Literature DB >> 6933925

Kinetics of benzene metabolism in rats in inhalation exposure.

I Gut, E Frantík.   

Abstract

Rats inhaling benzene concentrations 400, 800, 2,000, or 4,000 mg m-3 for 6 h excreted similar amounts of phenol in urine; hence benzene metabolism was already capacity-limited at 400 mg m-3. The rate of phenol elimination in the course of 12 h inhalation of benzene, 2,000 mg m-3, was increasing; the in vitro rate of hepatic microsomal benzene metabolism was increasing accordingly. Phenobarbital (PB) pretreatment significantly increased phenol excretion in rats exposed to benzene at 800 mg m-3 and higher concentrations. This effect disappeared during 12 h benzene inhalation, although the in vitro hepatic microsomal benzene metabolism in PB rats was significantly higher than in the controls.

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Year:  1980        PMID: 6933925     DOI: 10.1007/978-3-642-67729-8_64

Source DB:  PubMed          Journal:  Arch Toxicol Suppl        ISSN: 0171-9750


  3 in total

1.  Possible implications from results of animal studies in human risk estimations for benzene: nonlinear dose-response relationship due to saturation of metabolism.

Authors:  S Grilli; W K Lutz; S Parodi
Journal:  J Cancer Res Clin Oncol       Date:  1987       Impact factor: 4.553

2.  Exposure to various benzene derivatives differently induces cytochromes P450 2B1 and P450 2E1 in rat liver.

Authors:  I Gut; Y Terelius; E Frantík; I Linhart; P Soucek; B Filipcová; H Klucková
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

Review 3.  Results of animal studies suggest a nonlinear dose-response relationship for benzene effects.

Authors:  S Parodi; W K Lutz; A Colacci; M Mazzullo; M Taningher; S Grilli
Journal:  Environ Health Perspect       Date:  1989-07       Impact factor: 9.031

  3 in total

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