Potential genotoxic/cytotoxic effects of the epoxiconazole/fenpropimorph-based fungicide were investigated using single cell gel electrophoresis and cytogenetic assays: chromosomal aberrations, sister chromatid exchanges, micronuclei and fluorescence in situ hybridization in cultured bovine lymphocytes. No statistically significant elevations of DNA damage and increases in cytogenetic endpoints were seen. However, evident cytotoxic effect presented as a decrease in mitotic and proliferation indices were recorded after exposure of bovine lymphocytes to the fungicide for 24 and 48 h at concentrations ranging from 3 to 15 µg mL?1 (P < 0.05, P < 0.01, P < 0.001). Similarly, for 24 h an inhibition in the cytokinesis block proliferation index (CBPI) was obtained after exposure to the fungicide at concentrations ranging from 1.5 to 15 µg mL?1 (P < 0.01, P < 0.001) in each donor. 相似文献
Health risks associated with inhalation of fine particulate matter of 2.5 µm in diameter or smaller depend on their atmospheric levels and physicochemical properties. The relationships between chemical compositions and genotoxic activities of particles emitted by mineral industries, traffic and urban sources during summer and winter in the region of Provence-Alpes-Côte d'Azur (France) were investigated.
The fine particles were separated in respect to water-soluble (13 minerals and metals) and organic-extractable (16 polycyclic aromatic hydrocarbons) components that were quantified. The chromosome damaging properties of the hydrophilic and lipophilic extracts were assessed using the centromeric micronucleus assay on a human lung fibroblast cell line.
The composition of the fine particulate matter was variable and depended upon the sources and seasons. Both the hydrophilic and lipophilic extracts induced chromosome damage: (1) in hydrophilic extracts, Ca and Zn affected chromosome losses induction; (2) acenapthylene affected chromosome damage (breakages and losses) induction and naphthalene affected chromosome damage and losses induction in lipophilic extracts without metabolic activation; and (3) benzo[a]pyrene affected chromosome losses induction in lipophilic extracts with metabolic activation. Fine particulate matter arising from coal-fired power station, road traffic, and other urban sources were the most efficient to induce chromosome breakage. 相似文献
Despite that the use of DDT has been restricted for more than 40 years to malaria affected areas, low doses of this pesticide and its metabolites DDE and DDD can be found in the environment around the world. Although it has been shown that these pollutants induce cell and DNA damage, the mechanisms of their cytogenotoxic activity remains largely unknown. This study looks into their possible genotoxic effects, at doses that can be found in body fluids, on human lymphocytes using the cytokinesis-block micronucleus assay and the comet assay. After exposure for 1, 6, and 24 h compounds p,p′-DDT (0.1 μg mL−1), p,p′-DDE (4.1 μg mL−1), and p,p′-DDD (3.9 μg mL−1) showed increase in DNA damage. The most significant results were observed at exposure period of 24 h where number of micronucleated cells increased from control 2.5 ± 0.71 to 23.5 ± 3.54, 13.5 ± 0.71, and 16.5 ± 6.36 for DDT, DDE, and DDD, respectively. Similar effect was observed using comet test where the percentage of DNA in comets tail increased from control 1.81 ± 0.16 to 17.24 ± 0.55, 11.21 ± 0.56 and 9.28 ± 0.50 for each compound, respectively. At the same time Fpg-comet assay failed to report induction of oxidative DNA damage of these pollutants. Additionally, the type of cell death was determined using diffusion assay and necrosis dominated. Our findings suggest that even at low concentrations, these pesticides could induce cytogenetic damage to human peripheral blood lymphocytes and in that manner have the impact on human health as well. 相似文献
Background, Aim and Scope
Perfluorooctane sulfonate (PFOS; C8F17SO3-) is a fully fluorinated organic compound which has been manufactured for decades
and was used widely in industrial and commercial products. The recent toxicological knowledge of PFOS mainly concerns mono-substance
exposures of PFOS to biological systems, leaving the potential interactive effects of PFOS with other compounds as an area
where understanding is significantly lacking. However, a recent study, reported the potential of PFOS to enhance the toxicity
of two compounds by increasing cell membrane permeability. This is of particular concern since PFOS has been reported to be
widely distributed in the environment where contaminants are known to occur in complex mixtures. In this study, PFOS was evaluated
alone and in combination with cyclophosphamide (CPP) to investigate whether a presence of PFOS leads to an increased genotoxic
potential of CPP towards hamster lung V79 cells. Genotoxicity was investigated using the micronucleus (MN) assay according
to the recent draft ISO/DIS 21427-2 method. PFOS alone demonstrated no genotoxicity up to a concentration of 12.5 mg/L. However,
PFOS combined with two different concentrations of CPP, with metabolic activation, caused a significant increase in the number
of micronucleated cells compared to treatments with CPP only. These results provide a first indication that PFOS has the potential
to enhance the genotoxic action of CPP towards V79 cells, suggesting that together with the alterations in cell membrane properties
shown previously, that genotoxicity of complex mixtures may be increased significantly by changes in chemical uptake. Together
with an earlier study performed by the own working group it can be concluded that PFOS alone is not genotoxic in this bioassay
using V79 cells up to 12.5 mg/L, but that further investigations are needed to assess the potential interaction between PFOS
and other substances, in particular regarding the impact of membrane alterations on the uptake of toxic substances.
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