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人结肠上皮细胞对肠内酯和肠二醇的摄取与代谢

Uptake and metabolism of enterolactone and enterodiol by human colon epithelial cells.

作者信息

Jansen Guus H E, Arts Ilja C W, Nielen Michel W F, Müller Michael, Hollman Peter C H, Keijer Jaap

机构信息

RIKILT-Institute of Food Safety, Wageningen, The Netherlands.

出版信息

Arch Biochem Biophys. 2005 Mar 1;435(1):74-82. doi: 10.1016/j.abb.2004.12.015.

Abstract

The enterolignans enterolactone and enterodiol are phytoestrogens that are formed from plant lignans by microorganisms in the human colon. Enterolignans circulate in plasma as conjugates. We hypothesized that conjugation of enterolignans takes place in colon epithelial cells, and studied the time course of uptake and metabolism of enterolactone and enterodiol in three human colon epithelial cell lines. In addition, the conjugates were identified by mass spectrometry with accurate mass measurement (LC/QTOFMS/MS). Intracellular levels of conjugated enterolactone and enterodiol in HT29 cells rose immediately after starting the exposure. This was accompanied by a rapid decrease in free enterolactone and enterodiol in the exposure medium of HT29 and (un)differentiated CaCo-2 but not of CCD841CoTr cells. Conjugation and excretion of enterolactone and enterodiol was complete within 8 h, except for enterodiol in CaCo-2 cells ( approximately 48 h). Enterolactone appears to be more rapidly metabolized and/or excreted than enterodiol, and also the appearance of conjugated enterolactone in medium is less affected by the presence of enterodiol than vice versa. Total (free plus conjugated) enterolignan concentrations remained constant throughout the experiments. Three conjugates were identified in exposure medium of HT29 cells: enterolactone-sulfate, enterolactone-glucuronide, and enterodiol-glucuronide. Taken together, our data suggest that phase II metabolism of enterolactone and enterodiol already may take place during uptake in the colon and that colon epithelial cells may be responsible for this metabolism.

摘要

肠内木脂素肠内酯和肠二醇是植物雌激素,由人体结肠中的微生物从植物木脂素转化而来。肠内木脂素以共轭物的形式在血浆中循环。我们推测肠内木脂素的共轭化发生在结肠上皮细胞中,并研究了三种人结肠上皮细胞系中肠内酯和肠二醇的摄取和代谢的时间进程。此外通过具有精确质量测量功能的质谱(液相色谱/四极杆飞行时间串联质谱)对共轭物进行了鉴定。在HT29细胞中,开始暴露后,共轭肠内酯和肠二醇的细胞内水平立即升高。与此同时,HT29和(未)分化的CaCo-2细胞暴露培养基中游离肠内酯和肠二醇迅速减少,但CCD841CoTr细胞则不然。除CaCo-2细胞中的肠二醇(约48小时)外,肠内酯和肠二醇的共轭化和排泄在8小时内完成。肠内酯似乎比肠二醇代谢和/或排泄得更快,而且培养基中共轭肠内酯的出现受肠二醇存在的影响也小于反之情况。在整个实验过程中,总(游离加共轭)肠内木脂素浓度保持恒定。在HT29细胞的暴露培养基中鉴定出三种共轭物:硫酸肠内酯、葡萄糖醛酸肠内酯和葡萄糖醛酸肠二醇。综上所述,我们的数据表明,肠内酯和肠二醇的II相代谢可能在结肠摄取过程中就已发生,并且结肠上皮细胞可能负责这种代谢。

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