Liu Tian-yang, Zhou Ling-ling, Zhou Cong, Liu Zhang-pu, Chen Chen, Feng Zhe, Zhou Xue-ping
Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Chin J Integr Med. 2015 Apr;21(4):291-8. doi: 10.1007/s11655-014-1839-x. Epub 2014 Sep 2.
To study the mechanism underlying the inhibitory effect of Qingluo Tongbi Granule (, QTG) on osteoclast differentiation in rheumatoid arthritis in rats.
Fibroblast and monocyte co-culture were used to induce osteoclast differentiation in adjuvant-induced arthritic (AIA) rats. Serum containing QTG was prepared and added to the osteoclasts, and activation of the tumor necrosis factor receptor-associated factor 6/mitogen-activated protein kinase/nuclear factor of activated T cells, cytoplasmic1 (TRAF6/MAPK/NFATc1) pathways was examined.
The induced osteoclasts were multinucleated and stained positive for tartrate-resistant acid phosphatase (TRAP) staining. Serum containing QTG at 14.4, 7.2 or 3.6 g/kg inhibited the activation of TRAF6, extracellular regulated protein kinase (ERK)1/2, c-Jun N-terminal kinase (JNK) and p38 and decreased the percentage of cells with nuclear NFATc1 in a dose-dependent manner, the high and middle doses exhibited clear inhibitory activity (P<0.01 and P<0.05, respectively). After the addition of MAPK inhibitors, the NFATc1 expression showed no significant difference compared with the control group (P>0.05).
Serum containing QTG could generally inhibit the TRAF6/MAPK pathways and possibly inhibit the NFATc1 pathway. In addition, QTG may regulate other signaling pathways that are related to osteoclast differentiation and maturation.
研究青络通痹颗粒(QTG)对类风湿关节炎大鼠破骨细胞分化抑制作用的机制。
采用成纤维细胞与单核细胞共培养的方法诱导佐剂性关节炎(AIA)大鼠破骨细胞分化。制备含QTG的血清并添加到破骨细胞中,检测肿瘤坏死因子受体相关因子6/丝裂原活化蛋白激酶/活化T细胞核因子细胞质1(TRAF6/MAPK/NFATc1)信号通路的激活情况。
诱导的破骨细胞为多核细胞,抗酒石酸酸性磷酸酶(TRAP)染色呈阳性。含14.4、7.2或3.6 g/kg QTG的血清以剂量依赖性方式抑制TRAF6、细胞外调节蛋白激酶(ERK)1/2、c-Jun氨基末端激酶(JNK)和p38的激活,并降低细胞核内NFATc1的细胞百分比,高剂量和中剂量表现出明显的抑制活性(分别为P<0.01和P<0.05)。加入MAPK抑制剂后,NFATc1表达与对照组相比无显著差异(P>0.05)。
含QTG的血清可普遍抑制TRAF6/MAPK信号通路,并可能抑制NFATc1信号通路。此外,QTG可能调节与破骨细胞分化和成熟相关的其他信号通路。