In vivo genotoxicity of 1,4-dioxane evaluated by liver and bone marrow micronucleus tests and Pig-a assay in rats

Itoh, S; Hattori, C

HERO ID

5072318

Reference Type

Journal Article

Year

2019

Language

English

PMID

30595213

HERO ID 5072318
In Press No
Year 2019
Title In vivo genotoxicity of 1,4-dioxane evaluated by liver and bone marrow micronucleus tests and Pig-a assay in rats
Authors Itoh, S; Hattori, C
Journal Mutation Research: Genetic Toxicology and Environmental Mutagenesis
Volume 837
Page Numbers 8-14
Abstract 1,4-Dioxane, used widely as a solvent in the manufacture of chemicals and as a laboratory reagent, induced liver adenomas and carcinomas in mice and rats, and nasal tumors in rats in several long-term studies. 1,4-Dioxane has been reported to be non-genotoxic in vitro, and there is no clear conclusion concerning its in vivo genotoxicity in rodents. In the present study, we investigated the ability of 1,4-dioxane to induce micronuclei in the liver and bone marrow of rats. For the liver micronucleus test, we performed the juvenile animal method and two methods using partial hepatectomy (PH), dosing before PH or dosing after PH. We also evaluated the in vivo mutagenicity of 1,4-dioxane by Pig-a gene mutation assay using rat peripheral blood. As a result, all methods of liver micronucleus test showed an increase in the frequency of micronucleated hepatocytes by 1,4-dioxane. The dosing before PH, a suitable method for detecting structural chromosome aberration inducers, showed the clearest response for micronucleated hepatocytes induction among the three methods. This finding is consistent with a previous report that 1,4-dioxane induces mainly chromosome breakage in the liver. Negative results were obtained in the bone marrow micronucleus test and Pig-a gene mutation assay in our study. These results suggested that 1,4-dioxane is clastogenic in the liver but not genotoxic in the bone marrow of rats.
Doi 10.1016/j.mrgentox.2018.09.004
Pmid 30595213
Wosid WOS:000457503900002
Url https://linkinghub.elsevier.com/retrieve/pii/S1383571818301013
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Is Peer Review Yes