Healing of fractures in osteoporotic rat mandible shown by the expression of bone morphogenetic protein-2 and tumour necrosis factor-α

被引:44
作者
Islam, AAS [1 ]
Rasubala, L [1 ]
Yoshikawa, H [1 ]
Shiratsuchi, Y [1 ]
Ohishi, M [1 ]
机构
[1] Kyushu Univ, Fac Dent Sci, Dept Oral & Maxillofacial Oncol, Fukuoka 8128582, Japan
关键词
TNF-alpha; BMP-2; osteoporosis; fracture healing;
D O I
10.1016/j.bjoms.2004.10.018
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
We studied the healing process of mandibular closed fractures in osteoporotic rats using specific antibodies to bone morphogenetic protein-2 (BMP-2) and tumour necrosis factor-alpha (TNF-alpha). We confirmed the osteoporosis in rats after oophorectomy by micro-CT, and then caused unilateral closed fractures in the mandible and monitored the healing process after 7, 14, 21, and 28 days. Data were compared simultaneously with those from a group of rats that had a sham operation. During healing of the fracture in the osteoporotic group there was a prolonged phase of endochondral ossification, with an increased number of osteoclasts (p < 0.01). Expressions of BMP-2 and TNF alpha were more pronounced in the osteoporotic group and there was an increase in the number of osteoblasts and TNF alpha(+) cells compared with the normal control (P < 0.01). BMP-2 was related to the differentiation of osteoblasts and the higher values of TNFa were correlated with the up-regulation of osteoclasts during the prolonged phase of bone turnover. We conclude that the healing of fractures in osteoporotic bone is delayed about a week compared with controls. In the healing of fractures in osteoporotic bone, there were more osteoblasts and osteoclasts but there was a predominance of osteoclasts probably induced by TNF alpha. The prolonged phase of bone turnover with osteoclast predominance in the osteoporotic group is suggestive of the cause of delay in the healing of the fracture. (c) 2005 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:383 / 391
页数:9
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