Phytoestrogens as inhibitors of the human progesterone metabolizing enzyme AKR1C1

MOLECULAR AND CELLULAR ENDOCRINOLOGY

卷:259

Article

Brozic, Petra ; Smuc, Tina ; Gobec, Stanislav ; Rizner, Tea Lanisnik

关键词: 20 alpha-hydroxysteroid dehydrogenases;    aldo-keto reductases;    progesterone;    3 alpha,5 alpha-tetrahydroprogesterone;    neurosteroids;   

DOI  :  10.1016/j.mce.2006.08.001

来源: Elsevier

【 摘 要 】

Phyroestrogens are plant-derived, non-steroidal constituents of our diets. They can act as agonists or antagonists of estrogen receptors, and they can modulate the activities of the key enzymes in estrogen biosynthesis. Much less is known about their actions on the androgen and progesterone metabolizing enzymes. We have examined the inhibitory action of phytoestrogens on the key human progesterone-metabolizing enzyme, 20 alpha-hydroxysteroid dehydrogenase (AKR1C1). This enzyme inactivates progesterone and the neuroactive 3 alpha,5 alpha-tetrahydroprogesterone, to form their less active counterparts, 20 alpha-hydroxyprogesterone and 5 alpha-pregnane-3 alpha,20 alpha-diol, respectively. We overexpressed recombinant human AKR1C1 in Escherichia coli, purified it to homogeneity, and examined the selected phytoestrogens as inhibitors of NADPH-dependent reduction of a common AKR substrate, 9, 10-phenantrenequinone, and progesterone. The most potent inhibitors were 7-hydroxyflavone, 3,7-dihydroxyflavone and flavanone natingenin with IC50 values in the low mu M range. Docking of the flavones in the active site of AKR1C1 revealed their possible binding modes, in which they are sandwiched between the Leu308 and Trp227 of AKR1C1. (c) 2006 Elsevier Ireland Ltd. All rights reserved.

【 授权许可】

Free