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Long-term pretreatment with alendronate inhibits calvarial defect healing in an osteoporotic rat model.
Zhang, Chenggui; Zhu, Junxiong; Jia, Jialin; Guan, Zhiyuan; Sun, Tiantong; Zhang, Wang; Yuan, Wanqiong; Wang, Hong; Song, Chunli.
Afiliación
  • Zhang C; Department of Orthopedics, Peking University Third Hospital, No. 49, Huayuan North Road, Haidian District, Beijing, 100191, China.
  • Zhu J; Beijing Key Laboratory of Spinal Diseases, Beijing, China.
  • Jia J; Department of Orthopedics, Peking University Third Hospital, No. 49, Huayuan North Road, Haidian District, Beijing, 100191, China.
  • Guan Z; Beijing Key Laboratory of Spinal Diseases, Beijing, China.
  • Sun T; Department of Orthopedics, Peking University Third Hospital, No. 49, Huayuan North Road, Haidian District, Beijing, 100191, China.
  • Zhang W; Beijing Key Laboratory of Spinal Diseases, Beijing, China.
  • Yuan W; Department of Orthopedics, Peking University Third Hospital, No. 49, Huayuan North Road, Haidian District, Beijing, 100191, China.
  • Wang H; Beijing Key Laboratory of Spinal Diseases, Beijing, China.
  • Song C; Department of Orthopedics, Peking University Third Hospital, No. 49, Huayuan North Road, Haidian District, Beijing, 100191, China.
J Bone Miner Metab ; 39(6): 925-933, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34091742
ABSTRACT

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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Densidad Ósea / Alendronato Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Bone Miner Metab Asunto de la revista: METABOLISMO Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Densidad Ósea / Alendronato Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Bone Miner Metab Asunto de la revista: METABOLISMO Año: 2021 Tipo del documento: Article País de afiliación: China