Use of in vitro bioassays to facilitate read-across assessment of nitrogen substituted heterocycle analogues of polycyclic aromatic hydrocarbons
Autor: | Patrick Serrant, Benoît Schilter, Mireille Moser, Claudine Cottet Fontannaz, Julie Mollergues, Harrie Besselink, Myriam Coulet, Fanny Minetto, Hélia Latado, Matthew Tate, Maricel Marin-Kuan, Dominique Piguet |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Nitrogen Chemical structure Toxicology Ring (chemistry) medicine.disease_cause 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Salmonella Cell Line Tumor medicine Bioassay Estrogen Receptor beta Humans Polycyclic Aromatic Hydrocarbons Cytotoxicity Chemistry Mutagenicity Tests In vitro toxicology Estrogen Receptor alpha General Medicine In vitro 030104 developmental biology Biochemistry Receptors Aryl Hydrocarbon Receptors Androgen 030220 oncology & carcinogenesis Pyrene Biological Assay Genotoxicity DNA Damage Mutagens |
Zdroj: | Toxicology in vitro : an international journal published in association with BIBRA. 59 |
ISSN: | 1879-3177 |
Popis: | Nitrogen-containing polycyclic aromatic hydrocarbons (PANHs or azaarenes) are compounds structurally similar to PAHs (carbon substituted by a nitrogen) reported to occur at low levels in food. Although limited, literature may suggest possible higher toxicity than for PAHs. Using a battery of in vitro assays, the toxicological properties of uncharacterized PANHs of increasing ring number were compared to those of characterized structural PAH analogues. The parameters measured covered key events relevant to the AOP developed for Benzo(a)pyrene: AhR activation, mutagenicity and DNA-damage with and without metabolic activation and endocrine receptors activation/inhibition. There was a strong correlation between the chemical structure and the biological activities of the compounds. AhR activation was the most sensitive parameter with a direct correlation between potency and ring number. The most potent genotoxic chemicals were found amongst the ones with the highest number of ring, and under metabolic activation. Such an approach allowed designing sub-groups based on biological properties in addition to structural similarities. Within a sub-group, toxicological data of tested chemicals may be used to characterize hazard of biologically similar but toxicologically uncharacterized substances. This indicates that in addition to structural properties, in vitro biological data may be useful to conduct read-across. |
Databáze: | OpenAIRE |
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