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Toxicological Sciences 60, 56-62 (2001)
Copyright © 2001 by the Society of Toxicology

ENDOCRINE TOXICOLOGY

Androgen Receptor Antagonism by the Organophosphate Insecticide Fenitrothion

Hiroto Tamura*,{dagger}, Susan C. Maness{dagger}, Kim Reischmann{dagger}, David C. Dorman{dagger}, L. Earl Gray{ddagger} and Kevin W. Gaido{dagger},1

* Department of Applied Biochemistry, Meijo University, Nagoya 468-8502, Japan; {dagger} CIIT Centers for Health Research, P. O. Box 12137, Research Triangle Park, North Carolina 27709; and {ddagger} U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27709

Organophosphate insecticides represent one of the most widely used classes of pesticides with high potential for human exposure in both rural and residential environments. We investigated the interaction of the organophosphothioate pesticide fenitrothion (O,O-dimethyl O-(4-nitro-m-tolyl) phosphorothioate) with the human androgen receptor (AR). Fenitrothion blocked dihydrotestosterone-dependent AR activity in a concentration-dependent and competitive manner in HepG2 human hepatoma liver cells transiently transfected with human AR and an AR-dependent luciferase reporter gene. Schild regression analysis yielded an equilibrium dissociation constant value of 2.18 x 10–8 M. To determine the antiandrogenic potential of fenitrothion in vivo, 7-week-old castrated Sprague-Dawley rats were dosed once a day for 7 days with testosterone propionate (50 µg/day, sc) plus gavage doses of either corn oil vehicle or fenitrothion (15 or 30 mg/kg/day). An additional group of rats was given testosterone propionate and flutamide (50 mg/kg/day). Motor activity and acetylcholinesterase activity in whole blood and brain were also assessed. Both fenitrothion and the reference antiandrogen flutamide caused significant decreases in the ventral prostate, seminal vesicle, and levator ani plus bulbocavernosus muscles tissue weights. In contrast, blood acetylcholinesterase activity, a standard biomarker of organophosphate poisoning, was only inhibited at the higher dose of fenitrothion (30 mg/kg). Our results demonstrate that fenitrothion is a competitive AR antagonist, comparable in potency to the pharmaceutical antiandrogen flutamide and more potent, based on in vitro assays, than the known environmental antiandrogens linuron and p,p'-, 2,2-bis(p-hydroxyphenyl)-1,1-dichloroethylene ( p,p'-DDE).

Key Words: androgen receptor; organophosphate pesticide; endocrine-active chemical; antiandrogen; HepG2 cells; Hershberger assay; transcriptional activation.


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