2型糖尿病对小鼠骨代谢的影响
Effect of type 2 diabetes mellitus on bone metabolism : an in vivo study
  
DOI:
中文关键词:  2型糖尿病;骨代谢  骨量减少
英文关键词:Type 2 diabetes mellitus  Bone metabolism  Osteopenia
基金项目:国家自然科学基金资助项目(81070691)
作者单位
徐飞 董永辉 黄鑫 郭风劲 陈安民 黄仕龙 华中科技大学同济医学院附属同济医院骨科.武汉430030 
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中文摘要:
      目的观察2型糖尿病小鼠的骨代谢及骨微结构的特点。方法采用雄性KK/UpMy/J小鼠(自发性2型糖尿病模型 小鼠)10只作为实验组,同时选用10只雄性C57BL/6小鼠作为对照组。两组小鼠均给予常规饲料喂养,确认KK/UpMy/J小 鼠发病,继续饲养12周后处死所有小鼠,测定血清骨碱性磷酸酶(BALP)及抗酒石酸酸性磷酸酶(TRAP)活性,并运用Micro- CT分析小鼠胫骨微结构定量参数。结果与对照组相比,2型糖尿病小鼠血清BALP活性明显下降(分别为对照组:0. 029 士 0.003 pU/min,T2DM 组:0. 014 ± 0. 003 pU/min,尸 <0.05),血清 TRAP 活性明显升高(分别为对照组:0. 513 ± 0. 034 U/L, T2DM 组:0. 701 ±0.054 U/L,尸 <0. 05),胫骨平台处骨密度明显下降(对照组:810. 000 ±21. 000 mg/cm3,T2DM 组:709. 000 士 18. 000 mgjm3,P <0.05)。结论 2型糖尿病小鼠的骨吸收加快而骨形成不足,导致其骨量下降及骨折风险增大。
英文摘要:
      Objective To observe the effect of type 2 diabetes mellitus (T2DM) on bone metabolism and bone microstructure in mice. Methods Ten male KK/Upj~Ay/J mice,a mouse model of T2DM,were selected as experimental group,and 10 male C57BL/6 mice were selected as control group. The mice in both groups were fed with routine fodder. After the confirmation of T2DM in KK/Upj-Ay/J mice,all mice were fed for another 12 weeks and then executed. The activity of serum bone alkaline phosphatase (BALP) and tartrate-resistant acid phosphatase (TRAP) were detected. The parameters of the tibia were analyzed using micro-CT. Results Compared with those in control group, the activity of serum BALP in T2DM mice decreased significantly (control group : 0. 029 士 0. 003 |jlU/min; T2DM group : 0. 014 士 0. 003 |jlU/min,P <0. 05),while the activity of serum TRAP increased significantly (control group : 0. 513 ± 0. 034 U/L ; T2DM group : 0. 701 ±0. 054 U/L,P < 0. 05). The bone mineral density of the tibial plateau decreased significantly in T2DM group compared with that in control group (control group : 810. 000 士 21. 000 mg/cm3 ; T2DM group : 709. 000 士18. 000 mg/cm3,P < 0. 05). Conclusion The bone resorption in mice with T2DM accelerates while the bone formation is deficient,resulting in osteopenia and increased risk of bone fracture.
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