Mammoto Takeo, Seerattan Ruth A, Paulson Kent D, Leonard Catherine A, Bray Robert C, Salo Paul T
McCaig Institute for Bone and Joint Health, Department of Surgery, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta, Canada.
J Orthop Res. 2008 Jul;26(7):957-64. doi: 10.1002/jor.20615.
Previous work has shown that innervation participates in normal ligament healing. The present study was performed to determine if exogenous nerve growth factor (NGF) would improve the healing of injured ligament by promoting reinnervation, blood flow, and angiogenesis. Two groups of 30 Sprague-Dawley rats underwent unilateral medial collateral ligament transection (MCL). One group was given 10 microg NGF and the other was given PBS via osmotic pump over 7 days after injury. After 7, 14, and 42 days, in vivo blood flow was measured using laser speckle perfusion imaging (LSPI). Morphologic assessments of nerve density, vascularity, and angiogenesis inhibitor production were done in three animals at each time point by immunohistochemical staining for the pan-neuronal marker PGP9.5, the endothelial marker vWF, and the angiogenesis inhibitor thrombospondin-2 (TSP-2). Ligament scar material and structural mechanical properties were assessed in seven rats at each time point. Increased nerve density was promoted by NGF at both 14 and 42 days. Exposure to NGF also led to increased ligament vascularity, as measured by histologic assessment of vWF immunohistochemistry, although LSPI-measured blood flow was not significantly different from controls. NGF treatment also led to decreased expression of TSP-2 at 14 days. Mechanical testing revealed that exposure to NGF increased failure load by 40%, ultimate tensile strength by 55%, and stiffness by 30% at 42 days. There were no detectable differences between groups in creep properties. The results suggest that local application of NGF can improve ligament healing by promoting both reinnervation and angiogenesis, and results in scars with enhanced mechanical properties.
先前的研究表明神经支配参与正常韧带愈合。本研究旨在确定外源性神经生长因子(NGF)是否会通过促进神经再支配、血流和血管生成来改善损伤韧带的愈合。两组各30只Sprague-Dawley大鼠接受单侧内侧副韧带横断术(MCL)。一组在损伤后7天通过渗透泵给予10微克NGF,另一组给予PBS。在7天、14天和42天后,使用激光散斑灌注成像(LSPI)测量体内血流。通过对泛神经元标志物PGP9.5、内皮标志物vWF和血管生成抑制剂血小板反应蛋白-2(TSP-2)进行免疫组织化学染色,在每个时间点对三只动物进行神经密度、血管形成和血管生成抑制剂产生的形态学评估。在每个时间点对七只大鼠的韧带瘢痕材料和结构力学性能进行评估。在14天和42天时,NGF均促进了神经密度增加。通过vWF免疫组织化学的组织学评估测量,暴露于NGF还导致韧带血管形成增加,尽管LSPI测量的血流与对照组无显著差异。NGF治疗在14天时还导致TSP-2表达降低。力学测试显示,在42天时,暴露于NGF使破坏载荷增加40%,极限拉伸强度增加55%,刚度增加30%。两组在蠕变特性方面无可检测到的差异。结果表明,局部应用NGF可通过促进神经再支配和血管生成来改善韧带愈合,并产生具有增强力学性能的瘢痕。