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Integrating Strategies of Herbal Metabolomics, Network Pharmacology, and Experiment Validation to Investigate Frankincense Processing Effects

机译:草药代谢组学,网络药理学和实验验证的整合策略,用于研究乳香的加工效果

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摘要

In-depth research on processing can promote the globalization of processed herbs. The purpose of this study is to propose an improved strategy for processing effect investigation. Frankincense and processed frankincense were used as research subjects. First, high-speed countercurrent chromatography (HSCCC) and preparation high-performance liquid chromatography (PHPLC) techniques were used for major compounds isolation and minor compounds concentration. Processed frankincense was subjected to two stepwise solvent systems, namely, n-hexane:ethanol:water (6:5:1) and n-hexane:methyl-acetate:acetonitrile:water (4:4:3:4), to yield 12 fractions, and 18 compounds were further separated. Second, a comprehensive metabolomic analysis conducted by ultrahigh-performance liquid-chromatography/electrospray-ionization mass spectrometry (UHPLC-Qtof-MS) coupled with multivariate statistics was performed to fully characterize the chemical components and discover the potential biomarkers between frankincense and processed frankincense. In total, 81 metabolites, including the 18 separated compounds, were selected as potential biomarkers between frankincense and processed frankincense among 153 detected compounds for their VIP values of greater than one. The tirucallane-type compounds and components with 9,11-dehydro structures clearly occurred at high levels in the processed frankincense, while lupine-type compounds and those with 11-keto structures were significantly higher in frankincense. Then, a network pharmacology model was constructed to decipher the potential mechanisms of processing. Intestinal absorption properties prediction indicated the possibility of processing-related absorption enhancement. A systematic analysis of the constructed networks showed that the C-T network was constructed with 18 potential biomarkers and 69 targets. TNF and IL-1β were among the top-ranked and were linked by 8 and 7 pathways, which were mainly involved in inflammation. The arachidonic acid metabolism pathway exhibited the highest number of target connections. Finally, the prediction was validated experimentally by an intestinal permeability and efficacy assay. The experiments provided convincing evidence that processed frankincense harbored stronger inhibition effects toward TNF-α-, IL-1β- and arachidonic acid-induced platelet aggregation. The processing procedure leads to changes of the chemical metabolites, which triggers the enhancement of absorption and cure efficiency. The global change of the metabolites, absorption and pharmacological effects of processing were depicted in a systematic manner.
机译:对加工的深入研究可以促进加工草药的全球化。这项研究的目的是为加工效果调查提出一种改进的策略。乳香和加工的乳香被用作研究对象。首先,使用高速逆流色谱(HSCCC)和制备型高效液相色谱(PHPLC)技术分离主要化合物和微量化合物。将加工后的乳香置于两个逐步溶剂体系中,即正己烷:乙醇:水(6:5:1)和正己烷:乙酸甲酯:乙腈:水(4:4:3:4)分离出12个馏分和18种化合物。其次,通过超高效液相色谱/电喷雾电离质谱(UHPLC-Qtof-MS)结合多元统计数据进行了全面的代谢组学分析,以充分表征化学成分并发现乳香和加工乳香之间的潜在生物标志物。总共选择了81种代谢物,包括18种分离出的化合物,作为153种检测到的VIP值大于1的化合物在乳香和加工乳香之间的潜在生物标记。在加工过的乳香中,具有9,11-脱氢结构的丁香烷型化合物和组分明显地以高水平出现,而在羽扇豆香中,羽扇豆型化合物和具有11-酮结构的化合物明显更高。然后,建立了网络药理模型来解释潜在的加工机理。肠道吸收特性的预测表明与加工有关的吸收增强的可能性。对构建的网络的系统分析表明,构建的C-T网络具有18个潜在的生物标记和69个靶标。 TNF和IL-1β排在首位,并通过8和7种途径相互联系,这些途径主要与炎症有关。花生四烯酸代谢途径表现出最高数量的靶标连接。最后,该预测通过肠通透性和功效测定进行了实验验证。实验提供了令人信服的证据,表明加工后的乳香对TNF-α-,IL-1β-和花生四烯酸诱导的血小板聚集具有更强的抑制作用。加工程序导致化学代谢物的变化,从而触发吸收和固化效率的提高。系统地描述了加工过程中代谢物的整体变化,吸收和药理作用。

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