Genotoxic and cytotoxic effects of carbofuran and furadan® on Chinese hamster ovary (CHOK1) cells
| Autor: | Miguel A. Reigosa, Sonia Soloneski, Marcelo L. Larramendy, Norma Viviana González, G. Molinari |
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| Rok vydání: | 2008 |
| Předmět: |
Neutral red
Mitotic index Cell Survival Health Toxicology and Mutagenesis Hamster Sister chromatid exchange CHO Cells Biology medicine.disease_cause Toxicology Carbofuran chemistry.chemical_compound Cricetulus Cricetinae Genetics medicine Animals Pesticides Mutagenicity Tests Chinese hamster ovary cell Molecular biology chemistry Micronucleus test Growth inhibition Lysosomes Sister Chromatid Exchange Genotoxicity |
| Zdroj: | Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 656:68-73 |
| ISSN: | 1383-5718 |
| DOI: | 10.1016/j.mrgentox.2008.07.007 |
| Popis: | The in vitro geno- and cytotoxicity exerted by the N-methylcarbamate pesticide carbofuran (CF) and its commercial formulation furadan (F) were studied in Chinese hamster ovary (CHO(K1)) cells by several bioassays for both genotoxicity (e.g., the sister chromatid exchange (SCE) and micronuclei (MNi) frequencies), and cytotoxicity (e.g., cell-cycle progression, mitotic index (MI), 3(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), and neutral red (NR)). Both CF and F activities were tested within the range of 5-100 microg/ml. CF within a 10-100 microg/ml concentration-range induced a significant dependent increase of SCE frequency and MNi over control values. At the same concentration-range, F increased significantly the SCE frequencies over control values although in a non-dependent manner while only an enhanced frequency of MNi was found in those 50 microg/ml-treated cultures. No binucleated cytokinesis-block cells were found in 100 microg/ml F-treated cultures. The NDI index revealed a delay in the onset of cell-division with 50 and 100 microg/ml of CF and F, respectively. The delayed rate of nuclear division induced by 100 microg/ml of F was higher than that induced by an equal concentration of CF. CF and F induced both a significant concentration-dependent delay in cell-cycle progression and a decrease in the proliferative replication index within 5-100 microg/ml and 50-100 microg/ml concentration-range, respectively. Decreased cell viability was found in up to 26% and 47% in 100 microg/ml CF- and F-treated cultures, respectively. The NR and MTT assays revealed a clear cell growth inhibition when concentrations of 50 and 100 microg/ml of either CF or F were employed. Accordingly, the results highlight that CF by itself and F, even in a greater extend exerts both genotoxicity and cytotoxicity in mammalian cells in culture, at least in CHOK1 cells. |
| Databáze: | OpenAIRE |
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