SUBCHRONIC INHALATION STUDIES OF STYRENE IN CD RATS AND CD-1 MICE

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 eff ect 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 c onfined 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 v apor 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 m ice were exposed to styrene vapors at 0, 50, 100, 150, or 200 ppm 6 hr per day 5 days per week for 13 Reeks. Two females exposed to 200 ppm died during the first week. Liver toxicity was evident in the decedent s and in some female survivors at 200 ppm. Changes were observed in th e lungs of mice exposed to 100, 150, or 200 ppm and in the nasal passa ges of all treatment groups, those exposed to 50 ppm being less affect ed. 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 prolifer ation (BrdU labeling). No increase in cell proliferation was found in liver of rats or mice or in cells of the bronchiolar or alveolar regio n of the lung of rats. No increase in labeling index of type II pneumo cytes 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 anim als 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 m ice. (C) 1997 Society of Toxicology.