Literature DB >> 3173399

Benzene and the genotoxicity of its metabolites. II. The effect of the route of administration on the micronuclei and bone marrow depression in mouse bone marrow cells.

R Ciranni1, R Barale, G Ghelardini, N Loprieno.   

Abstract

Benzene (880 mg/kg) and 4 of its metabolites, i.e., phenol (265 mg/kg), hydroquinone (80 mg/kg), catechol (40 mg/kg), and p-benzoquinone (5-20 mg/kg) have been tested for their capability to induce micronuclei in bone marrow cells of male mice after oral administration or intraperitoneal injection. Oral administration of benzene shows more activity than intraperitoneal injection, whereas the metabolites show more activity if administered by the latter method. The respective genotoxic strengths of the benzene metabolites are the following: hydroquinone much greater than phenol greater than catechol = p-benzoquinone. This last is active when administered orally.

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Year:  1988        PMID: 3173399     DOI: 10.1016/0165-7992(88)90105-4

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  3 in total

1.  Mortality study of employees engaged in the manufacture and use of hydroquinone.

Authors:  J W Pifer; F T Hearne; F A Swanson; J L O'Donoghue
Journal:  Int Arch Occup Environ Health       Date:  1995       Impact factor: 3.015

Review 2.  Mechanistic considerations in benzene physiological model development.

Authors:  M A Medinsky; E M Kenyon; M J Seaton; P M Schlosser
Journal:  Environ Health Perspect       Date:  1996-12       Impact factor: 9.031

Review 3.  Comparative activity of human carcinogens and NTP rodent carcinogens in the mouse bone marrow micronucleus assay: an integrative approach to genetic toxicity data assessment.

Authors:  H Tinwell; J Ashby
Journal:  Environ Health Perspect       Date:  1994-09       Impact factor: 9.031

  3 in total

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