
pmid: 22269833
Numerous studies have indicated that inflammatory cytokines play a major role in osteoclastogenesis, leading to the bone resorption that is frequently associated with osteoporosis. D-pinitol, a 3-methoxy analogue of D-chiroinositol, was identified as an active principle in soy foods and legumes. Here we found that D-pinitol markedly inhibited the receptor activator of nuclear factor kappa B ligand (RANKL)-induced osteoclastic differentiation from bone marrow stromal cells and RAW264.7 macrophage cells. In addition, D-pinitol also reduced RANKL-induced p38 and JNK phosphorylation. Furthermore, RANKL-mediated increase of IKK, IκBα, and p65 phosphorylation and NF-κB-luciferase activity was inhibited by D-pinitol. However, D-pinitol did not affect the proliferation and differentiation of osteoblasts. In addition, D-pinitol also prevented the bone loss induced by ovariectomy in vivo. Our data suggest that D-pinitol inhibits osteoclastogenesis from bone marrow stromal cells and macrophage cells via attenuated RANKL-induced p38, JNK, and NF-κB activation, which in turn protect bone loss from ovariectomy.
MAP Kinase Kinase 4, Macrophages, Ovariectomy, Blotting, Western, RANK Ligand, NF-kappa B, Osteoclasts, Bone Marrow Cells, Cell Differentiation, Flow Cytometry, Growth Inhibitors, Rats, Rats, Sprague-Dawley, Osteogenesis, Animals, Osteoporosis, Female, Bone Resorption, Inositol, Cell Proliferation
MAP Kinase Kinase 4, Macrophages, Ovariectomy, Blotting, Western, RANK Ligand, NF-kappa B, Osteoclasts, Bone Marrow Cells, Cell Differentiation, Flow Cytometry, Growth Inhibitors, Rats, Rats, Sprague-Dawley, Osteogenesis, Animals, Osteoporosis, Female, Bone Resorption, Inositol, Cell Proliferation
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