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基于超高效液相色谱/电喷雾电离四极杆飞行时间质谱的茵陈二炔酮肝保护作用的代谢组学研究。

Metabolomics study on the hepatoprotective effect of scoparone using ultra-performance liquid chromatography/electrospray ionization quadruple time-of-flight mass spectrometry.

机构信息

National TCM Key Lab of Serum Pharmacochemistry, Heilongjiang University of Chinese Medicine, and Key Pharmacometabolomics Platform of Chinese Medicines, Heping Road 24, Harbin 150040, China.

出版信息

Analyst. 2013 Jan 7;138(1):353-61. doi: 10.1039/c2an36382h. Epub 2012 Nov 14.

Abstract

Scoparone is an important constituent of Yinchenhao (Artemisia annua L.), a famous medicinal plant, and displayed bright prospects in the prevention and therapy of liver injury. However, the precise molecular mechanism of hepatoprotective effects has not been comprehensively explored. Here, metabolomics techniques are the comprehensive assessment of endogenous metabolites in a biological system and may provide additional insight into the mechanisms. The present investigation was designed to assess the effects and possible mechanisms of scoparone against carbon tetrachloride-induced liver injury. Ultra-performance liquid chromatography/electrospray ionization quadruple time-of-flight mass spectrometry (UPLC/ESI-Q-TOF/MS) combined with pattern recognition approaches including principal component analysis (PCA) and partial least squares-discriminant analysis (PLS-DA) were integrated to discover differentiating metabolites. Results indicate five ions in the positive mode as differentiating metabolites. Functional pathway analysis revealed that the alterations in these metabolites were associated with primary bile acid biosynthesis, pyrimidine metabolism. Of note, scoparone has a potential pharmacological effect through regulating multiple perturbed pathways to the normal state. Our findings also showed that the robust metabolomics techniques are promising for getting biomarkers and clarifying mechanisms of disease, highlighting insights into drug discovery.

摘要

茅术酮是茵陈蒿(Artemisia annua L.)的重要组成部分,茵陈蒿是一种著名的药用植物,在预防和治疗肝损伤方面显示出广阔的前景。然而,其肝保护作用的确切分子机制尚未得到全面探讨。代谢组学技术是对生物系统内内源性代谢物的全面评估,可能为机制提供更多的见解。本研究旨在评估茅术酮对四氯化碳诱导的肝损伤的作用及可能的机制。超高效液相色谱/电喷雾电离四极杆飞行时间质谱联用(UPLC/ESI-Q-TOF/MS)结合主成分分析(PCA)和偏最小二乘判别分析(PLS-DA)等模式识别方法,用于发现差异代谢物。结果表明,正模式下有 5 个离子为差异代谢物。功能途径分析表明,这些代谢物的变化与初级胆汁酸生物合成、嘧啶代谢有关。值得注意的是,茅术酮通过调节多个受扰途径恢复正常状态,具有潜在的药理作用。我们的研究结果还表明,强大的代谢组学技术有望获得生物标志物并阐明疾病机制,为药物发现提供新的见解。

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