Qian Yuwangxuan, Yu Yihe, Yang Fan, Liang Qixing, Xu Dan, Chen Jiaxiang, Hu Xueqin
The Second Clinical Medical College of Zhejiang, Chinese Medical University, Hangzhou, 310053, China.
The First Clinical Medical College of Zhejiang, Chinese Medical University, Hangzhou, 310053, China.
J Orthop Surg Res. 2025 Feb 5;20(1):141. doi: 10.1186/s13018-025-05542-4.
The primary objective of this study was to elucidate the underlying pharmacological mechanisms by which Jingui Shenqi Wan (JGSQW) alleviates postmenopausal osteoporosis (PMOP). Through a systematic investigation, we sought to identify the specific molecular pathways through which JGSQW modulates the progression of PMOP, thereby providing a scientific basis for its clinical application.
We established an ovariectomized (OVX) mouse model to simulate estrogen deficiency-induced PMOP. Initially, micro-CT imaging and Alcian blue hematoxylin/orange G (ABH/OG) staining were employed to assess the effects of JGSQW on bone microarchitecture and bone mass preservation. Immunohistochemistry (IHC) was then utilized to evaluate the expression of osteogenic markers, including Osterix (OSX), Runx2, and Osteopontin (OPN). Additionally, Tartrate - Resistant Acid Phosphatase (TRAP) staining was performed to visualize and quantify osteoclasts. We further investigated the potential role of JGSQW in modulating the pyroptosis pathway.
JGSQW effectively alleviates the destruction of bone microstructure and the loss of bone mass caused by estrogen deficiency, an effect that appears to be mediated by promoting osteogenesis. Additionally, JGSQW significantly downregulates the expression of GSDMD in osteoblasts and mitigates the abnormal release of inflammatory factors, thereby maintaining the normal functional activities of osteoblasts.
JGSQW may effectively mitigate the progression of estrogen deficiency-induced PMOP by inhibiting the dysregulated activation of osteoblast pyroptosis.
本研究的主要目的是阐明金匮肾气丸(JGSQW)缓解绝经后骨质疏松症(PMOP)的潜在药理机制。通过系统研究,我们试图确定JGSQW调节PMOP进展的具体分子途径,从而为其临床应用提供科学依据。
我们建立了去卵巢(OVX)小鼠模型以模拟雌激素缺乏诱导的PMOP。最初,采用显微CT成像和阿尔新蓝苏木精/橘黄G(ABH/OG)染色来评估JGSQW对骨微结构和骨量保留的影响。然后利用免疫组织化学(IHC)评估成骨标志物,包括osterix(OSX)、Runx2和骨桥蛋白(OPN)的表达。此外,进行抗酒石酸酸性磷酸酶(TRAP)染色以可视化和量化破骨细胞。我们进一步研究了JGSQW在调节焦亡途径中的潜在作用。
JGSQW有效地减轻了雌激素缺乏引起的骨微结构破坏和骨量丢失,这一作用似乎是通过促进成骨作用介导的。此外,JGSQW显著下调成骨细胞中GSDMD的表达,并减轻炎症因子的异常释放,从而维持成骨细胞的正常功能活动。
JGSQW可能通过抑制成骨细胞焦亡的失调激活来有效减轻雌激素缺乏诱导的PMOP的进展。