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Identification of Triterpene Acids in Poria cocos Extract as Bile Acid Uptake Transporter Inhibitorss

机译:作为胆汁酸摄取运输抑制剂鉴定茯苓提取物中的三萜酸

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Literature reports that Poria cocos reduces blood lipid levels; however, the underlying mechanism remains unclear. Blood lipid levels are closely related to the enterohepatic circulation of bile acids, where uptake transporters playing a significant role. P. cocos extract is commonly used in traditional prescriptions and food supplements in China. We investigated the effects of P. cocos and its five triterpene acids on bile acid uptake transporters, including intestinal apical sodium-dependent bile acid transporter (ASBT) and hepatic sodium/taurocholate cotransporting polypeptide (NTCP). Triterpene acids were fingerprinted by high-performance liquid chromatography-TripleTOF and quantified by ultraperformance liquid chromatography/tandem mass spectrometry. The inhibitory effect of P. cocos and its five major representative triterpene acids on ASBT and NTCP was investigated by in vitro assays using Xenopus oocytes expressing ASBT and NTCP. P. cocos extract exhibited significant inhibitory effects with half-maximum inhibition constants of 5.89 mg/ml and 14.6 mg/ml for NTCP and ASBT, respectively. Among five triterpene acids, poricoic acid A, poricoic acid B, and polyporenic acid C significantly inhibited NTCP function. Poricoic acid A, poricoic acid B, and dehydrotumulosic acid significantly inhibited ASBT function. The representative triterpene acid, poricoic acid A, was identified as a competitive inhibitor of NTCP with an inhibitory constant of 63.4 6 18.7 mM. In conclusion, our results indicate that both P. cocos extract and its major triterpenes are competitive inhibitors of ASBT and NTCP. Accordingly, it was suggested that competitive inhibition of these bile acid transporters is one of the underlying mechanisms for the hypolipi-demic effect of P. cocos.
机译:文献报道茯苓降低血脂水平;然而,潜在的机制仍不清楚。血脂水平与胆汁酸的肠肝循环密切相关,胆汁酸的摄取转运蛋白在肠肝循环中起着重要作用。椰子提取物在中国的传统处方和食品补充剂中普遍使用。我们研究了椰子及其五种三萜酸对胆汁酸摄取转运体的影响,包括肠道顶端钠依赖性胆汁酸转运体(ASBT)和肝脏钠/牛磺胆酸共转运多肽(NTCP)。三萜酸通过高效液相色谱-三联法进行指纹图谱分析,并通过超高效液相色谱/串联质谱进行定量。利用表达ASBT和NTCP的爪蟾卵母细胞进行体外实验,研究了椰子及其五种主要代表性三萜酸对ASBT和NTCP的抑制作用。椰子提取物对NTCP和ASBT的半最大抑制常数分别为5.89 mg/ml和14.6 mg/ml,表现出显著的抑制作用。在五种三萜酸中,茯苓酸A、茯苓酸B和聚戊烯酸C显著抑制NTCP功能。茯苓酸A、茯苓酸B和脱氢肉桂酸显著抑制ASBT功能。具有代表性的三萜酸poricoacid A被鉴定为NTCP的竞争性抑制剂,其抑制常数为63.4 6 18.7 mM。总之,我们的结果表明,椰子提取物及其主要三萜是ASBT和NTCP的竞争性抑制剂。因此,有人认为竞争性抑制这些胆汁酸转运体是椰子降血脂作用的潜在机制之一。

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