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淫羊藿素:一种具有成骨诱导潜力的骨组织工程化合物。

Icariin: a potential osteoinductive compound for bone tissue engineering.

机构信息

Department of Chemistry and Biotechnology, School of Engineering, University of Tokyo, Tokyo, Japan.

出版信息

Tissue Eng Part A. 2010 Jan;16(1):233-43. doi: 10.1089/ten.TEA.2009.0165.

Abstract

To effectively treat bone diseases using bone regenerative medicine, there is an urgent need to develop safe and cheap drugs that can potently induce bone formation. Here, we demonstrate the osteogenic effects of icariin, the main active compound of Epimedium pubescens. Icariin induced osteogenic differentiation of preosteoblastic cells. The combination of icariin and a helioxanthin-derived small compound synergistically induced osteogenic differentiation of MC3T3-E1 cells to a similar extent to bone morphogenetic protein-2. Icariin enhanced the osteogenic induction activity of bone morphogenetic protein-2 in a fibroblastic cell line. Mineralization was enhanced by treatment with a combination of icariin and calcium-enriched medium. The in vivo anabolic effect of icariin was confirmed in a mouse calvarial defect model. Eight-week-old male C57BL/6N mice were transplanted with icariin-calcium phosphate cement (CPC) tablets or CPC tablets only (n = 5 for each), and bone regeneration was evaluated after 4 and 6 weeks. Significant new bone formation was observed in the icariin-CPC group at 4 weeks, and the new bone thickness had increased by 6 weeks. Obvious blood vessel formation was observed in the icariin-induced new bone. Treatment of senescence-accelerated mouse prone 1 and senescence-accelerated mouse prone 6 models further demonstrated that icariin was able to enhance bone formation in vivo. Therefore, icariin is a strong candidate for an osteogenic compound for use in bone tissue engineering.

摘要

为了有效利用骨再生医学治疗骨疾病,迫切需要开发安全且廉价的药物来强力诱导骨形成。在这里,我们展示了淫羊藿素(Epimedium pubescens 的主要活性化合物)的成骨作用。淫羊藿素诱导前成骨细胞的成骨分化。淫羊藿素与来源于海罂粟酮的小分子化合物的组合协同诱导 MC3T3-E1 细胞的成骨分化,其程度与骨形态发生蛋白-2 相似。淫羊藿素增强了成纤维细胞系中骨形态发生蛋白-2 的成骨诱导活性。用淫羊藿素和富含钙的培养基的组合处理可增强矿化。在小鼠颅骨缺损模型中证实了淫羊藿素的体内合成代谢作用。将 8 周龄雄性 C57BL/6N 小鼠移植淫羊藿素-磷酸钙水泥(CPC)片剂或仅 CPC 片剂(每组各 5 只),并在 4 和 6 周后评估骨再生情况。在 4 周时,在淫羊藿素-CPC 组中观察到明显的新骨形成,并且新骨厚度在 6 周时增加。在淫羊藿素诱导的新骨中观察到明显的血管形成。衰老加速小鼠易感 1 和衰老加速小鼠易感 6 模型的治疗进一步表明,淫羊藿素能够增强体内骨形成。因此,淫羊藿素是用于骨组织工程的成骨化合物的有力候选物。

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