Cytoprotective effect of the fruits of Lycium chinense Miller against oxidative stress-induced hepatotoxicity

被引:56
作者
Zhang, Rui [1 ,2 ]
Kang, Kyoung Ah [1 ,2 ]
Piao, Mei Jing [1 ,2 ]
Kim, Ki Cheon [1 ,2 ]
Kim, Areum Daseul [3 ]
Chae, Sungwook [4 ]
Park, Jong Sang [5 ]
Youn, Ui Joung [6 ]
Hyun, Jin Won [1 ,2 ]
机构
[1] Jeju Natl Univ, Sch Med, Jeju Si 690756, South Korea
[2] Jeju Natl Univ, Appl Radiol Sci Res Inst, Jeju Si 690756, South Korea
[3] Jeju Natl Univ, Sch Marine Biomed, Jeju Si 690756, South Korea
[4] Korea Inst Oriental Med, Dept Herbal Resources Res, Taejon 305811, South Korea
[5] Life Engn Inc, Haklimsu Res Inst, Taejon 302220, South Korea
[6] Ewha Womans Univ, Coll Pharm, Ctr Cell Signaling & Drug Discovery Res, Seoul 120750, South Korea
关键词
Reactive oxygen species; Lycium chinense; Chang liver cells; Antioxidant enzyme; DNA damage; Lipid peroxidation; Protein carbonyl; HYDROGEN-PEROXIDE; LIPID-PEROXIDATION; STRAND BREAKS; FREE-RADICALS; DNA-DAMAGE; IN-VITRO; CELLS; ANTIOXIDANTS; GENERATION; ASSAY;
D O I
10.1016/j.jep.2010.05.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Fruits of Lycium chinense Miller (Solanaceae), distributed in northeast Asia, have gained attraction for their hepatoprotective role in traditional oriental medicine. The excessive production of reactive oxygen species (ROS) is hazardous for living organisms and damage major cellular constituents such as DNA, lipid, and protein. The cytoprotective effect of Lycium chinense fruits (Lycium extract) was assessed against H2O2-induced Chang liver cell damage. Materials and methods: The effect of Lycium extract against H2O2-induced cell death was determined by the MIT assay. Radical scavenging activity was determined through the assessments of 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals, intracellular ROS, hydroxyl radicals, and superoxide. The inductions of antioxidant enzymes were determined via their protein expressions and activities. DNA damage was measured using comet assay and expression of phospho-histone H2A.X. Lipid peroxidation was measured using 8-isoprostane level and fluorescent probe. Protein modification was measured using protein carbonyl moiety. Results and conclusion: Lycium extract scavenged the DPPH free radicals, intracellular ROS, hydroxyl radicals, and superoxide. Lycium extract recovered activities of catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) decreased by H2O2. Lycium extract decreased DNA damage, lipid peroxidation and protein carbonyl values increased by H2O2 exposure. In addition, Lycium extract increased the cell viability of Chang liver cells exposed to H2O2 via inhibition of apoptosis. These results show that Lycium extract protected Chang liver cells against oxidative stressed cell damage by H2O2 via scavenging ROS and enhancing antioxidant enzyme activity. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:299 / 306
页数:8
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