基于 UPLC-QTOF-MS 的靶向代谢组学揭示 Swertia chirayita 的保肝标志化合物。

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED
Dhriti Verma, Saloni Thakur, Hitesh Shrimal, Satish Kumar, Joydeep Das, Biswatrish Sarkar, Deepak N Kapoor, Prashanta Kumar Deb
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引用次数: 0

摘要

在 "阿育吠陀 "中,Swertia chirayita 是一种广受欢迎的保肝草药。本研究采用靶向代谢组学方法对 S. chirayita 植物中具有肝脏保护特性的植物化学物质进行了表征。对 S. chirayita 水醇提取物的不同馏分进行了体外抗氧化和 HepG2 细胞保肝特性评估。此外,还对活性馏分进一步进行了基于 UPLC-QTOF-MS 的靶向代谢组学研究,以确定与生物活性相关的植物化学物质。此外,还进行了一项补充性硅学实验,以了解已鉴定分子与 CYP2E1 酶之间的相互作用。结果表明,正丁醇馏分能显著(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
UPLC-QTOF-MS based targeted metabolomics to unravel the hepatoprotective marker compounds of Swertia chirayita.

Swertia chirayita is a popular hepatoprotective herb according to 'Ayurveda'. This study characterises the phytochemicals of S. chirayita responsible for hepatoprotective properties was executed using targeted metabolomics approach. Different fractions of hydro-alcoholic extract of S. chirayita were subjected to assess in-vitro antioxidant and hepatoprotective properties in HepG2 cells. Furthermore, active fraction was further subjected to UPLC-QTOF-MS based targeted metabolomics to identify the phytochemicals linked to bioactivity. A complementary in-silico experiment was also performed to understand the interactions of identified molecules with CYP2E1 enzyme. It was observed that, n-butanol fraction deciphers significant (p < .05) and maximum antioxidant and hepatocyte protection compared to other fractions. UPLC-QTOF-HRMS analysis reveals that it contains 17 secondary metabolites various classes. Identified molecules showed potential interactions with the crucial amino acid residues in the active site of CYP2E1 protein indicate the possibility of inhibition which may counter APAP induced toxicity in HepG2 cells.

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来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
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