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Effects of thermal degradation products of polystyrene on drug biotransformation and tissue glutathione in rat and mouse
ANTTI ZITTING, PIRKKO PFÄFFLI and HARRI VAINIO
Scandinavian Journal of Work, Environment & Health
Vol. 4, Supplement 2. Proceedings of the International Symposium on Styrene: Occupational and Toxicological Aspects (1978), pp. 60-66
Published by: the Scandinavian Journal of Work, Environment & Health, the Finnish Institute of Occupational Health, the Danish National Research Centre for the Working Environment, and the Norwegian National Institute of Occupational Health
Stable URL: http://www.jstor.org/stable/40964658
Page Count: 7
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Rats and mice were exposed to the fumes of oxidative thermal degradation of polystyrene (350°C). A decrease in the reduced glutathione (GSH) in both liver and lung was detected immediately after both the acute (mice, 3 h) and subacute (rats, 3 weeks) exposures were stopped. Later on an elevation in the amount of GSH due to the increased synthesis (rebound effect) could be seen. Cytochrome P-450 content in mouse liver was initially decreased after acute exposure, but the prolonged treatment doubled the amount of the P-450 hemoprotein in liver microsomes. After acute exposure 7-ethoxycoumarin O-deethylase activity in mouse liver was doubled in 24 h. When the exposures were continued, this enhancement in ethoxycoumarin O-deethylase activity gradually disappeared. O-deethylase activity was also enhanced in rat liver and lung after subacute exposure. The exposures given had no effect on diphenyloxazole hydroxylase, and the effects on the conjugating enzymes (epoxide hydratase, UDPglucuronosyltransferase, glutathione S-transferase) were insignificant in rat liver.
Scandinavian Journal of Work, Environment & Health © 1978 Scandinavian Journal of Work, Environment & Health