Substrate Specificity and Inhibitor Sensitivity of Rabbit 20α-Hydroxysteroid Dehydrogenase

• Published in: Biological & pharmaceutical bulletin 2013/09/01, Vol.36(9), pp.1514-1518
• Main Authors: Endo, Satoshi, Arai, Yuki, Hara, Akira, Kitade, Yukio, Bunai, Yasuo, El-Kabbani, Ossama, Matsunaga, Toshiyuki
• Format: Article
• Language: English
• Subjects: 17β-hydroxysteroid dehydrogenase; 20-alpha-Hydroxysteroid Dehydrogenase - antagonists & inhibitors; 20-alpha-Hydroxysteroid Dehydrogenase - genetics; 20-alpha-Hydroxysteroid Dehydrogenase - metabolism; 20α-hydroxysteroid dehydrogenase; 4-oxo-2-nonenal; Aldehydes - metabolism; aldo-keto reductase 1C5; Animals; dehydroepiandrosterone; Enzyme Inhibitors - pharmacology; Flavonoids - pharmacology; Hydroxysteroids - metabolism; isatin; Isatin - metabolism; Ketones - metabolism; Ketosteroids - metabolism; Quinones - metabolism; Rabbits; Recombinant Proteins - metabolism; Substrate Specificity; Xenobiotics - metabolism
• ISSN: 0918-6158; 1347-5215
• DOI: 10.1248/bpb.b13-00342

In this study, we examined the substrate specificity and inhibitor sensitivity of rabbit 20α-hydroxysteroid dehydrogenase (AKR1C5), which plays a role in the termination of pregnancy by progesterone inactivation. AKR1C5 moderately reduced the 3-keto group of only 5α-dihydrosteroids with 17β- or 20α/β-hydroxy group among 3-ketosteroids. In contrast, the enzyme reversibly and efficiently catalyzed the reduction of various 17- and 20-ketosteroids, including estrogen precursors (dehydroepiandrosterone, estrone and 5α-androstan-3β-ol-17-one) and tocolytic 5β-pregnane-3,20-dione. In addition to the progesterone inactivation, the formation of estrogens and metabolism of the tocolytic steroid by AKR1C5 may be related to its role in rabbit parturition. AKR1C5 also reduced various non-steroidal carbonyl compounds, including isatin, an antagonist of the C-type natriuretic peptide receptor, and 4-oxo-2-nonenal, suggesting its roles in controlling the bioactive isatin and detoxification of cytotoxic aldehydes. AKR1C5 was potently and competitively inhibited by flavonoids such as kaempferol and quercetin, suggesting that its activity is affected by ingested flavonoids.