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首页> 外文期刊>RSC Advances >Cholestatic liver injury model of bile duct ligation and the protection of Huang-Lian-Jie-Du decoction by NMR metabolomic profiling
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Cholestatic liver injury model of bile duct ligation and the protection of Huang-Lian-Jie-Du decoction by NMR metabolomic profiling

机译:胆汁肝损伤的胆管结扎与核苷酸代谢分析汤的胆管结扎与保护

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摘要

Cholestatic liver injury has been increasingly recognized as a cause for high morbidity and mortality of some diseases in humans. This model could be established by bile duct ligation (BDL), which led to the toxic accumulation of bile acids in animals, resulting in cholestatic liver injury. In this study, rats were intragastrically administrated with an extract of Huang-Lian-Jie-Du decoction once a day for seven consecutive weeks to study its therapeutic effect. Serum and urine samples were collected and subjected to H-1 NMR-based metabolomic analysis. Perturbations on energy metabolism, amino acid metabolism, gut bacteria metabolism and oxidative stress were observed in BDL rats. The metabolomic pattern showed a distinct biphasic feature of the BDL model. Most of these metabolic disturbances occurred in the acute phase (week 1) were greatly attenuated in the long run. HLJDD ameliorated the disturbed metabolism throughout this model, showing bilateral adjustment of some metabolites varied in opposite direction in the two phases. This study demonstrated that H-1 NMR-based metabolomic approach is a powerful and feasible tool to study the pathological changes of a disease model dynamically and holistically and for the understanding of the therapeutic effects of complex Chinese herbal medicine formulae.
机译:胆汁淤积肝损伤越来越被认为是人类某些疾病的发病率和死亡率的原因。该模型可以通过胆管结扎(BDL)建立,这导致动物中胆汁酸的毒性积累,导致胆汁淤积肝损伤。在这项研究中,大鼠每天患有一次胃肠肠道,每天患有一次汤剂,连续七周进行治疗效果。收集血清和尿液样品并进行H-1 NMR基代谢分析。在BDL大鼠中观察到能量新陈代谢,氨基酸代谢,肠道细菌代谢和氧化应激的扰动。代谢物模式显示了BDL模型的不同双相特征。这些代谢障碍中的大部分发生在急性期(第1周)中大大衰减。 HLJDD在该模型中改善了干扰的新陈代谢,显示了两阶段在相反方向上变化的一些代谢物的双侧调节。本研究表明,基于H-1 NMR的代谢方法是一种强大而可行的工具,可以在动态和全面地研究疾病模型的病理变化,并用于了解复杂的中草药公式的治疗效果。

著录项

  • 来源
    《RSC Advances》 |2015年第81期|共12页
  • 作者单位

    China Pharmaceut Univ Dept Nat Med Chem State Key Lab Nat Med Nanjing 210009 Jiangsu Peoples R China;

    China Pharmaceut Univ Dept Nat Med Chem State Key Lab Nat Med Nanjing 210009 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Ctr Mol Metab Nanjing 210094 Jiangsu Peoples R China;

    China Pharmaceut Univ Dept Nat Med Chem State Key Lab Nat Med Nanjing 210009 Jiangsu Peoples R China;

    China Pharmaceut Univ Dept Nat Med Chem State Key Lab Nat Med Nanjing 210009 Jiangsu Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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