Andreen O, Larsson S E
Acta Orthop Scand. 1983 Dec;54(6):805-9. doi: 10.3109/17453678308992913.
Fracture healing was studied in male, adult Sprague-Dawley rats. Closed bilateral tibial fractures were observed to be clinically stable after 3 weeks. Parathyroidectomy (PTX) resulted in impaired fracture healing and several delayed unions. Fracture tensile strength, elastic stiffness and failure energy were significantly lower at the beginning of the healing period compared to that of control fracture rats. Treatment with low doses (60 ng/kg/day) of 1,25-dihydroxycholecalciferol (1,25(OH)2D3) increased early fracture bone formation and mineralization. However, these events did not result in a corresponding increase of tensile strength or failure energy compared with that of the controls. Increased bone turnover seemed to be the dominant characteristic and resulted in early resorption of periosteal callus. Toward the end of the healing period, fracture strength measured as tensile strength and failure energy actually decreased compared to that of the control rats. Elastic stiffness initially rose above control values due to increased mineralization, but declined later to control values.
在成年雄性斯普拉格-道利大鼠中研究骨折愈合情况。观察到闭合性双侧胫骨骨折在3周后临床稳定。甲状旁腺切除术(PTX)导致骨折愈合受损和多处延迟愈合。与对照骨折大鼠相比,在愈合期开始时,骨折的抗张强度、弹性刚度和破坏能量显著降低。用低剂量(60 ng/kg/天)的1,25-二羟基胆钙化醇(1,25(OH)2D3)治疗可增加早期骨折部位的骨形成和矿化。然而,与对照组相比,这些情况并未导致抗张强度或破坏能量相应增加。骨转换增加似乎是主要特征,并导致骨膜骨痂早期吸收。在愈合期接近尾声时,以抗张强度和破坏能量衡量的骨折强度实际上比对照大鼠降低了。弹性刚度最初因矿化增加而高于对照值,但后来又降至对照值。