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Cytochrome P/sub 450/ dependent monooxygenases in nasal epithelial membranes: effect of phenobarbital and benzo(a)pyrene

Journal Article · · Proc. West. Pharmacol. Soc.; (United States)
OSTI ID:6521495
The cytochrome P-450 content of microsomes isolated from nasal membranes, lungs, and livers of the mouse, rat, guinea pig, hamster, rabbit, and dog was measured. The cytochrome P-450 dependent monooxygenase activity (MO) was assayed in microsomes from dog nasal membrane, lung, and liver using aniline, p-nitroanisole, aminopyrine and hexamethylphosphoramide (HMPA) as substrates. Phenobarbital was administered as a saturated drinking water solution for 8 days or as an aerosol for 30 minutes on 4 successive days. Benzo(a)pyrene was administered as an aerosol for 1 h on 4 successive days. The drinking water was removed 12 h before sacrifice and the last aerosol exposure was 24 h before sacrifice. All species nasal membranes contained cytochrome P-450. The hamster nasal membranes contained the highest concentrations. All substrates used were metabolized (as measured by MO activity) by the nasal membrane microsomes except for aminopyrine by the maxilloturbinate microsomes. HMPA was the most rapidly metabolized substrate. Liver cytochrome P-450 was induced more than 2 times by the phenobarbital administered in the drinking water, but no induction of nasal membrane cytochrome P-450 was found. Neither the phenobarbital nor benzo(a)pyrene aerosols induced the liver, lung, or nasal membrane cytochrome P-450 content. (RJC)
Research Organization:
Lovelace Inhalation Toxicology Research Inst., Albuquerque, NM
DOE Contract Number:
AC04-76EV01013
OSTI ID:
6521495
Journal Information:
Proc. West. Pharmacol. Soc.; (United States), Journal Name: Proc. West. Pharmacol. Soc.; (United States) Vol. 25; ISSN PWPSA
Country of Publication:
United States
Language:
English