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磷酸钙骨水泥与锂和阿司匹林共同改性以实现骨质疏松性股骨髁缺损的快速骨再生

Co-modification of calcium phosphate cement to achieve rapid bone regeneration in osteoporotic femoral condyle defect with lithium and aspirin.

作者信息

Tao Zhou-Shan, Zhou Wan-Shu, Zhang Rou-Tian, Li Yang, Xu Hong-Guang, Wei Shan, Wang Zheng-Yu, Yang Min

机构信息

Department of Trauma Orthopedics, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital Wuhu 241001, Anhui, People's Republic of China.

Department of Geriatrics, The Second Affiliated Hospital of Wannan Medical College Wuhu 241000, Anhui, People's Republic of China.

出版信息

Am J Transl Res. 2021 Mar 15;13(3):952-966. eCollection 2021.

Abstract

Local application of lithium or aspirin with biological scaffold has been identified as a potent means to improve bone formation. In this study, lithium and aspirin modified calcium phosphate cement (Asp-Li/CPC) was prepared, and the feasibility of this biological scaffold in the treatment of osteoporotic bone defect was observed in vivo and in vitro. In vitro experiments confirmed that Asp-Li/CPC had better ability to promote MC3T3-E1 cells differentiation into osteoblasts, osteoblast mineralization and viability, and promote cell expression of ALP, OP, RUNX-2, OC and COL-1 protein than simple CPC or lithium modified CPC by MTT, Alizarin red staining and Western blot evaluation. In vivo experiments confirmed that Asp-Li/CPC presented the strongest effect on bone regeneration and bone mineralization through the comparison with CPC group and Li/CPC group with X-ray images, Micro-CT and Histological evaluation. RT-qPCR analysis showed that Asp-Li/CPC, Li/CPC group and CPC group demonstrated increased BMP2, Smad1, OPG than the OVX group (P<0.05), while Asp-Li/CPC exhibited decreased TNF-α, IFN-γ and RANKL than the OVX group (P<0.05). Experiments in vivo and in vitro show that Asp-Li/CPC is a scheme for rapid repair of femoral condylar defects, and these effects may be achieved by inhibiting local inflammation and through BMP-2/Smad1 and OPG/RANKL signaling pathway.

摘要

锂或阿司匹林与生物支架的局部应用已被确认为改善骨形成的有效手段。在本研究中,制备了锂和阿司匹林改性的磷酸钙骨水泥(Asp-Li/CPC),并在体内和体外观察了这种生物支架治疗骨质疏松性骨缺损的可行性。体外实验证实,通过MTT、茜素红染色和蛋白质印迹评估,与单纯的CPC或锂改性的CPC相比,Asp-Li/CPC具有更好的促进MC3T3-E1细胞分化为成骨细胞、成骨细胞矿化和活力的能力,并能促进细胞表达碱性磷酸酶(ALP)、骨钙蛋白(OP)、核心结合因子α1(RUNX-2)、骨桥蛋白(OC)和I型胶原蛋白(COL-1)。体内实验通过X射线图像、显微CT和组织学评估与CPC组和Li/CPC组比较,证实Asp-Li/CPC对骨再生和骨矿化具有最强的作用。逆转录-定量聚合酶链反应(RT-qPCR)分析表明,Asp-Li/CPC组、Li/CPC组和CPC组与去势骨质疏松(OVX)组相比,骨形态发生蛋白2(BMP2)、Smad1、骨保护素(OPG)表达增加(P<0.05),而Asp-Li/CPC组与OVX组相比,肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)和核因子κB受体活化因子配体(RANKL)表达降低(P<0.05)。体内和体外实验表明,Asp-Li/CPC是一种快速修复股骨髁缺损的方案,这些作用可能是通过抑制局部炎症以及通过BMP-2/Smad1和OPG/RANKL信号通路实现的。

相似文献

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[ study of strontium-doped calcium phosphate cement for biological properties].掺锶磷酸钙骨水泥生物学性能的研究
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