Nutrients · 2020 · 20 citations · 21 references
MedicineEndocrinologyPharmacologyBiochemical PharmacologyBone MetabolismMineral MetabolismBone Density RegulationBone MineralizationBone ResorptionOsteoclast BiologyOsteogenesisOsteoporosisBone Mineral DensityBone Mineral Density DeclineBone Mineral LossBone Resorption InhibitionCompound IdentificationExtractOsteoclast InhibitionPhosphatase Enzyme Activity
cortex (LRC) extract inhibited ovariectomized (OVX)-induced bone loss in mice. This study investigated the anti-osteoporotic effects of bioactive constituent(s) from the LRC extract. The effective compound(s) were screened, and a single compound, scopolin, which acts as a phytoalexin, was chosen as a candidate component. Scopolin treatment enhanced alkaline phosphatase activity and increased mineralized nodule formation in MC3T3-E1 pre-osteoblastic cells. However, osteoclast differentiation in primary-cultured monocytes was reduced by treatment with scopolin. Consistently, scopolin treatment increased osteoblast differentiation in the co-culture of monocytes (osteoclasts) and MC3T3-E1 (osteoblast) cells. Scopolin treatment prevented bone mineral density loss in OVX-induced osteoporotic mice. These results suggest that scopolin could be a therapeutic bioactive constituent for the treatment and prevention of osteoporosis.
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Multilineage Potential of Adult Human Mesenchymal Stem Cells
Mark F. Pittenger, Alastair M. Mackay, Stephen C. Beck et al. · Science · 1999 · 21.1K citations
FSH Directly Regulates Bone Mass
Li Sun, Yuanzhen Peng, Allison C. Sharrow et al. · Cell · 2006 · 731 citations · Full text