Abstract |
Bioactivity-guided fractionation led to the successful isolation of antiosteoporotic components, i.e. physicion (1), rubiadin-1-methyl ether (2), 2-hydroxy-1-methoxy- anthraquinone (3), 1,2-dihydroxy-3-methylanthraquinone (4), 1,3,8-trihydroxy-2-methoxy- anthraquinone (5), 2-hydroxymethyl-3-hydroxyanthraquinone (6), 2-methoxyanthraquinone (7) and scopoletin (8) from an ethanolic extract of the roots of Morinda officinalis. Compounds 4-8 are isolated for the first time from M. officinalis. Among them, compounds 2 and 3 promoted osteoblast proliferation, while compounds 4, 5 increased osteoblast ALP activity. All of the isolated compounds inhibited osteoclast TRAP activity and bone resorption, and the inhibitory effects on osteoclastic bone resorption of compounds 1 and 5 were stronger than that of other compounds. Taken together, antiosteoporotic activity of M. officinalis and its anthraquinones suggest therapeutic potential against osteoporosis.
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Authors | Yan-Bin Wu, Cheng-Jian Zheng, Lu-Ping Qin, Lian-Na Sun, Ting Han, Lei Jiao, Qiao-Yan Zhang, Jin-Zhong Wu |
Journal | Molecules (Basel, Switzerland)
(Molecules)
Vol. 14
Issue 1
Pg. 573-83
(Jan 23 2009)
ISSN: 1420-3049 [Electronic] Switzerland |
PMID | 19169204
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anthraquinones
- Bone Density Conservation Agents
- Alkaline Phosphatase
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Topics |
- Alkaline Phosphatase
(metabolism)
- Animals
- Anthraquinones
(chemistry, pharmacology, therapeutic use)
- Bone Density Conservation Agents
(chemistry, pharmacology, therapeutic use)
- Bone Resorption
(drug therapy)
- Cell Proliferation
(drug effects)
- Cells, Cultured
- Molecular Structure
- Morinda
(chemistry)
- Osteoblasts
(cytology, drug effects)
- Osteoclasts
(cytology, drug effects)
- Rats
- Rats, Wistar
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