Analysis of gene expression changes of drug metabolizing enzymes in the livers of F344 rats following oral treatment with kava extract

被引:36
作者
Guo, Lei [1 ]
Li, Quanzhen [2 ]
Xia, Qingsu [3 ]
Dial, Stacey [1 ]
Chan, Po-Chuen [4 ]
Fu, Peter [3 ]
机构
[1] US FDA, Natl Ctr Toxicol Res, Div Syst Toxicol, Jefferson, AR 72079 USA
[2] Univ Texas SW Med Ctr Dallas, Microarray Core Facil, Dallas, TX 75390 USA
[3] US FDA, Natl Ctr Toxicol Res, Div Biochem Toxicol, Jefferson, AR 72079 USA
[4] NIEHS, Res Triangle Pk, NC 27709 USA
关键词
Drug metabolizing enzyme; Drug metabolizing gene; Gene expression; Kava extract; Microarray; TaqMan assay; ST-JOHNS-WORT; DIETARY-SUPPLEMENTS; PIPER-METHYSTICUM; PYRROLIZIDINE ALKALOIDS; GINKGO-BILOBA; IN-VIVO; CYTOCHROME-P450; KAVALACTONES; TOXICITY; PHARMACOKINETICS;
D O I
10.1016/j.fct.2008.11.037
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The association of kava product use with liver-related risks has prompted regulatory action in many countries. We studied the changes in gene expression of drug metabolizing enzymes in the livers of Fischer 344 male rats administered kava extract by gavage for 14 weeks. Analysis of 22,226 genes revealed that there were 14, 41, 110, 386, and 916 genes significantly changed in the 0.125, 0.25, 0.5, 1.0, and 2.0 g/kg treatment groups, respectively. There were 16 drug metabolizing genes altered in all three high-dose treatment groups, among which seven genes belong to cytochrome P450 isozymes. While gene expression of Cyp1a1, 1a2, 26, 3a1, and 3a3 increased: Cyp 2c23 and 2c40 decreased, all in a dose-dependent manner. Real-time PCR analyses of several genes verified these results. Our results indicate that kava extract can significantly modulate drug metabolizing enzymes, particularly the CYP isozymes, which could cause herb-drug interactions and may potentially lead to hepatotoxicity. Published by Elsevier Ltd.
引用
收藏
页码:433 / 442
页数:10
相关论文
共 52 条
[1]   Pharmacokinetic and pharmacodynamic drug interactions with Kava (Piper methysticum Forst. f.) [J].
Anke, J ;
Ramzan, I .
JOURNAL OF ETHNOPHARMACOLOGY, 2004, 93 (2-3) :153-160
[2]   Kava hepatotoxicity: Are we any closer to the truth? [J].
Anke, J ;
Ramzan, I .
PLANTA MEDICA, 2004, 70 (03) :193-196
[3]  
[Anonymous], 2001, FDA ADV DIET SUPPL M
[4]  
Brauer R-B., 2001, Z GASTROENTEROL, V39, P491
[5]  
Bressler R, 2005, GERIATRICS, V60, P24
[6]   Kava-induced fulminant hepatic failure [J].
Campo, JV ;
McNabb, J ;
Perel, JM ;
Mazariegos, GV ;
Hasegawa, SL ;
Reyes, J .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2002, 41 (06) :631-632
[7]  
*CFSAN, 2002, KAV DIET SUPPL MAY A
[8]   Ginkgo biloba leave extract:: Biological, medicinal, and toxicological effects [J].
Chan, Po-Chuen ;
Xia, Qingsu ;
Fu, Peter P. .
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART C-ENVIRONMENTAL CARCINOGENESIS & ECOTOXICOLOGY REVIEWS, 2007, 25 (03) :211-244
[9]  
Chan PC, 2007, J FOOD DRUG ANAL, V15, P416
[10]   Gene expression profiles distinguish the carcinogenic effects of aristolochic acid in target (kidney) and non-target (liver) tissues in rats [J].
Chen, Tao ;
Guo, Lei ;
Zhang, Lu ;
Shi, Leming ;
Fang, Hong ;
Sun, Yongming ;
Fuscoe, James C. ;
Mei, Nan .
BMC BIOINFORMATICS, 2006, 7 (Suppl 2)