Red ginseng abrogates oxidative stress via mitochondria protection mediated by LKB1-AMPK pathway

被引:51
作者
Dong, Guang-Zhi [1 ]
Jang, Eun Jeong [1 ]
Kang, Seung Ho [2 ]
Cho, Il Je [1 ]
Park, Sun-Dong [1 ]
Kim, Sang Chan [1 ]
Kim, Young Woo [1 ]
机构
[1] Daegu Haany Univ, Coll Oriental Med, Med Res Ctr Globalizat Herbal Formulat, Taegu 706828, South Korea
[2] Sunlin Univ, Pohang 791712, Kyungsangbuk Do, South Korea
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2013年 / 13卷
基金
新加坡国家研究基金会;
关键词
Arachidonic acid; Red ginseng; AMPK; Oxidative stress; Mitochondria; ACTIVATED PROTEIN-KINASE; ARACHIDONIC-ACID; ENDOTHELIAL-CELLS; IRON HOMEOSTASIS; PANAX-GINSENG; INHIBITION; APOPTOSIS; DYSFUNCTION; TRANSPORT; OLTIPRAZ;
D O I
10.1186/1472-6882-13-64
中图分类号
R [医药、卫生];
学科分类号
100218 [急诊医学];
摘要
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.
引用
收藏
页数:9
相关论文
共 36 条
[1]
Ginseng pharmacology - Multiple constituents and multiple actions [J].
Attele, AS ;
Wu, JA ;
Yuan, CS .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (11) :1685-1693
[2]
Oxidative stress and arachidonic acid mobilization [J].
Balboa, Maria A. ;
Balsinde, Jesas .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (04) :385-391
[3]
Caro AA, 2001, MOL PHARMACOL, V60, P742
[5]
AMPK-mediated GSK3β inhibition by isoliquiritigenin contributes to protecting mitochondria against iron-catalyzed oxidative stress [J].
Choi, Song Hwa ;
Kim, Young Woo ;
Kim, Sang Geon .
BIOCHEMICAL PHARMACOLOGY, 2010, 79 (09) :1352-1362
[6]
Arachidonic acid interaction with the mitochondrial electron transport chain promotes reactive oxygen species generation [J].
Cocco, T ;
Di Paola, M ;
Papa, S ;
Lorusso, M .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (1-2) :51-59
[7]
Metformin prevents high-glucose-induced endothelial cell death through a mitochondrial permeability transition-dependent process [J].
Detaille, D ;
Guigas, B ;
Chauvin, C ;
Batandier, C ;
Fontaine, E ;
Wiernsperger, N ;
Leverve, X .
DIABETES, 2005, 54 (07) :2179-2187
[8]
Orchestration of iron homeostasis [J].
Fleming, RE ;
Bacon, BR .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (17) :1741-1744
[9]
Galaris D, 2008, CRIT REV CL LAB SCI, V45, P1, DOI [10.1080/10408360701713104, 10.1080/10408360701713104 ]
[10]
Regulation of arachidonic acid release and cytosolic phospholipase A2 activation [J].
Gijón, MA ;
Leslie, CC .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 65 (03) :330-336