p-Nitrophenol and glutathione response in medaka (Oryzias latipes) exposed to MX, a drinking water carcinogen

被引:15
作者
Geter, DR [1 ]
Fournie, JW
Brouwer, MH
DeAngelo, AB
Hawkins, WE
机构
[1] Univ So Mississippi, Dept Coastal Sci, Gulf Coast Res Lab, Ocean Springs, MS 39564 USA
[2] US EPA, Natl Hlth & Environm Effects Res Lab, Off Res & Dev, Gulf Breeze, FL 32561 USA
[3] US EPA, Natl Hlth & Environm Effects Res Lab, Off Res & Dev, Res Triangle Pk, NC 27711 USA
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 2003年 / 134卷 / 03期
关键词
chlorinated furanone; cytochrome P450 2E1 (CYP2E1); drinking water disinfection by-products; glutathione; methylazoxymethanol acetate; medaka; 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX);
D O I
10.1016/S1532-0456(03)00003-6
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
When chlorine is introduced into public drinking water for disinfection, it can react with organic compounds in surface waters to form toxic by-products such as 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX). We investigated the effect of exposure to MX on cytochrome P450 2E1 (CYP2E1)-like activity and total glutathione (GSH) in the liver of the small fish model, medaka (Oryzias latipes). The multi-site carcinogen methylazoxymethanol acetate (MAMAc) was the positive control compound. Both medaka liver microsome preparations and S-9 fractions catalyzed the hydroxylation of p-nitrophenol (PNP), suggesting CYP2E1-Iike activity in the medaka. Male medaka exposed for 96 It to the CYP2E1 inducers ethanol and acetone under fasted conditions showed significant increases in PNP-hydroxylation activity. Furthermore, total reduced hepatic GSH was reduced in fish fasted for 96 h, indicating that normal feeding is a factor in maintaining xenobiotic defenses. Exposure to MX and MAMAc induced significant increases in hepatic CYP2E1-like activity, however MX exposure did not alter hepatic GSH levels. These data strengthen the role of the medaka as a suitable species for examining cytochrome P450 and GSH detoxification processes and the role these systems play in chemical carcinogenesis. (C) 2003 Elsevier Science Inc. All rights reserved.
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页码:353 / 364
页数:12
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