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  4. Molecular dosimetry of endogenous and ethylene oxide-induced N7-(2-hydroxyethyl) guanine formation in tissues of rodents
 
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Molecular dosimetry of endogenous and ethylene oxide-induced N7-(2-hydroxyethyl) guanine formation in tissues of rodents

Journal
Carcinogenesis
Journal Volume
20
Journal Issue
9
Pages
1787-1792
Date Issued
1999
Author(s)
KUEN-YUH WU  
Ranasinghe A.
Upton P.B.
Walker V.E.
Swenberg J.A.
DOI
10.1093/carcin/20.9.1787
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0032841761&doi=10.1093%2fcarcin%2f20.9.1787&partnerID=40&md5=4443cb8c40d443ec1a6d4420941cdb3b
https://scholars.lib.ntu.edu.tw/handle/123456789/601701
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 ≥ 10 p.p.m. concentrations of ethylene oxide (EO) using fluorescence-linked high-performance liquid chromatography. In order to study the dose-responses for 7-HEG at lower exposures, a highly sensitive and specific gas chromatography coupled with high-resolution mass spectrometry (GC-HRMS) 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/μmol guanine in tissues of rats and mice. 7-HEG exhibited tissue- and species-specific dose-response relationships in EO-exposed animals. Linear dose-response 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 5.3-12.5 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 exposure-response 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.
Type
journal article

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