超高效液相色谱-四极杆-精确轨道-高分辨质谱法快速综合鉴定大鼠体内体外维萨胺代谢物。

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aichun Gao, Hongjin Wang, Xiaoge Cheng, Caihong Li, Lixin Sun
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引用次数: 0

摘要

背景:长春酰胺是一种从officinalis中提取的吲哚类生物碱,具有抗肿瘤、抗菌和抗炎等药理活性。然而,尽管其具有良好的治疗应用前景,但在研究vincosavide的代谢途径方面存在明显的差距。目的:研究长春酰胺在大鼠体内和体外的代谢情况,阐明其代谢途径。方法:采用超高效液相色谱-四极柱-高分辨质谱法(UHPLC-Q-Exactive Orbitrap HRMS)对长春新胺给药后的肝微粒体孵育、血浆、胆汁、尿液和粪便进行分析。采用Compound Discovery 3.2软件和分子网络方法对收集的数据进行分析。通过这些方法鉴定的代谢物随后使用Xcalibur 4.1软件进行验证,该软件提供了保留时间、亲本离子和特征片段离子的信息。结果:共鉴定出37种代谢物,其中体外代谢物8种,体内代谢物32种(血浆代谢物3种,胆汁代谢物7种,尿液代谢物22种,粪便代谢物17种)。虽然大鼠体内和体外对维新胺的代谢不同,但所发生的代谢反应的类型是明确的。主要的代谢途径是氧化、还原、去糖基化、水化、葡萄糖醛酸化、甲基化、磺化、甘氨酸偶联、半胱氨酸偶联、牛磺酸偶联和复合反应。结论:本研究阐明了大鼠体内和体外对维科沙胺的代谢,从而扩大了维科沙胺的代谢谱。这些发现为开发以维科沙胺为基础的新药奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid and Comprehensive Identification of Vincosamide Metabolites in vitro and in vivo in Rats by Ultra-High Performance Liquid Chromatography-Quadrupole- Exactive Orbitrap-High Resolution Mass Spectrometry.

Background: Vincosamide, an indole alkaloid extracted from Nauclea officinalis, exhibits a range of pharmacological activities, such as anti-tumor, antibacterial, and anti-inflammatory properties. However, despite its promising therapeutic applications, there is a notable gap in research focused on the metabolic pathways of vincosamide.

Objective: This study aims to investigate the metabolism of vincosamide both in vitro and in vivo in rats, and to elucidate its metabolic pathways.

Methods: Samples of liver microsomal incubation, plasma, bile, urine, and feces following vincosamide ad-ministration were analyzed by ultra-high performance liquid chromatography-quadrupole-Exactive Orbitrap-high resolution mass spectrometry (UHPLC-Q-Exactive Orbitrap HRMS). The collected data were analyzed using Compound Discovery 3.2 software and the molecular network method. The metabolites identified through these methodologies were subsequently validated using Xcalibur 4.1 software, which provided infor-mation on retention times, parent ions, and characteristic fragment ions.

Results: A total of 37 metabolites were identified, including 8 in vitro and 32 in vivo (3 in plasma, 7 in bile, 22 in urine, and 17 in feces). While the metabolism of vincosamide differs in vitro and in vivo in rats, the type of metabolic reaction that occurs is well-defined. The predominant metabolic pathways are oxidation, reduc-tion, deglycosylation, hydration, glucuronidation, methylation, sulfation, glycine conjugation, cysteine conju-gation, taurine conjugation, and complex reactions.

Conclusion: This study elucidates the metabolism of vincosamide in vitro and in vivo in rats, thereby expand-ing the metabolite profile of vincosamide. These findings provide a foundation for the potential development of new drugs based on vincosamide.

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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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