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Bone lengthening osteogenesis, a combination of intramembranous and endochondral ossification: an experimental study in sheep

机译:骨延长成骨,膜内和软骨内骨化的结合:绵羊的实验研究

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We evaluated the morphological features of the newly formed tissue in an experimental model of tibial callotasis lengthening on 24 lambs, aged from 2 to 3?months at the time of operation. A unilateral external fixator prototype Monotube Triax? (Stryker Howmedica Osteonics, New Jersey) was applied to the left tibia. A percutaneous osteotomy was performed in a minimally traumatic manner using a chisel. Lengthening was started 7?days after surgery and was continued to 30?mm. The 24 animals were randomly divided into three groups of 8 animals each: in Group 1, lengthening took place at a rate of 1?mm/day for 30?days; in Group 2, at a rate of 2?mm/day for 15?days; in Group 3, at a rate of 3?mm/day for 10?days. In each group, 4 animals were killed 2?weeks after end of lengthening, and the other 4 animals at 4?weeks after end of lengthening. To assess bony formation in the distraction area, radiographs were taken every 2?weeks from the day of surgery. To study the process of vascularization, we used Spalteholz’s technique. After killing, the tibia of each animal was harvested, and sections were stained with hematoxylin and eosin, Masson’s trichrome, and Safranin-O. Immunohistochemistry was performed, using specific antibodies to detect collagens I and II, S100 protein, and fibronectin. A combination of intramembranous and endochondral ossification occurred together at the site of distraction. Our study provides a detailed structural characterization of the newly formed tissue in an experimental model of tibial lengthening in sheep and may be useful for further investigations on callotasis.
机译:我们在24只羔羊的胫骨愈伤组织延长实验模型中评估了新形成的组织的形态特征,这些羊羔在手术时年龄为2至3个月。将单侧外固定器原型Monotube Triax (新泽西州Stryker Howmedica Osteonics)应用于左胫骨。使用凿子以最小的创伤方式进行经皮截骨术。手术后7天开始加长,持续30mm。将24只动物随机分为三组,每组8只动物:在第1组中,以1?mm /天的速度加长30?天;在第2组中,以2毫米/天的速度持续15天;在第3组中,速率为3?mm /天,持续10天。在每组中,在延长结束后2周杀死4只动物,在延长结束后4周杀死另外4只动物。为了评估牵张区的骨形成情况,从手术当天起每2周进行X射线照相。为了研究血管化过程,我们使用了Spalteholz的技术。杀死后,收集每只动物的胫骨,并用苏木精和曙红,Masson三色和Safranin-O染色。使用特异性抗体进行免疫组织化学,以检测I型和II型胶原蛋白,S100蛋白和纤连蛋白。分散部位同时发生膜内和软骨内骨化。我们的研究在绵羊胫骨延长实验模型中提供了新形成组织的详细结构特征,可能对进一步研究骨call病有用。

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