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Oxidative damage to biological macromolecules in Prague bus drivers and garagemen: impact of air pollution and genetic polymorphisms
Y. Bagryantseva, B. Novotna, P. Rossner, I. Chvatalova, A. Milcova, V. Svecova, Z. Lnenickova, I. Solansky, RJ. Sram,
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Dinoprost analogs & derivatives urine MeSH
- DNA Glycosylases genetics metabolism MeSH
- DNA drug effects MeSH
- Genetic Predisposition to Disease MeSH
- Glutathione Transferase genetics MeSH
- Guanine analogs & derivatives urine MeSH
- Protein Carbonylation drug effects MeSH
- Comet Assay MeSH
- Air Pollutants, Occupational toxicity MeSH
- Humans MeSH
- Lymphocytes chemistry drug effects MeSH
- Oxidative Stress drug effects MeSH
- Lipid Peroxidation drug effects MeSH
- Polycyclic Aromatic Hydrocarbons analysis toxicity MeSH
- Polymorphism, Genetic MeSH
- DNA Damage MeSH
- Volatile Organic Compounds analysis toxicity MeSH
- Vasoconstrictor Agents urine MeSH
- Vehicle Emissions toxicity MeSH
- Xeroderma Pigmentosum Group D Protein genetics MeSH
- Air Pollution MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
DNA integrity was investigated in the lymphocytes of 50 bus drivers, 20 garagemen and 50 controls using the comet assay with excision repair enzymes. In parallel, 8-oxo-7,8-dihydro-2'-deoxyguanosine and 15-F(2t)-isoprostane levels in the urine and protein carbonyl levels in the plasma were assessed as markers of oxidative damage to DNA, lipids and proteins. Exposure to carcinogenic polycyclic aromatic hydrocarbons (cPAHs) and volatile compounds was measured by personal samplers for 48 and 24h, respectively, before the collection of biological specimens. Both exposed groups exhibited a higher levels of DNA instability and oxidative damage to biological macromolecules than the controls. The incidence of oxidized lesions in lymphocyte DNA, but not the urinary levels of 8-oxodG, correlated with exposure to benzene and triglycerides increased this damage. Oxidative damage to lipids and proteins was associated with exposure to cPAHs and the lipid peroxidation levels positively correlated with age and LDL cholesterol, and negatively with vitamin C. The carriers of at least one variant hOGG1 (Cys) allele tended to higher oxidative damage to lymphocyte DNA than those with the wild genotype, while XPD23 (Gln/Gln) homozygotes were more susceptible to the induction of DNA strand breaks. In contrast, GSTM1 null variant seemed to protect DNA integrity.
References provided by Crossref.org
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