Fixation compliance in a mouse osteotomy model induces two different processes of bone healing but does not lead to delayed union

被引:39
作者
Groengroeft, Ina [2 ]
Heil, Petra [2 ]
Matthys, Romano [3 ]
Lezuo, Patrick [2 ]
Tami, Andrea [2 ]
Perren, Stephan [2 ,3 ]
Montavon, Pierre [4 ]
Ito, Keita [1 ,2 ]
机构
[1] Eindhoven Univ Technol, Dept Biomed Engn, NL-5600 MB Eindhoven, Netherlands
[2] AO Res Inst, Davos, Switzerland
[3] AO Dev Inst, Davos, Switzerland
[4] Univ Zurich, Vet Clin Small Anim Surg, CH-8006 Zurich, Switzerland
关键词
Fracture healing; Delayed union; Endochondral ossification; Intramembranous ossification; Mice; FRACTURE REPAIR; RAT;
D O I
10.1016/j.jbiomech.2009.06.004
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Delayed unions are a problematic complication of fracture healing whose pathophysiology is not well understood. Advanced molecular biology methods available with mice would be advantageous for investigation. In humans, decreased fixation rigidity and poor reduction are generally associated with delayed unions. In this study, these two factors were combined to observe their effect on bone healing in mice. Two plates with locking screws, one with 1/4 the bending stiffness of the other, were used to stabilize a 0.45 mm gap osteotomy. mu CT, radiographs, 4pt-bending tests and histological analysis demonstrated that the different plate types led to two different healing pathways. The less flexible bridging plate induced only intramembranous ossification whereas the more flexible bridging plate induced a mixture of endochondral and intramembranous ossification. However, the different plates led to a delay in healing of only 3-5 days in the period between 14 and 21 post-operative days. In mice, considerable fixation flexibility is necessary to induce secondary bone healing similar to that which occurs in humans, but this was not sufficient to induce a substantial delay in bone healing as would be expected in humans. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2089 / 2096
页数:8
相关论文
共 31 条
[1]   An externally fixed femoral fracture model for mice [J].
Cheung, KMC ;
Kaluarachi, K ;
Andrew, G ;
Lu, W ;
Chan, D ;
Cheah, KSE .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2003, 21 (04) :685-690
[2]   Influence of size and stability of the osteotomy gap on the success of fracture healing [J].
Claes, L ;
Augat, P ;
Suger, G ;
Wilke, HJ .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1997, 15 (04) :577-584
[3]   Altered fracture repair in the absence of MMP9 [J].
Colnot, C ;
Thompson, Z ;
Miclau, T ;
Werb, Z ;
Helms, JA .
DEVELOPMENT, 2003, 130 (17) :4123-4133
[4]  
Einhorn TA, 1998, CLIN ORTHOP RELAT R, pS7
[5]  
EINHORN TA, 1995, J BONE MINER RES, V10, P1272
[6]   Does adult fracture repair recapitulate embryonic skeletal formation? [J].
Ferguson, C ;
Alpern, E ;
Miclau, T ;
Helms, JA .
MECHANISMS OF DEVELOPMENT, 1999, 87 (1-2) :57-66
[7]   Osteogenic growth peptide modulates fracture callus structural and mechanical properties [J].
Gabet, Y ;
Müller, R ;
Regev, E ;
Sela, J ;
Shteyer, A ;
Salisbury, K ;
Chorev, M ;
Bab, I .
BONE, 2004, 35 (01) :65-73
[8]   Fracture healing as a post-natal developmental process: Molecular, spatial, and temporal aspects of its regulation [J].
Gerstenfeld, LC ;
Cullinane, DM ;
Barnes, GL ;
Graves, DT ;
Einhorn, TA .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 88 (05) :873-884
[9]   Differential inhibition of fracture healing by non-selective and cyclooxygenase-2 selective non-steroidal anti-inflammatory drugs [J].
Gerstenfeld, LC ;
Thiede, M ;
Seibert, K ;
Mielke, C ;
Phippard, D ;
Svagr, B ;
Cullinane, D ;
Einhorn, TA .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2003, 21 (04) :670-675
[10]  
Goldhahn S, 2000, Swiss Surg, V6, P315, DOI 10.1024/1023-9332.6.6.315