Arosarena Oneida A, Falk Arthur, Malmgren Leslie, Bookman Linda, Allen Matthew J, Schoonmaker Joanne, Tatum Sherard, Kellman Robert
Division of Otolaryngology, Department of Surgery, University of Kentucky Medical Center, 800 Rose St, Room C236, Lexington, KY 40536-0293, USA.
Arch Facial Plast Surg. 2003 Jan-Feb;5(1):103-8. doi: 10.1001/archfaci.5.1.103.
To investigate the ability of a bone growth factor mixture and bone marrow cells to repair a critical size defect of the rat mandibular body.
Prospective, randomized controlled trial.
Thirty-seven male Fischer rats.
Critical size defects 4 mm in diameter were created in the left mandibular bodies of the rats. The defects were filled with a bone marrow cell suspension (group 1), a synthetic bone matrix consisting of bovine collagen and calcium hydroxyapatite cement (group 2), the matrix and marrow cells (group 3), the matrix with 100 micro g of bone growth factor mixture (group 4), or the matrix with bone growth factor mixture and marrow cells (group 5). Animals were killed after 8 weeks, and the nondemineralized specimens were processed histologically. Specimens from group 1 were not processed because there was no grossly appreciable bone regeneration. Stereologic techniques were used to determine and compare the volume fractions and volume estimates of mature bone, new bone, osteoid, marrow, remaining cement, and fibrous tissue in each defect.
Volumes of mature bone, new bone, and remaining cement did not differ significantly among the groups (P =.30 for mature bone, P =.17 for new bone, and P =.34 for cement). However, group 4 and 5 specimens contained significantly more osteoid and larger marrow spaces than did the group 2 and 3 specimens (P<.001 for both). The specimens in groups 2 and 3 contained significantly more fibrous tissue ingrowth than did those in groups 4 and 5 (P<.001).
The synthetic bone substitute containing bone growth factor mixture was effective in stimulating new bone and osteoid development in the rat mandibular model.
研究骨生长因子混合物与骨髓细胞修复大鼠下颌骨体临界尺寸缺损的能力。
前瞻性随机对照试验。
37只雄性Fischer大鼠。
在大鼠左侧下颌骨体制造直径4mm的临界尺寸缺损。缺损处分别填充骨髓细胞悬液(第1组)、由牛胶原蛋白和羟基磷灰石水泥组成的合成骨基质(第2组)、该基质与骨髓细胞(第3组)、含有100μg骨生长因子混合物的基质(第4组)或含有骨生长因子混合物与骨髓细胞的基质(第5组)。8周后处死动物,对未脱钙标本进行组织学处理。第1组标本未进行处理,因为未观察到明显的骨再生。采用体视学技术测定并比较各缺损处成熟骨、新骨、类骨质、骨髓、剩余水泥和纤维组织的体积分数及体积估计值。
各组成熟骨、新骨和剩余水泥的体积无显著差异(成熟骨P = 0.30,新骨P = 0.17,水泥P = 0.34)。然而,第4组和第5组标本中的类骨质和骨髓腔明显多于第2组和第3组标本(两者P均<0.001)。第2组和第3组标本中的纤维组织向内生长明显多于第4组和第5组(P<0.001)。
含骨生长因子混合物的合成骨替代物在大鼠下颌骨模型中能有效刺激新骨和类骨质的形成。