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 ...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.展开更多
Bone mass is a key determinant of osteoporosis and fragility fractures.Epidemiologic studies have shown that a 10%increase in peak bone mass(PBM)at the population level reduces the risk of fracture later in life by 50...Bone mass is a key determinant of osteoporosis and fragility fractures.Epidemiologic studies have shown that a 10%increase in peak bone mass(PBM)at the population level reduces the risk of fracture later in life by 50%.Low PBM is possibly due to the bone loss caused by various conditions or processes that occur during adolescence and young adulthood.Race,gender,and family history(genetics)are responsible for the majority of PBM,but other factors,such as physical activity,calcium and vitamin D intake,weight,smoking and alcohol consumption,socioeconomic status,age at menarche,and other secondary causes(diseases and medications),play important roles in PBM gain during childhood and adolescence.Hence,the optimization of lifestyle factors that affect PBM and bone strength is an important strategy to maximize PBM among adolescents and young people,and thus to reduce the low bone mass or osteoporosis risk in later life.This review aims to summarize the available evidence for the common but important factors that influence bone mass gain during growth and development and discuss the advances of developing high PBM.展开更多
基金2020 Youth Training Fund Project of the First Affiliated Hospital of Hainan Medical University(No.202010)
文摘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.
基金supported by the Zhejiang Provincial Natural Science Foundation for Distinguished Young Scholars of China(No.LR17H070001)the National Natural Science Foundation of China(No.81871831).
文摘Bone mass is a key determinant of osteoporosis and fragility fractures.Epidemiologic studies have shown that a 10%increase in peak bone mass(PBM)at the population level reduces the risk of fracture later in life by 50%.Low PBM is possibly due to the bone loss caused by various conditions or processes that occur during adolescence and young adulthood.Race,gender,and family history(genetics)are responsible for the majority of PBM,but other factors,such as physical activity,calcium and vitamin D intake,weight,smoking and alcohol consumption,socioeconomic status,age at menarche,and other secondary causes(diseases and medications),play important roles in PBM gain during childhood and adolescence.Hence,the optimization of lifestyle factors that affect PBM and bone strength is an important strategy to maximize PBM among adolescents and young people,and thus to reduce the low bone mass or osteoporosis risk in later life.This review aims to summarize the available evidence for the common but important factors that influence bone mass gain during growth and development and discuss the advances of developing high PBM.
