Comprehensive Study of In vivo and In vitro Metabolites of Cycloastragenol Based on UHPLC-Q-Exactive Orbitrap Mass Spectrometer.

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Current drug metabolism Pub Date : 2023-01-01 DOI:10.2174/1389200224666230202150436
Huajian Li, Shaoping Wang, Hong Wang, Haoran Li, Yanan Li, Pingping Dong, Xianming Lan, Jiayu Zhang, Long Dai
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Abstract

Background: Cycloastragenol (CAG) is a sapogenin derived from the main bioactive constituents of Astragali Radix (AR). However, the current research on CAG metabolism in vivo and in vitro is still inadequate, and the metabolite cluster is incomplete due to incomplete analysis strategy.

Objective: The objective of this study was to screen and identify the metabolic behavior of CAG in vivo and in vitro.

Methods: A simple and rapid analysis strategy based on UHPLC-Q-Exactive Orbitrap mass spectrometry combined with data-mining processing technology was developed and used to screen and identify CAG metabolites in rat body fluids and tissues after oral administration.

Results: As a result, a total of 82 metabolites were fully or partially characterized based on their accurate mass, characteristic fragment ions, retention times, corresponding Clog P values, and so on. Among the metabolites, 61 were not been reported in previous reports. These metabolites (6 metabolites in vitro and 91 in vivo) were generated through reactions of hydroxylation, glucuronidation, sulfation, hydrogenation, hydroxylation, demethylation, deisopropylation, dehydroxylation, ring cleavage, and carboxyl substitution and their composite reactions, and the hydroxylation might be the main metabolic reaction of CAG. In addition, the characteristic fragmentation pathways of CAG were summarized for the subsequent metabolite identification.

Conclusion: The current study not only clarifies the metabolite cluster-based and metabolic regularity of CAG in vivo and in vitro, but also provides ideas for metabolism of other saponin compounds.

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环黄芪醇体内、体外代谢物的uhplc - q -精确轨道阱质谱综合研究
背景:环黄芪醇(Cycloastragenol, CAG)是从黄芪(Astragali Radix, AR)的主要生物活性成分中提取的皂苷元。然而,目前对CAG体内外代谢的研究仍然不足,由于分析策略不完善,代谢物簇也不完整。目的:筛选和鉴定CAG在体内和体外的代谢行为。方法:建立一种基于UHPLC-Q-Exactive Orbitrap质谱联用数据挖掘处理技术的简单快速分析策略,用于大鼠口服给药后体液及组织中CAG代谢物的筛选鉴定。结果:基于准确的质量、特征片段离子、保留时间、对应的Clog P值等,对82种代谢物进行了全部或部分表征。其中61种代谢物在既往报道中未见报道。这些代谢物(体外6个,体内91个)是通过羟基化、葡萄糖醛酸化、磺化、氢化、羟基化、去甲基化、去异丙基化、去羟基化、环裂解、羧基取代等反应及其复合反应产生的,羟基化可能是CAG的主要代谢反应。此外,总结了CAG的特征断裂途径,为后续的代谢物鉴定提供依据。结论:本研究不仅阐明了CAG体内外代谢产物簇基及其代谢规律,而且为其他皂苷类化合物的代谢提供了思路。
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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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