Notoginsenoside R1 suppresses wear particle-induced osteolysis and RANKL mediated osteoclastogenesis in vivo and in vitro

被引:24
作者
Zhao, Shuai [1 ]
Yan, Lianqi [1 ]
Li, Xiaolei [1 ]
Zhang, Zhen [2 ]
Sun, Yu [1 ]
Wang, Jingcheng [1 ]
机构
[1] Yangzhou Univ, Subei Peoples Hosp Jiangsu Prov, Clin Med Coll, Dept Orthoped, Yangzhou 225001, Jiangsu, Peoples R China
[2] Dalian Med Univ, Dalian 116044, Liaoning, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Osteolysis; Aseptic prosthesis loosening; Notoginsenoside R1; Mitogen-activated protein kinase; NF-kappa B; Osteoclast; TOTAL JOINT REPLACEMENT; PERIPROSTHETIC OSTEOLYSIS; BONE-RESORPTION; INFLAMMATION; HIP; CHALLENGES; DENOSUMAB; BIOLOGY; DEBRIS;
D O I
10.1016/j.intimp.2017.03.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aseptic periprosthetic osteolysis Is a complication induced by wear particles after hip joint replacement, which shortens the service life of prostheses. Although many methods have been applied to prevent this complication, the results were not always successful. In the present study, we explored the prophylactic effect of notoginsenoside R1 (NG-R1) on a Ti particle-induced mouse calvarial osteolysis model and the inhibitory effect on RANKL-mediated osteoclastogenesis and osteoclast bone resorption. Our results indicated that intraperitoneal injection of NG-R1 (10 or 20 m g/kg/day), a constituent of notoginseng, alleviates Ti particle-induced mouse calvarial osteolysis after twelve days post-treatment. In vitro, we observed that NG-R1 inhibits RANKL-mediated mitogen-activated protein kinases (MAPKs), including the phosphorylation levels of JNK1/2, P38, ERK1/2 and NF-kappa B (NF-kappa B) signalling pathways, and suppresses RANKL-mediated osteoclastogenesis and osteoclast bone resorption. These results suggest that NG-R1 may be a promising therapeutic agent for preventing wear particle-induced periprosthetic osteolysis. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 125
页数:8
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