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

Authors
Shin, Byong-kyuKim, JinheeKang, Ki SungPiao, Hui-ShanPark, Jeong HillHwang, Gwi Seo
Issue Date
Nov-2015
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
Chimaphila umbellata; 2,7-Dimethyl-1,4-dihydroxynaphthalene-1-O-beta-D-glucopyranoside; Osteoclast; Receptor activator of nuclear factor-kappa B ligand; Tartrate-resistant acid phosphatase
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.38, no.11, pp.2059 - 2065
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
38
Number
11
Start Page
2059
End Page
2065
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/9973
DOI
10.1007/s12272-015-0598-3
ISSN
0253-6269
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-beta-d-glucopyranoside (DMDHNG), based on spectroscopic evidence. DMDHNG significantly inhibited the receptor activator of nuclear factor-kappa B 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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Kang, Ki Sung
College of Korean Medicine (Premedical course of Oriental Medicine)
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