Abstract
A new naphthalene glycoside was isolated from the leaves and stems of Chimaphila umbellata Barton. Its chemical structure was elucidated to be 2,7-dimethyl-1,4-dihydroxynaphthalene-1-O-β-d-glucopyranoside (DMDHNG), based on spectroscopic evidence. DMDHNG significantly inhibited the receptor activator of nuclear factor-κB ligand (RANKL)-induced tartrate-resistant acid phosphatase (TRAP) activity and the formation of multinucleated osteoclasts in a dose-dependent manner. In addition, the new glycoside inhibited the RANKL-induced mRNA expression of osteoclast-associated genes that encode TRAP, cathepsin K, and another transcription factor—nuclear factor of activated T-cells c1. We believe that the inhibitory effects of DMDHNG on the osteoclast differentiation may be exploited for a therapeutic benefit.
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Acknowledgments
This work was supported by the Bio-Synergy Research Project (NRF-2012M3A9C4048796) of the Ministry of Science, ICT and Future Planning through the National Research Foundation. The authors wish to acknowledge the financial support of Gachon University Research Fund.
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The authors declare no conflict of interest.
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Byong-kyu Shin and Jinhee Kim contributed equally to this work.
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Shin, Bk., Kim, J., Kang, K.S. et al. A new naphthalene glycoside from Chimaphila umbellata inhibits the RANKL-stimulated osteoclast differentiation. Arch. Pharm. Res. 38, 2059–2065 (2015). https://doi.org/10.1007/s12272-015-0598-3
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DOI: https://doi.org/10.1007/s12272-015-0598-3