Integrating 2D NMR-based metabolomics and in vitro assays to explore the potential viability of cultivated Ophiocordyceps sinensis as an alternative to the wild counterpart

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Xiu Gu , Yanping Li , Yang Li , Xiaohui Duan , Youfan Hu , Jialuo Chen , Huan Du , Jing Bai , Chengyan He , Caihong Bai , Jinlin Guo , Jiahui Yang , Kaifeng Hu
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引用次数: 0

Abstract

Ophiocordyceps sinensis is widely used to treat various diseases and as a health supplement. The present study comprehensively compared the metabolic differences between wild and cultivated O. sinensis through 2D 1H-13C HSQC-based metabolomics, and assessed their anti-lung cancer activity on A549 cells. To characterize the global metabolic profile, sample preparation was scrutinously optimized, and both polar (1:4 methanol-water) and non-polar (1:4 methanol-chloroform) extracts of O. sinensis were investigated. A total of 47 and 10 metabolites were identified in the polar and non-polar extracts, respectively. Principal Component Analysis (PCA) revealed greater differences between the two types of O. sinensis in the polar extracts than in the non-polar extracts. Orthogonal Partial Least Squares-Discriminant Analysis (OPLS-DA) together with univariate tests captured 23 and 19 differential spectral features (with 22 and 11 of them assigned) between wild and cultivated O. sinensis in the polar and non-polar extracts, respectively. Meanwhile, the anti-lung cancer activities of both polar and non-polar extracts of wild and cultivated O. sinensis were assessed by MTS assay on A549 cells, and the sterols found in non-polar extracts, such as ergosterol, ergosterol peroxide, and 9,11-dehydroergosterol peroxide, and β-sitosterol, are the active ingredients with potential anti-lung cancer properties. In this study, we introduced a comprehensive strategy integrating 2D NMR-based metabolomics with in vitro assays for comparing the chemical composition and assessing the pharmacological activity of wild and cultivated O. sinensis. Our results provided a scientific basis for the potential viability of cultivated O. sinensis as an alternative to the wild counterpart.
整合基于二维核磁共振的代谢组学和体外试验,探索栽培的冬虫夏草作为野生冬虫夏草替代品的潜在可行性。
冬虫夏草被广泛用于治疗各种疾病和作为保健品。本研究通过基于二维 1H-13C HSQC 的代谢组学,全面比较了野生和栽培的冬虫夏草代谢差异,并评估了它们对 A549 细胞的抗肺癌活性。为了描述总体代谢特征,对样品制备进行了严格的优化,并研究了野生中华皂苷的极性(1:4 甲醇-水)和非极性(1:4 甲醇-氯仿)提取物。在极性和非极性提取物中分别鉴定出 47 种和 10 种代谢物。主成分分析(PCA)显示,极性萃取物与非极性萃取物之间的差异更大。正交偏最小二乘法判别分析(OPLS-DA)和单变量检验分别捕获了极性和非极性提取物中野生和栽培中药材的 23 个和 19 个差异光谱特征(其中 22 个和 11 个为指定特征)。同时,利用 MTS 法对 A549 细胞进行了抗肺癌活性评估,结果表明非极性提取物中的麦角甾醇、过氧化麦角甾醇、9,11-脱氢过氧化麦角甾醇、β-谷甾醇等甾醇类化合物是具有潜在抗肺癌活性的有效成分。在这项研究中,我们引入了一种综合策略,将基于二维核磁共振的代谢组学与体外检测相结合,用于比较野生和栽培的中华皂苷的化学成分并评估其药理活性。我们的研究结果为栽培的中华皂苷替代野生中华皂苷的潜在可行性提供了科学依据。
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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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