| Literature DB >> 28245158 |
Marize de Lourdes Marzo Solano1, Noeme Souza Rocha2, Luis Fernando Barbisan3, Carla Adriene da Silva Franchi1, Ana Lúcia Tozzi Spinardi-Barbisan1, Maria Luiza Cotrim Sartor de Oliveira1, Daisy Maria Fávero Salvadori1, Lúcia Regina Ribeiro1, João Lauro Viana de Camargo1.
Abstract
The medium-term multiorgan initiation-promotion chemical bioassay (diethylnitrosamine, methyl-nitrosourea, butyl-hydroxybutylnitrosamine, dihydroxypropylnitrosamine, dimethylhydrazine [DMBDD]) with the Fischer 344 rat was proposed as an alternative to the conventional 2-year carcinogenesis bioassay for regulatory purposes. The acronym DMBDD stands for the names of five genotoxic agents used for initiation of multiorgan carcinogenesis. The Brazilian Agency for the Environment officially recognized a variation of this assay (DMBDDb) as a valid method to assess the carcinogenic potential of agrochemicals. Different from the original protocol, this DMBDDb is 30-week long, uses Wistar rats and two positive control groups exposed to carcinogenesis promoters sodium phenobarbital (PB) or 2-acetylaminofluorene (2-AAF). This report presents the experience of an academic laboratory with the DMBDDb assay and contributes to the establishment of this alternative DMBDD bioassay in a different rat strain. Frequent lesions observed in positive groups to evaluate the promoting potential of pesticides and the immunohistochemical expressions of liver cytochrome P450 (CYP) 2B1/2B2 and CYP1A2 enzymes were assessed. Commonly affected organs were liver, kidney, intestines, urinary bladder, and thyroid. PB promoting activity was less evident than that of 2-AAF, especially in males. This study provides a repository of characteristic lesions occurring in positive control animals submitted to a modified alternative 2-stage multiorgan protocol for carcinogenesis in Wistar rat.Entities:
Keywords: DMBDD bioassay; Wistar rats; agrochemicals; carcinogenesis; histological lesions; initiation–promotion; multiorgan assay; regulatory toxicology
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Year: 2016 PMID: 28245158 DOI: 10.1177/0192623316678931
Source DB: PubMed Journal: Toxicol Pathol ISSN: 0192-6233 Impact factor: 1.902