Literature DB >> 10575436

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

J Błasiak1, P Jałoszynski, A Trzeciak, K Szyfter.   

Abstract

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 microM 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 microM, 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.

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Year:  1999        PMID: 10575436     DOI: 10.1016/s1383-5718(99)00132-1

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  20 in total

1.  Cytogenetic evaluation of malathion-induced toxicity in Sprague-Dawley rats.

Authors:  Pamela D Moore; Anita K Patlolla; Paul B Tchounwou
Journal:  Mutat Res       Date:  2011-08-02       Impact factor: 2.433

2.  Agricultural pesticide use and risk of t(14;18)-defined subtypes of non-Hodgkin lymphoma.

Authors:  Brian C-H Chiu; Bhavana J Dave; Aaron Blair; Susan M Gapstur; Shelia Hoar Zahm; Dennis D Weisenburger
Journal:  Blood       Date:  2006-04-18       Impact factor: 22.113

3.  Cytogenotoxicity assessment of monocrotophos and butachlor at single and combined chronic exposures in the fish Catla catla (Hamilton).

Authors:  S Anbumani; Mary N Mohankumar
Journal:  Environ Sci Pollut Res Int       Date:  2014-11-08       Impact factor: 4.223

4.  Ecotoxicity of malathion pesticide and its genotoxic effects over the biomarker comet assay in Daphnia magna.

Authors:  Luís F O Knapik; Wanessa Ramsdorf
Journal:  Environ Monit Assess       Date:  2020-04-04       Impact factor: 2.513

5.  [Genotoxic effects of insecticides in current use on mucosal epithelial cells from human tonsil tissue].

Authors:  M Tisch; M Faulde; H Maier
Journal:  HNO       Date:  2007-05       Impact factor: 1.284

6.  Application of comet assay in the study of DNA damage and recovery in rohu (Labeo rohita) fingerlings after an exposure to phorate, an organophosphate pesticide.

Authors:  G Mohanty; J Mohanty; A K Nayak; S Mohanty; S K Dutta
Journal:  Ecotoxicology       Date:  2010-12-09       Impact factor: 2.823

7.  Geostatistical analysis of DNA damage in oysters, Crassostrea virginica, in Lavaca Bay, Texas.

Authors:  Wesley Bissett; Lauren Smith; James A Thompson
Journal:  Ecotoxicology       Date:  2008-09-01       Impact factor: 2.823

8.  Geostatistical analysis of biomarkers of genotoxicity in cattle, Bos taurus and Bos taurus x Bos indicus, sentinels near industrial facilities.

Authors:  Wesley Bissett; Roger Smith; L Garry Adams; Robert Field; William Moyer; Tim Phillips; H Morgan Scott; James A Thompson
Journal:  Ecotoxicology       Date:  2008-09-01       Impact factor: 2.823

9.  Malathion-induced oxidative stress, cytotoxicity, and genotoxicity in human liver carcinoma (HepG2) cells.

Authors:  Pamela D Moore; Clement G Yedjou; Paul B Tchounwou
Journal:  Environ Toxicol       Date:  2010-06       Impact factor: 4.119

10.  Lipid peroxidative damage on malathion exposure in rats.

Authors:  Jucéla J Fortunato; Fabiano R Agostinho; Gislaine Z Réus; Fabrícia C Petronilho; Felipe Dal-Pizzol; João Quevedo
Journal:  Neurotox Res       Date:  2006-01       Impact factor: 3.911

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