Identification of metabolites from the Himalayan herbal medicine Meconopsis integrifolia total flavonoids fraction in rats using UPLC-Q-exactive orbitrap-MS analysis

IF 3.4 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Enhui Ji , Yuan Liu , Yifan Tian , Limin Li , Pei Qun , Zhengming Yang , Chaoqin Ren , Yanfei Huang , Yongcang Zhang
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引用次数: 0

Abstract

Meconopsis integrifolia total flavonoids (MITF) have been identified as the hepatoprotective fraction of M. integrifolia, with its main components being flavonoid glycosides, along with lower levels of phenolic acids and alkaloids. Since flavonoid glycosides are poorly absorbed in vivo, metabolism serves as a crucial pathway for their biotransformation. However, the metabolism and material basis of pharmacological effects of MITF in vivo remain unknown. In this study, ultra-performance liquid chromatography coupled with triple quadrupole mass spectrometry was used to investigate the metabolic profiles of MITF. A total of 61 absorbed prototype compounds were identified, including 54 in feces (43 flavonoids, 8 phenolic acids, and 3 alkaloids), 8 in urine (2 flavonoids, 3 phenolic acids, 3 alkaloids), and 6 in plasma (2 flavonoids, 4 phenolic acids). Furthermore, 113 metabolites were characterized, including 64 in feces (38 flavonoids, 11 phenolic acids, 15 alkaloids), 46 in urine (17 flavonoids, 16 phenolic acids, 13 alkaloids), and 14 in plasma (5 flavonoids, 9 phenolic acids). The major metabolic pathways were dehydroxylation, hydroxylation, reduction, dehydrogenation, hydration, dehydration, methylation, sulfation, and glucuronidation. The results indicated that the biotransformation and absorption of flavonoids in vivo were limited. In contrast, phenolic acids and alkaloids were extensively absorbed. This research provides crucial insights into the metabolic fate of MITF in rats, thereby clarifying the pharmacologically active substances derived from M. integrifolia.

Data availability

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
用uplc - q -高通量轨道谱-质谱法鉴定喜马拉雅草药绿绒蒿总黄酮大鼠代谢产物
综合Meconopsis integrifolia total flavonoids (MITF)是综合Meconopsis integrifolia的保肝成分,其主要成分为黄酮类苷,酚酸和生物碱含量较低。由于黄酮类苷在体内吸收较差,代谢是其生物转化的重要途径。然而,MITF在体内的代谢和药理作用的物质基础尚不清楚。本研究采用超高效液相色谱联用三重四极杆质谱法研究了MITF的代谢谱。共鉴定出61种吸收原型化合物,其中粪便54种(43种黄酮类化合物、8种酚酸类化合物和3种生物碱)、尿液8种(2种黄酮类化合物、3种酚酸类化合物、3种生物碱)和血浆6种(2种黄酮类化合物、4种酚酸类化合物)。共鉴定出113种代谢物,其中粪便64种(38种黄酮类化合物,11种酚酸,15种生物碱),尿液46种(17种黄酮类化合物,16种酚酸,13种生物碱),血浆14种(5种黄酮类化合物,9种酚酸)。主要代谢途径为去羟基化、羟基化、还原、脱氢、水化、脱水、甲基化、磺化和葡萄糖醛酸化。结果表明,黄酮类化合物在体内的生物转化和吸收是有限的。相反,酚酸和生物碱被广泛吸收。本研究为了解MITF在大鼠体内的代谢命运提供了重要的见解,从而阐明了来自整合芽孢杆菌的药理活性物质。数据可获得性支持本研究结果的数据可根据通讯作者的要求提供。由于隐私或道德限制,这些数据不会公开。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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