Publication Cover
Xenobiotica
the fate of foreign compounds in biological systems
Volume 51, 2021 - Issue 9
157
Views
6
CrossRef citations to date
0
Altmetric
General Xenobiochemistry

Roles of cytochrome P450 2A6 in the oxidation of flavone, 4′-hydroxyflavone, and 4′-, 3′-, and 2′-methoxyflavones by human liver microsomes

ORCID Icon, , , , ORCID Icon, , ORCID Icon, ORCID Icon & ORCID Icon show all
Pages 995-1009 | Received 01 Jun 2021, Accepted 28 Jun 2021, Published online: 04 Aug 2021
 

Abstract

  1. Nine forms of recombinant cytochrome P450 (P450 or CYP) enzymes were used to study roles of individual P450 enzymes in the oxidation of flavone and some other flavonoids, 4-hydroxyflavone and 4-, 3-, and 2-methoxyflavones, by human liver microsomes using LC-MS/MS analysis.

  2. As has been reported previously , 4-, 3-, and 2-methoxyflavones were preferentially O-demethylated by human liver P450 enzymes to form 4-, 3-, and 2-hydroxylated flavones and also 3′,4-dihydroxyflavone from the former two substrates.

  3. In comparisons of product formation by oxidation of these methoxylated flavones, CYP2A6 was found to be a major enzyme catalysing flavone 4- and 3-hydroxylations by human liver microsomes but did not play significant roles in 2-hydroxylation of flavone, O-demethylations of three methoxylated flavones, and the oxidation of 4-hydroxyflavone to 3′,4-dihydroxyflavone.

  4. The effects of anti-CYP2A6 IgG and chemical P450 inhibitors suggested that different P450 enzymes, as well as CYP2A6, catalysed oxidation of these flavonoids at different positions by liver microsomes.

  5. These studies suggest that CYP2A6 catalyses flavone 4- and 3-hydroxylations in human liver microsomes and that other P450 enzymes have different roles in oxidizing these flavonoids.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This study was supported in part by JSPS KAKENHI [16K21710] (to H. N), [15K07770] (to S. T.), [JP18K06000] (to M. K.), [20K07139] (to N. M.), and [20K07164] (to H. Y.), National Research Foundation of Korea [NRF-2019R1A2C1004722] (to D. K.), and United States Public Health Service grant [R01 GM118122] (to F. P. G.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.