INVESTIGADORES
DI VIRGILIO Ana Laura
congresos y reuniones científicas
Título:
Genotoxicity of the isoflavone Phytoestrogens Daidzein and Genistein in V79 cells
Autor/es:
DI VIRGILIO A.L.; DEGEN G.H.; BOLT H.M
Lugar:
Karlsruhe, Alemania
Reunión:
Congreso; XIII Congreso de Nutrición. “Phytoestrogens: benefits and risk for human health”.; 2003
Resumen:
The presence of hormonally active chemicals in the human diet , such as man-made estrogenic or plant derived compounds (phytoestrogens), has become a matter of concern. A significant part of the human exposure to phytoestrogens is attributable to soy isoflavones. Apart from the hormonal activity of daidzein and genistein, the question of genotoxicity has been raised for these compounds. Cytotoxicity of daidzein and genistein was assessed with the Neutral Red uptake and BCA assay in Chinese hamster fibroblast V79 cells. Cells were seeded into a 96 well plate (104  cells/well in 200 µl DMEM medium) in the presence of different concentrations of phytoestrogens. The dose range for daidzein and genistein was 25-150 µM and 5-100 µM, respectively. Genistein and daidzein caused no overt cytotoxicity within the dose range investigated. The alkaline elution (COMET) assay was used to detect DNA damage such as double and single strand breaks and alkali labile sites. When V79 cells were treated with isoflavones for 3, 12 and 18 h, a weak positive trend was observed for daidzein (25-100 µM), but not for genistein (5-50 µM). The micronucleus (MN) assay in V79 cells was then used to study chromosomal genotoxicity. V79 cells were grown in 25 cm2 flasks and treated with solutions of the test compounds in DMSO for 18 h. Cells were harvested, fixed on slides and stained with Acridine Orange for fluorescence microscopy. Genistein caused a clear dose-related induction of MN within the range of 5-25 µM. MN rates were declining at higher concentrations. By contrast, daidzein caused a comparatively shallow increase in the number of MN between 25-100 µM. Additional staining with the anti-kinetochore (CREST) antibodies served to determine if the micronuclei contain whole chromosomes or acentric fragments. Genistein induced mostly CREST (-) micronuclei, i.e., MN containing chromosomal fragments, thus indicative of clastogenic mode of action. MN induced by high concentrations of daidzein were partly CREST (+) and CREST(-). In essence, this points a differential genotoxicity of daidzein and genistein. Data on equol which is presently under investigation in these assays will be presented also.