Resveratrol affects CYP1A expression in rainbow trout hepatocytes

被引:20
作者
Aluru, Neelakanteswar [1 ]
Vijayan, Mathilakath M. [1 ]
机构
[1] Univ Waterloo, Dept Biol, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
aryl hydrocarbon receptor; AhR signaling; beta-naphthoflavone; fish; salmonid; CYP1A1; Oncorhynchus mykiss;
D O I
10.1016/j.aquatox.2005.12.010
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Resveratrol (RVT), a polyphenolic phytoalexin found in a variety of food products, including grapes and peanuts, is a well-characterized aryl hydrocarbon receptor (AhR) antagonist in mammalian cell lines. The lack of a reliable tool to block AhR signaling in rainbow trout (Oncorhynchus mykiss) prompted this study to evaluate the utility of RVT as an AhR antagonist in a piscine system. Trout hepatocytes in primary culture were exposed to varying doses of RVT (10(-5)-10(-12) M) either in the presence or absence of a well-established AhR agonist, beta-naphthoflavone (BNF). Indeed, BNF significantly elevated CYP1A and AhR protein expression in trout hepatocytes, and this response was inhibited at high (10(-5)-10(-7) M), but not low (10(-8)-10(-10) M), RVT doses. However, RVT alone at low doses (10(-8)-10(-10) M) significantly elevated CYP1A protein expression compared to control hepatocytes. This higher protein response with RVT was completely abolished with actinomycin D and cycloheximide suggesting transcriptional and translational regulation of CYP1A induction. Also, RVT at low (10(-9) M), but not high (10(-5) M), dose significantly elevated CYP1A1 mRNA transcript levels in BNF-primed hepatocytes supporting transcriptional modulation. Taken together, RVT is an effective AhR antagonist, but induces CYP1A expression at lower doses (< 10(-8) M) in trout hepatocytes. (c) 2006 Elsevier B.V All rights reserved.
引用
收藏
页码:291 / 297
页数:7
相关论文
共 45 条
[21]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[22]   Involvement of a post-transcriptional mechanism in the inhibition of CYP1A1 expression by resveratrol in breast cancer cells [J].
Lee, JE ;
Safe, S .
BIOCHEMICAL PHARMACOLOGY, 2001, 62 (08) :1113-1124
[23]   Effects of aryl hydrocarbon receptor null mutation and in utero and lactational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure on prostate and seminal vesicle development in C57BL/6 mice [J].
Lin, TM ;
Ko, K ;
Moore, RW ;
Simanainen, U ;
Oberley, TD ;
Peterson, RE .
TOXICOLOGICAL SCIENCES, 2002, 68 (02) :479-487
[24]   Evaluation of chemicals as inhibitors of trout cytochrome P450s [J].
Miranda, CL ;
Henderson, MC ;
Buhler, DR .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 148 (02) :237-244
[25]  
Mollerup S, 2001, INT J CANCER, V92, P18, DOI 10.1002/1097-0215(200102)9999:9999<::AID-IJC1156>3.3.CO
[26]  
2-5
[27]  
Navas JM, 2003, ENVIRON TOXICOL CHEM, V22, P830, DOI [10.1002/etc.5620220422, 10.1897/1551-5028(2003)022&lt
[28]  
0830:IOCBTN&gt
[29]  
2.0.CO
[30]  
2]