首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Analysis of Therapeutic Effect of Ilex hainanensis Merr. Extract on Nonalcoholic Fatty Liver Disease through Urine Metabolite Profiling by Ultraperformance Liquid Chromatography/Quadrupole Time of Flight Mass Spectrometry
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Analysis of Therapeutic Effect of Ilex hainanensis Merr. Extract on Nonalcoholic Fatty Liver Disease through Urine Metabolite Profiling by Ultraperformance Liquid Chromatography/Quadrupole Time of Flight Mass Spectrometry

机译:海南冬青树的治疗效果分析。超高效液相色谱/四极杆飞行时间质谱通过尿液代谢物谱分析提取非酒精性脂肪性肝病

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Nonalcoholic fatty liver disease (NAFLD), the most common form of chronic liver disease, is increased worldwide in parallel with the obesity epidemic. Our previous studies have showed that the extract of I. hainanensis (EIH) can prevent NAFLD in rat fed with high-fat diet. In this work, we aimed to find biomarkers of NAFLD and investigate the therapeutic effects of EIH. NAFLD model was induced in male Sprague-Dawley rats by high-fat diet. The NAFLD rats were administered EIH orally (250 nag/kg) for two weeks. After the experimental period, samples of 24 h urine were collected and analyzed by ultraperformance liquid chromatography/quadrupole time of flight mass spectrometry (UPLC-Q-TOF). Orthogonal partial least squares analysis (OPLSs) models were built to find biomarkers of NAFLD and investigate the therapeutic effects of EIH. 22 metabolites, which are distributed in several metabolic pathways, were identified as potential biomarkers of NAFLD. Taking these biomarkers as screening indexes, EIH could reverse the pathological process of NAFLD through regulating the disturbed pathway of metabolism. The metabolomic results not only supply a systematic view of the development and progression of NAFLD but also provide a theoretical basis for the prevention or treatment of NAFLD.
机译:非酒精性脂肪性肝病(NAFLD)是慢性肝病的最常见形式,在世界范围内与肥胖症流行同时发生。我们以前的研究表明,海南岛提取物(EIH)可以预防高脂饮食喂养的大鼠的NAFLD。在这项工作中,我们旨在寻找NAFLD的生物标记并研究EIH的治疗效果。通过高脂饮食在雄性Sprague-Dawley大鼠中建立NAFLD模型。给NAFLD大鼠口服EIH(250纳克/千克),持续2周。实验期过后,收集24小时尿液样品,并通过超高效液相色谱/四极飞行时间质谱(UPLC-Q-TOF)进行分析。建立正交偏最小二乘分析(OPLSs)模型以发现NAFLD的生物标记并研究EIH的治疗效果。分布在几种代谢途径中的22种代谢物被鉴定为NAFLD的潜在生物标志物。以这些生物标志物为筛选指标,EIH可以通过调节代谢途径的紊乱来逆转NAFLD的病理过程。代谢组学结果不仅为NAFLD的发生和发展提供系统的观点,而且为预防或治疗NAFLD提供了理论基础。

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