Inhibition of methyleugenol bioactivation by the herb-based constituent nevadensin and prediction of possible in vivo consequences using physiologically based kinetic modeling
| Autor: | Ivonne M.C.M. Rietjens, Alicia Paini, Jacques Vervoort, Wasma Alhusainy, Ans Punt, Ala′ A.A. Al-Subeihi, Peter J. van Bladeren |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
Male
medicine.disease_cause Toxicology Biochemistry estragole Rats Sprague-Dawley chemistry.chemical_compound DNA Adducts Bioassay rat Tissue Distribution Enzyme Inhibitors Biotransformation chemistry.chemical_classification methyl eugenol General Medicine Hep G2 Cells Methyleugenol dna-adducts Female Sulfotransferases Stereochemistry salmonella mutagenicity tests Biochemie Flavones Models Biological Risk Assessment In vivo Eugenol medicine Animals Anticarcinogenic Agents Humans colorimetric assay Carcinogen Toxicologie VLAG Dose-Response Relationship Drug human hepatoma-cells mouse-liver mass-spectrometry Rats Inbred F344 Rats safrole chemistry Safrole Carcinogens Hepatocytes Estragole Genotoxicity Food Science |
| Zdroj: | Food and Chemical Toxicology, 59, 564-571 Food and Chemical Toxicology 59 (2013) |
| ISSN: | 1873-6351 0278-6915 |
| Popis: | Methyleugenol (ME) occurs naturally in a variety of spices, herbs, including basil, and their essential oils. ME induces hepatomas in rodent bioassays following its conversion to a DNA reactive metabolite. In the present study, the basil constituent nevadensin was shown to be able to inhibit SULT-mediated DNA adduct formation in HepG2 cells exposed to the proximate carcinogen 1'-hydroxymethyleugenol in the presence of nevadensin. To investigate possible in vivo implications of SULT inhibition by nevadensin on ME bioactivation, the rat physiologically based kinetic (PBK) model developed in our previous work to describe the dose-dependent bioactivation and detoxification of ME in male rat was combined with the recently developed PBK model describing the dose-dependent kinetics of nevadensin in male rat. The resulting binary ME–nevadensin PBK model was used to predict the possible nevadensin mediated reduction in ME DNA adduct formation and resulting carcinogenicity at the doses of ME used by the NTP carcinogenicity study. Using these data an updated risk assessment using the Margin of Exposure (MOE) approach was performed. The results obtained point at a potential reduction of the cancer risk when rodents are orally exposed to ME within a relevant food matrix containing SULT inhibitors compared to exposure to pure ME. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect