Demirag Burak, Sarisozen Bartu, Ozer Ozgur, Kaplan Tolga, Ozturk Cagatay
Department of Orthopaedic Surgery, Uludag University Medical School, 16059, Görükle, Bursa, Turkey.
J Bone Joint Surg Am. 2005 Nov;87(11):2401-10. doi: 10.2106/JBJS.D.01952.
The use of soft-tissue grafts for anterior cruciate ligament reconstruction delays the healing process. This delay may be due to biochemical and/or biomechanical insults. We hypothesized that the blocking effect of alpha2-macroglobulin on synovial matrix metalloproteinase activity may enhance the healing of tendon graft in a bone tunnel.
The study was performed on twenty-eight healthy, skeletally mature New Zealand White rabbits. Each rabbit underwent bilateral anterior cruciate ligament reconstruction with use of the ipsilateral semitendinosus tendon. Alpha-2-macroglobulin (alpha2-macroglobulin) was injected into the knee joint in one limb, and the contralateral limb served as a control. The rabbits were killed two weeks (fourteen rabbits) or five weeks (fourteen rabbits) after the operative procedures. The presence of matrix metalloproteinases in synovial fluid, and the blocking effect of alpha2-macroglobulin on them, were determined with enzymatic assays. Healing between the tendon and the bone tunnel was assessed morphologically by determining the presence of fibrovascular tissue and collagen fibers. Healing also was assessed quantitatively by measuring the ultimate load to failure of the reconstructed complex.
There was an increase in matrix metalloproteinases in the control group; in contrast, there was a decrease in the study group (p < 0.05). In the control specimens, the fibrovascular tissue at the bone-tendon interface had developed into dense connective tissue with poor vascularization. In the treated specimens, the bone tunnel had more areas of denser connective-tissue ingrowth. The interface tissue was more mature and contained numerous perpendicular collagen bundles (Sharpey fibers). The ultimate load to failure was significantly greater in the alpha2-macroglobulin-treated specimens than in the untreated controls at both two and five weeks.
The present study demonstrated that alpha2-macroglobulin blockade of matrix metalloproteinases can enhance bone-tendon healing. This effect of alpha2-macroglobulin could occur through its effect solely on collagenase or on a subset of matrix metalloproteinases that are present at the healing interface.
使用软组织移植物进行前交叉韧带重建会延迟愈合过程。这种延迟可能是由于生化和/或生物力学损伤所致。我们假设α2-巨球蛋白对滑膜基质金属蛋白酶活性的阻断作用可能会促进肌腱移植物在骨隧道内的愈合。
对28只健康、骨骼成熟的新西兰白兔进行了研究。每只兔子均使用同侧半腱肌肌腱进行双侧前交叉韧带重建。在一侧肢体的膝关节内注射α2-巨球蛋白,对侧肢体作为对照。术后两周(14只兔子)或五周(14只兔子)处死兔子。通过酶学分析测定滑液中基质金属蛋白酶的存在情况以及α2-巨球蛋白对它们的阻断作用。通过确定纤维血管组织和胶原纤维的存在情况,从形态学上评估肌腱与骨隧道之间的愈合情况。还通过测量重建复合体的最终破坏载荷对愈合情况进行定量评估。
对照组中基质金属蛋白酶增加;相比之下,研究组中则减少(p < 0.05)。在对照标本中,骨-肌腱界面处的纤维血管组织已发展为血管化不良的致密结缔组织。在处理过的标本中,骨隧道有更多区域出现更致密的结缔组织长入。界面组织更成熟,包含许多垂直的胶原束(沙比纤维)。在两周和五周时,α2-巨球蛋白处理组标本的最终破坏载荷均显著高于未处理的对照组。
本研究表明,α2-巨球蛋白对基质金属蛋白酶的阻断作用可促进骨-肌腱愈合。α2-巨球蛋白的这种作用可能仅通过其对胶原酶或对愈合界面处存在的一部分基质金属蛋白酶的作用而发生。