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首页> 外文期刊>Journal of liquid chromatography and related technologies >Serum metabonomics characterization of liver fibrosis induced by bile duct-ligated in rats and the intervention effects of herb compound 861
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Serum metabonomics characterization of liver fibrosis induced by bile duct-ligated in rats and the intervention effects of herb compound 861

机译:大鼠胆管连接的肝纤维化血清代谢物理学表征及草药化合物861的干预作用

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摘要

Liver fibrosis has been increasingly recognized as a cause for high morbidity and mortality of some diseases in humans. Herbal medicines have received great attention due to their low side effects and high safety. Herbal compound 861 (Cpd 861) has been effectively used for treating hepatic fibrosis for long time. Yet, its exact mechanism is still in fancy. Herein, we first established a liver fibrosis model by bile duct ligation (BDL), which led to the toxic accumulation of bile acids in animals, resulting in hepatic fibrosis. A serum metabonomics study on BDL-induced liver fibrosis rats after Cpd 861 treatment was performed using UHPLC-QTOF/MS. Multivariate analysis showed that Cpd 861 significantly reversed the metabolic perturbation induced by BDL to normal state, which is in agreement with the serum biochemical and histopathological findings. 15 metabolites were screened as potential biomarkers. Eight metabolic pathways were recognized as the most relevant pathways, involving dysfunction of amino acids metabolism and synthesis, fatty acid metabolism, phospholipids metabolism, and others. This is the first study to reveal the underlying mechanism of Cpd 861 based on metabonomics, which is complementary to biochemical analysis, and more importantly, a potentially powerful tool to interpret the mechanisms of extremely complex systems.
机译:肝纤维化越来越被认为是人类某些疾病的发病率和死亡率的原因。由于其低副作用和高安全性,草药受到极大的关注。 Herbal化合物861(CPD 861)已经有效地用于长时间治疗肝纤维化。然而,其确切的机制仍在花哨上。在此,我们首先通过胆管结扎(BDL)建立了肝纤维化模型,从而导致动物中胆汁酸的毒性积累,导致肝纤维化。使用UHPLC-QTOF / MS进行CPD 861处理后BDL诱导的肝纤维化大鼠的血清代谢物理学研究。多变量分析表明,CPD 861显着逆转了BDL诱导的正常状态诱导的代谢扰动,这与血清生化和组织病理学发现一致。将15个代谢物筛选为潜在的生物标志物。八种代谢途径被认为是最相关的途径,涉及氨基酸代谢和合成,脂肪酸代谢,磷脂代谢等的功能障碍。这是第一研究,揭示基于代谢族的CPD 861的潜在机制,这与生化分析互补,更重要的是,一种解释极其复杂系统的机制的潜在强大的工具。

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