Biochemical and Biophysical Research Communications, Vol.477, No.4, 673-677, 2016
Echinocystic acid inhibits RANKL-induced osteoclastogenesis by regulating NF-kappa B and ERK signaling pathways
Receptor activator of nuclear factor-kappa B ligand (RANKL) is a key factor in the differentiation and activation of osteoclasts. Echinocystic acid (EA), a pentacyclic triterpene isolated from the fruits of Gleditsia sinensis Lam, was reported to prevent reduction of bone mass and strength and improve the cancellous bone structure and biochemical properties in ovariectomy rats. However, the molecular mechanism of EA on the osteoclast formation has not been reported. The purpose of this study was to investigate the effects and mechanism of EA on RANKL-induced osteoclastogenesis. Our results showed that EA inhibited the formation of osteoclast, as well as the expression of osteoclastogenesis-related marker proteins in bone marrow macrophages (BMMs). At molecular levels, EA inhibited RANKL-induced NF-kappa B activation and ERK phosphorylation in BMMs. In conclusion, the present study demonstrated that EA can suppress osteoclastogenesis in vitro. Moreover, we clarified that these inhibitory effects of EA occur through suppression of NF-kappa B and ERK activation. Therefore, EA may be a potential agent in the treatment of osteoclast-related diseases such as osteoporosis. (C) 2016 Elsevier Inc. All rights reserved.
Keywords:Echinocystic acid (EA);Receptor activator of nuclear factor kappa B ligand (RANKL);Bone marrow macrophages (BMMs)