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一种使用高分辨率质谱和多种数据处理工具研究多成分草药暴露、代谢和处置的综合方法。

An Integrated Approach for Studying Exposure, Metabolism, and Disposition of Multiple Component Herbal Medicines Using High-Resolution Mass Spectrometry and Multiple Data Processing Tools.

作者信息

Wu Caisheng, Zhang Haiying, Wang Caihong, Qin Hailin, Zhu Mingshe, Zhang Jinlan

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China (C.Wu., C.Wa., H.Q., J.Z.); Department of Biotransformation, Bristol-Myers Squibb Company, Princeton, New Jersey (H.Z., M.Z.).

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China (C.Wu., C.Wa., H.Q., J.Z.); Department of Biotransformation, Bristol-Myers Squibb Company, Princeton, New Jersey (H.Z., M.Z.)

出版信息

Drug Metab Dispos. 2016 Jun;44(6):800-8. doi: 10.1124/dmd.115.068189. Epub 2016 Mar 24.

Abstract

A typical prescription of traditional Chinese medicine (TCM) contains up to a few hundred prototype components. Studying their absorption, metabolism, distribution, and elimination (ADME) presents great challenges. The objective of this study was to develop a practical approach for investigating ADME of individual prototypes in TCM. An active fraction of Xiao-Xu-Ming decoction (AF-XXMD) as a model TCM prescription was orally administered to rats. AF-XXMD-related components in plasma, urine, bile, and feces were detected using high-resolution mass spectrometry and background subtraction, an untargeted data-mining tool. Components were then structurally characterized on the basis of MS(n) spectral data. Connection of detected AF-XXMD metabolites to their precursor species, either prototypes or upstream metabolites, were determined on the basis of mass spectral similarity and the matching of biotransformation reactions. As a result, 247 AF-XXMD-related components were detected and structurally characterized in rats, 134 of which were metabolites. Among 198 AF-XXMD prototypes dosed, 65 were fully or partially absorbed and 13 prototypes and 34 metabolites were found in the circulation. Glucuronidation, isomerization, and deglycosylation followed by biliary and urinary excretions and direct elimination of prototypes via kidney and liver were the major clearance pathways of AF-XXMD prototypes. As an example, the ADME profile of H56, the single major AF-XXMD component in rat plasma, was elucidated on the basis of profiles of H56-related components in plasma and excreta. The results demonstrate that the new analytical approach is a useful tool for rapid and comprehensive detection and characterization of TCM components in biologic matrix in a TCM ADME study.

摘要

一剂典型的中药方剂中可能含有多达数百种原型成分。研究它们的吸收、代谢、分布和排泄(ADME)面临着巨大挑战。本研究的目的是开发一种实用方法来研究中药中单个原型成分的ADME。将小续命汤活性部位(AF-XXMD)作为模型中药方剂口服给予大鼠。采用高分辨率质谱和背景扣除法(一种非靶向数据挖掘工具)检测血浆、尿液、胆汁和粪便中与AF-XXMD相关的成分。然后根据MS(n)光谱数据对成分进行结构表征。根据质谱相似性和生物转化反应的匹配,确定检测到的AF-XXMD代谢产物与其前体物质(原型或上游代谢产物)之间的联系。结果,在大鼠体内检测并鉴定了247种与AF-XXMD相关的成分,其中134种为代谢产物。在给药的198种AF-XXMD原型成分中,65种被完全或部分吸收,在循环系统中发现了13种原型成分和34种代谢产物。葡萄糖醛酸化、异构化和去糖基化,随后经胆汁和尿液排泄以及原型成分经肾脏和肝脏直接排泄是AF-XXMD原型成分的主要清除途径。例如,根据血浆和排泄物中与H56相关成分的情况,阐明了大鼠血浆中单一主要AF-XXMD成分H56的ADME特征。结果表明,这种新的分析方法是中药ADME研究中快速、全面检测和鉴定生物基质中中药成分的有用工具。

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