Studies on the mechanism of benzene toxicity.
Author(s) -
Robert Snyder,
Evangelos A. Dimitriadis,
Robert L. Guy,
Peidi Hu,
Keith R. Cooper,
Heinrich Bauer,
Guillaume Witz,
Bernard D. Goldstein
Publication year - 1989
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.898231
Subject(s) - hydroquinone , benzene , benzoquinone , chemistry , catechol , toxicity , pharmacology , toluene , phenol , micronucleus test , biochemistry , biology , organic chemistry
Using the 59Fe uptake method of Lee et al. it was shown that erythropoiesis in female mice was inhibited following IP administration of benzene, hydroquinone, p-benzoquinone, and muconaldehyde. Toluene protected against the effects of benzene. Coadministration of phenol plus either hydroquinone or catechol resulted in greatly increased toxicity. The combination of metabolites most effective in reducing iron uptake was hydroquinone plus muconaldehyde. We have also shown that treating animals with benzene leads to the formation of adducts of bone marrow DNA as measured by the 32P-postlabeling technique.
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