ToxSci Advance Access originally published online on March 7, 2003
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Toxicological Sciences 72, 359-362 (2003)
Copyright © 2003 by the Society of Toxicology
SAFETY EVALUATION |
The Mutagenic Potential of the Furylethylene Derivative 2-Furyl-1-nitroethene in the Mouse Bone Marrow Micronucleus Test



* Grup de Mutagènesi, Departament de Genètica i de Microbiologia, Facultat de Ciències, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain; and
Centro de Investigación y Desarrollo Aplicado, Cida s.a.l., 08130 Santa Perpètua de Mogoda, Barcelona, Spain
The compound 2-furyl-1-nitroethene (G-0) has been tested to determine its ability to induce clastogenic or aneugenic effects in vivo, through the induction of micronucleated polychromatic erythrocytes (MNPCE) in mouse bone marrow. Groups of five CD-1 male mice were administered once intraperitoneally at a dose range of 520 mg/kg and bone marrow was sampled at 24 and 48 h after the treatment. G-0 was dissolved in corn oil, thus a vehicle control group received only corn oil at 10 ml/kg. The positive control group was administered with cyclophosphamide (40 mg/kg). All animals dosed with the highest concentration of the test agent (20 mg/kg) showed evident clinical symptoms of toxicity. Although evidences of bone marrow toxicity were observed, no statistically significant increases in the incidence of MNPCE over the vehicle control group were observed at any sampling time with any of the assayed doses of the G-0 compound. Cyclophosphamide treatment increased the incidence of MNPCE in all treated animals, demonstrating the sensitivity of the assay conditions in which it was carried out. From the results obtained, it is concluded that the test agent G-0 is neither clastogenic nor aneugenic in the erythrocytes from the bone marrow of treated mice at the doses tested.
Key Words: micronucleus assay; mice; furylethylenes; polychromatic erythrocytes; bone marrow.
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