代谢肥胖对雄性大鼠骨代谢影响
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1.山东第一医科大学第二附属医院;2.日照市人民医院;3.潍坊市益都中心医院

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R587

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山东省医药卫生科技发展计划项目(202003061132,202103061110);山东第一医科大学学术提升计划项目(2019QL017);潍坊市卫健委科研项目(wfwsjk_2019_121);潍坊市益都中心医院科研创新基金项目(ydky2021ms01, ydky2021ms06)


Effect of metabolic obesity on bone metabolism in male rats
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1.The Second Affiliated Hospital of Shandong First Medical University;2.Rizhao People'3.'4.s Hospital;5.Weifang Yidu Central Hospital

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    摘要:

    [目的] 探讨代谢肥胖对雄性SD大鼠青年期(17周龄)和成年期(27周龄)骨代谢的影响。[方法]5周龄雄性SD大鼠,按随机数字表法随机分成普食组(ND组)、高脂组(HFD组)。代谢肥胖造模成功后,检测不同时期各组P1NP、CTX-1及钙、磷水平。采用三点弯曲实验观察骨强度变化;采用微型CT检查观察骨微结构变化。[结果] 1.27周龄大鼠P1NP水平HFD组(426.57 ± 35.22 pg/ml)较ND组(578.82 ± 23.96pg/ml)下降(P<0.01),CTX-1水平较ND组升高(88.44±8.73 vs 142.60±13.74 pg/ml)(P<0.05)。2.与ND组相比,17周龄HFD组大鼠的小梁骨结构参数如Tb.vBMD(0.135±0.011 vs 0.105±0.007 g/mm3)、Tb.BV/TV(34.64±2.766 vs 27.16±1.808 %)、Tb.N(2.454±0.145 vs1.907±0.143 1/mm )明显下降(P<0.05),Tb. Sp(0.329±0.014 vs 0.538±0.068 um)明显升高(P<0.05);27周龄HFD组大鼠上述参数变化趋势更明显(P<0.01)。3.与ND组相比,27周龄HFD组大鼠最大负荷(300.46 ± 7.13 vs 242.54 ± 11.78 N )、最大断裂负荷(285.58± 10.09 vs 227.44 ± 14.17 N )、极限拉伸强度(11.24±0.28vs 9.07 ± 0.66 MPa )、韧性(779.90± 41.99 vs595.14 ± 31.13 N/mm )、能量吸收(192.89± 13.42 vs 138.61 ± 12.67 N*m )均降低(P<0.01或0.05) [结论] 代谢肥胖可降低骨形成标志物,升高骨吸收标志物,自青少年开始出现骨微结构改变,至成年骨微结构损伤加重,并出现了骨强度下降。

    Abstract:

    [Objective] To investigate the effect of metabolic obesity on bone metabolism in juvenile (17 weeks) and adulthood (27weeks) male SD rats. [Methods] Five week old male SD rats were randomly divided into normal control diet group (ND group) or high fat diet group (HFD group) according to random number table. After metabolic obesity models were successfully established, Type 1 procollagen N-terminal propeptide (P1NP), type 1 collagen C-terminal peptide (CTX-1)and the serum calcium and phosphorus levels were detected in different periods. Three-point bending test was performed to observe changes in bone strength. MicroCT examination was conducted to observe changes in bone microstructure. [Results] 1.Compared with ND group(578.82 ± 23.96pg/ml), P1NP(426.57 ± 35.22 pg/ml) was decreased (P<0.01), and CTX-1 (88.44±8.73 vs 142.60±13.74 pg/ml)was increased (P<0.05) in 27 week old HFD group. 2. Trabecular bone markers such as Tb. vBMD,(0.135±0.011 vs 0.105±0.007 g/mm3)、Tb.BV/TV(34.64±2.766 vs 27.16±1.808 %)、Tb.N(2.454±0.145 vs1.907±0.143 1/mm )were decreased, Tb. Sp(0.329±0.014 vs 0.538±0.068 um)was increased in 17 week old HFD group compared with ND group. The change trend of the above parameters was more obvious in 27 week old HFD group (P<0.01). 3.The maximum load(300.46 ± 7.13 vs 242.54 ± 11.78 N ), maximum fracture load(285.58± 10.09 vs 227.44 ± 14.17 N ), ultimate tensile strength(11.24±0.28vs 9.07 ± 0.66 MPa ), stiffness(779.90± 41.99 vs595.14 ± 31.13 N/mm ) and energy absorption(192.89± 13.42 vs 138.61 ± 12.67 N*m ) were decreased (P<0.01 or P<0.05) in 27 week old HFD group compared with ND group. [Conclusion] Metabolic obesity can reduce marker of bone formation and increase marker of bone resorption. Bone microstructural changes begin in adolescents, and bone microstructural damage increases and bone strength decreases in adults.

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  • 收稿日期:2022-04-07
  • 最后修改日期:2022-07-07
  • 录用日期:2022-10-09
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