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牵张成骨的大鼠模型。

Rat model of distraction osteogenesis.

作者信息

Aronson J, Shen X C, Skinner R A, Hogue W R, Badger T M, Lumpkin C K

机构信息

Department of Orthopaedics, University of Arkansas for Medical Sciences, Little Rock, USA.

出版信息

J Orthop Res. 1997 Mar;15(2):221-6. doi: 10.1002/jor.1100150210.

DOI:10.1002/jor.1100150210
PMID:9167624
Abstract

Prior studies of distraction osteogenesis in dog and rabbit models have shown predominantly intramembranous bone formation. Other models of fracture healing normally display mixtures of both endochondral and intramembranous bone formation. We have established a rat model of tibial lengthening that reliably reproduces the pattern of zonal osteogenesis previously observed in dog and rabbit models. A distraction rate of 0.25 mm twice a day with a 0-day latency period produced intramembranous bone with zones of progressive mineralization from collagen. With this protocol, rats bridged the distraction gap with a 25% increase in the tibial bone length. After 20 days of distraction and 50 days of consolidation, the three-point bending stiffness, as a percentage of the contralateral control, reached a level equivalent to that measured in the canine model for a 15% lengthening (28-day distraction and 84-day consolidation). Radiodensitometric analysis of the regenerate bones measured 97% of the unaffected contralateral tibial densities, and mineral analyses demonstrated that calcium and phosphorus levels in the regenerate bone reached 78% of contralateral tibial levels by day 70. We concluded that a rat model of distraction osteogenesis will be useful for a wide range of studies involving rapid intramembranous bone formation.

摘要

先前在狗和兔子模型中进行的牵张成骨研究主要显示为膜内成骨。其他骨折愈合模型通常同时显示软骨内成骨和膜内成骨。我们建立了一种大鼠胫骨延长模型,该模型能够可靠地重现先前在狗和兔子模型中观察到的区域性成骨模式。每天两次以0.25毫米的牵张速率,潜伏期为0天,可产生从胶原蛋白开始逐渐矿化区域的膜内成骨。按照此方案,大鼠填补了牵张间隙,胫骨长度增加了25%。在牵张20天和巩固50天后,三点弯曲刚度相对于对侧对照的百分比达到了与犬类模型中15%延长(牵张28天和巩固84天)时测量的水平相当。对再生骨的放射密度分析测得其密度为未受影响的对侧胫骨密度的97%,矿物质分析表明,到第70天时,再生骨中的钙和磷水平达到对侧胫骨水平的78%。我们得出结论,牵张成骨大鼠模型将有助于开展涉及快速膜内成骨的广泛研究。

相似文献

1
Rat model of distraction osteogenesis.牵张成骨的大鼠模型。
J Orthop Res. 1997 Mar;15(2):221-6. doi: 10.1002/jor.1100150210.
2
Development of tensile strength during distraction osteogenesis in a rat model.大鼠模型牵张成骨过程中拉伸强度的发展
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Histomorphometry of distraction osteogenesis in a caprine tibial lengthening model.山羊胫骨延长模型中牵张成骨的组织形态计量学研究
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Preliminary studies of mineralization during distraction osteogenesis.
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Effects of pulsed electromagnetic field stimulation on distraction osteogenesis in the rabbit tibial leg lengthening model.脉冲电磁场刺激对兔胫骨延长模型中牵张成骨的影响。
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Intermittent parathyroid hormone (1-34) enhances mechanical strength and density of new bone after distraction osteogenesis in rats.间歇性甲状旁腺激素(1-34)可增强大鼠牵张成骨后新骨的机械强度和密度。
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Distraction osteogenesis in the Cbfa-1+/- mouse.Cbfa-1+/-小鼠中的牵引成骨
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The effect of low intensity pulsed ultrasound applied to rabbit tibiae during the consolidation phase of distraction osteogenesis.低强度脉冲超声在兔胫骨牵张成骨巩固期的应用效果。
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Zoledronic acid prevents osteopenia and increases bone strength in a rabbit model of distraction osteogenesis.唑来膦酸可预防牵张成骨兔模型中的骨质减少并增强骨强度。
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Linear increase in axial stiffness of regenerate callus during limb lengthening.
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Systemic Administration of G-CSF Accelerates Bone Regeneration and Modulates Mobilization of Progenitor Cells in a Rat Model of Distraction Osteogenesis.粒细胞集落刺激因子全身给药加速牵引成骨过程中的骨再生并调节祖细胞的动员。
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MicroRNA-144-3p inhibits bone formation in distraction osteogenesis through targeting Connexin 43.
微小RNA-144-3p通过靶向连接蛋白43抑制牵张成骨中的骨形成。
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An Efficient and Reproducible Protocol for Distraction Osteogenesis in a Rat Model Leading to a Functional Regenerated Femur.一种在大鼠模型中实现牵张成骨并形成功能性再生股骨的高效且可重复的方案。
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Comprehensive Review of Adipose Stem Cells and Their Implication in Distraction Osteogenesis and Bone Regeneration.脂肪干细胞综述及其在牵张成骨和骨再生中的意义
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Rosiglitazone disrupts endosteal bone formation during distraction osteogenesis by local adipocytic infiltration.罗格列酮通过局部脂肪细胞浸润干扰牵张成骨过程中的骨内膜骨形成。
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Inhibin A enhances bone formation during distraction osteogenesis.抑制素 A 可增强牵张成骨过程中的骨形成。
J Orthop Res. 2012 Feb;30(2):288-95. doi: 10.1002/jor.21501. Epub 2011 Aug 1.
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Analysis of the biomechanical properties of the mandible after unilateral distraction osteogenesis.分析单侧牵引成骨术后下颌骨的生物力学特性。
Plast Reconstr Surg. 2010 Aug;126(2):533-542. doi: 10.1097/PRS.0b013e3181de2240.
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Direct bone formation during distraction osteogenesis does not require TNFalpha receptors and elevated serum TNFalpha fails to inhibit bone formation in TNFR1 deficient mice.在牵张成骨过程中直接的骨形成并不需要 TNFalpha 受体,并且升高的血清 TNFalpha 并不能抑制 TNFR1 缺陷型小鼠的骨形成。
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