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垂盆草总黄酮及异鼠李素对对乙酰氨基酚诱导的L02细胞损伤的保护作用
引用本文:蒋志涛,王雪,王建春,陈晓峰,王建平,潘金火. 垂盆草总黄酮及异鼠李素对对乙酰氨基酚诱导的L02细胞损伤的保护作用[J]. 中国实验方剂学杂志, 2018, 24(6): 121-125
作者姓名:蒋志涛  王雪  王建春  陈晓峰  王建平  潘金火
作者单位:南京中医药大学 附属张家港医院 江苏省企业研究生工作站, 江苏 张家港 215600,南京中医药大学 药学院, 南京 210023,南京中医药大学 附属张家港医院 江苏省企业研究生工作站, 江苏 张家港 215600,南京中医药大学 附属张家港医院 江苏省企业研究生工作站, 江苏 张家港 215600,南京中医药大学 附属张家港医院 江苏省企业研究生工作站, 江苏 张家港 215600,南京中医药大学 药学院, 南京 210023
基金项目:江苏省科技支撑计划社会发展项目(BE2009682);苏州市科技计划项目(SYSD2017161)
摘    要:目的:探讨垂盆草总黄酮及异鼠李素对对乙酰氨基酚(APAP)诱导的人正常肝细胞(L02)损伤的保护作用。方法:以不同浓度的APAP刺激L02细胞,制备损伤模型,筛选APAP的有效刺激浓度;复制APAP诱导的L02细胞损伤模型,用细胞增殖与活性试剂(CCK-8)检测细胞存活能力,分析盆草总黄酮及异鼠李素对APAP诱导的L02细胞活性的影响;检测细胞上清液中丙二醛(MDA),谷胱甘肽(GSH)含量,超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-Px)活性,丙氨酸氨基转移酶(ALT)和天门冬氨酸氨基转移酶(AST)的含量。结果:与正常组比较,不同浓度的APAP处理的L02细胞活力显著降低,筛选出的造模条件为10 mmol·L-1APAP孵育24 h,模型组肝细胞上清液中MDA含量升高(P0.05,P0.01),GSH含量降低,SOD,GSH-Px活性降低,AST和ALT含量升高;与模型组比较,垂盆草总黄酮、异鼠李素均能显著提高APAP损伤细胞的存活率,降低MDA含量,提高GSH含量,提高SOD,GSH-Px活性,降低ALT和AST的释放量(P0.05,P0.01)。结论:垂盆草总黄酮及异鼠李素对APAP损伤的L02细胞具有较好的保护作用。

关 键 词:垂盆草  总黄酮  异鼠李素  对乙酰氨基酚  人正常肝细胞
收稿时间:2017-09-30

Effect of Sedi Herba Total Flavanones and Isorhamnetin on APAP-induced Injured L02 Cells
JIANG Zhi-tao,WANG Xue,WANG Jian-chun,CHEN Xiao-feng,WANG Jian-ping and PAN Jin-huo. Effect of Sedi Herba Total Flavanones and Isorhamnetin on APAP-induced Injured L02 Cells[J]. China Journal of Experimental Traditional Medical Formulae, 2018, 24(6): 121-125
Authors:JIANG Zhi-tao  WANG Xue  WANG Jian-chun  CHEN Xiao-feng  WANG Jian-ping  PAN Jin-huo
Affiliation:Zhangjiagang Hospital of Traditional Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Graduate Workstation of Enterprises in Jiangsu Province, Zhangjiagang 215600, China,Nanjing University of Chinese Medicine, Nanjing 210023, China,Zhangjiagang Hospital of Traditional Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Graduate Workstation of Enterprises in Jiangsu Province, Zhangjiagang 215600, China,Zhangjiagang Hospital of Traditional Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Graduate Workstation of Enterprises in Jiangsu Province, Zhangjiagang 215600, China,Zhangjiagang Hospital of Traditional Chinese Medicine, Affiliated Hospital of Nanjing University of Chinese Medicine, Graduate Workstation of Enterprises in Jiangsu Province, Zhangjiagang 215600, China and Nanjing University of Chinese Medicine, Nanjing 210023, China
Abstract:Objective: To study the protective effect of Sedi Herba total flavanones and isorhamnetin on the acetaminophen (APAP)-induced injury of human normal hepatocytes (L02).Method: L02 cells were stimulated with different concentrations of APAP to prepare the injury model, and the effective stimulating concentration of APAP was screened. APAP-induced L02 cell injury models were thencopied, and the effect of Sedi Herba total flavanones and isorhamnetin on the activity of L02 cells induced by APAP was analyzed by cell counting kit-8 (CCK-8) method.The contents of malondialdehyde (MDA) and glutathione (GSH), activity of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), and levels of alanine aminotransferase (ALT), andaspartate aminotransferase (AST) in supernatant were measured.Result: As compared with the normal group, the activity of L02 cells treated with different concentrations of APAP was significantly decreased, and the selected modeling condition was 10 mmol · L-1 for 24 h. The MDA content in the supernatant of the model group was increased and the GSH content was decreased, SOD and GSH-Px activity decreased, AST and ALT levels increased(P<0.05,P<0.01). As compared with the model group, the Sedi Herba total flavanones and isorhamnetin could significantly increase the survival rate of APAP-injured cells, decrease the content of MDA, increase the content of GSH, increase the activity of SOD and GSH-Px activity, and lower the release of ALT and AST(P<0.05,P<0.01).Conclusion: The Sedi Herba total flavanones and isorhamnetin have a good protective effect on APAP-injured L02 cells.
Keywords:Sedi Herba  total flavanones  isorhamnetin  acetaminophen (APAP)  L02 cells
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