Incorporation of S-9 activation into an ER-α transactivation assay

被引:17
作者
Charles, GD
Bartels, MJ
Gennings, C
Zacharewski, TR
Freshour, NL
Gollapudi, BB
Carney, EW
机构
[1] Dow Chem Co USA, Toxicol & Environm Res & Consulting, Midland, MI 48674 USA
[2] Virginia Commonwealth Univ, Dept Biostat, Richmond, VA 23298 USA
[3] Michigan State Univ, Dept Biochem, E Lansing, MI 48824 USA
[4] Michigan State Univ, Natl Food Safety & Toxicol Ctr, E Lansing, MI 48824 USA
关键词
reporter gene; methoxychlor; metabolism; S-9; activation; estrogenicity; MCF-7; cells; endocrine toxicity; HPTE;
D O I
10.1016/S0890-6238(00)00070-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We evaluated the feasibility of incorporating an exogenous metabolic activating system into an estrogen receptor-a transactivation assay. 17 beta-estradiol (E2), and the proestrogenic pesticide methoxychlor (MXC) were evaluated for activity in the presence and absence of Aroclor-1254 induced rat liver S-9 fractions. Both E2 and MXC responded consistently in the assay with average EC50 values of 9.6 x 10(-11) M and 1.2 X 10(-5) M, respectively. In the presence of a 0.1% S-9 fraction, the EC50 for E2 was increased to 1.4 x 10(-9) M and that for MXC decreased to 4.9 X 10(-7) M, with both compounds demonstrating increased secondary metabolite formation as evidenced by HPLC analysis. Consistent with these data, metabolites of E2 and MXC exhibited decreased and increased potencies, respectively, in the assay system relative to the parent molecules. S-9 was compatible with the MCF-7 reporter assay and has the potential to enhance detection of proestrogenic materials. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:207 / 216
页数:10
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