| Literature DB >> 30146787 |
Lilei He1,2, Guoju Hong3,4,5, Lin Zhou6, Jianguo Zhang2, Jian Fang2, Wei He3, Jennifer Tickner4, Xiaorui Han7, Lilian Zhao2, Jiake Xu3,4.
Abstract
Identification of natural compounds that inhibit osteoclastogenesis will facilitate the development of antiresorptive treatment of osteolytic bone diseases. Asiaticoside is a triterpenoid derivative isolated from Centella asiatica, which exhibits varying biological effects like angiogenesis, anti-inflammation, wound healing, and osteogenic differentiation. However, its role in osteoclastogenesis remains unknown. Here, we show that Asiaticoside can suppress RANKL-induced osteoclast formation and bone resorption in a dose-dependent manner. Asiaticoside attenuated the expression of osteoclast marker genes including Ctsk, Atp6v0d2, Nfatc1, Acp5, and Dc-stamp. Furthermore, Asiaticoside inhibited RANKL-mediated NF-κB and NFATc1 activities, and RANKL-induced calcium oscillation. Collectively, this study demonstrates that Asiaticoside inhibited osteoclast formation and function through attenuating RANKL-induced key signaling pathways, which may indicate that Asiaticoside is a potential antiresorptive agent against osteoclast-related osteolytic bone diseases.Entities:
Keywords: NF-κB; NFAT pathway; RANKL; asiaticoside; osteoclast
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Year: 2018 PMID: 30146787 DOI: 10.1002/jcp.27195
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384