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槐花中黄酮类化合物和黄酮糖苷的抗血小板作用

Anti-platelet effects of flavonoids and flavonoid-glycosides from Sophora japonica.

作者信息

Kim Jeong Mi, Yun-Choi Hye Sook

机构信息

Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul, Korea.

出版信息

Arch Pharm Res. 2008 Jul;31(7):886-90. doi: 10.1007/s12272-001-1242-1. Epub 2008 Aug 14.

Abstract

A methanol extract of Sophora japonica was subjected to anti-platelet activity guided fractionation affording the isolation of four flavonoids and six flavonoid-glycosides: biochanin A (1), irisolidone (2), genistein (3), sissotrin (4), sophorabioside (5), genistin (6), tectoridin (7), apigenin (8), quercitrin (9), and rutin (10). The structure of each compound was determined by a variety of spectroscopic methods. Among the compounds, 1, 3, and 7 showed approximately 2.5-6.5 fold greater inhibitory effects on arachidonic acid (AA) and U46619 induced platelet aggregation (IC50: 19.9 and 99.8 microM; 20.3 and 53.8 microM; 25.9 and 123.4 microM, respectively) than acetylsalicylic acid (ASA, IC50: 63.0 and 350.0 microM). Compound 2 was an approximately 22-40 fold stronger inhibitor than ASA on AA and U46619 induced aggregation (IC50: 1.6 and 15.6 microM, respectively).

摘要

对槐米的甲醇提取物进行抗血小板活性导向分级分离,从中分离出四种黄酮类化合物和六种黄酮苷:鹰嘴豆芽素A(1)、鸢尾酮(2)、染料木黄酮(3)、异鼠李素(4)、槐二糖甙(5)、染料木苷(6)、鸢尾黄素(7)、芹菜素(8)、槲皮苷(9)和芦丁(10)。通过多种光谱方法确定了每种化合物的结构。在这些化合物中,1、3和7对花生四烯酸(AA)和U46619诱导的血小板聚集的抑制作用比阿司匹林(ASA,IC50:63.0和350.0 microM)分别高约2.5 - 6.5倍(IC50:19.9和99.8 microM;20.3和53.8 microM;25.9和123.4 microM)。化合物2对AA和U46619诱导的聚集的抑制作用比ASA强约22 - 40倍(IC50分别为1.6和15.6 microM)。

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