RRC ID 43770
著者 Kwak EJ, Lee YS, Choi EM.
タイトル Effect of magnolol on the function of osteoblastic MC3T3-E1 cells.
ジャーナル Mediators Inflamm
Abstract OBJECTIVES:In the present study, the ability of magnolol, a hydroxylated biphenyl compound isolated from Magnolia officinalis, to stimulate osteoblast function and inhibit the release of bone-resorbing mediators was investigated in osteoblastic MC3T3-E1 cells.
METHODS:Osteoblast function was measured by cell growth, alkaline phosphatase activity, collagen synthesis, and mineralization. Glutathione content was also measured in the cells. Bone-resorbing cytokines, receptor activator of nuclear factor-κB ligand (RANKL), TNF-α, and IL-6 were measured with an enzyme immunoassay system.
RESULTS:Magnolol caused a significant elevation of cell growth, alkaline phosphatase activity, collagen synthesis, mineralization, and glutathione content in the cells (P < 0.05). Skeletal turnover is orchestrated by a complex network of regulatory factors. Among cytokines, RANKL, TNF-α, and IL-6 were found to be key osteoclastogenetic molecules produced by osteoblasts. Magnolol significantly (P < 0.05) decreased the production of osteoclast differentiation inducing factors such as RANKL, TNF-α, and IL-6 in the presence of antimycin A, which inhibits mitochondrial electron transport and has been used as an ROS generator.
CONCLUSION:Magnolol might be a candidate as an agent for the prevention of bone disorders such as osteoporosis.
巻・号 2012
ページ 829650
公開日 2012-1-1
DOI 10.1155/2012/829650
PMID 22474400
PMC PMC3306956
MeSH Alkaline Phosphatase / metabolism Animals Antimycin A / pharmacology Biphenyl Compounds / pharmacology* Cell Line Collagen / metabolism Cytokines / metabolism Glutathione / metabolism Interleukin-6 / metabolism Lignans / pharmacology* Mice Osteoblasts / drug effects* Osteoblasts / metabolism* RANK Ligand / metabolism Tumor Necrosis Factor-alpha / metabolism
IF 3.758
引用数 14
リソース情報
ヒト・動物細胞 MC3T3-E1(RCB1126)