Suppr超能文献

倍半萜内酯及含倍半萜内酯的植物制剂在人血液、血浆和人血清白蛋白溶液中的体外行为

In vitro behaviour of sesquiterpene lactones and sesquiterpene lactone-containing plant preparations in human blood, plasma and human serum albumin solutions.

作者信息

Wagner Steffen, Kratz Felix, Merfort Irmgard

机构信息

Institut für Pharmazeutische Wissenschaften, Lehrstuhl für Pharmazeutische Biologie, Universität Freiburg, Freiburg, Germany.

出版信息

Planta Med. 2004 Mar;70(3):227-33. doi: 10.1055/s-2004-815539.

Abstract

The interactions of the three sesquiterpene lactones (SLs) dihydrohelenalin acetate, dihydrohelenalin methacrylate and helenalin isobutyrate from Arnica montana and of parthenolide from Tanacetum parthenium as well as of three ethanolic Arnica preparations with human blood proteins using different matrices, human serum albumin (HSA), plasma and whole blood, were investigated. The extent of protein binding in human plasma or to human albumin differed significantly between individual SLs (dihydrohelenalin methacrylate < dihydrohelenalin acetate < helenalin isobutyrate << parthenolide), e. g., 30 % to 50 % of the SLs were bound to plasma. On the whole, SLs in the ethanolic preparations showed a lower degree of protein binding. Interestingly, although HSA has a reactive thiol group at its cysteine-34 position which is prone to react with the alpha,beta-unsaturated carbonyl of SLs, our studies showed that less than 6 % of SLs are bound to this position within 60 minutes. Thus, a reaction with other amino acids as well as non-covalent interactions with plasma proteins have to be considered. Considering the biological activity of SLs in whole blood, our studies demonstrate that knowledge of their plasma protein binding is important for interpreting the reported data of in vitro and ex vivo assays.

摘要

研究了来自山金车的三种倍半萜内酯(SLs)——醋酸二氢堆心菊素、甲基丙烯酸二氢堆心菊素和异丁酸堆心菊素,以及来自小白菊的小白菊内酯,还有三种山金车乙醇制剂与人类血液蛋白在不同基质(人血清白蛋白(HSA)、血浆和全血)中的相互作用。不同的SLs在人血浆中或与人白蛋白结合的程度存在显著差异(甲基丙烯酸二氢堆心菊素<醋酸二氢堆心菊素<异丁酸堆心菊素<<小白菊内酯),例如,30%至50%的SLs与血浆结合。总体而言,乙醇制剂中的SLs显示出较低的蛋白结合程度。有趣的是,尽管HSA在其半胱氨酸-34位置有一个易与SLs的α,β-不饱和羰基发生反应的活性硫醇基团,但我们的研究表明,在60分钟内,不到6%的SLs与该位置结合。因此,必须考虑与其他氨基酸的反应以及与血浆蛋白的非共价相互作用。考虑到SLs在全血中的生物活性,我们的研究表明,了解它们与血浆蛋白的结合对于解释体外和离体试验的报告数据很重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验