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首页> 外文期刊>Frontiers in Pharmacology >Huangqi Decoction Alleviates Alpha-Naphthylisothiocyanate Induced Intrahepatic Cholestasis by Reversing Disordered Bile Acid and Glutathione Homeostasis in Mice
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Huangqi Decoction Alleviates Alpha-Naphthylisothiocyanate Induced Intrahepatic Cholestasis by Reversing Disordered Bile Acid and Glutathione Homeostasis in Mice

机译:黄芪汤通过逆转小鼠胆汁酸和谷胱甘肽的体内稳态,减轻α-萘基异硫氰酸酯诱导的肝内胆汁淤积

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摘要

Intrahepatic cholestasis is a serious symptom of liver disorders with limited therapies. In this study, we investigated the efficacy of Huangqi decoction (HQD), a two-herb classic traditional Chinese medicine (TCM), in the treatment of alpha-naphthylisothiocyanate (ANIT)-induced intrahepatic cholestasis in mice. HQD treatment ameliorated impaired hepatic function and tissue damage. A metabolomics study revealed that the endogenous metabolites significantly affected by HQD were related to bile acid (BA) biosynthesis and glutathione metabolism pathways. HQD treatment decreased the intrahepatic accumulation of cytotoxic BAs, normalized serum BA levels, and increased biliary and urinary BA excretion. Additionally, HQD restored the hepatic glutathione content and suppressed reactive oxygen species (ROS) in cholestatic mice. Protein and gene analysis revealed that HQD increased the expression of the hepatic metabolizing enzymes cytochrome P450 (CYP) 2B10 and UDP glucuronosyltransferase family 1 member A1 (UGT1A1), as well as multidrug resistance-associated protein 2 (Mrp2), Mrp3, and Mrp4, which play crucial roles in BA homeostasis. Further, HQD increased the protein expression of glutamate-cysteine ligase, which is involved in the synthesis of glutathione. Importantly, HQD increased the nuclear expression of nuclear factor-E2-related factor-2 (Nrf2). In conclusion, HQD protects against intrahepatic cholestasis by reversing the disordered homeostasis of BAs and glutathione.
机译:肝内胆汁淤积是肝脏疾病的严重症状,治疗方法有限。在这项研究中,我们调查了黄芪汤(HQD),一种两种草药的传统中药(TCM)在治疗α-萘基异硫氰酸酯(ANIT)诱导的小鼠肝内胆汁淤积中的功效。 HQD治疗改善了肝功能受损和组织损伤。代谢组学研究表明,受HQD显着影响的内源性代谢产物与胆汁酸(BA)的生物合成和谷胱甘肽代谢途径有关。 HQD治疗可降低细胞毒性BA的肝内蓄积,血清BA水平正常化以及胆汁和尿液BA排泄增加。此外,HQD可恢复胆汁淤积小鼠的肝谷胱甘肽含量并抑制活性氧(ROS)。蛋白质和基因分析显示,HQD增加了肝代谢酶细胞色素P450(CYP)2B10和UDP葡萄糖醛酸转移酶家族1成员A1(UGT1A1)的表达,以及多药耐药相关蛋白2(Mrp2),Mrp3和Mrp4的表达,在BA动态平衡中起着至关重要的作用。此外,HQD增加了谷氨酸-半胱氨酸连接酶的蛋白质表达,这与谷胱甘肽的合成有关。重要的是,HQD增加了核因子E2相关因子2(Nrf2)的核表达。总之,HQD通过逆转BA和谷胱甘肽的稳态紊乱来预防肝内胆汁淤积。

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