COMPARISON OF THE DISPOSITION OF BUTADIENE EPOXIDES IN SPRAGUE-DAWLEYRATS AND B6C3F(1) MICE FOLLOWING A SINGLE AND REPEATED EXPOSURES TO 1,3-BUTADIENE VIA INHALATION

Citation
Jr. Thorntonmanning et al., COMPARISON OF THE DISPOSITION OF BUTADIENE EPOXIDES IN SPRAGUE-DAWLEYRATS AND B6C3F(1) MICE FOLLOWING A SINGLE AND REPEATED EXPOSURES TO 1,3-BUTADIENE VIA INHALATION, Toxicology, 123(1-2), 1997, pp. 125-134
Citations number
34
Categorie Soggetti
Toxicology,"Pharmacology & Pharmacy
Journal title
ISSN journal
0300483X
Volume
123
Issue
1-2
Year of publication
1997
Pages
125 - 134
Database
ISI
SICI code
0300-483X(1997)123:1-2<125:COTDOB>2.0.ZU;2-R
Abstract
1,3-Butadiene (BD), a compound used extensively in the rubber industry , is a potent carcinogen in mice and a weak carcinogen in rats in chro nic carcinogenicity bioassays. While many chemicals are known to alter their own metabolism after repeated exposures, the effect of exposure prior to BD on its in vivo metabolism has not been reported. The purp ose of the present research was to examine the effect of repeated expo sure to BD on tissue concentrations of two mutagenic BD metabolites, b utadiene monoepoxide (BDO) and butadiene diepoxide (BDO2). Concentrati ons of BD epoxides were compared in several tissues of rats and mice f ollowing a single exposure or ten repeated exposures to a target conce ntration of 62.5 ppm BD. Female Sprague-Dawley rats and female B6C3F(1 ) mice were exposed to BD for 6 h or 6 h x 10 days. BDO and BDO2 were quantified in blood and several other tissues following preparation by cryogenic vacuum distillation and analysis by multidimensional gas ch romatography-mass spectrometry. Blood and lung BDO concentrations did not differ significantly (P less than or equal to 0.05) between the tw o exposure regimens in either species. Following multiple exposures to BD, BDO levels were 5- and 1.6-fold higher (P less than or equal to 0 .05) in mammary tissue and 2- and 1.4-fold higher in fat tissue of rat s and mice, respectively, as compared with single exposures. BDO2 leve ls also increased in rat fat tissue following multiple exposures to BD . However, in mice, levels of this metabolite decreased by 15% in fat, by 28% in mammary tissue and by 34% in lung tissue following repeated exposures to BD. The finding that the mutagenic epoxide BDO, which is the precursor to the highly mutagenic BDO2, accumulates in rodent fat may be important in assessing the potential risk to humans from inhal ation of BD. (C) 1997 Elsevier Science Ireland Ltd.