咬合支持改变对幼年大鼠骨代谢及骨微结构影响的研究
Effects of occlusal support changes on bone metabolism and bone microstructure in juvenile rats
  
DOI:10.3969/j.issn.1006-7108.2022.02.011
中文关键词:  幼年大鼠  咬合支持改变  应激  HPA轴  骨小梁
英文关键词:young rats  occlusal support changes  stress  HPA axis  trabecular bone
基金项目:新疆维吾尔自治区自然科学基金(2016D01C316)
作者单位
刘艳飞1,2 李伯琦1,2 陈朝旭1,2 刘奕杉1,2* 1.新疆医科大学第一附属医院(附属口腔医院)儿童口腔科-口腔预防科新疆 乌鲁木齐 830054 2.新疆维吾尔自治区口腔医学研究所新疆 乌鲁木齐 830054 
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中文摘要:
      目的 研究咬合支持改变对幼年大鼠骨骼生长的影响及其与应激有关HPA轴的作用机制。方法 4~5周龄雄性SD大鼠,随机分为正常对照组(A组)、单侧上颌磨牙拔除组(B组)、双侧上颌磨牙拔除组(C组),每组6只;记录大鼠术后4、8周体重,ELISA检测大鼠术后4、8周HPA轴及骨代谢相关激素水平,术后8周用HE染色检测股骨骨小梁组织学改变及Micro-CT检测股骨骨小梁骨微结构的改变。结果 各组大鼠体重差异无统计学意义。术后4、8周实验组大鼠血浆CRH、ACTH、CORT水平显著升高,BGP水平显著下降趋势。造模8周后实验组股骨骨小梁数量明显减少,骨小梁变细,排列疏松。BV/TV和Tb.Th及TN显著降低,Tb.Sp显著升高。结论 幼年大鼠牙齿咬合支持改变使股骨骨小梁形态改变、增加骨质丢失,其机制与脑区HPA轴功能异常影响骨代谢有关。
英文摘要:
      Objective To study the effects of occlusal disharmony on the growth and development of bone in young rats and the mechanism with HPA axis related to stress. Methods 4-5-week male SD rats were randomly divided into normal control group, unilateral maxillary molar extraction group, and bilateral maxillary molar extraction group, with 6 rats in each group, After 4 and 8 weeks of operation, the levels of HPA axis and bone metabolism related hormones were detected using ELISA. Histological changes of the femoral trabecular were detected with HE staining. The microstructural changes in trabecular bone of the femur were detected with micro-CT after 8 weeks. Results There was no significant difference in body weight among rats in each group. Serum levels of CRH, ACTH, and CORT in the experimental group increased significantly and the BGP level decreased significantly after 4 and 8 weeks. The number of trabeculae of the femoral bone decreased obviously after 8 weeks of modeling. The trabeculae became thinner and loose. BV/TV, Tb.Th, and TN decreased significantly, and Tb.Sp increased significantly. Conclusion The changes of dental occlusal support in juvenile rats result in changes of trabecular bone morphology and increase in bone loss. The mechanism is related to the abnormal HPA axis function in brain region.
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