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Evaluation of Fish Models of Soluble Epoxide Hydrolase Inhibition

John W. Newman, Debra L. Denton, Christophe Morisseau, Cory S. Koger, Craig E. Wheelock, David E. Hinton and Bruce D. Hammock
Environmental Health Perspectives
Vol. 109, No. 1 (Jan., 2001), pp. 61-66
DOI: 10.2307/3434922
Stable URL: http://www.jstor.org/stable/3434922
Page Count: 6
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Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Evaluation of Fish Models of Soluble Epoxide Hydrolase Inhibition
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Abstract

Substituted ureas and carbamates are mechanistic inhibitors of the soluble epoxide hydrolase (sEH). We screened a set of chemicals containing these functionalities in larval fathead minnow (Pimphales promelas) and embryo/larval golden medaka (Oryzias latipes) models to evaluate the utility of these systems for investigating sEH inhibition in vivo. Both fathead minnow and medaka sEHs were functionally similar to the tested mammalian orthologs (murine and human) with respect to substrate hydrolysis and inhibitor susceptibility. Low lethality was observed in either larval or embryonic fish exposed to diuron [N-(3,4-dichlorophenyl), N′-dimethyl urea], desmethyl diuron [N-(3,4-dichlorophenyl), N′-methyl urea], or siduron [N-(1-methylcyclohexyl), N′-phenyl urea]. Dose-dependent inhibition of sEH was a sublethal effect of substituted urea exposure with the potency of siduron < desmethyl diuron = diuron, differing from the observed in vitro sEH inhibition potency of siduron > desmethyl diuron > diuron. Further, siduron exposure synergized the toxicity of trans-stilbene oxide in fathead minnows. Medaka embryos exposed to diuron, desmethyl diuron, or siduron displayed dose-dependent delays in hatch, and elevated concentrations of diuron and desmethyl diuron produced developmental toxicity. The dose-dependent toxicity and in vivo sEH inhibition correlated, suggesting a potential, albeit undefined, relationship between these factors. Additionally, the observed inversion of in vitro to in vivo potency suggests that these fish models may provide tools for investigating the in vivo stability of in vitro inhibitors while screening for untoward effects.

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