Literature DB >> 9038236

Subchronic inhalation studies of styrene in CD rats and CD-1 mice.

G Cruzan1, J R Cushman, L S Andrews, G C Granville, R R Miller, C J Hardy, D W Coombs, P A Mullins.   

Abstract

Groups of 10 male and 10 female Charles River (CRL) CD (Sprague-Dawley-derived) rats were exposed to styrene vapor at 0, 200, 500, 1000, or 1500 ppm 6 hr per day 5 days per week for 13 weeks. Styrene had no effect on survival, hematology, or clinical chemistry. Males at 1500 ppm weighed 10% less after 13 weeks and males and females at 1000 and 1500 ppm consumed more water than controls. Histopathologic changes were confined to the olfactory epithelium of the nasal mucosa. Groups of 20 male and 20 female CRL CD-1 and B6C3F1 mice were exposed to styrene vapor at 0, 15, 60, 250, or 500 ppm 6 hr per day 5 days per week for 2 weeks. Mortality was observed in both CD-1 and B6C3F1 mice exposed to 250 or 500 ppm; more female mice, but not males, died from exposure to 250 ppm than from 500 ppm. Groups of 10 male and 10 female CRL CD-1 mice were exposed to styrene vapors at 0, 50, 100, 150, or 200 ppm 6 hr per day 5 days per week for 13 weeks. Two females exposed to 200 ppm died during the first week. Liver toxicity was evident in the decedents and in some female survivors at 200 ppm. Changes were observed in the lungs of mice exposed to 100, 150, or 200 ppm and in the nasal passages of all treatment groups, those exposed to 50 ppm being less affected. Satellite groups of 15 male rats and 30 male mice were exposed as described above for 2, 5, or 13 weeks for measurement of cell proliferation (BrdU labeling). No increase in cell proliferation was found in liver of rats or mice or in cells of the bronchiolar or alveolar region of the lung of rats. No increase in labeling index of type II pneumocytes was seen in mouse lungs, while at 150 and 200 ppm, an increased labeling index of Clara cells was seen after 2 weeks and in occasional mice after 5 weeks. Large variations in the labeling index among animals emphasize the need for large group sizes. For nasal tract effects, a NOAEL was not found in CD-1 mice, but in CD rats, the NOAEL was 200 ppm. For other effects, the NOAEL was 500 ppm in rats and 50 ppm in mice.

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Year:  1997        PMID: 9038236     DOI: 10.1006/faat.1996.2273

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  7 in total

1.  Evidence for cellular protein covalent binding derived from styrene metabolite.

Authors:  Wei Yuan; Hua Jin; Jou-Ku Chung; Jiang Zheng
Journal:  Chem Biol Interact       Date:  2010-05-12       Impact factor: 5.192

2.  Structure-toxicity relationship study of para-halogenated styrene analogues in CYP2E1 transgenic cells.

Authors:  Jou-Ku Chung; Shuijie Shen; Zhiteng Jiang; Wei Yuan; Jiang Zheng
Journal:  Toxicol Lett       Date:  2012-02-16       Impact factor: 4.372

Review 3.  Non-malignant respiratory disease among workers in industries using styrene-A review of the evidence.

Authors:  Randall J Nett; Jean M Cox-Ganser; Ann F Hubbs; Avima M Ruder; Kristin J Cummings; Yuh-Chin T Huang; Kathleen Kreiss
Journal:  Am J Ind Med       Date:  2017-02       Impact factor: 2.214

4.  Deaths from Nonmalignant Respiratory Disease in Styrene-Exposed Workers: Does Obliterative Bronchiolitis Contribute to Mortality?

Authors:  Randall J Nett; Nicole T Edwards; Avima M Ruder; Stephen J Bertke; Isna Keumala; Jean Cox-Ganser; Kristin J Cummings
Journal:  Ann Am Thorac Soc       Date:  2017-05

Review 5.  Pulmonary toxicity and carcinogenicity of trichloroethylene: species differences and modes of action.

Authors:  T Green
Journal:  Environ Health Perspect       Date:  2000-05       Impact factor: 9.031

6.  The Weight of Evidence Does Not Support the Listing of Styrene as "Reasonably Anticipated to be a Human Carcinogen" in NTP's Twelfth Report on Carcinogens.

Authors:  Lorenz R Rhomberg; Julie E Goodman; Robyn L Prueitt
Journal:  Hum Ecol Risk Assess       Date:  2013-01-02       Impact factor: 5.190

Review 7.  Olfactory dysfunction revisited: a reappraisal of work-related olfactory dysfunction caused by chemicals.

Authors:  Sabine Werner; Eberhard Nies
Journal:  J Occup Med Toxicol       Date:  2018-09-04       Impact factor: 2.646

  7 in total

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