Induction of antioxidant and phase 2 drug-metabolizing enzymes by falcarindiol isolated from Notopterygium incisum extract, which activates the Nrf2/ARE pathway, leads to cytoprotection against oxidative and electrophilic stress

被引:27
作者
Ohnuma, Tomokazu [1 ]
Komatsu, Takao [2 ]
Nakayama, Shinji [3 ]
Nishiyama, Takahito [1 ]
Ogura, Kenichiro [1 ]
Hiratsuka, Akira [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, Dept Drug Metab & Mol Toxicol, Hachioji, Tokyo 1920392, Japan
[2] Nippon Chemiphar Co Ltd, Chiyoda Ku, Tokyo 1018678, Japan
[3] Toyama Chem Co Ltd, Shinjuku Ku, Tokyo 1600023, Japan
关键词
Falcarindiol; Nrf2; ARE; Drug-metabolizing enzyme; Menadione; Cytotoxicity; CHINESE CRUDE DRUG; INDUCIBLE EXPRESSION; UNDERGROUND PARTS; QUINONE REDUCTASE; DT-DIAPHORASE; BASAL LEVEL; KEAP1; GENE; IDENTIFICATION; PROTECTION;
D O I
10.1016/j.abb.2009.06.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, we isolated falcarindiol from Notopterygium incisum and investigated the effect of falcarindiol on the expression of antioxidant enzymes (AOEs), such as catalase, and phase 2 drug-metabolizing enzymes (DMEs), such as glutathione S-transferase and NAD(P)H:quinone oxidoreductase 1, in a cultured cell line from normal rat liver, Clone 9 cells. Exposure of Clone 9 cells to falcarindiol resulted in the significant induction of AOEs and phase 2 DMEs. Western blot analysis and transfection studies using a luciferase reporter construct demonstrated that the induction of AOEs and phase 2 DMEs by falcarindiol was caused through the Nrf2/ARE (nuclear factor-E2-related factor 2/antioxidant response element) pathway. Pretreatment of cells with falcarindiol accelerated the detoxification of a potentially toxic quinone (menadione) and mitigated menadione-induced cytotoxicity. We found that falcarindiol was a novel inducer of ACEs and phase 2 DMEs and falcarindiol might exhibit chemopreventive activity. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 41
页数:8
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