Literature DB >> 10490505

Glutathione conjugation of electrophilic metabolites of 1-nitronaphthalene in rat tracheobronchial airways and liver: identification by mass spectrometry and proton nuclear magnetic resonance spectroscopy.

K C Watt1, D M Morin, M J Kurth, R S Mercer, C G Plopper, A R Buckpitt.   

Abstract

1-Nitronaphthalene (1-NN) is a mutagenic nitroaromatic which has been detected in emissions from both heavy- and light-duty diesel engines, as well as in urban airborne particles. 1-NN is a cytochrome P450-bioactivated, nonciliated bronchiolar epithelial (Clara) cell cytotoxicant. These studies examined the metabolism of 1-NN to electrophilic metabolites which were trapped as glutathione conjugates in highly susceptible (lung) and less susceptible (liver) tissues of the rat. Significant depletion of reduced glutathione was observed at all levels of tracheobronchial airways of rats treated with 200 mg/kg 1-NN, ip. This observation of depleted glutathione was consistent with the HPLC radioactivity profiles demonstrating six glutathione conjugates isolated from liver and lung microsomal incubations with 1-NN, [(3)H]glutathione, and glutathione S-transferase. Mass spectrometry of all six metabolites in electrospray positive ion mode yielded an ion of m/z 497 (M + H), and daughter ions of m/z 479 (loss of water), m/z 306 (glutathione), and m/z 177 (loss of the nitro group and formation of hydroxy naphthalene thiolate ion), demonstrating the formation of hydroxy-dihydroglutathionyl derivatives presumably via intermediate epoxide(s). Proton nuclear magnetic resonance spectroscopy identified four different regioisomeric conjugates from lung and liver microsomal incubations: 1-nitro-7-glutathionyl-8-hydroxy-7, 8-dihydronaphthalene, 1-nitro-7-hydroxy-8-glutathionyl-7, 8-dihydronaphthalene, 1-nitro-5-hydroxy-6-glutathionyl-5, 6-dihydronaphthalene, and 1-nitro-5-glutathionyl-6-hydroxy-5, 6-dihydronaphthalene. HPLC radioactivity profiles demonstrated that major conjugates generated in the lung were derived from the C(7), C(8)-epoxide, whereas the most prominent metabolites in the liver were derived from the C(5),C(6)-epoxide.

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Year:  1999        PMID: 10490505     DOI: 10.1021/tx990023v

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  5 in total

1.  Detection of protein adduction derived from styrene oxide to cysteine residues by alkaline permethylation.

Authors:  Jieyu Dai; Fan Zhang; Jiang Zheng
Journal:  Anal Biochem       Date:  2010-05-06       Impact factor: 3.365

2.  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

3.  In vivo effects of ozone exposure on protein adduct formation by 1-nitronaphthalene in rat lung.

Authors:  Asa M Wheelock; Bridget C Boland; Margaret Isbell; Dexter Morin; Teresa C Wegesser; Charles G Plopper; Alan R Buckpitt
Journal:  Am J Respir Cell Mol Biol       Date:  2005-04-21       Impact factor: 6.914

Review 4.  Toxicity and metabolism of methylnaphthalenes: comparison with naphthalene and 1-nitronaphthalene.

Authors:  Ching Yu Lin; Asa M Wheelock; Dexter Morin; R Michael Baldwin; Myong Gong Lee; Aysha Taff; Charles Plopper; Alan Buckpitt; Arlean Rohde
Journal:  Toxicology       Date:  2009-03-18       Impact factor: 4.221

5.  The role of inflammatory mediators in the synergistic toxicity of ozone and 1-nitronaphthalene in rat airways.

Authors:  Kara R Schmelzer; Asa M Wheelock; Katja Dettmer; Dexter Morin; Bruce D Hammock
Journal:  Environ Health Perspect       Date:  2006-09       Impact factor: 9.031

  5 in total

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