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Tea Polyphenols Inhibit Rat Osteoclast Formation and Differentiation

Authors :
Yoshiomi Oka
Shinichi Iwai
Hitoshi Amano
Yuko Irie
Kentaro Yatomi
Kakei Ryu
Shoji Yamada
Katsunori Inagaki
Katsuji Oguchi
Source :
Journal of Pharmacological Sciences, Vol 118, Iss 1, Pp 55-64 (2012)
Publication Year :
2012
Publisher :
Elsevier, 2012.

Abstract

Matrix metalloproteinases (MMPs) play an important role in degeneration of the matrix associated with bone and cartilage. Regulation of osteoclast activity is essential in the treatment of bone disease, including osteoporosis and rheumatoid arthritis. Polyphenols in green tea, particularly epigallocatechin-3-gallate (EGCG), inhibit MMPs expression and activity. However, the effects of the black tea polyphenol, theaflavin-3,3′-digallate (TFDG), on osteoclast and MMP activity are unknown. Therefore, we examined whether TFDG and EGCG affect MMP activity and osteoclast formation and differentiation in vitro. TFDG or EGCG (10 and 100 μM) was added to cultures of rat osteoclast precursors cells and mature osteoclasts. Numbers of multinucleated osteoclasts and actin rings decreased in polyphenol-treated cultures relative to control cultures. MMP-2 and MMP-9 activities were lower in TFDG- and EGCG-treated rat osteoclast precursor cells than in control cultures. MMP-9 mRNA levels declined significantly in TFDG-treated osteoclasts in comparison to control osteoclasts. TFDG and EGCG inhibited the formation and differentiation of osteoclasts via inhibition of MMPs. TFDG may suppress actin ring formation more effectively than EGCG. Thus, TFDG and EGCG may be suitable agents or lead compounds for the treatment of bone resorption diseases. Keywords:: theaflavin-3,3′-digallate (TFDG), epigallocatechin-3-gallate (EGCG), rat osteoclast, rat osteoclast precursor cell, matrix metalloproteinase (MMP)-9

Subjects

Subjects :
Therapeutics. Pharmacology
RM1-950

Details

Language :
English
ISSN :
13478613
Volume :
118
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Pharmacological Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.94ceb1b6b9f84a7b828907b3127346fc
Document Type :
article
Full Text :
https://doi.org/10.1254/jphs.11082FP