© 1990 Oxford University Press
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Vinyl chloride-induced DNA adducts II: Formating and persistence of 7-(2'oxoethyl)guanine and N2 ,3 ethenoguanine in rat tissue DNA
Chemical Industry Institute of Toxicology, Department of Biochemical Toxicology and Pathobiology PO Box 12137, Research Triangle Park, NC 27709 USA
1Present address: Hüls AG, PS Biologie und Toxikologie, Postfach 1320, D-4370 Marl, FRG
2Present address: Department of Pathology, Campus Box 7095, University of North Carolina, Chapel Hill, NC 27599, USA
3To whom correspondence should be addressed
The formation and persistence of the DNA adducts 7-(2'-oxo-ethyl)guanine (OEG) and N2 ,3-ethenoguanine (EG) were investigated in preweanling SpragueDawley rats exposed to chloride (VC). Lactating female CD rats with 10 day old pups were exposed to 600 p.p.m. VC by inhalation for 5 days, 4 /day. Groups of rats were killed immediately and 3, 7 and 14 days after exposure. The concentrations of OEG and EG were measured in liver, lung, kidney, brain and spleen. HPLC with fluorescence detection was used for OEG detection, and gas chromatographynegative ion chemical ionization mass spectrometry was used for EG detection. In tissues of neonatal rats, the concentrations of both DNA adducts, expressed as pmo/µmol unmodified guanine, were highest in liver (OEG 162 ± 36, EG 1.81 ± 0.25), followed by kidney (OEG 29 ± 1, EG 0.31 ± 0.02), and lung (OEG 20 ± 7, EG 0.21 ± 0.08). No adducts were found in brain or spleen. DNA adducts were detected only In liver (OEG 43 ± 7, EG 0.47 ± 0.14) and lung (OEG 20 ± 5, EG 0.27 ± 0.03) of the dams. The ratio between EG and OEG was
1:100 in all tissues immediately after exposure. In the liver of the preweanling rats, this ratio increased to 1:14 1 week after exposure, reflecting a greater persistence of EG. A half-life of 62 h was calculated for OEG, and the estimated half-life for EG was >30 days. In view of the slow loss of EG and its high efficiency for causing base-pair mismatch, these results suggest that EG may be an important DNA adduct in VC-induced carcinogenesis.
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