兰克尔
破骨细胞
化学
去卵巢大鼠
NF-κB
体内
MAPK/ERK通路
体外
骨质疏松症
细胞生物学
激活剂(遗传学)
信号转导
药理学
内分泌学
生物化学
受体
生物
生物技术
激素
作者
Yuting Zhang,Hu Chen,Songxuan Zhang,Huihao Zhou,Jun Xu,Jian‐Da Ma,Lie Dai,Qiong Gu
标识
DOI:10.1016/j.bioorg.2021.105511
摘要
Euphoesulatin A (Eup A), a new jatrophane diterpenoid isolated from the Euphorbia esula L. (Euphorbiaceae), was reported to inhibit RANKL-induced osteoclastogenesis. However, the underlying mechanism and the effect in osteoporosis mouse model are still unclear. This study is the first to demonstrate that Eup A inhibits osteoclastogenesis in vitro and in vivo. Mechanistic analysis suggested that Eup A (3, 6, 12 μM) dose-dependently inhibited osteoclastogenesis by down-regulating the activation of NFATc1 and NF-κB and MAPKs signal pathways. Moreover, Eup A (10 mg/kg) significantly prevented bone loss in ovariectomized mice. This work provides in vitro and in vivo evidence that Eup A could be a potential candidate for the development of anti-osteoporosis agents.
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