Vegger Jens Bay, Brüel Annemarie, Sørensen Thomas Givskov, Thomsen Jesper Skovhus
Department of Biomedicine, Health, Aarhus University, Wilhelm Meyers Allé 3, 8000, Aarhus C, Denmark.
Calcif Tissue Int. 2016 Feb;98(2):206-14. doi: 10.1007/s00223-015-0077-3. Epub 2015 Nov 5.
Strontium ranelate (SrR) has both bone anabolic and anti-resorption properties and has therefore the potential to increase the healing of bone defects. The aim of the present study was to investigate the effect of systemic treatment with SrR during the healing of cortical bone defects in rats. In addition, the vertebral bodies were examined in order to elucidate the effect of short-term treatment with SrR on intact trabecular bone. Sixty 16-week-old female Wistar rats were randomized into four groups. A cylindrical defect was drilled through the anterior cortex of the mid-femoral diaphysis in both hind limbs. Two of the groups were treated with SrR (900 mg/kg b.w.) mixed into the food and two groups served as controls. The animals were euthanized after either 3 or 8 weeks of treatment. Healing of the defects was analyzed with µCT, mechanical testing, and stereology. Treatment with SrR resulted in increased thickness of the defects after 3 weeks of treatment, whereas no effect on bone volume fraction (BV/TV), mechanical properties (maximum strength and maximum stiffness), periosteal callus volume, or osteoclast-covered bone surfaces (Oc.S/BS) after either 3 or 8 weeks of treatment was found. Furthermore, SrR increased the bone material density (ρ) of the vertebral bodies, and tended to increase BV/TV after 8 weeks of treatment (p = 0.087). The mechanical properties of the vertebral bodies were not influenced by SrR treatment. In conclusion, 3 weeks of treatment with SrR increased the thickness of the healing mid-femoral cortical bone defects in rats, but did not influence BV/TV, mechanical properties, periosteal callus volume, or Oc.S/BS after either 3 or 8 weeks. Furthermore, SrR had no effect on the microstructure and mechanical properties of the vertebral bodies.
雷奈酸锶(SrR)具有骨合成代谢和抗骨吸收特性,因此有增加骨缺损愈合的潜力。本研究的目的是调查在大鼠皮质骨缺损愈合过程中全身应用SrR的效果。此外,对椎体进行检查,以阐明短期应用SrR对完整小梁骨的影响。将60只16周龄雌性Wistar大鼠随机分为四组。在双侧后肢股骨骨干中段的前皮质钻一个圆柱形缺损。其中两组用混入食物中的SrR(900 mg/kg体重)治疗,两组作为对照。治疗3周或8周后对动物实施安乐死。用μCT、力学测试和体视学分析缺损的愈合情况。治疗3周后,SrR治疗导致缺损厚度增加,而在治疗3周或8周后,未发现对骨体积分数(BV/TV)、力学性能(最大强度和最大刚度)、骨膜骨痂体积或破骨细胞覆盖骨表面(Oc.S/BS)有影响。此外,SrR增加了椎体的骨材料密度(ρ),并且在治疗8周后有增加BV/TV的趋势(p = 0.087)。SrR治疗对椎体的力学性能没有影响。总之,SrR治疗3周增加了大鼠股骨中段皮质骨缺损愈合的厚度,但在治疗3周或8周后未影响BV/TV、力学性能、骨膜骨痂体积或Oc.S/BS。此外,SrR对椎体的微观结构和力学性能没有影响。