[Effect of accordion technique and deferoxamine on promoting bone regeneration in distraction osteogenesis].

Kai Liu, Lingyun Shi, Sulong Wang, Ainizier Yalikun, Yimurang Hamiti, Aihemaitijiang Yusufu
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引用次数: 0

Abstract

Objective: To compare the effects of hypoxia-inducible drugs using deferoxamine (DFO) and accordion technique (AT) on activating the hypoxia-inducible factor 1α (HIF-1α)/vascular endothelial growth factor (VEGF) signaling pathway to promote bone regeneration and remodelling during consolidation phase of distraction osteogenesis (DO).

Methods: Forty-five specific-pathogen-free adult male Sprague-Dawley (SD) rats were randomly divided into the control group, DFO group, and AT group, with 15 rats in each group. All rats underwent osteotomy to establish a right femur DO model. Then, continuous distraction was started for 10 days after 5 days of latency in each group. During the consolidation phase after distraction, no intervention was performed in the control group; DFO was locally perfused into the distraction area in the DFO group starting at the 3rd week of consolidation phase; cyclic stress stimulation was given in the AT group starting at the 3rd week of consolidation phase. The general condition of rats in each group was observed. X-ray films were conducted at the end of the distraction phase and at the 2nd, 4th, and 6th weeks of the consolidation phase to observe the calcification in the distraction area. At the 4th and 6th weeks of the consolidation phase, peripheral blood was taken for ELISA detection (HIF-1α, VEGF, CD31, and Osterix), femoral specimens were harvested for gross observation, histological staining (HE staining), and immunohistochemical staining [HIF-1α, VEGF, osteopontin (OPN), osteocalcin (OCN)]. At the 6th week of the consolidation phase, Micro-CT was used to observe the new bone mineral density (BMD), bone volume/tissue volume (BV/TV), trabecular separation (Tb.Sp), trabecular number (Tb.N), and trabecular thickness (Tb.Th) in the distraction area, and biomechanical test (ultimate load, elastic modulus, energy to failure, and stiffness) to detect bone regeneration in the distraction area.

Results: The rats in all groups survived until the termination of the experiment. ELISA showed that the contents of HIF-1α, VEGF, CD31, and Osterix in the serum of the AT group were significantly higher than those of the DFO group and control group at the 4th and 6th weeks of the consolidation phase ( P<0.05). General observation, X-ray films, Micro-CT, and biomechanical test showed that bone formation in the femoral distraction area was significantly better in the DFO group and AT group than in the control group, and complete recanalization of the medullary cavity was achieved in the AT group, and BMD, BV/TV, Tb.Sp, Tb.N, and Tb.Th, as well as ultimate load, elastic modulus, energy to failure, and stiffness in the distraction area, were better in the AT group than in the DFO group and control group, and the differences were significant ( P<0.05). HE staining showed that trabecular bone formation and maturation in the distraction area were better in the AT group than in the DFO group and control group. Immunohistochemical staining showed that at the 4th week of consolidation phase, the expression levels of HIF-1α, VEGF, OCN, and OPN in the distraction area of the AT group were significantly higher than those of the DFO group and control group ( P<0.05); however, at 6th week of consolidation phase, the above indicators were lower in the AT group than in the DFO group and control group, but there was no significant difference between groups ( P>0.05).

Conclusion: Both continuous local perfusion of DFO in the distraction area and AT during the consolidation phase can activate the HIF-1α/VEGF signaling pathway. However, AT is more effective than local perfusion of DFO in promoting the process of angiogenesis, osteogenesis, and bone remodelling.

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[风琴技术和去氧胺对促进牵张成骨中骨再生的影响]。
目的比较缺氧诱导药物去铁胺(DFO)和手风琴技术(AT)对激活缺氧诱导因子1α(HIF-1α)/血管内皮生长因子(VEGF)信号通路以促进牵张成骨(DO)巩固期骨再生和重塑的作用:将 45 只无特异性病原体的成年雄性 Sprague-Dawley (SD) 大鼠随机分为对照组、DFO 组和 AT 组,每组 15 只。所有大鼠均接受截骨术以建立右股骨 DO 模型。然后,每组大鼠在潜伏 5 天后开始持续牵引 10 天。在牵引后的巩固阶段,对照组不进行任何干预;DFO组在巩固阶段第3周开始向牵引区域局部灌注DFO;AT组在巩固阶段第3周开始给予周期性应力刺激。观察各组大鼠的一般状况。在牵引阶段结束时和巩固阶段的第 2、4 和 6 周拍摄 X 光片,观察牵引区域的钙化情况。在巩固阶段的第 4 周和第 6 周,抽取外周血进行 ELISA 检测(HIF-1α、VEGF、CD31 和 Osterix),采集股骨标本进行大体观察、组织学染色(HE 染色)和免疫组化染色[HIF-1α、VEGF、骨生成素(OPN)、骨钙素(OCN)]。在巩固期的第 6 周,使用 Micro-CT 观察牵引区域的新骨矿物质密度(BMD)、骨体积/组织体积(BV/TV)、骨小梁分离度(Tb.Sp)、骨小梁数量(Tb.N)和骨小梁厚度(Tb.Th),并进行生物力学测试(极限载荷、弹性模量、破坏能量和刚度)以检测牵引区域的骨再生情况:各组大鼠均存活至实验结束。ELISA显示,在巩固期的第4周和第6周,AT组血清中HIF-1α、VEGF、CD31和Osterix的含量明显高于DFO组和对照组(PPPP>0.05):结论:在牵张区持续局部灌注DFO和在巩固期灌注AT都能激活HIF-1α/VEGF信号通路。但在促进血管生成、成骨和骨重塑过程中,AT 比局部灌注 DFO 更有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中国修复重建外科杂志
中国修复重建外科杂志 Medicine-Medicine (all)
CiteScore
0.80
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11334
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