INVITRO STUDIES OF THE METABOLISM OF ATRAZINE, SIMAZINE, AND TERBUTRYN IN SEVERAL VERTEBRATE SPECIES

被引:62
作者
ADAMS, NH [1 ]
LEVI, PE [1 ]
HODGSON, E [1 ]
机构
[1] N CAROLINA STATE UNIV,DEPT TOXICOL,BOX 7633,RALEIGH,NC 27695
关键词
D O I
10.1021/jf00096a025
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The metabolism of three triazine herbicides (atrazine, simazine, and terbutryn) was studied in rat (Sprague-Dawley and Fischer strains), mouse, goat, sheep, pig, rabbit, and chicken by using in vitro hepatic 10000g supernatant or microsomal systems. Principal phase I metabolites were 4- or 6-monodealkylated-s-triazines; several observations, including studies with purified enzymes, demonstrated that phase I reactions were cytochrome P-450 mediated. There were species-related variations in rates of metabolism and in ratios of primary metabolites, although no strain-or sex-related differences were noted. Phase II products were glutathione conjugates of the parent compound and of the two monodealkylated products. Experiments with Fenton’s reagent, which generates hydroxyl radicals, gave dealkylated 2-chloro-s-triazine, supporting the possible role of active oxygen radicals in the cytochrome P-450 mediated reactions. © 1990, American Chemical Society. All rights reserved.
引用
收藏
页码:1411 / 1417
页数:7
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