Anti-inflammatory effect of Calycosin glycoside on lipopolysaccharide-induced inflammatory responses in RAW 264.7 cells

被引:48
作者
Dong, Lin [1 ,4 ,5 ]
Yin, Lei [2 ]
Chen, Rong [1 ]
Zhang, Yuanbin [3 ]
Hua, Shiyao [1 ]
Quan, Hongfeng [1 ]
Fu, Xueyan [1 ,4 ,5 ]
机构
[1] Ningxia Med Univ, Sch Pharm, Yinchuan 750004, Peoples R China
[2] Shizuishan Family Planning Serv Ctr Maternal & Ch, 125 Jianshexi Rd, Shizuishan 753000, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Jiangsu, Peoples R China
[4] Ningxia Engn & Technol Res Ctr Modernizat Hui Med, Yinchuan 750004, Peoples R China
[5] Ningxia Med Univ, Minist Educ, Key Lab Hui Ethn Med Modernizat, Yinchuan 750004, Peoples R China
关键词
Calycosin glycoside; Anti-inflammatory effect; Western blotting; MAPK; NF-kappa B; NF-KAPPA-B; MAPK SIGNALING PATHWAYS; ASTRAGALUS-MONGHOLICUS; NITRIC-OXIDE; PC12; CELLS; MACROPHAGES; ISOFLAVONOIDS; ACTIVATION; EXPRESSION; PROTECTION;
D O I
10.1016/j.gene.2018.06.057
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Objective to find the Calycosin glycoside (CG) potential anti-inflammatory effect. The anti-inflammatory activity of CG was evaluated by lipopolysaccharide (LPS)-induced RAW 264.7 cells, and the IL-6, IL-1 beta, TNF-alpha and PGE2 level were measured by ELISA; NO levels in the culture media were determined using the Griess reaction. The iNOS and COX-2 mRNA expressions were measured by qRT-PCR and the phosphorylation of I kappa B alpha, 65, ERK, JNK, and p38 was determined by western blotting. The CG could markedly inhibit the productions of NO and PGE(2) and markedly inhibit the productions of TNF-alpha, IL-1 beta and IL-6. CG could suppress mRNA expression of iNOS, COX-2 and protein phosphorylation of I kappa B alpha, p65, ERK, JNK, and p38 in LPS-induced RAW 264.7 cells. These findings indicate that CG exhibited potent anti-inflammatory activity through the NF-kappa B and MAPK signal pathway, and as a potential therapeutic agent against inflammatory diseases.
引用
收藏
页码:94 / 101
页数:8
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