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Metabolism of butadiene by mice, rats, and humans: a comparison of physiologically based toxicokinetic model predictions and experimental data.

作者信息

Bond J A, Himmelstein M W, Seaton M, Boogaard P, Medinsky M A

机构信息

Chemical Industry Institute of Toxicology, Research Triangle Park, NC 27709, USA.

出版信息

Toxicology. 1996 Oct 28;113(1-3):48-54. doi: 10.1016/0300-483x(96)03426-9.

DOI:10.1016/0300-483x(96)03426-9
PMID:8901882
Abstract

1,3-Butadiene is a carcinogen in rats and mice, with mice being substantially more sensitive than rats. Our recent research is directed toward obtaining a better understanding of the cancer risk of butadiene in humans by evaluating species-dependent differences in the formation of the toxic metabolites epoxybutene and diepoxybutane. The recent data include in vitro studies on butadiene metabolism using tissues from humans, rats, and mice as well as experimental data and physiological model predictions for butadiene in blood and butadiene epoxides in blood, lung, and liver after exposure of rats and mice to inhaled butadiene. The findings suggest that humans would be more like rats and less like mice regarding the formation of butadiene epoxides. These research findings permit a reassessment of some default options that are used in carcinogen risk assessments. The research approach employed can be a useful strategy for developing mechanistic and toxicokinetic data to supplant default assumptions used in carcinogen risk assessments.

摘要

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1
Metabolism of butadiene by mice, rats, and humans: a comparison of physiologically based toxicokinetic model predictions and experimental data.
Toxicology. 1996 Oct 28;113(1-3):48-54. doi: 10.1016/0300-483x(96)03426-9.
2
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Quantitative and qualitative differences in the metabolism of 14C-1,3-butadiene in rats and mice: relevance to cancer susceptibility.
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PBPK model for butadiene metabolism to epoxides: quantitative species differences in metabolism.用于丁二烯代谢生成环氧化物的生理药代动力学(PBPK)模型:代谢中的定量物种差异
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IARC Sci Publ. 1993(127):45-55.
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