Effect of dithiocarbamate pesticide zineb and its commercial formulation, azzurro IV.: DNA damage and repair kinetics assessed by single cell gel electrophoresis (SCGE) assay on Chinese hamster ovary (CHO) cells

被引:23
作者
González, M [1 ]
Soloneski, S [1 ]
Reigosa, MA [1 ]
Larramendy, ML [1 ]
机构
[1] Natl Univ La Plata, Fac Ciencias Nat & Museo, Lab Citogenet, Catedra Citol, RA-1900 La Plata, Argentina
关键词
comet assay; Chinese hamster ovary (CHO) cells; zineb; azzurro; dithiocarbamates; repair kinetics;
D O I
10.1016/S1383-5718(02)00257-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Single cell gel electrophoresis (SCGE) was used to analyse dithiocarbamate zineb- and the zineb-containing technical formulation azzurro-induced DNA damage and repair in CHO cells. Cells were treated with zineb (50.0 mug/ml) or azzurro (100.0 mug/ml) for 80 min, washed and reincubated in pesticide-free medium for 0-12 It until SCGE. Viability of treated cells (0 h) did not differ from control remaining unchanged up to 6 h of incubation. After 12 h, viability decreased up to 70 and 54% in zineb- and azzurro-treated cultures, respectively. SCGE revealed at 0 h the absence of undamaged cells and an increase of slightly damaged and damaged cells in zineb-treated cultures or by an increase in damaged cells in azzurro-treated cultures. For both chemicals, a time-dependent repair of pesticide-induced DNA damage within a 0-12 h post-treatment incubation period was observed. Overall, damaged cells decreased as a function of the repair time for both pesticides while the slightly damaged cells decreased as a function of the repair time of zineb-induced DNA damage. Concomitantly, a time-dependent increase of undamaged cells was observed within the 0.5-12 h repair time for both pesticides. At 12 h after treatment, no differences in the frequencies of undamaged, slightly damaged and damaged cells were found between both zineb- or azzurro-treated cultures and control values as well as between zineb- and azzurro-treated cells. Immediately after exposure, nuclear DNA from zineb and azzurro-treated cells were larger and wider than nuclear DNA from untreated cells. When damaged cells were allowed to repair, a time-dependent decrease of the amount of free DNA migrating fragments was observed committed only to damaged cells but not in slightly or undamaged cells. On the other hand, no time-dependent alteration on nuclear DNA width within the 0-12 h repair period was observed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 154
页数:10
相关论文
共 30 条
  • [1] ANDRIANOVA M M, 1970, Voprosy Pitaniya, V29, P71
  • [2] [Anonymous], MON EV CARC RISKS HU
  • [3] [Anonymous], MON EV CARC RISK CHE
  • [4] Banu BS, 2001, FOOD CHEM TOXICOL, V39, P361, DOI 10.1016/S0278-6915(00)00141-1
  • [5] BLACKWELLSMITH R, 1953, J PHARMACOL EXP THER, V109, P159
  • [6] In vitro studies on the genotoxicity of the organophosphorus insecticide malathion and its two analogues
    Blasiak, J
    Jaloszynski, P
    Trzeciak, A
    Szyfter, K
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1999, 445 (02) : 275 - 283
  • [7] Chernov OV, 1969, VOP ONKOL, V15, P71
  • [8] Della Croce C, 1996, J Environ Pathol Toxicol Oncol, V15, P21
  • [9] Analysis of DNA alkylation damage and repair in mammalian cells by the comet assay
    Fortini, P
    Raspaglio, G
    Falchi, M
    Dogliotti, E
    [J]. MUTAGENESIS, 1996, 11 (02) : 169 - 175
  • [10] GENOTOXICITY OF DITHIOCARBAMATES AND THEIR METABOLITES
    FRANEKIC, J
    BRATULIC, N
    PAVLICA, M
    PAPES, D
    [J]. MUTATION RESEARCH LETTERS, 1994, 325 (2-3): : 65 - 74