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青络通痹颗粒对佐剂性关节炎大鼠滑膜成纤维细胞与单核细胞共培养诱导破骨细胞分化的抑制机制

Inhibition mechanism of Qingluo Tongbi Granule () on osteoclast differentiation induced by synovial fibroblast and monocytes co-culture in adjuvant-induced arthritic rats.

作者信息

Liu Tian-yang, Zhou Ling-ling, Zhou Cong, Liu Zhang-pu, Chen Chen, Feng Zhe, Zhou Xue-ping

机构信息

Nanjing University of Chinese Medicine, Nanjing, 210023, China.

出版信息

Chin J Integr Med. 2015 Apr;21(4):291-8. doi: 10.1007/s11655-014-1839-x. Epub 2014 Sep 2.

DOI:10.1007/s11655-014-1839-x
PMID:25182154
Abstract

OBJECTIVE

To study the mechanism underlying the inhibitory effect of Qingluo Tongbi Granule (, QTG) on osteoclast differentiation in rheumatoid arthritis in rats.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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