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
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
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.