高级检索
佟宇, 王晶. 黄芪甲苷对脂多糖诱导肝细胞损伤保护作用[J]. 中国公共卫生, 2014, 30(6): 753-755. DOI: 10.11847/zgggws2014-30-06-18
引用本文: 佟宇, 王晶. 黄芪甲苷对脂多糖诱导肝细胞损伤保护作用[J]. 中国公共卫生, 2014, 30(6): 753-755. DOI: 10.11847/zgggws2014-30-06-18
TONG Yu, WANG Jing. Effects of astragaloside IV on lipopolysaccharide-induced hepatocytes injury in vitro[J]. Chinese Journal of Public Health, 2014, 30(6): 753-755. DOI: 10.11847/zgggws2014-30-06-18
Citation: TONG Yu, WANG Jing. Effects of astragaloside IV on lipopolysaccharide-induced hepatocytes injury in vitro[J]. Chinese Journal of Public Health, 2014, 30(6): 753-755. DOI: 10.11847/zgggws2014-30-06-18

黄芪甲苷对脂多糖诱导肝细胞损伤保护作用

Effects of astragaloside IV on lipopolysaccharide-induced hepatocytes injury in vitro

  • 摘要: 目的观察黄芪甲苷(AsIV)对脂多糖诱导体外培养肝细胞损伤的保护作用及其可能机制。方法将原代培养大鼠肝细胞分为对照组,模型组和低、中、高黄芪甲苷(16、32、64 μmol/L)组,作用24 h后,噻唑蓝法检测细胞存活率,上清液测谷草转氨酶(AST)、谷丙转氨酶(ALT)活性,酶联免疫吸附法测定肿瘤坏死因子(TNF-α),白细胞介素-6(IL-6)水平,Western blot测定肝细胞中p65、IκBα表达。结果与对照组比较,模型组细胞存活率下降34.9%,AST、ALT活性增高,TNF-α,IL-6 含量增加,p65表达增高65.9%,IκBα表达降低34.5%;与模型组比较,32、64 μmol/L黄芪甲苷组细胞存活率(分别为38.9%和48.1%)升高,AST、ALT活性降低,TNF-α,IL-6水平降低,p65表达降低35.6%和57.8%,而IκBα表达增高56.1%和89.2%。结论黄芪甲苷对脂多糖诱导的肝细胞损伤具有保护作用,且这种保护作用可能与黄芪甲苷抑制核因子-κB通路进而降低炎症因子表达有关。

     

    Abstract: ObjectiveTo study the protective effect of astragaloside IV(AsIV)on lipopolysaccharide(LPS)-induced hepatocytes injury and to explore its possible mechanism.MethodsThe cultured hepatocytes were divided into 5 groups:normal group,model group,and different does of AsIV groups(16,32,and 64 μmol/L).After 24 hours of incubation,the cell viability rates were detected by(3-(4,5-dimethylthiazol-2yl)-2,5 diphenyleterazolium bromide(MTT)assay.The activity of serum aspartate aminotransferase(AST)and alanine aminotransferase(ALT)were detected.The content of tumor necrosis factor α(TNF-α)and interleukin-6(IL-6)were determined by enzyme-linked immunosorbent assay(ELISA).The expression of p65 and IκBα were measured by Western blot.ResultsCompared with the normal group,the cell viability rate was decreased by 34.9%,the contents of ALT,AST,TNF-α,and IL-6 were increased and the expression of p65 was increased by 65.9%,while the expression of IκBα was decreased by 34.5%.AsIV at doses of 32 and 64 μmol/L could obviously reduce the activities of ALT,AST,the content of TNF-α,IL-6 and the expression of p65(35.6% and 57.8%),increase the the expression of IκBα(56.1% and 89.2%)and cell viability rates(38.9% and 48.1%)compared with those of the model group.ConclusionAsIV has a protective effect on LPS-induced hepatocyte injury,which is partially via attenuating inflammatory effect and the NF-κB signling pathway.

     

/

返回文章
返回