Herbal formulation, Yukmi-jihang-tang-Jahage, regulates bone resorption by inhibition of phosphorylation mediated by tyrosine kinase Src and cyclooxygenase expression

被引:36
作者
Jin, Un-Ho
Kim, Dong-Il
Lee, Tae-Kyun
Lee, Dong-Nyung
Kim, June-Ki
Lee, In-Seon
Kim, Cheorl-Ho [1 ]
机构
[1] Sungkyunkwan Univ, Dept Biol Sci, Suwon 440746, South Korea
[2] Sungkyunkwan Univ, Natl Res Lab Glycobiol, Suwon 440746, South Korea
[3] Dongguk Univ, Coll Oriental Med, Kyungbuk 780714, South Korea
[4] LeeTaeKyun Hanuiwon & Hanbang Clin, Taegu, South Korea
[5] Seimyung Univ, Coll Oriental Med, Dept Gynecol, Chungbuk, South Korea
[6] Keimyung Univ, Ctr Tradit Microorganism Resources, Taegu 704701, South Korea
关键词
Yitkmi-jihang-tang-Jahage; bone resorption; osteoporosis; prostaglandin E2; IL-1; beta; osteoblast; protein tyrosinekinase inhibitor; IL-6; TNF-alpha; TGF-beta;
D O I
10.1016/j.jep.2006.01.012
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Anti-bone resorption properties of the Korean herbal medicine, Yukmi-jihang-tang (YJ), which is comprised of seven herbs such as Rehmannia glutinosa Libosch, Dioscorea japonica THUNB, Cornus officinalis SIEB et. ZUCC, Smilax glabra ROXB, Paeonia suffruticosa ANDR, Alisma platago-aquatica var. orientale SAMUELS and Hominis placenta, were investigated. Cyclooxygenase-2 (COX-2) and tyrosine kinase involve on prostaglandin E2 (PGE2) production in mouse calvarial osteoblasts stimulated by cytokine interleukin-1 beta (IL-1 beta), tumor necrosis factor-alpha (TNF-alpha) and/or interleukin-6 (M-6). IL-1 beta and IL-6 and to a lesser extent TNF-alpha, enhanced COX-2 mRNA levels in calvarial osteoblasts. TGF-beta, YJ (100 mu g/ml) and their combinations of YJ + TGF-beta reduced the COX-2 mRNA level, PGE2 biosynthesis and bone resorption induced by IL-1 beta, TNF-alpha, IL-6 or their combination. Finally, YJ inhibits in vitro and in vivo bone resorption by inhibition of phosphorylation of peptide substrates. The parathyroid hormone-induced bone resorption in mouse fetal long bone cultures was inhibited with an IC50 of 16 mu g/ml. YJ dose-dependently reduced the hypercalcemia induced in mice by IL-1 beta and partly prevented bone loss and microarchitectural changes in young ovariectomized rats, showing that the protective effect on bone was exerted via the inhibition of bone resorption. These results indicate that the synergy between IL-beta, TNF-alpha, IL-6 on PGE2 production is due to an enhanced gene expression of COX-2 and that tyrosine kinase(s) are involved in the signal transduction of COX-2 in mouse calvarial osteoblasts. Thus, YJ as a possible Src family kinase inhibitor may be useful for the treatment of diseases associated with elevated bone loss. This result also suggested that the YJ extracts is effective for bone resorptive action in bone cells. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:333 / 343
页数:11
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