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人脑中胆固醇 24-羟化酶 CYP46A1 对口服特力补的代谢。

Metabolism of oral turinabol by the human brain cholesterol 24-hydroxylase CYP46A1.

机构信息

Institute of Biochemistry, Saarland University, D-66123, Saarbruecken, Germany.

Center for Bioinformatics, Saarland University, D-66123, Saarbruecken, Germany.

出版信息

J Steroid Biochem Mol Biol. 2021 Sep;212:105927. doi: 10.1016/j.jsbmb.2021.105927. Epub 2021 Jun 2.

Abstract

The human microsomal cytochrome P450 enzyme CYP46A1 plays a crucial role in cholesterol elimination from the brain. It performs a 24-hydroxylation of cholesterol and is of outstanding significance for memory and cognition. This study demonstrates the catalytic activity of human CYP46A1 towards an anabolic androgenic steroid, oral turinabol (dehydrochloromethyltestosterone, 4-chloro-17β-dihydroxy,17α-methylandrosta-1,4-dien-3-one), which is a doping substance. CYP46A1 is the first human microsomal steroid-converting P450 showing activity towards this xenobiotic compound. Furthermore, the inhibitory effect of oral turinabol on the cholesterol conversion has been investigated in vitro demonstrating competition of the two substrates on the active site of CYP46A1 which might be of importance for potential pathogenic effects of oral turinabol. The conversion of oral turinabol was found to be selective resulting in the formation of only one product, as shown by HPLC analysis. To produce sufficient amounts of this product for NMR analysis, a system expressing human full-length CYP46A1 and CPR on a bicistronic vector was successfully developed realizing the selective cholesterol 24-hydroxylation in E. coli in mg amounts. Using this novel whole-cell system, the conversion of oral turinabol was performed and the product of this conversion by CYP46A1 was isolated and identified as 16β-hydroxy oral turinabol by NMR.

摘要

人细胞色素 P450 酶 CYP46A1 在胆固醇从大脑中消除中起着至关重要的作用。它对胆固醇进行 24-羟化作用,对记忆和认知具有重要意义。本研究证明了人 CYP46A1 对同化雄激素类固醇,口服 Turinabol(去氢氯甲基睾酮,4-氯-17β-二羟基,17α-甲基-雄甾-1,4-二烯-3-酮)的催化活性,这是一种兴奋剂物质。CYP46A1 是第一个对这种外源化合物表现出活性的人微粒体甾体转化 P450。此外,还研究了口服 Turinabol 对胆固醇转化的抑制作用,证明了两种底物在 CYP46A1 的活性部位竞争,这可能对口服 Turinabol 的潜在致病作用很重要。口服 Turinabol 的转化是选择性的,如 HPLC 分析所示,仅形成一种产物。为了获得足够量的用于 NMR 分析的产物,成功开发了一种在双顺反子载体上表达人全长 CYP46A1 和 CPR 的系统,在 mg 级水平上实现了大肠杆菌中选择性的胆固醇 24-羟化。使用这种新型全细胞系统进行了口服 Turinabol 的转化,并通过 NMR 将 CYP46A1 转化的产物分离并鉴定为 16β-羟基口服 Turinabol。

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Cholesterol 24-hydroxylase: Brain cholesterol metabolism and beyond.胆固醇24-羟化酶:脑胆固醇代谢及其他
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