Regulation Effects of Isoquercitrin on Inflammatory in LPS-induced RAW264.7 Cell
10.3870/j.issn.1004-0781.2017.06.003
- VernacularTitle:异槲皮苷对脂多糖诱导RAW264.7细胞产生炎症因子的调控
- Author:
Tianxu LIU
;
Juan LI
;
Guojun JIANG
;
Xiaomin DONG
;
Zhaoming ZHU
;
Guihong HUANG
- Keywords:
Isoquercitrin;
RAW264.7 cell;
Inflammatory factors;
Tumor necrosis factor α
- From:
Herald of Medicine
2017;36(6):601-605
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the influence of isoquercitrin on the inflammatory factors in LPS-induced RAW264.7 cells.Methods MTT method was used to detect inhibition ratio of RAW264.7 cells induced by isoquercitrin.The level of TNF-α in culture medium was measured by ELISA.Nitric oxide (NO) was detected by Nitrate Assay Kit.Western blotting was used to investigate the influence on the productions of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2).Results The half inhibitory concentration (IC50) of isoquercitrin was 65.73 μmol·L-1.LPS had no inhibitory effect on the cells.Compared with LPS group,the level of TNF-α was decreased to 74.80% and 60.57% in isoquercitrin (20,10 μmol·L-1) groups in a dose-dependent manner.The results measured by Nitrate Assay Kit revealed that isoquercitrin (20,10 μmol·L-1) could suppress production of NO,the level of NO decreased to 79.34% and 68.81%(P<0.05).The Western blotting results showed that isoquercitrin (20,15,10 μmol·L-1) inhibited the productions of iNOS and COX-2 (P<0.05).Conclusion Isoquercitrin has anti-inflammatory effects by inhibiting the productions of TNF-α,NO,iNOS and COX-2,and the most effective dose for the inhibition is 10 μmol·L-1.
