In vitro studies on the genotoxicity of the organophosphorus insecticide malathion and its two analogues

被引:108
作者
Blasiak, J
Jaloszynski, P
Trzeciak, A
Szyfter, K
机构
[1] Univ Lodz, Dept Mol Genet, PL-90237 Lodz, Poland
[2] Polish Acad Sci, Inst Human Genet, PL-60479 Poznan, Poland
关键词
organophosphorus insecticide; malathion; DNA damage; comet assay; DNA repair; human peripheral blood lymphocyte;
D O I
10.1016/S1383-5718(99)00132-1
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
Malathion [S-(1,2-dicarboethoxyethyl)O,O-dimethyl phosphorodithioate] is a commonly used organophosphorus insecticide reported to be genotoxic both in vivo and in vitro, but the reports are conflicting. In order to elucidate the genotoxic potency of the main compounds present in commercial preparations of malathion, the DNA-damaging effect of this insecticide, its major metabolite malaoxon [S-(1,2-dicarboethoxyethyl)O,O-dimethyl phosphorothiolate] and its isomer isomalathion [S-(1,2-dicarboethoxyethyl)O,S-dimethyl phosphorodithioate], all at purity of at least 99.8%, was investigated by use of the alkaline single cell gel electrophoresis (comet assay). Freshly isolated human peripheral blood lymphocytes were incubated with 25, 75 and 200 mu M of the chemicals for 1 h at 37 degrees C. The concentrations used are comparable to those found in blood following various non-lethal human exposures to pesticides. Malathion did not cause any significant changes in the comet length of the lymphocytes, throughout the range of concentrations tested. Malaoxon and isomalathion introduced damage to DNA in a dose-dependent manner. The effect induced by malaoxon was more pronounced than that caused by isomalathion. Treated cells were able to recover within a 60-min incubation in insecticide-free medium at 37 degrees C except the lymphocytes exposed to malaoxon at 200 mu M, which did not show measurable DNA repair. The latter result suggests a considerable cytotoxic effect (cell death) of malaoxon at the highest concentration used. The reported genotoxicity of malathion might, therefore, be a consequence of its metabolic biotransformation to malaoxon or the presence of malaoxon and/or isomalathion as well as other unspecified impurities in commercial formulations of malathion. In this regard, the results of our study clearly indicate that malathion used as commercial product, i.e., containing malaoxon and isomalathion, can be considered as a genotoxic substance in vitro. This means that it may also produce DNA disturbances in vivo, such as DNA breakage at sites of oncogenes or tumor suppressor genes, thus playing a role in the induction of malignancies in individuals exposed to this agent. Therefore, malathion can be regarded as a potential mutagen/carcinogen and requires further investigation. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:275 / 283
页数:9
相关论文
共 45 条
  • [1] THE SINGLE-CELL GEL-ELECTROPHORESIS ASSAY FOR INDUCED DNA-DAMAGE (COMET ASSAY) - MEASUREMENT OF TAIL LENGTH AND MOMENT
    ASHBY, J
    TINWELL, H
    LEFEVRE, PA
    BROWNE, MA
    [J]. MUTAGENESIS, 1995, 10 (02) : 85 - 90
  • [2] BAKER EL, 1978, LANCET, V1, P31
  • [3] CYTOGENETIC EFFECT OF MALATHION IN INVITRO CULTURE OF HUMAN PERIPHERAL-BLOOD
    BALAJI, M
    SASIKALA, K
    [J]. MUTATION RESEARCH, 1993, 301 (01): : 13 - 17
  • [4] SYNTHESIS, ABSOLUTE-CONFIGURATION, AND ANALYSIS OF MALATHION, MALAOXON, AND ISOMALATHION ENANTIOMERS
    BERKMAN, CE
    THOMPSON, CM
    PERRIN, SR
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1993, 6 (05) : 718 - 723
  • [5] COMPARATIVE-STUDIES ON CYTOTOXIC AND GENOTOXIC EFFECTS OF 2 ORGANIC MERCURY-COMPOUNDS IN LYMPHOCYTES AND GASTRIC-MUCOSA CELLS OF SPRAGUE-DAWLEY RATS
    BETTI, C
    BARALE, R
    POOLZOBEL, BL
    [J]. ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1993, 22 (03) : 172 - 180
  • [6] BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
  • [7] The comet assay: What can it really tell us?
    Collins, AR
    Dobson, VL
    Dusinska, M
    Kennedy, G
    Stetina, R
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 375 (02) : 183 - 193
  • [8] CYTOGENETIC BIOMONITORING OF AN ITALIAN POPULATION EXPOSED TO PESTICIDES - CHROMOSOME ABERRATION AND SISTER-CHROMATID EXCHANGE ANALYSIS IN PERIPHERAL-BLOOD LYMPHOCYTES
    DEFERRARI, M
    ARTUSO, M
    BONASSI, S
    BONATTI, S
    CAVALIERI, Z
    PESCATORE, D
    MARCHINI, E
    PISANO, V
    ABBONDANDOLO, A
    [J]. MUTATION RESEARCH, 1991, 260 (01): : 105 - 113
  • [9] *DHS, 1991, HLTH RISK ASS AER AP
  • [10] CYTOGENETIC EFFECT OF MALATHION ASSESSED BY THE MICRONUCLEUS TEST
    DULOUT, FN
    OLIVERO, OA
    VONGURADZE, H
    PASTORI, MC
    [J]. MUTATION RESEARCH, 1982, 105 (06): : 413 - 416