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11β-羟基类固醇脱氢酶1型:从人肝脏中纯化并鉴定为外源性物质的羰基还原酶

11Beta-hydroxysteroid dehydrogenase type 1: purification from human liver and characterization as carbonyl reductase of xenobiotics.

作者信息

Maser E, Wsol V, Martin H-J

机构信息

Institute of Toxicology and Pharmacology for Natural Scientists, University Medical School Schleswig-Holstein, Kiel, Germany.

出版信息

Mol Cell Endocrinol. 2006 Mar 27;248(1-2):34-7. doi: 10.1016/j.mce.2005.10.019. Epub 2005 Dec 15.

Abstract

11Beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) catalyzes the interconversion of 11-oxo glucocorticoids to their 11-hydroxy metabolites, thereby controlling access of glucocorticoid hormones to the glucocorticoid receptor. Interestingly, evidence is emerging that 11beta-HSD1 fulfills an additional role in the metabolism of xenobiotic carbonyl compounds. In our studies, 11beta-HSD1 was identified as a microsomal reductase that initiates the final detoxification of xenobiotics by reducing them to alcohols that are easier to conjugate and eliminate. With its pluripotent substrate specificities for glucocorticoids and xenobiotics, 11beta-HSD1 adds to an expanding list of those hydroxysteroid dehydrogenases which, on the one hand, are capable of catalyzing the carbonyl reduction of non-steroidal carbonyl compounds, and which, on the other hand, exhibit great specificity to their physiological steroid substrates. It is conceivable that large interferences must occur between endogenous steroid metabolism and the detoxification of xenobiotic compounds on the level of hydroxysteroid dehydrogenases.

摘要

11β-羟基类固醇脱氢酶1型(11β-HSD1)催化11-氧代糖皮质激素与其11-羟基代谢产物之间的相互转化,从而控制糖皮质激素进入糖皮质激素受体。有趣的是,越来越多的证据表明,11β-HSD1在异生物质羰基化合物的代谢中发挥着额外作用。在我们的研究中,11β-HSD1被鉴定为一种微粒体还原酶,它通过将异生物质还原为更易于结合和消除的醇类,启动异生物质的最终解毒过程。凭借其对糖皮质激素和异生物质的多能底物特异性,11β-HSD1加入了越来越多的羟基类固醇脱氢酶行列,这些酶一方面能够催化非甾体羰基化合物的羰基还原,另一方面对其生理类固醇底物表现出高度特异性。可以想象,在内源性类固醇代谢和羟基类固醇脱氢酶水平上的异生物质化合物解毒过程之间必然会发生大量干扰。

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