华西口腔医学杂志

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XW630促进去势大鼠骨组织成骨作用的实验研究

费伟,王大章,郑虎,翁玲玲   

  1. 610072 四川省人民医院口腔颌面外科(费 伟), 四川大学华西口腔医学院口腔颌面外科学教研室(王大章),四川大学华西药学院药物化学研究室(郑 虎,翁玲玲)
  • 收稿日期:2001-12-25 修回日期:2001-12-25 出版日期:2001-12-20 发布日期:2001-12-20
  • 基金资助:
    本课题为国家自然科学基金资助项目(编号39430120)

Effects of XW630 on Mechanical Properties and Trabecular Structure Parameters of Bone Tissue in Ovariectomized Rats

Fei Wei, Wang Dazhang, Zheng Hu, et al.   

  1. Fei Wei Department of Oral andMaxillofacialSurgery, Sichuan Provincial Peoplecs Hospital Wang Dazhang, Zheng Hu, Weng Lingling West China University of MedicalSciences
  • Received:2001-12-25 Revised:2001-12-25 Online:2001-12-20 Published:2001-12-20

摘要:

目的:探讨抗骨质疏松新药XW630在去势大鼠骨组织成骨中的作用。方法:3月龄SD雌性大鼠36只,随机分为4组,即Sham组、OVX组、OVX加雌酚酮组和OVX加XW630组,每组3只。术后30、60、90 d各处死1组动物, 取两侧胫骨作HE和SEM组织学观察,取1侧股骨作三点弯曲力学强度测试。结果:HE和SEM观察发现,OVX组胫骨干骺端术后30 d即呈骨丢失状态,并持续至整个观察期。应用雌酚酮和XW630治疗后,干骺端骨小梁出现不同程度的骨修复现象,整个观察期内XW630组成骨活动明显较雌酚酮治疗组活跃。整个观察期内,OVX组股骨三点弯曲强度呈下降趋势,与Sham组存在显著性差异(P<0101),两个治疗组骨强度则呈上升趋势,与OVX组存在显著性差异(P<0105和P<0101)。结论:XW630能有效地促进去势大鼠骨组织的成骨和预防骨质疏松性骨折的发生。

关键词: 骨质疏松症, 抗骨质疏松药, 成骨作用, 骨质量

Abstract:

Objective:The study aimed at investigating the effects of a new anti-osteoporotic drug, XW630 on promoting the osteogenic activity of bone tissue in ovariectomized rats.Methods:Thirty-six female SD rats, three months old, were randomly divided into four groups: sham-operated group (sham), the ovariectomized group (OVX), the esterone-therapy group (OVX+CFT) and the XW630-therapy group (OVX+XW630). Three rats in each group were killed on the 30th, 60th, and 90th day after the opera- tion. The femur of one side was taken for the three-point bending resistance test, and the bilateral tibias were taken for the HE stain and scanning electronic microscopy (SEM) examination.Results:The HE and SEM results indicated that the bone loss ap- peared in the OVX group 30 days after the operation, which lasted for the whole observing period. While after application of es- terone and XW630, there were different degrees of bone repairing around the trabeculae, and the osteogenic activity was obviously active in the XW630 group than that in the esterone group. During the experimental period, the three-point bending resistance of the OVX group gradually decreased and there was a significantdifference comparedwith thatof the shamgroup (P<0.01), while the three-point bending resistance of the two therapy group gradually increased and there was significant difference between the OVX group and the XW630 group (P<0.05 andP<0.01).Conclusion:XW630 can effectively promote osteogenic action and prevent osteoporostic fracture in ovariectomized rats.

Key words: osteoporosis, anti-osteoporostic drugs, osteogenic activity, bone quality