首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Exploring the interaction between Salvia miltiorrhiza and human serum albumin: Insights from herb-drug interaction reports, computational analysis and experimental studies
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Exploring the interaction between Salvia miltiorrhiza and human serum albumin: Insights from herb-drug interaction reports, computational analysis and experimental studies

机译:探索丹参与人血清白蛋白之间的相互作用:草药-药物相互作用报告,计算分析和实验研究的启示

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Human serum albumin (HSA) binding is one of important pharmacokinetic properties of drug, which is closely related to in vivo distribution and may ultimately influence its clinical efficacy. Compared to conventional drug, limited information on this transportation process is available for medicinal herbs, which significantly hampers our understanding on their pharmacological effects, particularly when herbs and drug are co-administrated as polytherapy to the ailment. Several lines of evidence suggest the existence of Salvia miltiorrhiza-Warfarin interaction. Since Warfarin is highly HSA bound in the plasma with selectivity to site I, it is critical to evaluate the possibility of HSA-related herb-drug interaction. Herein an integrated approach was employed to analyze the binding of chemicals identified in S. miltiorrhiza to HSA. Molecular docking simulations revealed filtering criteria for HSA site I compounds that include docking score and key molecular determinants for binding. For eight representative ingredients from the herb, their affinity and specificity to HSA site I was measured and confirmed fluorometrically, which helps to improve the knowledge of interaction mechanisms between this herb and HSA. Our results indicated that several compounds in S. miltiorrhiza were capable of decreasing the binding constant of Warfarin to HSA site I significantly, which may increase free drug concentration in vivo, contributing to the herb-drug interaction observed clinically. Furthermore, the significance of HSA mediated herb-drug interactions was further implied by manual mining on the published literatures on S. miltiorrhiza. (C) 2016 Elsevier B.V. All rights reserved.
机译:人血清白蛋白(HSA)结合是药物的重要药代动力学特性之一,与体内分布密切相关,并可能最终影响其临床疗效。与传统药物相比,有关草药的运输过程的信息有限,这极大地妨碍了我们对其药理作用的理解,尤其是在将草药和药物作为综合疗法共同用于该疾病时。几条证据表明丹参与华法林之间存在相互作用。由于华法林在血浆中高度结合HSA,对位置I具有选择性,因此评估HSA相关草药与药物相互作用的可能性至关重要。在本文中,采用综合方法来分析在乳链球菌中鉴定的化学物质与HSA的结合。分子对接模拟揭示了HSA I位化合物的过滤标准,包括对接得分和结合的关键分子决定因素。对于来自该草药的八种代表性成分,通过荧光分析法测定并证实了它们对HSA I位点的亲和力和特异性,这有助于提高对该草药与HSA之间相互作用机理的了解。我们的结果表明,沙门氏菌中的几种化合物能够显着降低华法林与HSA位点的结合常数,这可能会增加体内的游离药物浓度,从而有助于临床上观察到的药草相互作用。此外,通过人工采矿进一步揭示了HSA介导的草药-药物相互作用的重要性。 (C)2016 Elsevier B.V.保留所有权利。

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