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通脉方在人肠道菌群作用下的生物转化及其跨Caco-2细胞单层的肠道通透性研究。

Study of the Biotransformation of Tongmai Formula by Human Intestinal Flora and Its Intestinal Permeability across the Caco-2 Cell Monolayer.

作者信息

Wu Shuai, Xu Wei, Wang Fu-Rong, Yang Xiu-Wei

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University Health Science Center, Peking University, No. 38, Xueyuan Road, Haidian District, Beijing 100191, China.

出版信息

Molecules. 2015 Oct 15;20(10):18704-16. doi: 10.3390/molecules201018704.

Abstract

Tongmai formula (TMF) is a well-known Chinese medicinal preparation that contains isoflavones as its major bioactive constituents. As traditional Chinese medicines (TCMs) are usually used by oral administration, their fate inside the intestinal lumen, including their biotransformation by human intestinal flora (HIF) and intestinal absorption deserves study. In this work TMF extract was incubated with human intestinal bacteria under anaerobic conditions and the changes in the twelve main constituents of TMF were then investigated. Their intestinal permeabilities, i.e., the transport capability across the intestinal brush border were investigated with a human colon carcinoma cell line (Caco-2) cell monolayer model to predict the absorption mechanism. Meanwhile, rapid HPLC-DAD methods were established for the assay. According to the biotransformation curves of the twelve constituents and the permeability coefficients, the intestinal absorption capacity of the typical compounds was elevated from the levels of 10(-7) cm/s to 10(-5) cm/s from those of the original compounds in TMF. Among them the main isoflavone glycosides puerarin (4), mirificin (6) and daidzin (7) were transformed into the same aglycone, daidzein (10). Therefore it was predicted that the aglycone compounds might be the real active ingredients in TMF. The models used can represent a novel path for the TCM studies.

摘要

通脉方(TMF)是一种著名的中药制剂,其主要生物活性成分是异黄酮。由于中药通常通过口服给药,它们在肠腔内的命运,包括它们被人类肠道菌群(HIF)的生物转化和肠道吸收值得研究。在这项工作中,TMF提取物在厌氧条件下与人肠道细菌一起孵育,然后研究TMF的十二种主要成分的变化。用人类结肠癌细胞系(Caco-2)细胞单层模型研究它们的肠道通透性,即跨肠道刷状缘的转运能力,以预测吸收机制。同时,建立了快速HPLC-DAD方法用于测定。根据十二种成分的生物转化曲线和渗透系数,典型化合物的肠道吸收能力从TMF中原始化合物的水平从10^(-7) cm/s提高到10^(-5) cm/s。其中主要的异黄酮苷葛根素(4)、米里菲辛(6)和大豆苷(7)被转化为相同的苷元大豆苷元(10)。因此,预计苷元化合物可能是TMF中的真正活性成分。所使用的模型可以代表中药研究的一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0198/6331934/9c533024b6d0/molecules-20-18704-g001.jpg

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