Su Hui, Liu Luyao, Yan Zechen, Guo WenXuan, Huang Guangxin, Zhuang Rujie, Pan Yu
The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, Zhejiang Province, 310053, China.
Orthopedic Department, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, 310053, China.
J Orthop Surg Res. 2025 Mar 11;20(1):260. doi: 10.1186/s13018-025-05665-8.
This study seeks to confirm the therapeutic effectiveness of TRFD in inhibiting adipogenesis and promoting osteogenesis in primary osteoporosis through the MAPK/HIF-1α signaling pathway. C57BL/6J mice underwent ovariectomy (OVX) to induce osteoporosis. Mice were administered TRFD (Low and high doses)estradiol for a duration of 12 weeks. Bone microarchitecture evaluated using Micro-CT, while serum biomarkers and protein expressions were analyzed through enzyme-linked immunosorbent assay, Western blotting, and immunohistochemistry. Furthermore, BMSC were isolated to show differentiation, Osteogenic and adipogenic induction were performed, including ALP activity and Oil Red O staining. Bioinformatics analysis of RNA sequencing data was conducted to identify differentially expressed genes.
Total flavonoids of Rhizoma Drynariae treatment significantly improved bone microarchitecture and reversed histopathological damage in OVX mice. It increased serum levels of osteogenesis markers (RUNX2, BMP-2) and enhanced MAPK and HIF-1α signaling pathways, The results also showed a significant dose, TFDR enhanced the osteogenic differentiation of BMSCs while suppressing adipogenic differentiation, as demonstrated by increased ALP activity and mineralization, alongside, the expression of lipid markers (PPAR-γ, C/EBPα) was inhibited. Furthermore, MAPK/HIF-1α pathway was confirmed be crucial in mediating these effects.
TRFD exhibits significant therapeutic potential in treating primary osteoporosis by promoting osteogenesis and inhibiting adipogenesis through the MAPK/HIF-1α pathway. These establish an investigation of TRFD as a natural treatment option for managing osteoporosis.
Not applicable.
本研究旨在通过丝裂原活化蛋白激酶/低氧诱导因子-1α(MAPK/HIF-1α)信号通路,证实骨碎补总黄酮(TRFD)抑制原发性骨质疏松症中脂肪生成和促进骨生成的治疗效果。对C57BL/6J小鼠进行卵巢切除术(OVX)以诱导骨质疏松症。给小鼠施用TRFD(低剂量和高剂量)、雌二醇,持续12周。使用显微计算机断层扫描(Micro-CT)评估骨微结构,同时通过酶联免疫吸附测定、蛋白质印迹法和免疫组织化学分析血清生物标志物和蛋白质表达。此外,分离骨髓间充质干细胞(BMSC)以显示其分化情况,进行成骨和成脂诱导,包括碱性磷酸酶(ALP)活性和油红O染色。对RNA测序数据进行生物信息学分析以鉴定差异表达基因。
骨碎补总黄酮治疗显著改善了OVX小鼠的骨微结构并逆转了组织病理学损伤。它提高了成骨标志物(RUNX2、骨形态发生蛋白-2)的血清水平,并增强了MAPK和HIF-1α信号通路。结果还显示出显著的剂量效应,TRFD增强了BMSC的成骨分化,同时抑制了成脂分化,这表现为ALP活性和矿化增加,同时脂质标志物(过氧化物酶体增殖物激活受体γ、CCAAT增强子结合蛋白α)的表达受到抑制。此外,证实MAPK/HIF-1α通路在介导这些效应中起关键作用。
TRFD通过MAPK/HIF-1α途径促进骨生成和抑制脂肪生成,在治疗原发性骨质疏松症方面具有显著的治疗潜力。这些结果确立了对TRFD作为治疗骨质疏松症的天然治疗选择的研究。
不适用。