AH RECEPTOR-BINDING PROPERTIES OF INDOLE CARBINOLS AND INDUCTION OF HEPATIC ESTRADIOL HYDROXYLATION

被引:159
作者
JELLINCK, PH
FORKERT, PG
RIDDICK, DS
OKEY, AB
MICHNOVICZ, JJ
BRADLOW, HL
机构
[1] QUEENS UNIV, DEPT ANAT, KINGSTON K7L 3N6, ONTARIO, CANADA
[2] UNIV TORONTO, DEPT PHARMACOL, TORONTO M5S 1A1, ONTARIO, CANADA
[3] INST HORMONE RES, NEW YORK, NY USA
关键词
D O I
10.1016/0006-2952(93)90258-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of route of administration on the ability of indole-3-carbinol (I3C), an anticarcinogen present in cruciferous vegetables, to induce estradiol 2-hydroxylase (EH) in female rat liver microsomes was investigated and compared to that of its main gastric conversion product, 3,3'-diindolylmethane (DIM). This dimer was more potent than I3C after either oral or intraperitoneal administration and was also a better in vitro inhibitor of EH in control and I3C-induced hepatic microsomes. The induction of both CYP1A1 and 1A2 in about equal amounts by I3C and DIM as well as of CYP2B1/2 was demonstrated using monoclonal antibodies. DIM, isosafrole, beta-naphthoflavone, 3-methylcholanthrene and naringenin added in vitro inhibited EH strongly in induced microsomes but gestodene was a better inhibitor of estrogen 2-hydroxylation in liver microsomes from untreated female rats. The binding affinities of I3C and DIM to the Ah receptor were compared to that of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) by competition studies, and the IC50, values were shown to be 2.0 x 10(-9) M, 5.0 x 10(-5) M and 2.3 x 10(-3) M for TCDD, DIM and I3C, respectively. The ability of I3C or DIM to cause in vitro transformation of the Ah receptor to a form able to bind to the dioxin-responsive element-3 (DRE3) was compared to that of TCDD and shown to parallel their abilities to compete for binding of [H-3]TCDD to the Ah receptor. These experiments confirm and extend the proposals that dietary indoles induce specific cytochrome P450s in rat liver by a mechanism possibly involving the Ah receptor. The induced monooxygenases, in turn, increase the synthesis of 2-hydroxylated estrogens in the competing pathways of 2- and 16alpha-hydroxylation which decreases the levels of 16alpha-hydroxyestrone able to form stable covalent adducts with proteins including the estrogen receptor. Such steroid-protein interaction has been correlated with mammary carcinogenesis.
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页码:1129 / 1136
页数:8
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