Characterization of multiple products of cytochrome P450 2A6-catalyzed cotinine metabolism

Sharon E Murphy, Lisa M. Johnson, Dominic A. Pullo

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

The primary metabolite of nicotine in smokers is cotinine. Cotinine is further metabolized to trans-3'-hydroxycotinine, the major urinary metabolite of nicotine in tobacco users. It was recently reported that cytochrome P450 2A6 catalyzes the conversion of cotinine to trans-3'-hydroxycotinine. In this work, we report that P450 2A6 metabolizes cotinine not only to trans-3'- hydroxycotinine but also to 5'-hydroxycotinine, norcotinine, and a fourth as yet unidentified metabolite. The products of baculovirus-expressed P450 2A6 [methyl-3H]cotinine metabolism were analyzed by radioflow HPLC. Three 3H- labeled metabolites were detected and were present in approximately equal amounts. The identities of two of the metabolites were confirmed to be 5'- hydroxycotinine and trans-3'-hydroxycotinine by LC/MS/MS and LC/MS analysis and comparison to standards. The third product was not identified. A fourth product of P450 2A6-catalyzed cotinine metabolism was detected by LC/MS. It was identified by cochromatography with a standard and MS and MS/MS data to be norcotinine. An attempt was made to further characterize the unidentified 3H-labeled metabolite by comparison to the cotinine metabolites generated by hamster liver microsomes. Hamster liver microsomes contain a P450, 2A8, which is closely related to P450 2A6, and have previously been shown to metabolize cotinine to three hydroxylated products, trans-3'-hydroxycotinine, 5'- hydroxycotinine, and N-(hydroxymethyl)-norcotinine. We were unable to confirm that N-(hydroxymethyl)norcotinine was the unidentified cotinine metabolite generated by P450 2A6.

Original languageEnglish (US)
Pages (from-to)639-645
Number of pages7
JournalChemical research in toxicology
Volume12
Issue number7
DOIs
StatePublished - 1999

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