Gushukang inhibits osteocyte apoptosis and enhances BMP-2/Smads signaling pathway in ovariectomized rats

被引:35
|
作者
Chai, Shuang [1 ]
Wan, Lei [2 ]
Wang, Ji-Li [1 ]
Huang, Jia-Chun [1 ]
Huang, Hong-Xing [2 ,3 ]
机构
[1] Guangzhou Univ Chinese Med, Guangzhou, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
[3] Guangzhou Univ Chinese Med, Natl Key Discipline Orthopaed & Traumatol Chinese, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Gushukang; BMP-2/Smads signaling pathway; Osteocyte apoptosis; Osteoporosis; BONE MORPHOGENETIC PROTEIN-2; OSTEOBLAST DIFFERENTIATION; REGULATES OSTEOBLAST; INDUCED OSTEOPOROSIS; ESTROGEN; GROWTH; BETA; ASSOCIATION; ALENDRONATE; EXPRESSION;
D O I
10.1016/j.phymed.2019.153063
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Traditional herbal formula Gushukang (GSK) has been clinically applied to treat primary osteoporosis, which can stimulate osteoblastogenesis and improve calcium homeostasis. However, it remains unknown the mechanism that GSK against ovariectomized (OVX) induced damage. Purpose: The aim of this study was to investigate the effect of GSK on BMP-2/Smsds signaling pathway and osteocyte apoptosis which has been reported to play a central role in bone remodeling. Study design: OVX in rat was established and GSK was administered. Results: BMP-2/Smsds signaling pathway was inhibited and the number of apoptotic osteocytes was increased in OVX rats. Treatment with GSK significantly enhanced BMP-2/Smsds signaling pathway by up-regulating the expression of BMP-2, p-Smad1 and p-Smad5, Osterix and Runx2, and inhibited osteocyte apoptosis by up-regulating Bcl-xl and down-regulating Bak, which were consistent with histological changes revealed by ALP, Trap and TUNEL staining. GSK treatment improved bone mass and micro-structure of trabecular bone at distal femur in OVX rats shown by BMD, micro-CT measurement and HE staining. Conclusion: These data suggest that GSK exhibited protective effects on promoting bone formation and precluding osteocyte apoptosis. The underlying mechanism may be attributed to its regulation on BMP-2/Smads signaling pathway and Bcl2 family.
引用
收藏
页数:9
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