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基于 UPLC-HRMS 和 DESI-MS 技术的鲫鱼中小儿消食丸吸收、分布、代谢和排泄的综合方法。

Integrated approach toward absorption, distribution, metabolism, and excretion of Xiaoke pills in zebrafish based on UPLC-HRMS and DESI-MS techniques.

机构信息

Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Sciences, Xiamen University, Xiang'an South Road, Xiamen, Fujian 361102, PR China.

State Key Laboratory of Coal Resources and Safe Mining, China University of Mining and Technology (Beijing), Beijing 100083, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Jun 1;1200:123276. doi: 10.1016/j.jchromb.2022.123276. Epub 2022 May 6.

Abstract

Traditional Chinese medicine (TCM) has been used in clinical settings for over 2000 years in China. The study of the absorption, distribution, metabolism, and excretion (ADME) of TCM in vivo could be beneficial for the discovery of the active components in TCM. However, the conventional strategies used for ADME research are based on rodent models and have the characteristics of lengthy experimental periods, complex processes, and extensive data processing, which make it difficult to perform rapid analyses and high-throughput ADME screening of the medicinal components of TCM. In this study, an integrated high-throughput research strategy for the in vivo ADME analysis of TCM was established based on a zebrafish model. Accordingly, a combination of ultra-performance liquid chromatography-high-resolution mass spectrometry (UPLC-HRMS), desorption electrospray ionization-mass spectrometry (DESI-MS) imaging, and in-house non-targeted precise-and-thorough background-subtraction (PATBS) data post-processing techniques were successfully applied for the analysis of the metabolism of zebrafish exposed to Xiaoke pills. A total of 49 compounds related to Xiaoke pills (including 13 prototypical components and 36 metabolites) were detected in zebrafish. In total, 32 of them, including puerarin, daidzein, deoxyschizandrin, formononetin, and glibenclamide, which have been identified to have hypoglycemic activity in our previous studies and are phase I and phase II metabolites resulting from the hydroxylation, demethylation, glucuronidation, sulfation, and glycosylation of the prototypical components in vivo, were found in rats treated with Xiaoke pills. Furthermore, the overall distribution of the known compounds in zebrafish exposed to Xiaoke pills was explored using DESI-MS. In summary, this study provides a practical approach for the high-throughput screening of the active components of TCM using a zebrafish model.

摘要

中医药在中国临床应用已有 2000 多年的历史。研究中药在体内的吸收、分布、代谢和排泄(ADME)有助于发现中药中的活性成分。然而,传统的 ADME 研究策略基于啮齿动物模型,具有实验周期长、过程复杂、数据处理广泛等特点,难以对中药的药用成分进行快速分析和高通量 ADME 筛选。在这项研究中,建立了一种基于斑马鱼模型的中药体内 ADME 分析的集成高通量研究策略。相应地,成功地将超高效液相色谱-高分辨率质谱(UPLC-HRMS)、解吸电喷雾电离质谱(DESI-MS)成像以及内部非靶向精确全面背景减除(PATBS)数据后处理技术相结合,用于分析暴露于消渴丸的斑马鱼的代谢情况。在斑马鱼中检测到与消渴丸相关的 49 种化合物(包括 13 种原型成分和 36 种代谢物)。其中,32 种化合物,包括葛根素、大豆苷元、五味子甲素、芒柄花素和格列本脲,在我们之前的研究中已被证实具有降血糖活性,并且是体内原型成分羟化、去甲基化、葡萄糖醛酸化、硫酸化和糖基化的 I 相和 II 相代谢物,在服用消渴丸的大鼠中被发现。此外,还使用 DESI-MS 探索了暴露于消渴丸的斑马鱼中已知化合物的总体分布。总之,本研究为利用斑马鱼模型进行中药活性成分的高通量筛选提供了一种实用方法。

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