Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, People's Republic of China.
Key Laboratory of Biomechanics and Mechanobiology (Beihang University), Ministry of Education, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing 100083, People's Republic of China.
Biomed Mater. 2023 May 5;18(4). doi: 10.1088/1748-605X/accf55.
Increased life expectancy has resulted in an increase in osteoporosis incidence worldwide. The coupling of angiogenesis and osteogenesis is indispensable for bone repair. Although traditional Chinese medicine (TCM) exerts therapeutic effects on osteoporosis, TCM-related scaffolds, which focus on the coupling of angiogenesis and osteogenesis, have not yet been used for the treatment of osteoporotic bone defects.saponin (PNS), the active ingredient of, was added to a poly (-lactic acid) (PLLA) matrix. Osteopractic total flavone (OTF), the active ingredient of, was encapsulated in nano-hydroxyapatite/collagen (nHAC) and added to the PLLA matrix. Magnesium (Mg) particles were added to the PLLA matrix to overcome the bioinert character of PLLA and neutralize the acidic byproducts generated by PLLA. In this OTF-PNS/nHAC/Mg/PLLA scaffold, PNS was released faster than OTF. The control group had an empty bone tunnel; scaffolds containing OTF:PNS = 100:0, 50:50, and 0:100 were used as the treatment groups. Scaffold groups promoted new vessel and bone formation, increased the osteoid tissue, and suppressed the osteoclast activity around osteoporotic bone defects. Scaffold groups upregulated the expression levels of angiogenic and osteogenic proteins. Among these scaffolds, the OTF-PNS (50:50) scaffold exhibited a better capacity for osteogenesis than the OTF-PNS (100:0 and 0:100) scaffolds. Activation of the bone morphogenic protein ()-/BMP receptor ()-/runt-related transcription factor ()-signaling pathway may be a possible mechanism for the promotion of osteogenesis. Our study demonstrated that the OTF-PNS/nHAC/Mg/PLLA scaffold could promote osteogenesis via the coupling of angiogenesis and osteogenesis in osteoporotic rats with bone defects, and activating thesignaling pathway may be an osteogenesis-related mechanism. However, further experiments are necessary to facilitate its practical application in the treatment of osteoporotic bone defects.
预期寿命的增加导致了全球骨质疏松症发病率的增加。血管生成和骨生成的耦联对于骨修复是必不可少的。虽然中药(TCM)对骨质疏松症有治疗作用,但尚未将关注血管生成和骨生成耦联的 TCM 相关支架用于治疗骨质疏松性骨缺损。
加入聚(-乳酸)(PLLA)基质中的。
封装在纳米羟基磷灰石/胶原(nHAC)中并添加到 PLLA 基质中的。
添加到 PLLA 基质中以克服 PLLA 的生物惰性特性并中和 PLLA 产生的酸性副产物。
在这种 OTF-PNS/nHAC/Mg/PLLA 支架中,PNS 的释放速度快于 OTF。对照组有空骨隧道;使用含有 OTF:PNS = 100:0、50:50 和 0:100 的支架作为治疗组。支架组促进新血管和骨形成,增加类骨质组织,并抑制骨质疏松性骨缺损周围的破骨细胞活性。支架组上调了血管生成和成骨蛋白的表达水平。在这些支架中,OTF-PNS(50:50)支架的成骨能力优于 OTF-PNS(100:0 和 0:100)支架。骨形态发生蛋白(BMP)-/BMP 受体(BMPR)-/ runt 相关转录因子(Runx2)-信号通路的激活可能是促进成骨的一种可能机制。我们的研究表明,OTF-PNS/nHAC/Mg/PLLA 支架可通过激活信号通路促进骨质疏松大鼠骨缺损中的血管生成和骨生成耦联,从而促进成骨,该信号通路可能是一种成骨相关机制。然而,需要进一步的实验来促进其在治疗骨质疏松性骨缺损中的实际应用。