Gambogic acid inhibits osteoclast formation and ovariectomy-induced osteoporosis by suppressing the JNK, p38 and Akt signalling pathways

被引:30
|
作者
Ma, Jianjun [1 ,2 ]
Ma, Yan [1 ,2 ]
Liu, Xuqiang [3 ]
Chen, Shuai [1 ,2 ]
Liu, Chao [1 ,2 ]
Qin, An [3 ]
Fan, Shunwu [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Orthopaed, Sir Run Run Shaw Hosp, Hangzhou 310016, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sir Run Run Shaw Inst Clin Med, Hangzhou 310016, Zhejiang, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Dept Orthopaed, Shanghai Key Lab Orthopaed Implant,Shanghai Peopl, Shanghai 200011, Peoples R China
关键词
Akt; gambogic acid; JNK; osteoclasts; osteoporosis; p38; PARTICLE-INDUCED OSTEOLYSIS; NF-KAPPA-B; BONE-RESORPTION; INDUCED APOPTOSIS; IN-VIVO; C-FOS; DIFFERENTIATION; RANKL; CANCER; BISPHOSPHONATES;
D O I
10.1042/BJ20150151
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Excessive osteoclast formation and bone resorption are key causes of osteoporosis. Natural compounds can serve as alternative therapeutic agents for the prevention and treatment of osteoporosis, and some natural compounds may have advantages over traditional drugs. In the present paper, we report that the natural compound GBA (gambogic acid), which is bioavailable, effective and less toxic, inhibits osteoclast formation, thereby attenuating osteoclastic bone resorption in vitro. Further in vivo studies demonstrated that GBA prevented ovariectomy-induced bone loss in a dose-dependent manner. Moreover, we demonstrated that GBA suppressed RANKL (receptor activator of nuclear factor kappa B ligand)-induced 2JNK (c-Jun N-terminal kinase), p38 and Akt phosphorylation. Taken together, our results demonstrate that GBA inhibits osteoclast formation in vitro and in vivo, suggesting that it is of potential value in the treatment of osteoclast-related diseases.
引用
收藏
页码:399 / 408
页数:10
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