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Effect of chronic sleep deprivation on peak bone mass in rats: An experimental study

机译:慢性睡眠剥夺对大鼠骨质峰骨质的影响:实验研究

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Objective:To investigate the effects of chronic sleep deprivation(CSD)on bone microstructure and peak bone mass(PBM)in SD rats.Methods:Twenty-four SD rats were randomly divided into CSD group and control group.In the CSD group,a CSD model was established using a new sleep deprivation instrument for rats and mice,and intervened for 5 weeks.Bone turnover markers including P1NP and CTX-1 before and after the experiment were observed.After the experiment,the left femur were scanned by Micro-CT,and the cortical bone and bone trabecula were three-dimensionally reconstructed,respectively.The bone mineral density(BMD)and relevant parameters were detected.Results:CT images of the femur(proximal ends)showed significant trabecular loss in CSD rats.Trabecular parameters including bone volume fraction(BV/TV),trabecular number(Tb.N)and trabecular separation(Tb.Sp)in the CSD group were all lower than those in the control group.The bone cortex of the middle segment of the femur and tibia in CSD rats was also lower than that in the control group.The parameters of bone cortex including total tissue area(Tt.Ar),cortical bone area(Ct.Ar)and cortical bone thickness(Ct.Th)in the CSD group were significantly lower than those in the control group(P<0.01).After chronic CSD,BMD of both bone trabecula and bone cortex of the femur was lower,while the corresponding P1NP and CTX-1 were significantly higher than those in the control group.Conclusion:Sleep plays an important role in PBM formation.CSD accelerates bone turnover and thus significantly reducing PBM in SD rats.
机译:目的:探讨慢性睡眠剥夺(CSD)对SD大鼠骨微观结构和峰骨质量(PBM)的影响。方法:将二十四只SD大鼠随机分为CSD组和对照组。在CSD组,a CSD模型是使用用于大鼠和小鼠的新睡眠剥夺仪器建立,并介入5周。在实验之前和之后,包括P1NP和CTX-1,包括P1NP和CTX-1的替换标记。通过微量扫描左股骨扫描左侧股骨CT,皮质骨和骨小梁分别是三维重建的。骨矿物密度(BMD)和相关参数被检测到。结果:股骨(近端)的CT图像在CSD大鼠中显示出显着的小梁损失。TRABURAL CSD组中的骨骼体积分数(BV / TV),小梁数(TB.SH)和小梁分离(TB.SP)的参数均低于对照组中的骨髓内部段的骨皮层和CSD大鼠的胫骨还低于对照组中的骨皮层参数,CSD组中的总组织区域(TT.AR),皮质骨区(CT.AR)和皮质骨厚度(CT.TH)显着低于对照组(P <0.01)。慢性CSD中,股骨骨的BMD和股骨的骨皮层较低,而相应的P1NP和CTX-1显着高于对照组中的P1NP和CTX-1。结论:睡眠在PBM Flowation中发挥重要作用.CSD加速骨质转换,从而显着减少了SD大鼠的PBM。

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