A polyacetylene from Gymnaster koraiensis exerts hepatoprotective effects in vivo and in vitro

被引:27
作者
Lee, Saet Byoul [1 ]
Kang, Kyungsu [1 ]
Oidovsambuu, Sarangerel [1 ]
Jho, Eun Hye [1 ]
Yun, Ji Ho [1 ]
Yoo, Ji-Hye [1 ]
Lee, En-Ha [1 ]
Pan, Cheol-Ho [1 ]
Lee, Jae Kwon [2 ]
Jung, Sang Noon [1 ]
Nho, Chu Won [1 ]
机构
[1] Korea Inst Sci & Technol, Nat Prod Res Ctr, Kangnung 210340, South Korea
[2] Chungbuk Natl Univ, Dept Biol Educ, Cheongju 361763, South Korea
关键词
Gymnasterkoreayne B; Quinone reductase; Glutathione reductase; Menadione; Nrf2; Hepatotoxicity; DRUG-METABOLIZING-ENZYMES; OXIDATIVE STRESS; TRANSCRIPTIONAL REGULATION; NAD(P)H-QUINONE REDUCTASE; INDUCIBLE EXPRESSION; RESPONSIVE ELEMENT; CANCER CELLS; BASAL LEVEL; PHASE-I; GENE;
D O I
10.1016/j.fct.2010.07.035
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In the present study, we isolated a polyacetylene, gymnasterkoreayne B (GKB), from Gymnaster koraiensis and investigated the effect of GKB on the protection from oxidative stress-induced cytotoxicity through induction of the expression of cellular defense enzymes. GKB induced mRNA expression and enzyme activity of NAD(P)H:quinone oxidoreductase (NQO1) in vitro and in vivo, and potently increased expression of many cellular defense genes including glutathione-S-transferases, UDP-glucuronosyltransferase, and glutathione reductase (GSR) in normal rat liver. The nuclear factor erythroid 2-related factor 2 (Nrf2) which is known to induce various antioxidant and cytoprotective genes, and the genes containing the antioxidant response element (ARE), including NQO1, hemeoxygenease-1, GSR were induced by GKB in HepG2 human hepatocarcinoma cells. Pre-treatment of the cells with GKB accelerated the production of glutathione and mitigated menadione-induced cytotoxicity in HepG2 cells. Taken together, we found that GKB was a novel inducer of phase II detoxification enzymes and cellular defense enzymes, resulting in protection of the cells from oxidative stress and hepatotoxicity through regulation of detoxifying and antioxidant systems. (C) 2010 Published by Elsevier Ltd.
引用
收藏
页码:3035 / 3041
页数:7
相关论文
共 35 条
[1]   IDENTIFICATION OF A 2ND REGION UPSTREAM OF THE MOUSE HEME OXYGENASE-1 GENE THAT FUNCTIONS AS A BASAL LEVEL AND INDUCER-DEPENDENT TRANSCRIPTION ENHANCER [J].
ALAM, J ;
CAMHI, S ;
CHOI, AMK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) :11977-11984
[2]   NAD(P)H::Quinone oxidoreductase 1 (NQO1) Pro187Ser polymorphism and the risk of lung, bladder, and colorectal cancers:: a meta-analysis [J].
Chao, Chun ;
Zhang, Zuo-Feng ;
Berthiller, Julien ;
Boffetta, Paolo ;
Hashibe, Mia .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (05) :979-987
[3]   Oxidant-induced hepatocyte injury from menadione is regulated by ERK and AP-1 signaling [J].
Czaja, MJ ;
Liu, HL ;
Wang, YJ .
HEPATOLOGY, 2003, 37 (06) :1405-1413
[4]   A physiological threshold for protection against menadione toxicity by human NAD(P)H:quinone oxidoreductase (NQO1) in Chinese hamster ovary (CHO) cells [J].
De Haan, LHJ ;
Boerboom, AMJF ;
Rietjens, IMCM ;
van Capelle, D ;
De Ruijter, AJM ;
Jaiswal, AK ;
Aarts, JMMJG .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (11) :1597-1603
[5]  
DELARCO JE, 2010, CANC BIOL THER, V9
[6]  
Fahey JW, 2004, METHOD ENZYMOL, V382, P243
[7]  
FAVREAU LV, 1991, J BIOL CHEM, V266, P4556
[8]   XENOBIOTIC-INDUCIBLE EXPRESSION OF MURINE GLUTATHIONE-S-TRANSFERASE YA-SUBUNIT GENE IS CONTROLLED BY AN ELECTROPHILE-RESPONSIVE ELEMENT [J].
FRILING, RS ;
BENSIMON, A ;
TICHAUER, Y ;
DANIEL, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6258-6262
[9]   Gene expression profiling in the liver of CD-1 mice to characterize the hepatotoxicity of triazole fungicides [J].
Goetz, Amber K. ;
Bao, Wenjun ;
Ren, Hongzu ;
Schmid, Judith E. ;
Tully, Douglas B. ;
Wood, Carmen ;
Rockett, John C. ;
Narotsky, Michael G. ;
Sun, Guobin ;
Lambert, Guy R. ;
Thai, Sheau-Fung ;
Wolf, Douglas C. ;
Nesnow, Stephen ;
Dix, David J. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2006, 215 (03) :274-284
[10]   Nrf2-regulated glutathione recycling independent of biosynthesis is critical for cell survival during oxidative stress [J].
Harvey, C. J. ;
Thimmulappa, R. K. ;
Singh, A. ;
Blake, D. J. ;
Ling, G. ;
Wakabayashi, N. ;
Fujii, J. ;
Myers, A. ;
Biswal, S. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 46 (04) :443-453