Sister chromatid exchanges and chromosomal aberrations in Chinese hamster ovary (CHO-K1) cells treated with the insecticide pirimicarb

被引:43
|
作者
Soloneski, Sonia [1 ]
Larramendy, Marcelo L. [1 ]
机构
[1] Univ Nacl La Plata, Fac Ciencias Nat & Museo, Catedra Citol, Lab Citogenet, RA-1900 La Plata, Argentina
关键词
Carbamates; Cytotoxicity; Genotoxicity; Mammalian cell lines; Technical formulations; LYMPHOCYTES IN-VITRO; DITHIOCARBAMATE PESTICIDE ZINEB; COMMERCIAL FORMULATION; DAPHNIA-MAGNA; DNA-DAMAGE; VITAMIN-E; GENOTOXICITY; BLEOMYCIN; TOXICITY; INDUCTION;
D O I
10.1016/j.jhazmat.2009.09.068
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Pirimicarb and its formulation Aficida (R) (50% pirimicarb) effects were studied on CHO-K1 cells employing sister chromatid exchange (SCE), chromosomal aberrations (CA), cell-cycle progression and mitotic index analyses. Continuous treatments were performed within 10-300 mu g/ml concentration-range. Pirimicarb, but not Aficida (R). induced a concentration-dependent increase of abnormal cells. Pirimicarb induced a greater frequency of chromatid/isochromatid breaks than Aficida (R) did. Regression analyses showed a concentration-dependent increase in the frequency of chromatid-type breaks for both compounds whereas only the frequency of isochromatid-type breaks did in those pirimicarb-treated cultures. SCEs in pirimicarb- or Aficida (R)-treated cultures were significantly higher than control values with concentrations of 100-200 mu g/ml. Both test compounds induced equivalent frequency of SCEs. A delay in cell-cycle kinetics was observed for pirimicarb and Aficida (R) within 100-300 and 200-300 mu g/ml concentration-range, respectively. An inhibition of MI was observed for both chemicals regardless of tested concentrations. Finally, the CAs appears to be a higher sensitive bioassay to detect DNA damage at lower concentrations of pirimicarb than SCEs does. The results demonstrated that pirimicarb and Aficida (R) exert geno-cytotoxicity, at least in CHO-K1 cells. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:410 / 415
页数:6
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