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Metabolic Profile of Obeticholic Acid and Endogenous Bile Acids in Rats with Decompensated Liver Cirrhosis

机译:代偿性肝硬化大鼠中奥贝胆酸和内源胆汁酸的代谢特征

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摘要

Obeticholic acid (OCA) is a semisynthetic bile acid (BA) analog and potent farnesoid X receptor agonist approved to treat cholestasis. We evaluated the biodistribution and metabolism of OCA administered to carbon tetrachloride‐induced cirrhotic rats. This was to ascertain if plasma and hepatic concentrations of OCA are potentially more harmful than those of endogenous BAs. After administration of OCA (30 mg/kg), we used liquid chromatography–mass spectrometry to measure OCA, its metabolites, and BAs at different timepoints in various organs and fluids. Plasma and hepatic concentrations of OCA and BAs were higher in cirrhotic rats than in controls. OCA and endogenous BAs had similar metabolic pathways in cirrhotic rats, although OCA hepatic and intestinal clearance were lower than in controls. BAs' qualitative and quantitative compositions were not modified by a single administration of OCA. In all the matrices studied, OCA concentrations were significantly lower than those of endogenous BAs, potentially much more cytotoxic.
机译:奥贝胆酸(OCA)是一种半合成胆汁酸(BA)类似物,是经批准用于治疗胆汁淤积的强效法呢类X受体激动剂。我们评估了四氯化碳诱导的肝硬化大鼠服用OCA的生物分布和代谢。这是为了确定血浆和肝中OCA浓度是否比内源性BA有害。施用OCA(30 mg / kg)后,我们使用液相色谱-质谱法在不同时间点在各种器官和体液中测量OCA,其代谢产物和BA。肝硬化大鼠的血浆和肝中OCA和BAs浓度高于对照组。肝硬化大鼠的OCA和内源性BA具有相似的代谢途径,尽管OCA的肝和肠清除率低于对照组。单次施用OCA不会改变BA的定性和定量组成。在所有研究的基质中,OCA浓度均显着低于内源性BA,可能具有更高的细胞毒性。

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