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异鼠李素及橙皮甙抑制LDL氧化修饰作用的研究

Inhibitory Effect of Isorhamnetin and Hesperidin on LDL Oxidation Induced by Cu2+

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【作者】 刘瑞; 孟芳; 刘宇; 白怀; 刘秉文;

【Author】 LIU Rui1,MENG Fang2,LIU Yu2,BAI Huai3,LIU Bing-wen2(1.Division of Peptides Related with Human Diseases,State Key Laboratory of Biotherapy,West China Hospital,Sichuan University,Chengdu 610041,China;2.Apolipoprotein Research Unit,Department of Biochemistry and Molecular Biology,West China School of Preclinical and Forensic Medicine,Sichuan University,Chengdu 610041,China;3.Unit of Laboratory Medicine,West China Second Hospital,Sichuan University, Chengdu 610041,China)

【机构】 四川大学华西医院生物治疗国家重点实验室及人类疾病相关多肽研究室; 四川大学基础医学与法医学院生物化学与分子生物学教研室及载脂蛋白研究室; 四川大学华西第二医院实验中心; 四川大学基础医学与法医学院生物化学与分子生物学教研室及载脂蛋白研究室 四川成都610041; 四川成都610041;

【摘要】 目的:研究黄酮类中药异鼠李素及橙皮甙是否具有抑制LDL氧化修饰的作用。方法:按一次性密度梯度超速离心法分离人血清LDL,分别加入5.0μmol/L异鼠李素及橙皮甙与LDL温育3 h,然后利用Cu2+介导体外氧化修饰脂蛋白的方法,观察LDL氧化修饰不同时间,其A234、REM、TBARS及蛋白质羰基的动力学改变,并与对照组比较。结果:Cu2+介导LDL氧化修饰时,在2、4、6、8、12及24 h后,其A234、REM、TBARS及蛋白质羰基含量均逐步增加;加入5.0μmol/L异鼠李素及橙皮甙的实验组,Cu2+LDL的氧化修饰分别延迟2~4 h和2 h,其A234、REM、TBARS及载脂蛋白羰基含量较对照组降低;异鼠李素实验组分别较对照组降低23.5%~40.4%、20.5%~37.7%、18.6%~30.3%及20.1%~52.4%(P<0.001);橙皮甙实验组分别降低11.1%~21.2%、9.2%~28.3%、13.7%~21.3%及5.0%~43.8%(P<0.001,P<0.01,P<0.001及P<0.05)。结论:异鼠李素及橙皮甙均可抑制Cu2+诱导的LDL的氧化修饰,且异鼠李素的抗氧化作用较及橙皮甙强。

【Abstract】 Objective: To evaluate the inhibitory effect of Isorhamnetin and Hesperidin on the LDL oxidation induced by Cu2+.Methods: The serum LDL was isolated by the one step density gradient ultracentrifugation.The LDL oxidation was induced by Cu2+ in vitro for different time periods.Isorhamnetin and Hesperidin at 5 μmol/L were added respectively,as the experimental groups,3 hours before oxidation.The oxidation of LDL in experimental and control groups was identified by measuring A234,REM,TBARS and protein carbonyls content.Results: The values of A234,REM,TBARS and protein carbonyls formation increased gradually during LDL oxidation induced by Cu2+ in vitro.During LDL oxidation induced by Cu2+ in vitro and incubation with each of Isorhamnetin and Hesperidin,the kinetic changes of A234,REM,TBARS and protein carbonyls formation showed lag phases of 2-4 h and 2 h respectively,and the corresponding values for each of the agents treated group were reduced by 23.5%~40.4%、20.5%~37.7%、18.6~30.3% and 20.1%~52.4%(P<0.001);and 11.1%~21.2%、9.2%~28.3%、13.7%~21.3% and 5.0%%~43.8% respectively(P<0.001,P<0.01,P<0.001 and P<0.05).Conclusion: It suggests that Isorhamnetin and Hesperidin can substantially inhibit LDL oxidation,and Isorhamnetin has antioxidation ability stronger than Hesperidin.

【基金】 四川省科技厅攻关项目(No03SG011-007-1)
  • 【文献出处】 中药材 ,Journal of Chinese Medicinal Materials , 编辑部邮箱 ,2007年06期
  • 【分类号】R285
  • 【被引频次】18
  • 【下载频次】199
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