Molecular dosimetry of endogenous and ethylene oxide-induced N7-(2-hydroxyethyl) guanine formation in tissues of rodents
Authors: Wu K-Y.1; Ranasinghe A.1; Upton P.B.1; Walker V.E.1, 2; Swenberg J.A.1
Source: Carcinogenesis, Volume 20, Number 9, September 1999 , pp. 1787-1792(6)
Publisher: Oxford University Press
Abstract:
The formation of N7-(2-hydroxyethyl)guanine (7-HEG) in DNA was investigated previously in target and non-target tissues of F-344 rats and B6C3F1 mice exposed to
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10 p.p.m. concentrations of ethylene oxide (EO) using fluorescence-linked high-performance liquid chromatography [V.E.Walker et al. (1992) Cancer Res., 52, 42384334]. In order to study the doseresponses for 7-HEG at lower exposures, a highly sensitive and specific gas chromatography coupled with high-resolution mass spectrometry (GCHRMS) assay was developed. DNA was extracted from liver, brain, lung and spleen of B6C3F1 mice and F-344 rats exposed to 0, 3, 10, 33 or 100 p.p.m. EO for 4 weeks (6 h/day, 5 days/week). Analysis of DNA from control rodents showed that endogenous 7-HEG varied from 0.2 ± 0.1 to 0.3 ± 0.2 pmol/
mol guanine in tissues of rats and mice. 7-HEG exhibited tissue- and species-specific doseresponse relationships in EO-exposed animals. Linear doseresponse relationships were evident in mouse liver, brain and spleen at exposures between 3 and 100 p.p.m.. Mouse lung exhibited a slightly sublinear response between 33 and 100 p.p.m. EO. The relationships were linear in liver and spleen of rats between 3 and 100 p.p.m. EO, but were slightly sublinear in brain and lung between 33 and 100 p.p.m. EO. The number of 7-HEG adducts present in rats exposed to 3 p.p.m. EO was 5.312.5 times higher than endogenous 7-HEG in unexposed controls. In contrast, mice exposed to 3 p.p.m. EO only had 1.3- to 2.5-fold greater numbers of 7-HEG adducts. The factors driving the exposureresponse relationships are also likely to affect carcinogenic and mutagenic responses of rodents to EO. Likewise, a better understanding of the relationships between 7-HEG derived from low exposures to EO and endogenously formed 7-HEG may be important for the accurate extrapolation of risk to humans.
Document Type: Original article
Affiliations: 1: Department of Environmental Sciences and Engineering, University of North Carolina, Chapel Hill, NC 27599 and 2: Wadsworth Center for Laboratory and Research, New York State Department of Health, Empire State Plaza, PO Box 509, Albany, NY 12201, USA

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