Intraosseous BMP implants in rabbits -: Inhibitory effect on bone formation

被引:32
作者
Jeppsson, C
Boström, M
Aspenberg, P [1 ]
机构
[1] Univ Lund Hosp, Dept Orthoped, SE-22185 Lund, Sweden
[2] Hosp Special Surg, New York, NY 10021 USA
来源
ACTA ORTHOPAEDICA SCANDINAVICA | 1999年 / 70卷 / 01期
关键词
D O I
10.3109/17453679909000963
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The bone harvest chamber is a model for rapid spontaneous bone healing in rabbits. We have previously shown inhibition of bone formation by using BMP-P on a collagen carrier in this intraosseous model, despite bone formation when depositing BMP-2 on a similar carrier subfascially in the same animals. The doses were 12 and 0.6 mu g/ 5 mm(3) chamber volume. As these findings conflicted with most other experiments dealing with the skeletal response to BMP-2, we repeated the previous experiments with variations. We studied: 1) a lower BMP-P dose, 2) a different type of BMP (BMP-7/OP-1), 3) a different carrier (hydroxyapatite), 4) a different chamber construction allowing contact with extraskeletal tissue and 5) BMP-2 on the original collagen carrier in an acutely inserted chamber in rats. We also studied the border between the BMP-P implant and the preexisting bone to see whether BMP-2 caused premature differentiation of the callus so that proliferation was stopped and a bone cyst formed, The low dose of BMP-2 reduced tissue ingrowth and tended to reduce bone formation. BMP-7 showed the same inhibitory effects as BMP-2. BMP-2 on a hydroxyapatite carrier also inhibited bone formation in the chamber. In the chamber that allowed contact with extraskeletal tissue, we observed no effects of BMP-2. The border between the BMP-2 implant and the preexisting bone did not look like a cyst wall. BMP-2, from the same batch, on a similar collagen carrier, regularly increased bone formation in the acutely inserted bone chamber in rats, thereby excluding major defects in the BMP-2 implants. The inhibition in this specific model is a consistent finding and not due to an overdose, a specific BMP-type, a specific carrier or premature callus differentiation.
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页码:77 / 83
页数:7
相关论文
共 16 条
[1]
ALBREKTSSON T, 1984, BIOMATERIALS BIOMECH, P283
[2]
[Anonymous], EUR J EXP MUSCULOSKE
[3]
Bone graft proteins influence osteoconduction - A titanium chamber study in rats [J].
Aspenberg, P ;
Tagil, M ;
Kristensson, C ;
Lidin, S .
ACTA ORTHOPAEDICA SCANDINAVICA, 1996, 67 (04) :377-382
[4]
Transforming growth factor beta and bone morphogenetic protein 2 for bone ingrowth: A comparison using bone chambers in rats [J].
Aspenberg, P ;
Jeppsson, C ;
Wang, JS ;
Bostrom, M .
BONE, 1996, 19 (05) :499-503
[5]
Bostrom MPG, 1998, CLIN ORTHOP RELAT R, P221
[6]
THE EFFECT OF RECOMBINANT HUMAN OSTEOGENIC PROTEIN-1 ON HEALING OF LARGE SEGMENTAL BONE DEFECTS [J].
COOK, SD ;
BAFFES, GC ;
WOLFE, MW ;
SAMPATH, TK ;
RUEGER, DC ;
WHITECLOUD, TS .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1994, 76A (06) :827-838
[7]
GOODMAN SB, 1994, ACTA ORTHOP SCAND S, V258, P65
[8]
BMP-2 can inhibit bone healing - Bone-chamber study in rabbits [J].
Jeppsson, C ;
Aspenberg, P .
ACTA ORTHOPAEDICA SCANDINAVICA, 1996, 67 (06) :589-592
[9]
Marcias D, 1997, DEVELOPMENT, V124, P1109
[10]
BONE AND CARTILAGE DIFFERENTIATION [J].
REDDI, AH .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (05) :737-744