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Evaluation of 4,4'-diaminodiphenyl ether in the rat comet assay: Part of the Japanese Center for the Validation of Alternative Methods (JaCVAM)-initiative international validation study of in vivo rat alkaline comet assay.
Priestley, Catherine C; Walker, Joanne S; O'Donovan, Michael R; Doherty, Ann T.
Afiliação
  • Priestley CC; Genetic Toxicology, Drug Safety And Metabolism, AstraZeneca R&D, Unit 310, Darwin Building, Cambridge Science Park CB4 0WG, United Kingdom. Electronic address: catherine.priestley@astrazeneca.com.
  • Walker JS; Genetic Toxicology, Drug Safety And Metabolism, AstraZeneca R&D, Unit 310, Darwin Building, Cambridge Science Park CB4 0WG, United Kingdom.
  • O'Donovan MR; Genetic Toxicology, Drug Safety And Metabolism, AstraZeneca R&D, Unit 310, Darwin Building, Cambridge Science Park CB4 0WG, United Kingdom.
  • Doherty AT; Genetic Toxicology, Drug Safety And Metabolism, AstraZeneca R&D, Unit 310, Darwin Building, Cambridge Science Park CB4 0WG, United Kingdom.
Mutat Res Genet Toxicol Environ Mutagen ; 786-788: 125-8, 2015 Jul.
Article em En | MEDLINE | ID: mdl-26212302
ABSTRACT
As a part of the Japanese Center for the Validation of Alternative Methods (JaCVAM)-initiative international validation study of the in vivo rat alkaline comet assay, 4,4'-diaminodiphenyl ether (DPE), a known rodent genotoxic carcinogen, was tested in this laboratory. Sprague Dawley rats (7-9 weeks of age) were given three oral doses of DPE, 24 and 21 h apart and liver or stomach sampled 3h after the final dose. Under the conditions of the test, no increases in DNA damage in liver and stomach were observed with DPE (up to 200 mg/kg/day). A dose-dependent decrease in DNA migration, compared to vehicle controls, was noted for DPE in rat stomach. Further analysis is required to elucidate fully whether this decrease is a consequence of the mode of action or due to the toxicity of DPE. What is perhaps surprising is the inability of the comet assay to detect a known rat genotoxic carcinogen in liver. Further investigation is needed to clarify whether this apparent lack of response results from limited tissue exposure or metabolic differences between species. This finding highlights a need for careful consideration of study design when evaluating assay performance as a measure of in vivo genotoxicity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éteres Fenílicos / Ensaio Cometa Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éteres Fenílicos / Ensaio Cometa Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article