Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota.
Division of Orthopedic Surgery, Oslo University Hospital, Norway & Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
J Cell Biochem. 2018 Jul;119(7):5715-5724. doi: 10.1002/jcb.26755. Epub 2018 Mar 25.
Tendon graft healing in bone tunnels for the fixation of intra-articular ligament reconstructions may limit clinical outcome by delaying healing. This study assesses the effects of hydrogel-mediated delivery of bone anabolic growth factors in a validated model of tendon-to-bone tunnel healing. Forty-five Wistar rats were randomly allocated into three groups (BMP2-treated, GSK126-treated, and placebo). All animals underwent a tendon-to-bone tunnel reconstruction. Healing was evaluated at 4 weeks by biomechanical assessment, micro-computed tomography (bone mineral density, bone volume, cross sectional area of bone tunnels), and traditional histology. Adverse events associated with the hydrogel-mediated delivery of drugs were not observed. Results of our biomechanical assessment demonstrated favorable trends in animals treated with bone anabolic factors for energy absorption (P = 0.116) and elongation (P = 0.054), while results for force to failure (P = 0.691) and stiffness (P = 0.404) did not show discernible differences. Cross sectional areas for BMP2-treated animals were reduced, but neither BMP2 nor GSK126 administration altered bone mineral density (P = 0.492) or bone volume in the bone tunnel. These results suggest a novel and positive effect of bone anabolic factors on tendon-to-bone tunnel healing. Histological evaluation confirmed absence of collagen fibers crossing the soft tissue-bone interface indicating immature graft integration as expected at this time point. Our study indicates that hydrogel-mediated delivery of BMP2 and GSK126 appears to be safe and has the potential to enhance tendon-to-bone tunnel healing in ligament reconstructions.
用于关节内韧带重建固定的骨隧道内肌腱移植物愈合可能会通过延迟愈合来限制临床结果。本研究评估了水凝胶介导的骨合成代谢生长因子在肌腱-骨隧道愈合的验证模型中的作用。将 45 只 Wistar 大鼠随机分配到三组(BMP2 治疗组、GSK126 治疗组和安慰剂组)。所有动物均接受肌腱-骨隧道重建。在第 4 周通过生物力学评估、微计算机断层扫描(骨矿物质密度、骨体积、骨隧道横截面积)和传统组织学评估来评估愈合情况。未观察到与水凝胶介导的药物输送相关的不良事件。生物力学评估的结果表明,接受骨合成代谢因子治疗的动物在能量吸收(P=0.116)和伸长(P=0.054)方面有良好的趋势,而在失效力(P=0.691)和刚度(P=0.404)方面的结果没有明显差异。BMP2 治疗动物的横截面积减小,但 BMP2 和 GSK126 给药均未改变骨隧道中的骨矿物质密度(P=0.492)或骨体积。这些结果表明骨合成代谢因子对肌腱-骨隧道愈合有新的积极作用。组织学评估证实没有胶原纤维穿过软组织-骨界面,表明在这个时间点预期的移植物不成熟整合。我们的研究表明,水凝胶介导的 BMP2 和 GSK126 输送似乎是安全的,并有可能增强韧带重建中的肌腱-骨隧道愈合。