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作 者:黄文文[1,2] 叶小利[3] 李学刚[1] 赵忠启[1] 蓝萍[1] 王亮[1] 柳明[1] 高英[1] 朱家颖[1] 李萍 冯平
机构地区:[1]西南大学药学院药用资源研究所,重庆400716 [2]国家海洋局第三海洋研究所,福建厦门361005 [3]西南大学生命科学学院,重庆400715 [4]北碚中医院,重庆400700
出 处:《中国中药杂志》2010年第18期2428-2431,共4页China Journal of Chinese Materia Medica
基 金:重庆市科委攻关项目[CSTC;2010AC5007];重庆市卫生局重点项目[渝中医(2008)38号]
摘 要:目的:研究山楂降血脂活性成分及作用机制。方法:以HMG-CoA还原酶活性为靶标,采用大孔树脂和硅胶等进行分离纯化,筛选HMG-CoA还原酶抑制剂。结果:获得4个对HMG-CoA还原酶活性具有较强抑制作用的化合物,为槲皮素、金丝桃苷、芦丁和绿原酸,4个化合物抑制率之和为50.01%,复配后的抑制活性为79.48%。结论:槲皮素和金丝桃苷为山楂中抑制HMG-CoA还原酶活性的主要活性成分,且单体之间存在协同作用。Objective: To study the hypolipidemic active compounds from Crataegus pinnatifida and mechanism of action of those.Method: Guided by the inhibitory activity to HMG-CoA reductase,the active compounds were separated and purified with macroporous resin and silica gel.Result: Four active compounds were obtained,which were quercetin,hyperoside,rutin and chlorogenic acid,the sum of their inhibitory rate was 50.01%,and the total inhibitory rate of the mixture of four active compounds matched was 79.48%.Conclusion: Quercetin and hyperoside were the principle active components inhibiting HMG-CoA reductase in Hawthorn fruit,and there were synergistic action among them.
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