Shen Gu An Capsule Inhibition of Postmenopausal Osteoporosis in Ovariectomized Mice Using Network Pharmacology-Based Mechanism Prediction and Pharmacological Validation

被引:0
|
作者
Du, Meilin [1 ]
Yuan, Shiguo [2 ,3 ]
Wang, Jiayang [4 ]
Zhao, Qiangqiang [5 ]
Ye, Baofei [2 ,3 ]
Wu, Haiyan [2 ,3 ]
Xu, Liangliang [5 ]
Hou, Yu [2 ,6 ]
机构
[1] Shandong Univ Tradit Chinese Med, Lab Gynecol, Jinan, Chin, Myanmar
[2] Guangzhou Univ Chinese Med, Hainan Hosp, Guangdong Prov Hosp Chinese Med, Dept Orthopaed, Guangzhou 510000, Guangdong, Peoples R China
[3] Hainan Med Univ, Hainan Tradit Chinese Med Hosp, Dept Orthopaed, Haikou, Hainan, Peoples R China
[4] Dalian Med Univ, Lab Orthopaed & Traumatol, Dalian, Liaoning, Peoples R China
[5] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Lingnan Med Res Ctr, Key Lab Orthopaed & Traumatol, Guangzhou, Guangdong, Peoples R China
[6] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Clin Coll 2, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
postmenopausal osteoporosis; Shen Gu An capsule; NF-kappa B signaling pathway; osteoclasts; bone; NF-KAPPA-B; TRANSCRIPTION FACTOR; SALVIA-MILTIORRHIZA; OSTEOCLAST; PREVENTION; DIFFERENTIATION; WOMEN;
D O I
10.1177/1934578X241297039
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background Postmenopausal osteoporosis (PMOP) is characterized by low bone mass and increased bone fragility in postmenopausal women. Shen Gu An capsule (SGA) has been clinically used to treat bone diseases, especially PMOP with kidney Yang deficiency.Objectives We aimed to study the effect of SGA on the treatment of PMOP.Methodology The key candidate targets and pathways of SGA for treating PMOP were predicted by Network pharmacology analysis. Then, in vivo validation using bilaterally ovariectomized C57BL/6 mice was performed, and the bone quality was analyzed by Micro-CT and histological analysis.Results In this study, we obtained 113 active compounds and 82 targets via the database of Traditional Chinese Medicine Systems Pharmacology. Subsequently, compound-target and protein-protein interaction networks were constructed. Then GO and KEGG analysis revealed that NF-kappa B signaling pathway might be the underlying mechanism as its well-known function in osteoclastogenesis. Furthermore, the in vivo experiments using ovariectomized mice demonstrated that SGA could decrease the number of osteoclasts and preserve bone mass through inhibiting the NF-kappa B signaling pathway.Conclusions SGA could prevent postmenopausal osteoporosis in ovariectomized mice through inhibiting NF-kappa B signaling pathway. The finding of this study provides more evidence for the clinical application of SGA to treat osteoporosis.
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页数:10
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