Liu Kai, Shi Lingyun, Wang Sulong, Yalikun Ainizier, Hamiti Yimurang, Yusufu Aihemaitijiang
Department of Trauma and Microreconstructive Surgery, the First Affiliated Hospital of Xinjiang Medical University, Urumqi Xinjiang, 830054, P. R. China.
Department of Orthopaedic Surgery, the First Affiliated Hospital of Xinjiang Medical University, Urumqi Xinjiang, 830054, P. R. China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2024 Aug 15;38(8):1001-1009. doi: 10.7507/1002-1892.202404073.
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).
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.
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 ( <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 ( <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 ( <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 ( >0.05).
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.
比较使用去铁胺(DFO)和手风琴技术(AT)的缺氧诱导药物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效果。
将45只无特定病原体成年雄性Sprague-Dawley(SD)大鼠随机分为对照组、DFO组和AT组,每组15只。所有大鼠均行截骨术建立右股骨DO模型。然后,每组在潜伏期5天后开始连续牵张10天。在牵张后的巩固期,对照组不进行干预;DFO组在巩固期第3周开始向牵张区域局部灌注DFO;AT组在巩固期第3周开始给予周期性应力刺激。观察每组大鼠的一般情况。在牵张期结束时以及巩固期第2、4、6周拍摄X线片,观察牵张区域的钙化情况。在巩固期第4周和第6周,采集外周血进行ELISA检测(HIF-1α、VEGF、CD31和osterix),取股骨标本进行大体观察、组织学染色(HE染色)和免疫组织化学染色[HIF-1α、VEGF、骨桥蛋白(OPN)、骨钙素(OCN)]。在巩固期第6周,使用Micro-CT观察牵张区域的新骨矿物质密度(BMD)、骨体积/组织体积(BV/TV)、骨小梁间距(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)以检测牵张区域的骨再生情况。
所有组的大鼠均存活至实验结束。ELISA结果显示,在巩固期第4周和第6周,AT组血清中HIF-1α、VEGF、CD31和osterix的含量显著高于DFO组和对照组(<0.05)。大体观察、X线片、Micro-CT和生物力学测试显示,DFO组和AT组股骨牵张区域的骨形成明显优于对照组,AT组实现了髓腔的完全再通,且牵张区域的BMD、BV/TV、Tb.Sp、Tb.N和Tb.Th以及极限载荷、弹性模量、破坏能量和刚度,AT组均优于DFO组和对照组,差异有统计学意义(<0.05)。HE染色显示,AT组牵张区域的骨小梁形成和成熟情况优于DFO组和对照组。免疫组织化学染色显示,在巩固期第4周,AT组牵张区域HIF-1α、VEGF、OCN和OPN的表达水平显著高于DFO组和对照组(<0.05);然而,在巩固期第6周,AT组上述指标低于DFO组和对照组,但组间差异无统计学意义(>0.05)。
在巩固期,牵张区域持续局部灌注DFO和AT均可激活HIF-1α/VEGF信号通路。然而,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。