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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Hepatic cytochrome P450 mediates interaction between warfarin and Coleus forskohlii extract in vivo and in vitro
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Hepatic cytochrome P450 mediates interaction between warfarin and Coleus forskohlii extract in vivo and in vitro

机译:肝细胞色素P450在体内和体外介导华法林与福寿草提取物之间的相互作用

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摘要

Objectives This study aimed to determine whether Coleus forskohlii extract (CFE) influences the anticoagulant action of warfarin in mice in vivo and its relationship with hepatic cytochrome P450 (CYP). Methods Mice were fed various doses of CFE standardised with 10% forskolin in a normal diet for one week, or in protein diets containing 7% and 20% casein (low and normal) for four weeks. They were then administered with warfarin by gavage on the last two days of the treatment regimen, and blood coagulation parameters, as well as hepatic CYP, were analysed at 18 h after the last dose. Direct interaction between CFE and forskolin with CYP2C was evaluated in vitro. Key findings CFE dose dependently increased hepatic total CYP content and S-warfarin 7-hydroxylase activity at a dietary level of ≥0.05%. Warfarin-induced anticoagulation was attenuated by CFE in parallel with CYP induction. The findings were similar in mice fed diets containing CFE and different ratios of protein. CFE directly inhibited CYP2C activity in mouse and human liver microsomes in vitro, whereas forskolin was only slightly inhibitory. Conclusions CFE attenuates the anticoagulant action of warfarin by inducing hepatic CYP2C; thus, caution is required with the combination of warfarin and dietary supplements containing CFE.
机译:目的这项研究旨在确定锦紫苏提取物(CFE)是否在体内影响华法林的抗凝作用及其与肝细胞色素P450(CYP)的关系。方法在正常饮食中,或在分别含7%和20%酪蛋白(低和正常)的蛋白质饮食中,给小鼠喂食各种剂量的10%福司可林标准化的CFE,持续4周。然后在治疗方案的最后两天通过管饲法向他们施用华法林,并在最后一次给药后18小时分析凝血参数以及肝CYP。体外评估了CFE和毛喉素与CYP2C的直接相互作用。主要发现在饮食水平≥0.05%的情况下,CFE剂量依赖性地增加了肝脏的总CYP含量和S-华法林7-羟化酶活性。华法林诱导的抗凝作用与CYP诱导同时被CFE减弱。在饲喂含CFE和不同比例蛋白质的饮食的小鼠中,发现相似。 CFE在体外直接抑制了小鼠和人肝微粒体的CYP2C活性,而福司可林仅具有轻微的抑制作用。结论CFE可诱导肝CYP2C减弱华法林的抗凝作用。因此,华法林和含有CFE的膳食补充剂的组合需要谨慎。

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