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中药复方“三拗汤”中激活过氧化物酶体增殖物激活受体γ的生物活性成分的分离、鉴定及剂量-效应关系。

Separation, characterization and dose-effect relationship of the PPARgamma-activating bio-active constituents in the Chinese herb formulation 'San-Ao decoction'.

机构信息

Jiangsu Key Laboratory for TCM Formulae Research, Nanjing University of Chinese Medicine, Nanjing 210046, China.

出版信息

Molecules. 2009 Oct 9;14(10):3942-51. doi: 10.3390/molecules14103942.

Abstract

San-ao decoction (SAD), comprising Herba Ephedrae, Radix et Rhizoma Glycyrrhizae and Seneb Armeniacae Amarum, is one of the most popular traditional Chinese medicine (TCM) formulae for asthma. Peroxisome proliferator-activated receptors (PPARs) areey regulators of lipid and glucose metabolism and have become important therapeutic targets for various deseases, PPARgamma activation might exhibit anti-inflammatory properties in different chronic inflammatory processes. The EtOAc fraction of SAD showed a significant effect on PPARgamma activation. A simple and rapid method has been established for separation and characterization of the main compounds in the PPARgamma-activating fraction of SAD by ultra-fast HPLC coupled with quadropole time-of-flight mass pectrometry (UPLC-Q-TOF/MS). A total of 10 compounds were identified in the activating fraction of SAD, including amygdalin (1), liquiritin (2), 6'-acetyliquiritin (3), liquiritigenin (4), isoliquiritigenin (5), formononetin (6), licoisoflavanone (7), glycycoumarin (8), glycyrol (9) and uercetin (10). The results also characterized formononetin as a predominant component in this fraction. The dose-effect relationship comparison study of formononetin and the EtOAc fraction of SAD by adding formononetin was performed, the results suggested that formononetin was the major component of the EtOAc fraction of SAD responsible for activating PPARgamma, and the method will possibly be applied to study the complex biological active constituents of other TCMs.

摘要

三拗汤(SAD)由麻黄、甘草和苦杏仁组成,是治疗哮喘最常用的中药方剂之一。过氧化物酶体增殖物激活受体(PPARs)是脂质和糖代谢的关键调节剂,已成为多种疾病的重要治疗靶点。PPARγ 激活可能在不同的慢性炎症过程中表现出抗炎特性。SAD 的乙酸乙酯部分对 PPARγ 激活具有显著作用。已经建立了一种超快速高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF/MS)联用的简单快速方法,用于分离和鉴定 SAD 中 PPARγ 激活部分的主要化合物。从 SAD 的激活部分中鉴定出 10 种化合物,包括苦杏仁苷(1)、甘草苷(2)、6'-乙酰甘草苷(3)、甘草素(4)、异甘草素(5)、芒柄花素(6)、大豆苷元(7)、甘草香豆素(8)、甘草醇(9)和槲皮素(10)。结果还表明芒柄花素是该部分的主要成分。通过添加芒柄花素对芒柄花素和 SAD 的乙酸乙酯部分进行剂量-效应关系比较研究,结果表明,芒柄花素是 SAD 的乙酸乙酯部分中负责激活 PPARγ 的主要成分,该方法可能适用于研究其他中药的复杂生物活性成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4992/6255477/95f3dab29798/molecules-14-03942-g001.jpg

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