Site-specific metabolism of naphthalene and 1-nitronaphthalene in dissected airways of rhesus macaques

Bridget Boland, Ching Yu Lin, Dexter Morin, Lisa Miller, Charles Plopper, Alan R Buckpitt

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Studies in rodents have demonstrated the importance of cytochrome P450 monooxygenases in generating reactive metabolites that produce Clara cell injury. Pulmonary P450 activities in rodents are much higher than those in primates, raising the issue of relevance of rodent data to primates. Few studies on P450-catalyzed activation of cytotoxicants in subcompartments of primate lung have been reported. Accordingly, infant monkey airway subcompartments, including trachea, proximal, midlevel, distal airways, and parenchyma, were incubated with naphthalene or 1-nitronaphthalene to define metabolism at both high (500 μM) and low (50 μM) substrate concentrations. There was a relatively even distribution of metabolizing activities for naphthalene across subcompartments, but at high concentrations of 1-nitronaphthalene, lower airways (midlevel airway through parenchyma) showed higher bioactivation than upper airways. Dihydrodiol was the predominant water-soluble metabolite of naphthalene generated by all subcompartments, whereas covalently bound metabolites accounted for the greatest percentage of 1-nitronaphthalene metabolites, especially in lower airways. As anticipated, the amounts of metabolite covalently bound as a percentage of total metabolite formed increased dramatically with the 10-fold increase in substrate concentration. With both substrates, the formation of water-soluble metabolites was approximately 100 times less than observed previously in rodents. We conclude that 1) there are significant quantitative differences between rhesus and rodents in substrate bioactivation; 2) the distribution of metabolizing activities for naphthalene but not 1-nitronaphthalene is significantly different for rodents and primates; and 3) a very high percentage of the metabolites generated, particularly for 1-nitronaphthalene, is bound covalently to cellular proteins.

Original languageEnglish (US)
Pages (from-to)546-554
Number of pages9
JournalJournal of Pharmacology and Experimental Therapeutics
Volume310
Issue number2
DOIs
StatePublished - Aug 2004

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Macaca mulatta
Rodentia
Primates
Lung
Water
Mixed Function Oxygenases
Trachea
Cytochrome P-450 Enzyme System
Haplorhini
1-nitronaphthalene
naphthalene
Wounds and Injuries
Proteins

ASJC Scopus subject areas

  • Pharmacology

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Site-specific metabolism of naphthalene and 1-nitronaphthalene in dissected airways of rhesus macaques. / Boland, Bridget; Lin, Ching Yu; Morin, Dexter; Miller, Lisa; Plopper, Charles; Buckpitt, Alan R.

In: Journal of Pharmacology and Experimental Therapeutics, Vol. 310, No. 2, 08.2004, p. 546-554.

Research output: Contribution to journalArticle

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