway |
title_sort | red ginseng abrogates oxidative stress via mitochondria protection mediated by lkb1-ampk pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635924/ https://www.ncbi.nlm.nih.gov/pubmed/23506615 http://dx.doi.org/10.1186/1472-6882-13-64 |
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