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甘草酸、甘草苷、异甘草素对醋氨酚人肝细胞损伤模型的保护作用比较
引用本文:陈云华,万新,孙建宁,王文全,张硕峰.甘草酸、甘草苷、异甘草素对醋氨酚人肝细胞损伤模型的保护作用比较[J].中国实验方剂学杂志,2012,18(4):245-248.
作者姓名:陈云华  万新  孙建宁  王文全  张硕峰
作者单位:1. 北京城市学院生物医药学部,北京,100094
2. 国家知识产权局专利审查协作中心化学处,北京,100083
3. 北京中医药大学中药学院,北京 ,100102
摘    要:目的:建立并验证醋氨酚人肝细胞损伤模型,进一步研究甘草酸、甘草苷、异甘草素的保肝作用.方法:20 mmol·L -醋氨酚作用HL-7702正常人肝细胞3h,以四氮溴盐(MTT)为考察指标,通过阳性药物双环醇验证该细胞模型并获得量效参考值,进而研究不同质量浓度的甘草酸、甘草苷、异甘草素对人肝细胞损伤的保护作用.结果:醋氨酚人肝细胞损伤模型成功、方法可靠,甘草酸、甘草苷、异甘草素3种成分对人肝细胞醋氨酚损伤均具一定的保护作用.甘草酸的最低有效浓度为0.001 6μmol· L-1,保肝的最大效能为47.0%,达到最大效能的浓度为0.2μmol·L-1.甘草苷的最低有效浓度为0.4μmol·L -1,保肝的最大效能为22.9%,达到最大效能的浓度为2μmol·L -1.异甘草素的最低有效浓度为0.4μmol·L -1,保肝的最大效能为72.6%,达到最大效能的浓度为250 μmol·L -1.结论:提供一种新的体外肝细胞损伤模型;在甘草用于保肝相关作用时,单纯以甘草酸、甘草苷作为质量评价指标是不够的.

关 键 词:甘草酸  甘草苷  异甘草素  醋氨酚人肝细胞损伤  保肝作用

Hepato-protective Activity of Glycyrrhizin, Liquiritin and Isoliquiritigenin on HL-7702 Cells Injury Induced by Acetaminophen
CHEN Yun-hu,WAN Xin,SUN Jian-ning,WANG Wen-quan and ZHANG Shuo-feng.Hepato-protective Activity of Glycyrrhizin, Liquiritin and Isoliquiritigenin on HL-7702 Cells Injury Induced by Acetaminophen[J].China Journal of Experimental Traditional Medical Formulae,2012,18(4):245-248.
Authors:CHEN Yun-hu  WAN Xin  SUN Jian-ning  WANG Wen-quan and ZHANG Shuo-feng
Institution:Biomedical School, Beijing City University, Beijing 100094, China;Patent Examination Cooperation Center of SIPO, Beijing 100083, China;Beijing University of Chinese Medicine, Beijing 100102, China;Beijing University of Chinese Medicine, Beijing 100102, China;Beijing University of Chinese Medicine, Beijing 100102, China
Abstract:Objective:To study the hepato-protective activity of glycyrrhizin,liquiritin and isoliquritigenin on a new HL-7702 cells injury model induced by acetaminophen.Method:HL-7702 cells injury induced by 20 mmol·L-1 acetaminophen for 3 hours were chosen as the liver cells injury model and the effect of glycyrrhizin,liquiritin and isoliquritigenin was assayed.The main index was MTT.Result:The new HL-7702 cells injury model induced by acetaminophen was successful.Glycyrrhizin,liquiritin and isoliquiritigenin had hepato-protective activity on the cell model.The minimum effective concentration of glycyrrhizin was 0.001 6 μmol·L-1.The hepato-protective maximum efficacy of glycyrrhizin was 47.0% at the concentration of 0.2 μmol·L-1.The minimum effective concentration of liquiritin was 0.4 μmol·L-1.The hepato-protective maximum efficacy of liquiritin was 22.9 % at the concentration of 2 μmol·L-1.The minimum effective concentration of isoliquritigenin was 0.4 μmol·L-1.The hepato-protective maximum efficacy of isoliquritigenin was 72.6%at the concentration of 250 μmol·L-1.Conclusion:The new HL-7702 cells injury model induced by acetaminophen could be applied on studying the hepato-protective effect of drugs.The hepato-protective activity of licorice has connection with not only glycyrrhizin,liquiritin but also isoliquritigenin.Therefore,it is not enough to treat glycyrrhizin,liquiritin as the quality evaluation index for licorice.
Keywords:glycyrrhizin  liquiritin  isoliquritigenin  liver cell injury  hepato-protective activity
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