Evaluation of EROD and CYP3A4 activities in earthworm Eisenia fetida as biomarkers for soil heavy metal contamination

被引:33
作者
Cao, Xiufeng [1 ,2 ]
Song, Yufang [1 ]
Kai, Jianrong [1 ,2 ]
Yang, Xiaoxia [1 ,2 ]
Ji, Puhui [3 ]
机构
[1] Chinese Acad Sci, Inst Appl Ecol, Key Lab Pollut Ecol & Environm Engn, Shenyang 110016, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] NW A&F Univ, Coll Nat Resources & Environm, Yangling 712100, Peoples R China
关键词
Earthworm; CYP1A1; CYP3A4; Heavy metals; Biomarkers; ECm; NEUTRAL-RED RETENTION; BIOCHEMICAL RESPONSES; MONOOXYGENASE ACTIVITIES; ARTIFICIAL SOIL; COPPER; CYTOCHROME-P450; EXPOSURE; CADMIUM; FISH; METABOLISM;
D O I
10.1016/j.jhazmat.2012.10.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, the effects of heavy metals (Cd, Cu, Pb, Zn) on EROD and CYP3A4 activities in the earthworm Eisenia fetida were evaluated to find out their possible induction and potential as biomarkers for soil heavy metal contamination. The earthworms were exposed to increasing concentrations of Cd (0.1-8 mg L-1), Cu (10-200 mg L-1), Pb (20-400 mg L-1) or Zn (50-400 mg L-1) in filter papers for 48 h. EROD activity was significantly changed in dose-dependent manners after exposure to each of the four metals. CYP3A4 activity was significantly induced by Cd and Pb, rather by Cu and Zn. This is the first report on heavy metal-induced changes of CYP3A4 activity in earthworms. Among the four heavy metals, Cd was the most potent inducing EROD and CYP3A4. While EROD and CYP3A4 activities showed a similar trend, EROD is more sensitive than CYP3A4 activity in E. fetida as a biomarker for heavy metals pollution. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 151
页数:6
相关论文
共 67 条
[1]   Recovery of cholinesterase activity in the earthworm Eisenia fetida savigny following exposure to chlorpyrifos [J].
Aamodt, Solveig ;
Konestabo, Heidi Sjursen ;
Sverdrup, Line Emilie ;
Gudbrandsen, Marius ;
Reinecke, Sophie A. ;
Reinecke, Adriaan J. ;
Stenersen, Jorgen .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2007, 26 (09) :1963-1967
[2]   PAH metabolites in bile, cytochrome P4501A and DNA adducts as environmental risk parameters for chronic oil exposure: a laboratory experiment with Atlantic cod [J].
Aas, E ;
Baussant, T ;
Balk, L ;
Liewenborg, B ;
Andersen, OK .
AQUATIC TOXICOLOGY, 2000, 51 (02) :241-258
[3]   Cytochrome P450 and dependent activities in unexposed and PAH-exposed terrestrial annelids [J].
Achazi, RK ;
Flenner, C ;
Livingstone, DR ;
Peters, LD ;
Schaub, K ;
Scheiwe, E .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1998, 121 (1-3) :339-350
[4]   Capillary electrophoretic investigation of the enantioselective metabolism of propafenone by human cytochrome P-450SUPERSOMES: Evidence for atypical kinetics by CYP2D6 and CYP3A4 [J].
Afshar, Minoo ;
Thormann, Wolfgang .
ELECTROPHORESIS, 2006, 27 (08) :1526-1536
[5]   Cytochrome P-450 levels and EROD activity in the Adriatic sturgeon (Acipenser naccarii, Chondrostei) and its induction by β-Naphthoflavone [J].
Agradi, E ;
Brevini, TAL ;
Bolla, M ;
Baga, R ;
Favetta, LA .
JOURNAL OF APPLIED ICHTHYOLOGY, 1999, 15 (4-5) :96-98
[6]   Environmental contaminants and biochemical response in eel exposed to Po river water [J].
Agradi, E ;
Baga, R ;
Cillo, F ;
Ceradini, S ;
Heltai, D .
CHEMOSPHERE, 2000, 41 (10) :1555-1562
[7]   Human CYP3A4-introduced HepG2 cells: In vitro screening system of new chemicals for the evaluation of CYP3A4-inhibiting activity [J].
Araki, N. ;
Tsuruoka, S. ;
Wang, N. ;
Hasegawa, G. ;
Yanagihara, H. ;
Ando, H. ;
Omasa, T. ;
Enosawa, S. ;
Nagai, H. ;
Fujimura, A. .
XENOBIOTICA, 2008, 38 (11) :1355-1364
[8]   Interlaboratory comparison of the assessment of P450 activities in human hepatic microsomal samples [J].
Boobis, AR ;
McKillop, D ;
Robinson, DT ;
Adams, DA ;
McCormick, DJ .
XENOBIOTICA, 1998, 28 (05) :493-506
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   Toxicological and biochemical responses of the earthworm Lumbricus rubellus to pyrene, a non-carcinogenic polycyclic aromatic hydrocarbon [J].
Brown, PJ ;
Long, SM ;
Spurgeon, DJ ;
Svendsen, C ;
Hankard, PK .
CHEMOSPHERE, 2004, 57 (11) :1675-1681