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人肝脏11β-羟基类固醇脱氢酶1型的纯化、表征及NNK羰基还原酶活性:酶的协同作用及在烟草衍生致癌物解毒中的意义

Purification, characterization and NNK carbonyl reductase activities of 11beta-hydroxysteroid dehydrogenase type 1 from human liver: enzyme cooperativity and significance in the detoxification of a tobacco-derived carcinogen.

作者信息

Maser Edmund, Friebertshäuser Jutta, Völker Bernhard

机构信息

Department of Experimental Toxicology, Faculty of Medicine, University of Kiel, Brunswiker Strasse 10, D-24105, Kiel, Germany.

出版信息

Chem Biol Interact. 2003 Feb 1;143-144:435-48. doi: 10.1016/s0009-2797(02)00180-1.


DOI:10.1016/s0009-2797(02)00180-1
PMID:12604230
Abstract

11beta-Hydroxysteroid dehydrogenase type 1 (11beta-HSD 1) physiologically catalyzes the interconversion of receptor-active 11-hydroxy glucocorticoids (cortisol) to their receptor-inactive 11-oxo metabolites (cortisone), thereby acting as important pre-receptor control device in regulating access of glucocorticoid hormones to the glucocorticoid receptor. Evidence is emerging that 11beta-HSD 1 fulfills an additional role in the detoxification of non-steroidal carbonyl compounds, by catalyzing their reduction to the corresponding hydroxy derivatives that are easier to conjugate and eliminate. Whereas a number of methods were ineffective in purifying 11beta-HSD 1 from human liver, this membrane-bound enzyme was successfully obtained in an active state by a purification procedure that took advantage of a gentle solubilization method as well as providing a favourable detergent surrounding during the various chromatographic steps. We could demonstrate that 11beta-HSD 1 is active as a dimeric enzyme which exhibits cooperativity with cortisone and dehydrocorticosterone (11-oxoreducing activity) as substrates. Accordingly, this enzyme dynamically adapts to low (nanomolar) as well as to high (micromolar) substrate concentrations, thereby providing the fine tuning required as a consequence of great variations in circadian plasma glucocorticoid levels. Due to this kinetic peculiarity, 11beta-HSD 1 is also able to even metabolize nanomolar concentrations of the tobacco-specific nitrosamine 4-methylnitrosamino-1-(3-pyridyl)-1-butanone (NNK), a fact which is important in view of the relatively low levels of this carcinogen observed in smokers. Finally, 11beta-HSD 1 is potently (in nM concentrations) inhibited by glycyrrhetinic acid, the main constituent of licorice. Licorice, however, in addition to being a confectionary, serves as a major cigarette additive, which is used in cigarette manufacturing as a taste and flavour intensifier. Hence, licorice exposure may affect NNK detoxification by inhibition of 11beta-HSD 1, a condition which may advance lung cancer incidence, especially in smokers expressing low levels of this enzyme. Collectively, our data expand insights into the multifunctional nature of hydroxysteroid dehydrogenases/carbonyl reductases and emphasize the importance of 11beta-HSD 1 in the detoxification of a tobacco-derived carcinogen, in addition to its endocrinological functions.

摘要

11β-羟基类固醇脱氢酶1型(11β-HSD 1)在生理上催化具有受体活性的11-羟基糖皮质激素(皮质醇)向其无受体活性的11-氧代代谢物(可的松)的相互转化,从而作为调节糖皮质激素进入糖皮质激素受体的重要受体前控制机制。越来越多的证据表明,11β-HSD 1在非甾体羰基化合物的解毒过程中发挥着额外作用,它通过催化这些化合物还原为更易于结合和消除的相应羟基衍生物来实现这一作用。虽然有多种方法无法从人肝脏中纯化出11β-HSD 1,但通过一种纯化程序成功获得了处于活性状态的这种膜结合酶,该程序利用了温和的增溶方法,并在各个色谱步骤中提供了有利的去污剂环境。我们能够证明11β-HSD 1作为一种二聚体酶具有活性,它以可的松和脱氢皮质酮(11-氧还原活性)为底物表现出协同作用。因此,这种酶能够动态适应低(纳摩尔)和高(微摩尔)底物浓度,从而提供由于昼夜血浆糖皮质激素水平的巨大变化而所需的精细调节。由于这种动力学特性,11β-HSD 1甚至能够代谢纳摩尔浓度的烟草特异性亚硝胺4-甲基亚硝氨基-1-(3-吡啶基)-1-丁酮(NNK),鉴于在吸烟者中观察到的这种致癌物水平相对较低,这一事实具有重要意义。最后,11β-HSD 1受到甘草次酸(甘草的主要成分)的强烈抑制(纳摩尔浓度)。然而,甘草除了作为一种糖果外,还是一种主要的香烟添加剂,在香烟制造中用作味道和风味增强剂。因此,接触甘草可能会通过抑制11β-HSD 1影响NNK的解毒,这种情况可能会增加肺癌发病率,尤其是在该酶表达水平较低的吸烟者中。总的来说,我们的数据扩展了对羟基类固醇脱氢酶/羰基还原酶多功能性质的认识,并强调了11β-HSD 1在烟草衍生致癌物解毒中的重要性,以及它的内分泌功能。

相似文献

[1]
Purification, characterization and NNK carbonyl reductase activities of 11beta-hydroxysteroid dehydrogenase type 1 from human liver: enzyme cooperativity and significance in the detoxification of a tobacco-derived carcinogen.

Chem Biol Interact. 2003-2-1

[2]
11 Beta-hydroxysteroid dehydrogenase type 1 from human liver: dimerization and enzyme cooperativity support its postulated role as glucocorticoid reductase.

Biochemistry. 2002-2-19

[3]
11Beta-hydroxysteroid dehydrogenase responsible for carbonyl reduction of the tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone in mouse lung microsomes.

Cancer Res. 1998-7-15

[4]
Expression and NNK reducing activities of carbonyl reductase and 11beta-hydroxysteroid dehydrogenase type 1 in human lung.

Chem Biol Interact. 2001-1-30

[5]
Carbonyl reduction of the tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in cytosol of mouse liver and lung.

Toxicology. 1999-11-29

[6]
Carbonyl reduction of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) by cytosolic enzymes in human liver and lung.

Cancer Lett. 2000-2-1

[7]
Interindividual variability in the expression and NNK carbonyl reductase activity of 11beta-hydroxysteroid dehydrogenase 1 in human lung.

Cancer Lett. 1999-10-18

[8]
11Beta-hydroxysteroid dehydrogenase type 1: purification from human liver and characterization as carbonyl reductase of xenobiotics.

Mol Cell Endocrinol. 2006-3-27

[9]
The identification of 11 beta-hydroxysteroid dehydrogenase as carbonyl reductase of the tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone.

Eur J Biochem. 1996-6-1

[10]
Role of type-1 11beta-hydroxysteroid dehydrogenase in detoxification processes.

Eur J Biochem. 1997-10-15

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[3]
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[6]
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[7]
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[8]
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[9]
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