N. Titenkoholland et al., GENOTOXICITY OF MALATHION IN HUMAN-LYMPHOCYTES ASSESSED USING THE MICRONUCLEUS ASSAY IN-VITRO AND IN-VIVO - A STUDY OF MALATHION-EXPOSED WORKERS, Mutation research. Genetic toxicology and environmental mutagenesis, 388(1), 1997, pp. 85-95
The aerial application of malathion, a widely used organophosphate ins
ecticide, has raised public concerns about potential adverse health ef
fects. We therefore studied micronucleus formation in human lymphocyte
s as a biomarker of genotoxicity both in vitro and in vivo. Lymphocyte
s were cultured either as whole blood or after Ficoll isolation and tr
eated with malathion in doses from 5 to 100 mu g/ml for 48 h. A signif
icant increase in micronucleated cells (47.5/1000 versus 16.0/1000 in
DMSO control, p < 0.001) was found in isolated lymphocytes at high dos
e levels (75-100 mu g/ml), concurrent with cytotoxicity and a strong i
nhibition of proliferation (p < 0.001). Many of the treated cells also
possessed multiple micronuclei. Antikinetochore-antibody staining rev
ealed that the majority of malathion-induced micronuclei were kinetoch
ore-negative. A significant dose-response was also observed in whole b
lood cultures, although the increase in micronucleated cells was lower
than in isolated lymphocyte cultures (p = 0.03). When the same techni
que was applied to lymphocytes of 38 intermittently malathion-exposed
workers involved in the Mediterranean Fruit Fly Eradication Program in
California, no change in either proliferation or micronucleus level w
as observed compared with an unexposed control group. We conclude that
malathion has a relatively low potential to cause chromosome damage i
n vitro, and corresponding doses are much higher than ones that even p
rofessional applicators are likely to be exposed to in vivo. The poten
tial risk of chromosome damage for malathion exposure in vivo is there
fore relatively low. More studies are needed to assess the possibility
of interaction of malathion with other pesticides through combined ex
posure.