@article {Schebbdmd.114.058206, author = {Nils H Schebb and Jaya B Muvvala and Dexter Morin and Alan R Buckpitt and Bruce D Hammock and Robert H Rice}, title = {Metabolic Activation of the Antibacterial Agent, Triclocarban, by Cytochrome P450 1A1 Yielding Glutathione Adducts}, elocation-id = {dmd.114.058206}, year = {2014}, doi = {10.1124/dmd.114.058206}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {Triclocarban (3,4,4{\textquoteright}-trichlorocarbanilide; TCC) is an antibacterial agent used in personal care products such as bar soaps. Small amounts of chemical are absorbed through the epidermis. Recent studies show that residues of reactive TCC metabolites are bound covalently to proteins in incubations with keratinocytes, raising concerns about the potential toxicity of this antimicrobial agent. To obtain additional information on metabolic activation of TCC, this study characterized the reactive metabolites trapped as glutathione conjugates. Incubations were carried out with 14C-labeled TCC, recombinant CYP1A1 or CYP1B1 coexpressed with P450 reductase, GSH, glutathione S-transferases and an NADPH generating system. Incubations containing CYP1A1, but not 1B1, led to formation of a single TCC-GSH adduct with a conversion rate of 1\% of parent compound in 2 hr. Using high resolution mass spectrometry and diagnostic fragmentation, the adduct was tentatively identified as 3,4-dichloro-3{\textquoteright}-glutathionyl-4{\textquoteright}-hydroxycarbanilide. These findings support the hypothesis that TCC is activated by oxidative dehalogenation and oxidation to a quinone imine. Incubations of TCDD-induced keratinocytes with 14C-TCC yielded a minor radioactive peak coeluting with TCC-GSH. Thus, we conclude that covalent protein modification by TCC in TCDD-induced human keratinocyte incubations is mainly caused by activation of TCC by CYP1A1 via a dehalogenated TCC derivative as reactive species.}, issn = {0090-9556}, URL = {https://dmd.aspetjournals.org/content/early/2014/04/14/dmd.114.058206}, eprint = {https://dmd.aspetjournals.org/content/early/2014/04/14/dmd.114.058206.full.pdf}, journal = {Drug Metabolism and Disposition} }