破骨细胞
成骨细胞
化学
抗酒石酸酸性磷酸酶
组织蛋白酶K
骨吸收
碱性磷酸酶
黄芪甲素
酸性磷酸酶
骨保护素
生物化学
骨重建
细胞生物学
内科学
内分泌学
生物
酶
医学
类黄酮
体外
山奈酚
抗氧化剂
激活剂(遗传学)
基因
作者
Ryuichiro Suzuki,Yoshiaki Shirataki,Akito Tomomura,Kenjiro Bandow,Hiroshi Sakagami,Mineko Tomomura
标识
DOI:10.3390/ijms242417479
摘要
Plants contain a large number of small-molecule compounds that are useful for targeting human health and in drug discovery. Healthy bone metabolism depends on the balance between bone-forming osteoblast activity and bone-resorbing osteoclast activity. In an ongoing study searching for 22 plant extracts effective against osteoporosis, we found that the crude extract of Euptelea polyandra Sieb. et Zucc (E. polyandra) had osteogenic bioactivity. In this study, we isolated two compounds, isoquercitrin (1) and astragalin (2), responsible for osteogenic bioactivity in osteoblastic MC3T3-E1 cells from the leaf of E. polyandra using column chromatography and the spectroscopic technique. This is the first report to isolate astragalin from E. polyandra. Compounds (1) and (2) promoted osteoblast differentiation by increasing alkaline phosphatase (ALP) activity and alizarin red S stain-positive calcium deposition, while simultaneously suppressing tartrate-resistant acid phosphatase (TRAP)-positive osteoclast differentiation in RAW264.7 cells at non-cytotoxic concentrations. Isoquercitrin (1) and astragalin (2) increased the expression of osteoblastic differentiation genes, Osterix, ALP, and Osteoprotegerin in the MC3T3-E1 cells, while suppressing osteoclast differentiation genes, TRAP, Cathepsin K, and MMP 9 in the RAW264.7 cells. These compounds may be ideal targets for the treatment of osteoporosis due to their dual function of promoting bone formation and inhibiting bone resorption.
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