Literature DB >> 33189850

Characterization of human adrenal cytochrome P450 11B2 products of progesterone and androstenedione oxidation.

Sarah M Glass1, Michael J Reddish2, Stella A Child1, Clayton J Wilkey1, Donald F Stec3, F Peter Guengerich4.   

Abstract

Cytochrome P450 (P450) 11B1 and 11B2 both catalyze the 11β-hydroxylation of 11-deoxycorticosterone and the subsequent 18-hydroxylation of the product. P450 11B2, but not P450 11B1, catalyzes a further C-18 oxidation to yield aldosterone. 11-Oxygenated androgens are of interest, and 11-hydroxy progesterone has been reported to be a precursor of these. Oxidation of progesterone by purified recombinant P450 11B2 yielded a mono-hydroxy derivative as the major product, and co-chromatography with commercial standards and 2-D NMR spectroscopy indicated 11β-hydroxylation. 18-Hydroxyprogesterone and a dihydroxyprogesterone were also formed. Similarly, oxidation of androstenedione by P450 11B2 yielded 11β-hydroxyandrostenedione, 18-hydroxyandrostenedione, and a dihydroxyandrostenedione. The steady-state kinetic parameters for androstenedione and progesterone 11β-hydroxylation were similar to those reported for the classic substrate 11-deoxycorticosterone. The source of 11α-hydroxyprogesterone in humans remains unresolved.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  11 β-Hydroxyandrostenedione; 11-Hydroxy steroids; 11β-Hydroxyprogesterone; 18-Hydroxy steroids; Androstenedione; Cytochrome P450 11B2; Progesterone

Mesh:

Substances:

Year:  2020        PMID: 33189850      PMCID: PMC7954869          DOI: 10.1016/j.jsbmb.2020.105787

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  39 in total

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Authors:  K H LOKE; G F MARRIAN; W S JOHNSON; W L MEYER; D D CAMERON
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2.  The in vitro metabolism of 11β-hydroxyprogesterone and 11-ketoprogesterone to 11-ketodihydrotestosterone in the backdoor pathway.

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Journal:  J Clin Endocrinol Metab       Date:  2015-04-07       Impact factor: 5.958

4.  Metabolism of androstenedione by porcine adrenal homogenates.

Authors:  A M Ling; K H Loke
Journal:  Steroids       Date:  1966-11       Impact factor: 2.668

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Authors:  Adina F Turcu; Aya T Nanba; Robert Chomic; Sunil K Upadhyay; Thomas J Giordano; James J Shields; Deborah P Merke; William E Rainey; Richard J Auchus
Journal:  Eur J Endocrinol       Date:  2016-02-10       Impact factor: 6.664

Review 6.  Steroid biomarkers in human adrenal disease.

Authors:  Juilee Rege; Adina F Turcu; Tobias Else; Richard J Auchus; William E Rainey
Journal:  J Steroid Biochem Mol Biol       Date:  2019-01-29       Impact factor: 4.292

7.  11 alpha- and 11 beta-hydroxyprogesterone, potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2), confer marked mineralocorticoid activity on corticosterone in the ADX rat.

Authors:  G W Souness; S A Latif; J L Laurenzo; D J Morris
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8.  The 11β-hydroxyandrostenedione pathway and C11-oxy C21 backdoor pathway are active in benign prostatic hyperplasia yielding 11keto-testosterone and 11keto-progesterone.

Authors:  Therina du Toit; Amanda C Swart
Journal:  J Steroid Biochem Mol Biol       Date:  2019-10-15       Impact factor: 4.292

Review 9.  New standards for collecting and fitting steady state kinetic data.

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Journal:  Beilstein J Org Chem       Date:  2019-01-02       Impact factor: 2.883

10.  Cyp27c1 Red-Shifts the Spectral Sensitivity of Photoreceptors by Converting Vitamin A1 into A2.

Authors:  Jennifer M Enright; Matthew B Toomey; Shin-ya Sato; Shelby E Temple; James R Allen; Rina Fujiwara; Valerie M Kramlinger; Leslie D Nagy; Kevin M Johnson; Yi Xiao; Martin J How; Stephen L Johnson; Nicholas W Roberts; Vladimir J Kefalov; F Peter Guengerich; Joseph C Corbo
Journal:  Curr Biol       Date:  2015-11-05       Impact factor: 10.834

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