Hypoxia During the Consolidation Phase of Distraction Osteogenesis Promotes Bone Regeneration

被引:14
作者
Liu, Yanshi [1 ]
Liu, Jialin [2 ]
Cai, Feiyu [1 ]
Liu, Kai [1 ]
Zhang, Xiaoxu [3 ]
Yusufu, Aihemaitijiang [1 ]
机构
[1] Xinjiang Med Univ, Affiliated Hosp 1, Dept Trauma & Microreconstruct Surg, Urumqi, Peoples R China
[2] Xinjiang Med Univ, Affiliated Hosp 1, Dept Prosthodont, Urumqi, Peoples R China
[3] Xinjiang Med Univ, Sch Publ Hlth, Urumqi, Peoples R China
基金
中国国家自然科学基金;
关键词
bone regeneration; consolidation; distraction osteogenesis; hypoxia; osteogenic-angiogenic coupling; IN-VITRO; TENSION; RECONSTRUCTION; ANGIOGENESIS; ACTIVATION; RESECTION; FRACTURE; GROWTH; REPAIR;
D O I
10.3389/fphys.2022.804469
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
BackgroundHypoxia is the critical driving force for angiogenesis and can trigger the osteogenic-angiogenic coupling followed by the enhancement of bone regeneration. While lots of studies showed that hypoxia administration can accelerate bone formation during distraction osteogenesis (DO), the therapeutic timing for the osteogenic purpose was concentrated on the distraction phase. The outcomes of hypoxia administration in the consolidation phase stay uncertain. The purpose of this study was to determine the osteogenic effectiveness of hypoxia therapy during the consolidation phase, if any, to enhance bone regeneration in a rat femoral DO model. MethodsA total of 42 adult male Sprague-Dawley rats underwent right femoral mid-diaphysis transverse osteotomy and were randomly divided into Control (NS administration, n = 21) and Group1 (deferoxamine therapy, n = 21) after distraction. During the consolidation phase, Group1 was treated with local deferoxamine (DFO) injection into the distraction zone, while the Control underwent the same dosage of NS. Animals were sacrificed after 2, 4, and 6 weeks of consolidation. The process of bone formation and remodeling was monitored by digital radiographs, and the regenerated bone was evaluated by micro-computed tomography (micro-CT), biomechanical test, and histological analysis. The serum content of hypoxia-inducible factor 1 alpha (HIF-1 alpha) and vascular endothelial growth factor (VEGF) were measured by enzyme linked immunosorbent assay (ELISA) for further analysis. ResultsBone regeneration was significantly enhanced after hypoxia therapy during the consolidation phase. The digital radiograph, micro-CT, and biomechanical evaluation showed better effects regarding volume, continuity, and mechanical properties of the regenerated bone in Group1. The histomorphological evaluation also revealed the hypoxia treatment contributed to accelerate bone formation and remodeling during DO. The higher positive expression of angiogenic and osteogenic markers were observed in Group1 after hypoxia administration according to the immunohistochemical analysis. The serum content of HIF-1 alpha and VEGF was also increased after hypoxia therapy as evidenced from ELISA. ConclusionHypoxia administration during the consolidation phase of distraction osteogenesis has benefits in enhancing bone regeneration, including accelerates the bone formation and remodeling.
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页数:11
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