Antioxidant and Hepatoprotective Effects of the Red Ginseng Essential Oil in H2O2-Treated HepG2 Cells and CCl4-Treated Mice

被引:92
作者
Bak, Min-Ji [1 ]
Jun, Mira [2 ]
Jeong, Woo-Sik [1 ]
机构
[1] Inje Univ, Coll Biomed Sci & Engn, Dept Food & Life Sci, Inst Phytochem Drug Interact, Gimhae 621749, South Korea
[2] Dong A Univ, Dept Food Sci & Nutr, Pusan 604714, South Korea
基金
新加坡国家研究基金会;
关键词
antioxidant enzymes; SOD; GPx; Catalase; MAPK; red ginseng essential oil; Panax ginseng; INDUCED LIVER-INJURY; OXIDATIVE STRESS; CARBON-TETRACHLORIDE; FREE-RADICALS; ERECTILE DYSFUNCTION; ROOT EXTRACT; DISEASE; RATS; MECHANISMS; EXPRESSION;
D O I
10.3390/ijms13022314
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The aim of this study was to evaluate the antioxidant mechanisms of red ginseng essential oil (REO) in cells as well as in an animal model. REO was prepared by a supercritical CO2 extraction of waste-products generated after hot water extraction of red ginseng. In HepG2 cells, REO diminished the H2O2-mediated oxidative stress and also restored both the activity and expression of antioxidant enzymes such as superoxide dismutase, catalase and glutathione peroxidase. Administration of REO inhibited the phosphorylation of upstream mitogen-activated protein kinases (MAPKs) such as c-Jun N-terminal kinase, extracellular signal-regulated kinase, and p38. In mice, the CCl4-mediated elevation of serum aspartate transaminase and alanine transaminase as well as the induction of hepatic lipid peroxidation were decreased by REO administration. REO treatments also resulted in up-regulation of the antioxidant enzyme expression in the liver. Moreover, increased phosphorylations of MAPKs were inhibited after REO administration. Overall, REO seems to protect the liver from oxidative stress through the activation and induction of antioxidant enzymes via inhibition of MAPKs pathways.
引用
收藏
页码:2314 / 2330
页数:17
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