破骨细胞
兰克尔
骨吸收
汤剂
机制(生物学)
PI3K/AKT/mTOR通路
药理学
抗酒石酸酸性磷酸酶
去卵巢大鼠
医学
骨质疏松症
骨髓
化学
信号转导
内科学
生物化学
受体
激活剂(遗传学)
雌激素
哲学
认识论
作者
Jianxin Shi,Xiao-Qun Cai,Zehao Zhao,Yu Deng,Zhikun Zhou
摘要
Osteoclasts (OCs) have been the unique cell type exhibiting the bone-resorption activity in body. It is important to identify drugs to resist osteoclastogenesis to manage the bone-loss disorders. Huangqi Sanxian decoction (HQSXD) is utilized for the treatment of postmenopausal osteoporosis (PMOP) for a long history in East Asia. This work aimed to examine HQSXD's activity in OC differentiation. Based on staining with tartrate-resistant acid phosphatase (TRAP), it was found that HQSXD suppressed OC generation under the induction of RANKL produced in the bone marrow-derived monocytes/macrophages (BMMs), with no cytotoxic effect. Later analysis like molecular exploration and network pharmacology (NP) suggested the role of HQSXD in suppressing genes associated with osteoclastogenesis via PI3K/Akt-mediated mechanism dose-dependently. This work might illustrate the molecular pharmacological mechanism involved in HQSXD's effect on treating OC-associated disorders. Moreover, NP was found to modernize traditional Chinese medicine (TCM) research.
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