EVALUATION OF GENOTOXIC POTENTIAL OF STYRENE IN FURNITURE WORKERS USING UNSATURATED POLYESTER RESINS

Citation
Ae. Karakaya et al., EVALUATION OF GENOTOXIC POTENTIAL OF STYRENE IN FURNITURE WORKERS USING UNSATURATED POLYESTER RESINS, Mutation research. Genetic toxicology and environmental mutagenesis, 392(3), 1997, pp. 261-268
Citations number
49
Categorie Soggetti
Toxicology,"Genetics & Heredity
ISSN journal
13835718
Volume
392
Issue
3
Year of publication
1997
Pages
261 - 268
Database
ISI
SICI code
1383-5718(1997)392:3<261:EOGPOS>2.0.ZU;2-3
Abstract
Styrene is a widely used chemical, mostly in making synthetic rubber, resins, polyesters, plastics and insulators. Increasing attention has been focused on this compound since experiments using cytogenetic end- points have implicated styrene as a potential carcinogen and mutagen. In order to perform biological monitoring of genotoxic exposure to sty rene monomer, we evaluated the urinary thioether (UT) excretion, and s ister chromatid exchanges (SCEs) and micronuclei (MN) in peripheral ly mphocytes from 53 furniture workers employed in small workplaces where polyester resin lamination processings were done and from 41 matched control subjects. The mean air concentration of styrene in the breathi ng zone of workers was 30.3 ppm. As a metabolic marker for styrene exp osure, mandelic acid + phenylglyoxylic acid was measured in the urine and the mean value was 207 mg/g creatinine. The mean +/- SD value of U T excretions of workers was 4.43 +/- 3.42 mmol SH-/mol creatinine and also mean UT for controls was found to be a 2.75 +/- 1.78 mmol SH-/mol creatinine. The mean +/- SD/cell values of SCE frequency in periphera l lymphocytes from the workers and controls were 6.20 +/- 1.56 and 5.2 3 +/- 1.23, respectively. The mean +/- SD frequencies (parts per thous and) of MN in the exposed and control groups were 1.98 +/- 0.50 and 2. 09 +/- 0.35, respectively. Significant effects of work-related exposur e were detected in the UT excretion and SCEs analyzed in peripheral bl ood lymphocytes (p < 0.05 and p < 0.01, respectively). The MN frequenc y in lymphocytes from the styrene-exposed group did not differ from th at in the controls (p > 0.05). Effect of smoking, age and duration of exposure on the genotoxicity parameters analyzed were also evaluated. In conclusion, although our data do not demonstrate a dose-response re lationship, they do suggest that styrene exposure was evident and that this styrene exposure may contribute to the observed genotoxic damage in furniture workers.