Long-term pretreatment with alendronate inhibits calvarial defect healing in an osteoporotic rat model

被引:2
作者
Zhang, Chenggui [1 ,2 ]
Zhu, Junxiong [1 ,2 ]
Jia, Jialin [1 ,2 ]
Guan, Zhiyuan [1 ,2 ]
Sun, Tiantong [1 ,2 ]
Zhang, Wang [1 ,2 ]
Yuan, Wanqiong [1 ,2 ]
Wang, Hong [1 ,2 ]
Song, Chunli [1 ,2 ]
机构
[1] Peking Univ Third Hosp, Dept Orthoped, 49 Huayuan North Rd, Beijing 100191, Peoples R China
[2] Beijing Key Lab Spinal Dis, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Alendronate; Osteoporotic; Calvarial defect; Inhibit; Parathyroid hormone; PARATHYROID-HORMONE; ZOLEDRONIC ACID; CANCELLOUS BONE; COMBINATION; EXPRESSION; INCREASE; REPAIR; BMP-7; GRAFT;
D O I
10.1007/s00774-021-01235-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction This study aimed to observe the effects of long-term alendronate pretreatment on the healing of osteoporotic calvarial defects, and further investigate the effect of alendronate combined with once-weekly parathyroid hormone following 12 weeks of alendronate treatment in ovariectomized rats. Materials and methods Thirty 3-month-old female rats were ovariectomized, and 24 rats received alendronate for 12 weeks. Then, a critical defect was created in the calvaria of all animals. Immediately after osteotomy, the animals received one of five treatments for 8 weeks: (1) continuation of vehicle (group E), (2) alendronate followed by vehicle (group A), (3) continuation of alendronate (group B), (4) alendronate followed by once-weekly parathyroid hormone alone (group C), or (5) continuation of alendronate combined with once-weekly parathyroid hormone (group D). Calvarial defect healing was assessed using dual-energy X-ray absorptiometry, micro-computed tomography, histology, and sequential fluorescence labeling. Results Group E showed a significantly higher volume of newly formed bone than groups A, B, C, and D. Evidence of new dense bone formation in group E was observed histologically. In addition, the immunohistochemical expression of runt-related transcription factor 2 was increased in group E but inhibited in groups A, B, C, and D. Sequential immunofluorescence also showed inhibited mineral apposition in groups A, B, C, and D compared with group E. Conclusion The present study shows that long-term pretreatment with alendronate inhibited calvarial defect healing in osteoporotic rats, and this effect could not be reversed by stopping alendronate, switching to parathyroid hormone, or combining with once-weekly parathyroid hormone.
引用
收藏
页码:925 / 933
页数:9
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