期刊文献+

牵张成骨矫治腭裂成骨区碱性磷酸酶表达的研究 被引量:1

Expression of Alkaline Phosphatase in New Bone Following Distraction Osteogenesis for Repair of Cleft Palate in Cats
下载PDF
导出
摘要 目的:研究牵张成骨术整复腭裂骨缺损新骨生成过程中碱性磷酸酶(ALP)的表达与分布,探讨新骨生成与改建的变化规律。方法:家猫20只为实验对象。实验组:建立腭裂模型后以0.4mm/次,2次/d速率牵张整复腭部组织缺损。术后第2、4、6、8及12周分别处死3只动物,分析ALP在新骨组织中表达与分布。结果与实验对照组及空白对照组比较。结果:术后2周为成骨早期,即出现ALP高水平表达;术后4~6周为成骨中期,ALP强表达于成骨细胞膜及骨基质;术后8~12周则为成骨后期,ALP表达趋于静止。结论:牵张成骨法以新生骨组织修复腭裂骨缺损并最终改建成熟。 Objective: To study the expression and distribution characteristics of alkaline phosphatase (ALP) in new formed bone following distraction osteogenesis (DO) correction for cleft palate (CP) bone defect and to discuss the patterns of new bone formation and remodeling. Methods: Twenty cats were divided randomly into 3 groups. For the experimental group, the bone defects of hard palate in CP animal models were corrected by DO technique at the rate of 0.4mm twice per day, until the transport disc (TD) reached the opposite edge across the defect region. The specimens were retrieved at 2, 4, 6, 8 and 12 weeks after completion of distraction. The expression and distribution of ALP were analyzed by means of enzyme histochemistry, and the results were then compared with those of experimental control and empty control groups. Results: A dynamic trend of new bone formation and remodeling was revealed: early bone formation stage in 2 weeks with early high level ALP expression, intermediate stage through 4 to 6 weeks with highest level ALP expression and later remodeling stage of 8 to 12 weeks with normal ALP expression. Conclusion: The correction of DO for CP could get steadily new bone formation and gradually remodeling to mature bone structure.
出处 《天津医药》 CAS 北大核心 2007年第4期270-271,F0003,共3页 Tianjin Medical Journal
基金 国家自然科学基金资助项目(项目编号:30500533) 天津市自然科学基金资助项目(项目编号:043609111)
关键词 骨生成 腭裂 模型 动物 碱性磷酸酶 osteogenesis cleft palate model, animal alkaline phosphatase
  • 相关文献

参考文献7

二级参考文献28

  • 1王常勇.人重组骨形成蛋白的研究进展[J].国外医学(口腔医学分册),1995,22(1):11-15. 被引量:2
  • 2金行晴.血管化和非血管化骨移植的实验比较研究(博士研究生论文)[M].上海:上海第二医科大学,1992.34-45.
  • 3[1]Karp NS, Thorne CHM, McCarthy JG, et al. Bone lengthening in the craniofacial skeleton. Ann Plast Surg, 1990,24:231
  • 4[2]Aronson J, Good B, Stewart C, et al. Preliminary studies of mineralization during distraction osteogenesis. Clin Orthop, 1990,250:43
  • 5[3]Delloye C, Delefortrie G, Coutelier L, et al. Bone regenerate formation in cortical bone during distraction osteogenesis. Clin Orthop, 1990,250:34
  • 6[4]Aronson J. Temporal and spatial increases in blood flow during distraction osteogenesis. Clin Orthop, 1993,301:124
  • 7[5]Karp NS, McCarthy JG, Schreiber JS, et al. Membranous bone lengthening: A serial histological study. Ann Plast Surg, 1992,29:2
  • 8[6]Rachmiel A, Potparic Z, Jackson IT, et al. Midface advancement by gradual distraction. Br J Plast Surg, 1993,46:201
  • 9[7]Rhee C, Smith R, Kobayashi K, et al. The use of tissue expansion to elongate the latissimus dorsi myocutaneous flap in the pig model. Eur J Plast Surg, 1995,18:281
  • 10[8]Oda T, Sawaki Y, Fukuta K, et al. Segmental mandibular reconstruction by distraction osteogenesis under skin flaps. Int J Oral Maxillofac Surg, 1998,27:9

共引文献27

同被引文献18

  • 1Wang DZ,Chen G,Liao YM,et al.A new approach to repairing cleft palate and acquired palatal defects with distraction ostongenesis.Int J Oral Maxillofac Surg,2006,35(8):718-726.
  • 2Livak K J,Schmittgen TD.Analysis of relative gene expression data using real-time quantitative PCB and the 2 (-Deha Delta C(T)) Method.Methods,2001,25(4):402-408.
  • 3Kuliwaba JS,Fazzalari NL,Findlay DM.Stability of RNA isolated from human trabecular bone at post-mertem and surgery.Binehim Biophys Acta,2005,1740(1):1-11.
  • 4Aronson J.Experimental and clinical experience with distrnetion ostcogenesis.Cleft Palate Craniofac,1994,31(6):473-482.
  • 5Carls FR,Schtlpbach P,Sailer HF,et al.Distraction coteogenesis for lengthening of the hard palate:Part Ⅱ.Histological studty of the hard and soft palate after distraction.Plast Reconstr Surg,1997,100 (7):1648-1654.
  • 6Jacobsen KA,AI-Aql ZS,Wan C,et al.Bone formation during distraction estcogenesis is dependent on both VEGFR1 and VEGFR2 signaling.Bone Miner Res,2008,23(5):596-609.
  • 7Yates KE,Troulis M J,Kaban LB,et al.IGF-I,TGF beta,and BMP-4 are expressed during distraction osteogenesis of the pig mandible,im J Oral Maxillofac Surg,2002,31(2):173-178.
  • 8Bail HJ,Kolbeck S,Lindner T,et al.The effect of growth hormone on insulin-like growth factor I and bone metabolism in distraction ostengenesis.Growth Horm IGF Res,2001,11 (5):314-323.
  • 9Haque T,Amako M,Nakada S,et al.An immunohistochemieal analysis of the temporal and spatial expression of growth factors FGF 1,2 and 18,IGF 1 and 2,and TGF betal during distraction osteogenesis.Histol Histopatbol,2007,22(2):119-228.
  • 10Theyse IF,Oosterlaken-Dijksterhuis MA,van Doom J.Expression of osteotropic growth factors and growth hormone receptor in a canine distraction ostcogenesis model.J Bone Miner Metab,2006,24(4):266-273.

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部