4.4 Article

Dried plum polyphenols inhibit osteoclastogenesis by downregulating NFATc1 and inflammatory mediators

Journal

CALCIFIED TISSUE INTERNATIONAL
Volume 82, Issue 6, Pages 475-488

Publisher

SPRINGER
DOI: 10.1007/s00223-008-9139-0

Keywords

bone; osteoclast; antioxidant; osteoporosis; macrophage

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Dried plums and their polyphenols have been shown to suppress bone resorption by downregulating receptor activator NF-KB ligand (RANYL). Due to the anti-iDflammatory and antioxidant properties of these compounds, this study was designed to investigate whether dried plum polyphenols exert additional, more direct effects on osteoclasts and their precursors. RAW 264.7 macrophages were used as a model to study osteoclast precursors and osteoclast differentiation and activity. Under inflammatory conditions induced by lipopolysaccharide (LPS), polyphenols extracted from dried plum (10, 20, and 30 tg/mQ downregulated osteoclast precursor cyclooxygenase expression and nitric oxide (NO) by inhibiting inducible NO synthase. NO and tumor necrosis factor (TNF)-a were also suppressed in the presence of RANKL during osteoclastogenesis by the polyphenols. Increased TNF-oc production in response to oxidative stress, but not LPS, was decreased over time. As expected, LPS and H2O2 significantly increased the number of tartrateresistant acid phosphatase-positive cells by 127% and 30%, respectively. Dried plum polyphenols decreased osteoclast differentiation under normal as well as inflammatory and oxidative stress conditions, coincident with the suppression of the transcription factor, nuclear factor for activated T cells (NFATcl). These inhibitory effects on osteoclastogenesis were confirmed in primary bone marrow cultures. Resorption pit formation was decreased to a similar extent as osteoclast differentiation, suggesting that dried plum polyphenols primarily affect osteoclast differentiation as opposed to activity. Our data demonstrate that dried plum polyphenols directly inhibit osteoclastogenesis, leading to a decrease in osteoclast activity, by downregulating NFATcl and inflammatory mediators.

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