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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Metabolomics research on the hepatoprotective effect of cultured bear bile powder in alpha-naphthylisothiocyanate-induced cholestatic mice
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Metabolomics research on the hepatoprotective effect of cultured bear bile powder in alpha-naphthylisothiocyanate-induced cholestatic mice

机译:α-萘噻噻唑烷酸胆汁胆汁小鼠培养熊胆汁粉末肝胆汁粉末的代谢组科研究

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摘要

Natural bear bile powder (NBBP) is a famous traditional medicine and has been widely used in clinic. However, access to the sources of bear bile is restricted; hence, it is essential to discover new substitutes for NBBP. Cultured bear bile powder (CBBP) is transformed from chicken bile and contains main ingredients as to NBBP. In the present study, the effect and potential mechanism of action of CBBP on cholestatic liver injury in-naphthylisothiocyanate (ANIT)-induced mouse model was explored using metabolomics. CBBP treatment ameliorated impaired hepatic dysfunction and tissue damage that induced by ANIT. Metabolomics showed there were 28 different metabolites induced by ANIT as compared with control mice, and 18 of which was reversed by CBBP. Pathway analysis revealed that those 18 metabolites are mainly involved in bile acid (BA) biosynthesis and Dglutamine and D-glutamate metabolism. Further LC-MS/MS analysis showed that CBBP and NBBP both reduced serum and liver levels of BAs, but increased their biliary levels. Additionally, CBBP and NBBP upregulated expression of BA efflux transporters, Mrp2, Mrp3, and Mrp4, and metabolic enzymes, Cyp2b10 and Ugt1a1 of liver tissue of cholestatic mice, increased the BA excretion and metabolism. Moreover, CBBP and NBBP treatment upregulated GCLc/GCLm expression, and restored glutathione metabolism. In conclusion, the protective effects of CBBP against cholestatic liver injury were similar to those of NBBP. Mechanistically, both CBBP and NBBP reversed the disruption in homeostasis of BAs and glutathione, alleviating damage to hepatocytes.
机译:天然熊胆汁粉(NBBP)是着名的传统医学,已广泛用于诊所。但是,限制了对熊胆来源的访问;因此,对于NBBP来说,必须发现新的替代品。培养的熊胆汁粉(CBBP)由鸡胆汁转化,并含有NbBP的主要成分。在本研究中,使用代谢组科探讨了含有代谢噻唑烷酸甲酯(ANIT)诱导的小鼠模型胆甾醇损伤的CBBP对胆汁肝损伤的影响和潜在机制。 CBBP治疗改善了肝功能障碍和由ANIT引起的组织损伤。代谢组学显示,与对照小鼠相比,Anit诱导的28种不同的代谢物,其中18个由CBBP反转。途径分析表明,那些18代谢物主要涉及胆汁酸(BA)生物合成和Dglutamine和D-谷氨酸代谢。此外,LC-MS / MS分析表明,CBBP和NBBP都减少了血清和肝脏水平,但增加了胆汁水平。另外,CBBP和NBBP的BA流出转运蛋白,MRP2,MRP3和MRP4的表达和胆汁淤积小鼠的肝组织的代谢酶,CYP2B10和UGT1A1增加,增加了BA排泄和代谢。此外,CBBP和NBBP处理上调了GCLC / GCLM表达,并恢复了谷胱甘肽代谢。总之,CBBP对胆汁淤积性肝损伤的保护作用与NBBP的保护作用类似。机械地,CBBP和NBBP都扭转了BAS和谷胱甘肽的稳态中断,减轻了对肝细胞的损害。

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    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

    Shanghai Univ Tradit Chinese Med Res Ctr Tradit Chinese Med Complex Syst Shanghai Peoples R China;

    Shanghai Kai Bao Pharmaceut CO Ltd Shanghai 201401 Peoples R China;

    Shanghai Univ Tradit Chinese Med Inst Chinese Mat Med Shanghai Key Lab Complex Prescript Shanghai 2012013 Peoples R China;

    Shanghai Univ Tradit Chinese Med Sch Pharm Dept Pharmacol 1200 Cailun Rd Shanghai 201203 Peoples R China;

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

    Metabolomics; Bile acid; Cholestasis; Cultured bear bile; Transporter;

    机译:代谢组学;胆汁酸;胆汁淤积;培养熊胆;运输器;

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