中药葛根素对青年大鼠峰值骨量的影响研究
Effect of Puerarin on peak bone mass in young rats
  
DOI:10.3969/j.issn.1006.7108.2018.04.019
中文关键词:  葛根素  峰值骨量  骨密度  青年大鼠
英文关键词:Puerarin  Peak bone mass  Bone mineral density  Young rats
基金项目:国家自然科学基金面上项目(81471090);甘肃省自然科学基金(1506RJZA306)
作者单位
葸慧荣1 李文苑1 杨芳芳1 马慧萍2 陈克明1* 1.兰州军区兰州总医院骨科研究所甘肃 兰州 730050 2.兰州军区兰州总医院药剂科甘肃 兰州 730050 
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中文摘要:
      目的 探究葛根素(puerarin,PR)是否能提高青年大鼠的峰值骨量,起到预防骨质疏松症的作用。方法 1月龄Wistar雌性健康大鼠36只,按随机数表法分为3组,每组12只,分别为对照组(control,CON)、淫羊藿苷组(icariin,ICA,阳性对照)和葛根素组(puerarin,PR)。ICA组灌胃淫羊藿苷25 mg/(kg·d),PR组灌胃葛根素15.4 mg/(kg·d),CON组灌胃等体积蒸馏水。待各组间骨密度有显著差异后(两个月后)处死所有大鼠,进行重要脏器的器官指数计算,采用HE染色进行病理学分析、双能X线骨密度仪检测椎骨和股骨离体骨密度、万能材料试验机进行骨生物力学检测、ELISA试剂盒进行血清骨代谢指标检测以及VG染色进行骨形态计量学的检测。结果 在实验期间各组大鼠体重均呈上升趋势,但组间无显著差异;各组间主要脏器肺、肾、子宫等的器官指数无明显差异,病理学观察也未见异常改变;骨密度结果显示:灌胃给药前,CON组、 ICA组和PR组大鼠全身骨密度均无统计学意义,灌胃4 w时,与CON组比较, ICA组和PR组大鼠全身骨密度有升高趋势,但无统计学意义(P均>0.05),灌胃8 w时ICA组和PR组大鼠骨密度显著升高,且差异具有统计学意义(P均<0.05);与CON组相比,ICA组和PR组股骨离体骨密度均显著升高(P均<0.01), 椎骨离体骨密度显著升高(P均<0.05);生物力学结果:与CON组相比,ICA组和PR组大鼠股骨和椎骨的最大载荷值均显著升高(P<0.01,P<0.05),弹性模量值也均显著升高(P均<0.05);骨形态计量学VG染色结果分析:与CON组相比,ICA组和PR组股骨中骨小梁数目(trabecular number,Tb.N)、骨小梁厚度(trabecular thickness,Tb.Th)和骨体积/组织体积(bone volume/tissue volume,BV/TV)值均显著升高(P均<0.05),而骨小梁分离度(trabecular Spacing,Tb.Sp)显著下降(P<0.01)。血清骨代谢指标检测结果:与CON组比较,ICA组和PR组骨钙素 (osteocalcin,OC) 含量值显著升高(P均<0.05),而抗酒石酸酸性磷酸酶 (tartrate-resistant acid phosphatase?5b,TRACP 5b)含量均显著降低(P均<0.05)。结论 葛根素能显著提高青年大鼠的峰值骨密度和骨质量,增强股骨和椎骨生物力学性能,改变骨形态计量学,其可能机制是具有提高骨形成和抑制骨吸收的双重活性。
英文摘要:
      Objective To investigate whether Puerarin (PR) can improve the peak bone mass of young rats and play a role in the prevention of osteoporosis. Methods Thirty-six Wistar female healthy rats were randomly divided into four groups: control group (CON), Icariin (ICA, positive control group) and Puerarin group (PR). ICA group was administered with icariin 25 mg/ (kg ? d), rats in the PR group were treated with Puerarin 15.4 mg/ (kg ? d), and the control group was administered with equal volume of distilled water. All rats were sacrificed after significant differences in bone mineral density (after 2 months) were observed among the groups. The organ index of vital organs was calculated. Pathological analysis was performed by HE staining. Vertebrae and femur were assessed by dual energy X-ray absorptiometry for bone mineral density, universal testing machine was used for bone biomechanical testing, ELISA kits were used to assess serum bone metabolism indicators and VG staining was used for bone morphometric examination. Results Body weight increased in all three groups, but here were no significant differences in body weight and organ index of lung, kidney and uterus among the groups during the experiment. No pathological changes were observed in the pathology examination. At baseline, there were no significant differences in bone mineral density among the CON group, ICA group and the PR group, and the increase in bone mineral density in ICA group and PR group was not significantly different from that of the CON group at 4 weeks after the intragastric administration (both P>0.05). However, compared with CON group, bone mineral density of ICA group and PR group significantly increased (both P<0.01) at the end of the 8 weeks. Biomechanical results: Compared with CON group, the maximum load values ??of femur and vertebrae of ICA group and PR group significantly increased (P <0.01, P<0.05). Bone histomorphometry VG staining analysis: compared with CON group, the number of trabecular (Tb.N), trabecular thickness (Tb.Th) and bone volume / tissue volume (BV/TV) values ?significantly increased (all P<0.05), and trabecular spacing (Tb.Sp) was significantly lower (P<0.01). Compared with CON group, the levels of osteocalcin (OC) in ICA group and PR group were significantly higher (both P<0.05), and of Tartrate-resistant acid phosphatase 5b (TRACP 5b) were significantly lower (both P<0.05). Conclusion Puerarin can significantly improve the peak bone mineral density and bone mass of young rats, enhance the biomechanical properties of femur and vertebrae, and change the bone histomorphometry properties. The possible mechanism is that it has the dual activity of improving bone formation and inhibiting bone resorption.
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