期刊：
International Immunopharmacology,2015年25(1):49-54 ISSN：1567-5769
通讯作者：
Wang, Haibin
作者机构：
[Wang, Haibin; Chen, Qunqun; Zhou, Chi; He, Wei] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Guangzhou 510405, Guangdong, Peoples R China.;[Liu, Wengang] 2nd Tradit Chinese Med Hosp Guangdong Prov, Guangzhou, Guangdong, Peoples R China.;[Song, Houpan] Hunan Univ Chinese Med, Inst TCM Diagnost, Changsha 410007, Hunan, Peoples R China.;[Wang, Haibin] Guangzhou Univ Chinese Med, Affiliated Hosp 1, 16 Airport Rd, Guangzhou 510405, Guangdong, Peoples R China.
通讯机构：
[Wang, Haibin] G;Guangzhou Univ Chinese Med, Affiliated Hosp 1, 16 Airport Rd, Guangzhou 510405, Guangdong, Peoples R China.
关键词：
MAPK;NF-kappaB;Osteoclast;RANKL;Saikosaponin a
摘要：
Inflammatory cytokines play an important role in osteoclastogenesis. Saikosaponin a (SSa) possesses anti-inflammatory activity. However, the role of SSa in osteoporosis is still unclear. Therefore, the objective of this study was to investigate the effects of SSa on receptor activator of the nuclear factor-kappa B ligand (RANKL)-induced osteoclastogenesis and signaling pathway by in vitro assay. In mouse bone marrow monocytes (BMMs), SSa suppressed RANKL plus macrophage colony-stimulating factor (M-CSF)-induced osteodast differentiation in a dose-dependent manner. Moreover, SSa decreased osteoclastogenesis-related marker proteins expression, including NFATcl, c-fos and cathepsin K At molecular levels, SSa inhibited RANKL-induced I kappa B alpha phosphotylation, p65 phosphorylation and NF-kappa B luciferase activity in RAW264.7 cells. And SSa also suppressed RANKL-induced p-38, extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK) phosphorylation. Taken together, these findings suggest that SSa suppresses osteoclastogenesis through inhibiting RANKL-induced p-38, ERK, JNK and NF-kappa B activation. SSa is a novel agent in the treatment of osteodast-related diseases, such as osteoporosis. (C) 2015 Elsevier B.V. All rights reserved.
