系统评价黄芪中不同成分的整体相互作用以改善糖尿病肾病的综合药代动力学策略。

IF 4.8 2区 医学 Q1 CHEMISTRY, MEDICINAL
Yu Duan, Ke Pei, Xue Liu, Xia Zhang, Peixiang Song, Sicong Tu, Hui Zhu, Hao Cai
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引用次数: 0

摘要

民族药理学相关性:黄芪(黄芪的干燥根,AR)-山茱萸(山茱萸的干燥成熟果实,FC)作为治疗糖尿病肾病(DKD)的草药配伍疗法已有上百年的历史。AR 中的多糖、皂苷和黄酮类化合物以及 FC 中的鸢尾苷被认为是能提供有益肾脏保护活性的主要生物活性成分。我们对 ARFC 药材配对、从药材配对中提取的主要生物活性成分及其不同比例的组合的肾保护作用进行了系统评价,CG6(多糖、黄酮、皂苷和鸢尾甙,比例为 2:3:1:2)是我们之前研究中筛选出的最佳配比:本研究旨在研究AR-FC药对在DKD大鼠体内的药代动力学特征,探讨AR-FC中各成分之间的相互作用以及不同成分的合理配伍:首先通过组织病理学检查验证了AR-FC和CG6对DKD引起的肾损伤的保护作用。然后,建立了基于 UHPLC-Q-TOF-MS 和 UHPLC-QqQ-MS/MS 的代谢物定性定量分析方法,无需参考标准,并将其应用于以下不同方面的药代动力学(PK)研究:单一组(多糖、黄酮、皂苷和鸢尾苷)与相容组(AR-FC、CG6)之间、正常大鼠与 DKD 大鼠、单剂量给药与长期给药:结果:病理学观察证实,AR-FC 可改善 DKD 大鼠的肾损伤。结果:病理学观察证实,AR-FC能改善DKD大鼠的肾损伤,获得了不同组别中9种原型和4种代谢物的PK谱,揭示了多种成分、病理状态的相容性,长期给药能改变AR-FC主要成分的PK特征,促进其吸收(Cmax、AUC0-t和AUC0-t增加)。值得注意的是,同时服用鸢尾甙可显著增加黄酮类化合物和皂苷在体内的吸收。基于同源化合物的药代动力学显示,皂苷首先起作用,然后其初始代谢产物影响黄酮类化合物,最终黄酮类化合物的代谢产物影响鸢尾苷:这项研究表明,AR-FC 药材配对中的成分之间存在相互作用,它们之间的合理配伍非常重要。它为开发基于 AR-FC(尤其是 CG6)的治疗药物以治疗 DKD 提供了实验证据。它还有望为其他中药的多成分药代动力学研究提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comprehensive pharmacokinetic strategy for systematic evaluation of whole interaction of different constituents in Astragali Radix -Fructus Corni to improve diabetic kidney disease.

Ethnopharmacological relevance: Astragali-Radix (the dried root of Astragalus mongholicus Bunge, AR) - Fructus Corni (the dried ripe fruit of Cornus officinalis Sieb. et Zucc., FC) has been used as a herb-pair remedy to treat diabetic kidney disease (DKD) for hundred years. Polysaccharides, saponins, and flavonoids in AR, and the iridoid glycosides in FC were deemed as the main bioactive constituents that can offer beneficial nephroprotective activities. A systematic evaluation of the nephroprotective effects of AR-FC herb pair, the main bioactive constituents extracted from the herb pair, and their combinations in different ratios was performed, CG6 (polysaccharides, flavonoids, saponins, and iridoid glycosides, in a ratio of 2:3:1:2) as the best compatibility proportion was screened out in our previous study.

Aim of the study: This study aimed to investigate the pharmacokinetic characteristics of AR-FC herb-pair in DKD rats, and explore the interactions between constituents from AR-FC and the rational compatibility of different constituents.

Materials and methods: The protective effect of AR-FC and CG6 on renal injury caused by DKD was first verified by histopathological examination. Then, an analytical method based on UHPLC-Q-TOF-MS and UHPLC-QqQ-MS/MS for qualitative and quantitative metabolites without reference standards was established and applied to pharmacokinetic (PK) studies in following different aspects: between single groups (polysaccharides, flavonoids, saponins and iridoid glycosides) and compatibility groups (AR-FC, CG6), in normal and DKD rats, in single-dose administration and long-term administration.

Results: Pathological observations confirmed that AR-FC could improve renal injury in DKD rats. PK profiles of nine prototypes and four metabolites in various groups were obtained, revealing the compatibility of multiple constitutes, pathological states, and long-term administration could alter PK characteristics of the main components from AR-FC, and promoting the absorption of them (Cmax, AUC0-t, and AUC0-t increased). Notably, co-administration of iridoid glycosides could significantly increase the absorption of flavonoids and saponins in vivo. The pharmacokinetics based on homologous compounds revealed that saponins first acted, then its initial metabolites affected flavonoids, and ultimately the metabolites of flavonoids influenced iridoid glycosides.

Conclusion: This study demonstrated the existence of interactions between constituents from AR-FC herb-pair and the importance of their rational compatibility. It provides experimental evidence for developing a therapeutic agent based on AR-FC (especially CG6) to treat DKD. It is also expected to provide a reference for the multi-component pharmacokinetic study of other herbal medicines.

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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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