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Strontium ranelate stimulates trabecular bone formation in a rat tibial bone defect healing process

机译:雷奈酸锶刺激大鼠胫骨骨缺损愈合过程中的骨小梁形成

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摘要

Strontium ranelate treatment is known to prevent fractures. Here, we showed that strontium ranelate treatment enhances bone healing and affects bone cellular activities differently in intact and healing bone compartments: Bone formation was increased only in healing compartment, while resorption was reduced in healing and normal bone compartments.INTRODUCTION: Systemic administration of strontium ranelate (SrRan) accelerates the healing of bone defects; however, controversy about its action on bone formation remains. We hypothesize that SrRan could affect bone formation differently in normal mature bone or in the bone healing process.METHODS: Proximal tibia bone defects were created in 6-month-old female rats, which orally received SrRan (625 mg/kg/day, 5/7 days) or vehicle (control groups) for 4, 8, or 12 weeks. Bone samples were analyzed by micro-computed tomography and histomorphometry in various regions, i.e., metaphyseal 2nd spongiosa, a region close to the defect, within the healing defect and in cortical defect bridging region. Additionally, we evaluated the quality of the new bone formed by quantitative backscattered electron imaging and by red picosirius histology.RESULTS: Healing of the bone defect was characterized by a rapid onset of bone formation without cartilage formation. Cortical defect bridging was detected earlier compared with healing of trabecular defect. In the healing zone, SrRan stimulated bone formation early and laterly decreased bone resorption improving the healing of the cortical and trabecular compartment without deleterious effects on bone quality. By contrast, in the metaphyseal compartment, SrRan only decreased bone resorption from week 8 without any change in bone formation, leading to little progressive increase of the metaphyseal trabecular bone volume.CONCLUSIONS: SrRan affects bone formation differently in normal mature bone or in the bone healing process. Despite this selective action, this led to similar increased bone volume in both compartments without deleterious effects on the newly bone-formed quality.
机译:雷奈酸锶治疗可预防骨折。在这里,我们显示了雷奈酸锶治疗可促进骨骼的愈合并在完整和愈合的骨腔中不同地影响骨细胞的活动:仅在愈合腔中增加骨形成,而在正常和正常骨腔中吸收则减少。雷奈酸盐(SrRan)促进骨缺损的愈合;然而,关于其对骨形成作用的争议仍然存在。我们假设SrRan可能在正常成熟骨骼或骨骼愈合过程中影响骨骼形成。方法:六个月大的雌性大鼠产生了胫骨近端骨缺损,该大鼠口服SrRan(625 mg / kg / day,5 / 7天)或车辆(对照组)持续4、8或12周。通过微计算机断层摄影术和组织形态学分析在各个区域,即干phy端第二海绵体,靠近缺损的区域,在愈合缺损内以及在皮质缺损桥接区域中的骨样品。此外,我们通过定量反向散射电子成像和红色皮西里斯氏组织学评估了新骨的质量。结果:骨缺损的愈合以迅速形成骨而无软骨形成为特征。与骨小梁缺损的修复相比,皮质缺损的桥接被发现得更早。在愈合区,SrRan早期刺激骨形成,后来又减少了骨吸收,从而改善了皮质和小梁腔的愈合,而对骨质没有有害影响。相比之下,在干phy端区中,SrRan从第8周开始仅降低骨吸收,而骨形成没有任何变化,导致干phy端小梁骨体积的逐渐增加。结论:SrRan对正常成熟骨或骨骼中骨形成的影响不同。康复过程。尽管有这种选择性的作用,这仍导致两个隔室中的骨量增加,而对新骨形成的质量没有有害影响。

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