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首页> 外文期刊>Molecular and Cellular Endocrinology >11beta-Hydroxysteroid dehydrogenase type 1: Purification from human liver and characterization as carbonyl reductase of xenobiotics.
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11beta-Hydroxysteroid dehydrogenase type 1: Purification from human liver and characterization as carbonyl reductase of xenobiotics.

机译:11β-羟基类固醇脱氢酶1:从人肝中纯化并将其表征为异生物的羰基还原酶。

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摘要

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.
机译:11β-羟基类固醇脱氢酶1(11beta-HSD1)催化11-氧代糖皮质激素向其11-羟基代谢产物的相互转化,从而控制糖皮质激素激素对糖皮质激素受体的访问。有趣的是,越来越多的证据表明11β-HSD1在异生物羰基化合物的代谢中起着额外的作用。在我们的研究中,11beta-HSD1被鉴定为微粒体还原酶,可通过将异源生物还原为更易于缀合和消除的醇类来启动异源生物的最终解毒。凭借其对糖皮质激素和异生物素的多能底物特异性,11beta-HSD1增加了这些羟类固醇脱氢酶的范围,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,对它们的生理类固醇底物表现出极大的特异性。可以想象,内源性类固醇代谢与异种化合物的解毒之间必须发生很大的干扰,这取决于羟基类固醇脱氢酶的水平。

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