new naphthalene glycoside from Chimaphila umbellata inhibits the RANKL-stimulated osteoclast differentiation

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 activato...

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Veröffentlicht in:Archives of pharmacal research 2015, 38(11), , pp.2059-2065
Hauptverfasser: Shin, Byong-kyu, Kim, Jinhee, Kang, Ki Sung, Piao, Hui-Shan, Park, Jeong Hill, Hwang, Gwi Seo
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Sprache:eng
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Zusammenfassung: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.
ISSN:0253-6269
1976-3786
DOI:10.1007/s12272-015-0598-3