同种异体骨髓间充质干细胞(MSCs)和血管内皮生长因子(VEGF)重建骨隧道模型前交叉韧带(ACL)的胶原蛋白分析

petrasama petrasama
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引用次数: 0

摘要

ACL重建措施的目的是获得稳定的膝关节,并减少进一步损伤半月板和关节表面的风险。加速肌腱移植物与骨隧道之间的融合过程将改善ACL重建的最终结果。本研究旨在探讨静脉注射同种异体骨髓间充质干细胞和血管内皮生长因子重建前交叉韧带骨隧道移植模型的胶原组成。本研究采用后验组设计,将20只家兔分为治疗组和对照组。在第3周和第6周进行胶原免疫组化评价。第3周评价高剂量组治疗时1型胶原面积(p < 0.05)。同种异体骨髓间充质干细胞和血管内皮生长因子在ACL重建中促进了1型胶原的形成,加速了移植物肌腱突与骨隧道的融合。关键词:前十字韧带,同种异体骨髓间充质干细胞,血管内皮生长因子,移植物,胶原
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COLLAGEN ANALYSIS OF GRAFT IN BONE TUNNEL MODEL ANTERIOR CRUCIATE LIGAMENT (ACL) RECONSTRUCTION WITH INTRATUNNEL ALLOGENIC BONE MARROW MESENCHYMAL STEM CELLS (MSCs) AND VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF)
ACL reconstruction measures aim to obtain stable knees, and reduce the risk of further injury to the meniscus and joint surfaces. Acceleration of the integration process between the tendon graft and the bone tunnel will improve the final result of ACL reconstruction. The purpose of this study was to investigate the collagen composition of the bone tunnel graft model of anterior cruciate ligament reconstruction with intravenous allogenic bone marrow mesenchymal stem cells and vascular endothelial growth factor in experimental animals. The design of this study was Post-test only Control Group Design using 20 rabbits divided into treatment group and control group. Collagen immunohistochemical evaluation was performed at weeks 3 and 6. Evaluation at week 3 obtained the area of collagen type-1 in the higher treatment group at treatment (p <0.001). In the 6th week evaluation, it was found that the area of collagen type-1 in the treatment group was higher (p <0.05). Type-1 collagen at week 6 did not differ significantly with week 3 (p> 0.05). Provision of allogenic bone marrow mesenchymal stem cells and intratonal vascular endothelial growth factor in ACL reconstruction enhanced the formation of collagen type-1 which is the acceleration of incorporation of the graft tendon process with bone tunnel.Keywords : Anterior Cruciate Ligament, allogenic bone marrow mesenchymal stemcells, vascular endothelial growth factor, graft and collagen.
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