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首页> 外文期刊>Analytical methods >Plasma metabolic profiling analysis of normal and ANIT-induced cholestasis rats after oral administration of Da-Huang-Xiao-Shi decoction using UHPLC-Q-Orbitrap MS coupled with pattern recognition
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Plasma metabolic profiling analysis of normal and ANIT-induced cholestasis rats after oral administration of Da-Huang-Xiao-Shi decoction using UHPLC-Q-Orbitrap MS coupled with pattern recognition

机译:使用UHPLC-Q-Orbitrap MS结合模式识别技术对大黄小石汤口服后正常和ANIT诱发的胆汁淤积大鼠血浆代谢谱分析

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Da-Huang-Xiao-Shi decoction (DHXSD) is a representative formula for treating jaundice and could have bright prospects owing to its liver protecting effects. DHXSD might synthetically result in a change in the metabolic profiles of cholestasis rats compared with that of normal rats after oral administration. Metabolic profiling analysis has gained significant attention ever since the field of metabolomics began to develop. In this study, a highly sensitive, rapid and high chromatographic resolution ultra-high performance liquid chromatography-hybrid quadrupole-Orbitrap mass spectrometry (UHPLC-Q-Orbitrap MS) combined with multivariate statistical analysis method was established to investigate the metabolic profiles of DHXSD in normal and alpha-naphthylisothiocyanate (ANIT)-induced cholestasis rats. In addition, serum biochemical indices and pathological observation analysis were utilized to evaluate the animal model. As a result, a total of 68 prototype compounds and metabolites in normal and cholestasis rats in vivo were screened and tentatively identified according to their exact mass and the relevant literature. Among these, 15 of the compounds were filtered out as potential chemical markers that may be responsible for the pharmacological effects of DHXSD, which offers a basic foundation for quality evaluation, pharmacokinetic research and the clinical safety of drug usage. In conclusion, this study provides an insight into the metabolism of DHXSD in vivo to enable understanding of the metabolic process and therapeutic mechanism of cholestasis.
机译:大黄消食汤(DHXSD)是一种治疗黄疸的典型配方,由于其对肝脏的保护作用,具有广阔的前景。 DHXSD可能会导致口服后胆汁淤积大鼠的代谢谱与正常大鼠相比发生变化。自从代谢组学领域开始发展以来,代谢谱分析一直备受关注。本研究建立了一种高灵敏度,快速,高分离度的超高效液相色谱-混合四极杆-Orbitrap质谱(UHPLC-Q-Orbitrap MS)结合多元统计分析方法,以研究DHXSD的代谢特征。正常和α-萘基异硫氰酸酯(ANIT)诱导的胆汁淤积大鼠。另外,利用血清生化指标和病理观察分析来评价动物模型。结果,根据它们的确切质量和相关文献,对体内和胆汁淤积症大鼠体内总共68种原型化合物和代谢物进行了筛选和初步鉴定。其中,有15种化合物作为潜在的化学标记物被滤出,可能是DHXSD的药理作用的原因,这为质量评估,药代动力学研究和药物使用的临床安全性提供了基础。总而言之,这项研究提供了体内DHXSD代谢的真知灼见,使人们能够了解胆汁淤积的代谢过程和治疗机制。

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