Notoya K, Yoshida K, Taketomi S, Yamazaki I, Kumegawa M
Pharmaceutical Research Laboratories II, Takeda Chemical Industries Ltd., Osaka, Japan.
Calcif Tissue Int. 1992;51 Suppl 1:S3-6. doi: 10.1007/BF02180241.
Effects of ipriflavone (7-isopropoxyisoflavone) on osteoclast-induced bone resorption were evaluated using an unfractionated bone cell culture system containing mature osteoclasts from the femur and tibia of newborn mice. When cells were cultured for 4 days on dentin slices in the presence of 5% fetal bovine serum and 10(-8) M 1 alpha, 25(OH)2D3, ipriflavone (3 x 10(-7) -3 x 10(-5) M) inhibited pit formation and caused a decrease in the number of tartrate-resistant acid phosphatase (TRAP)-positive multinucleated cells (MNCs). The lowest significant effect was observed at a concentration of 10(-6) M. Unlike ipriflavone, calcitonin inhibited pit formation 4 days after the culture was started without affecting the number of TRAP-positive MNCs. Ipriflavone still inhibited pit formation when the culture period was 13 days, when new osteoclasts were expected to be formed. These findings suggest that ipriflavone inhibits new osteoclast formation and bone resorption at the cellular level.
使用包含新生小鼠股骨和胫骨成熟破骨细胞的未分级骨细胞培养系统,评估了依普黄酮(7 - 异丙氧基异黄酮)对破骨细胞诱导的骨吸收的影响。当细胞在含有5%胎牛血清和10(-8) M 1α,25(OH)2D3的条件下于牙本质切片上培养4天时,依普黄酮(3×10(-7) - 3×10(-5) M)抑制了蚀斑形成,并导致抗酒石酸酸性磷酸酶(TRAP)阳性多核细胞(MNCs)数量减少。在10(-6) M浓度下观察到最低显著效应。与依普黄酮不同,降钙素在培养开始4天后抑制蚀斑形成,但不影响TRAP阳性MNCs的数量。当培养期为13天时,预计会形成新的破骨细胞,依普黄酮仍能抑制蚀斑形成。这些发现表明,依普黄酮在细胞水平上抑制新破骨细胞的形成和骨吸收。