黄芪散对肥胖模型大鼠胫骨骨结构的研究
The effect of astragalus powder on the tibia structure in obesity rats
  
DOI:10.3969/j.issn.1006-7108.2019.05.011
中文关键词:  黄芪散  肥胖  骨组织形态计量学  胫骨  大鼠  动物实验
英文关键词:astragalus powder  obesity  bone histomorphometry  tibia  rats  animal experiments
基金项目:国家自然科学基金面上项目(81473439);广东药科大学“创新强校工程资助项目”(2016KQNCX087)
作者单位
王芳1 陈珺2 曾煦欣3 陈艳芬1 李卫民4* 1.广东药科大学中药学院广东 广州 510006 2.广东药科大学生命科学与生物制药学院广东 广州 510006 3.佛山科学技术学院口腔医学院(医药工程学院)广东 佛山 528000 4.广州中医药大学中药学院广东 广州 510006 
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中文摘要:
      目的 观察黄芪散对肥胖模型大鼠胫骨上段松质骨和中段皮质骨的影响。方法 180~200 g雄性SD大鼠,实验分为正常组、高脂模型组、立普妥组(2 mg/kg)、黄芪散低剂量组(1.2 g/kg,10 mL/kg)、黄芪散高剂量组(2.4 g/kg,10 mL/kg);通过高脂饲料喂养诱导肥胖模型7周,造模成功后开始给药,持续给药15周,处死大鼠,对胫骨松质骨和皮质骨进行骨组织形态计量学考察。结果 与正常对照组相比,模型组胫骨松质骨骨小梁面积百分数(Tb.Ar%)、骨小梁宽度(Tb.Th)显著减少;胫骨中段骨皮质面积百分数(Ct.Ar%)明显增加,骨髓腔面积百分数(Ma.Ar%)明显减小,骨外膜面骨形成率(P-BFR/BS)降低。与模型组相比,黄芪散使胫骨上段的Tb.Ar%、Tb.Th、Tb.N均增加;新骨年形成率(BFR/BV)和中段骨Ma.Ar%明显减少,P-BFR/BS显著增加。结论 肥胖可致模型大鼠胫骨松质骨结构发生明显变化,呈现骨质疏松状态;皮质骨骨量增加。黄芪散可抑制肥胖引起大鼠胫骨松质骨的骨丢失,可维持肥胖引起大鼠胫骨皮质骨的促生长作用。其机制可能与抑制骨吸收有关,但对皮质骨无明显作用。
英文摘要:
      Objective To observe the effect of astragalus powder (HQS) on the cancellous bone and cortical bone of the tibia in obese rats. Methods Male SD rats (180-200g) were divided into normal group, high fat model group, Lipitor group (2 mg/kg), low-dose HQS group (1.2 g/kg, 10 mL/kg), and high-dose HQS group (2.4 g/kg, 10 mL/kg). Obesity model was established by high fat diet for 7 weeks. HQS was administrated after the modelling for 15 weeks and the rats were then sacrificed. Histomorphometric study of the cancellous bone and cortical bone of the tibia was performed. Results Compared with those in the normal control group, the percentage of trabecular area (Tb.Ar%) and bone trabecular width (Tb.Th) of the tibial cancellous bone in the model group decreased significantly, the percentage of cortical area in the middle section of the tibia (Ct.Ar%) increased significantly, and the percentage of bone marrow cavity area (Ma.Ar%) and the rate of bone formation of the outer membrane(P-BFR/BS) decreased. Compared with those in the model group, Tb.Ar%, Tb.Th, and Tb.Nof the upper segment of the tibia in HQS group increased, the annual formation rate of the new bone (BFR/BV) and Ma.Ar (%) of the middle segment decreased significantly, and P-BFR/BS increased significantly. Conclusion Obesity causes obvious changes in the structure of the tibial cancellous bone in the model rats, showing osteoporosis and increased cortical bone volume. HQS inhibits bone loss of the tibia cancellous bone caused by obesity, and maintains the promoting effect of obesity on the tibial cortical bone of rats. The mechanism may be related to the inhibition of bone resorption, but has no obvious effect on cortical bone.
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