Oroxin B Attenuates Ovariectomy-Induced Bone Loss by Suppressing Osteoclast Formation and Activity

被引:5
|
作者
Huang, Jun-ming [1 ]
Wang, Chen-zhong [1 ]
Lu, Shun-yi [1 ]
Wang, Zhe [1 ]
Yan, Zuo-qin [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Orthopaed, Shanghai 200032, Peoples R China
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2021年 / 15卷
基金
中国国家自然科学基金;
关键词
osteoclast; Oroxin B; MAPK; NF-kappa B; RANKL; osteoporosis; T-CELLS C1; NUCLEAR FACTOR; ACTIVATION; DIFFERENTIATION; RECEPTOR; PATHWAY; ICARIIN;
D O I
10.2147/DDDT.S328238
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Osteoclasts are the major players in bone resorption and have always been studied in the prevention and treatment of osteoporosis. Previous studies have confirmed that a variety of flavonoids inhibit osteoporosis and improve bone health mainly through inhibiting osteoclastogenesis. Oroxin B (OB) is a flavonoid compound extracted from traditional Chinese herbal medicine Oroxylum indicum (L.) Vent, exerts potent antitumor and anti inflammation effect, but its effect on osteoclastogensis remains unknown. Methods: We comprehensively evaluated the effect of OB on the formation and function of osteoclasts and the underling mechanism by bone marrow-derived macrophage in vitro. In vivo, we used mice ovariectomized model to verify the protective effect of OB. Results: OB was found to inhibit osteoclast formation and bone resorption function in vitro, in a dose-dependent manner and the increased osteoclastic-related genes induced by RANKL (NFATc1, c-fos, cathepsin K, RANK, MMP9 and TRAP) were also attenuated following OB treatment. Mechanistical investigation showed OB abrogated the increased phosphorylation level of MAPK and NF-kappa B pathway, and diminished the expression of the vital transcription factors for osteoclastogenesis. OB also prevented ovariectomy (OVX)-induced bone loss by inhibiting osteoclast formation and activity in mice. Conclusion: Our study demonstrated that OB may act as an anti-osteoporosis agent by inhibiting osteoclast maturation and attenuating bone resorption.
引用
收藏
页码:4811 / 4825
页数:15
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