期刊文献+

脱蛋白骨联合VEGF基因转染治疗股骨头缺血坏死 被引量:2

Deproteinized bone with VEGF gene transfer for avascular necrosis of the femoral head
下载PDF
导出
摘要 目的探索一种新的方法治疗股骨头早期缺血性坏死(avascular necrosis of the femoral head,AVNFH)。方法69只AVNFH造模成功后的新西兰大白兔随机分成3组。第1组,将脱蛋白骨(deprotein ized bone,DPB)复合pcDNA3.1/VEGF165质粒植入坏死的股骨头内,第2组植入DPB,第3组仅在股骨头内钻一隧道。术后3 d,1、2、4、8和16周获取标本。RT-PCR、W estern b lot和免疫组化技术分别检测VEGF165 mRNA、蛋白的表达及安全性。X线大体观察成骨情况,组织形态学分析血管发生和股骨头修复。结果第1组VEGF165 mRNA和蛋白表达术后1周达到高峰,时间持续超过3周,第1组动物术后远膈脏器未检测到VEGF165的表达。血管形成术后2,4周增加,骨形成术后2,4和8周增加,与另两组相比差异有显著性(P<0.01)。结论VEGF165基因转染可促进局部血管的早期形成,DPB-VEGF复合物可增加骨形成,VEGF基因治疗兔AVNFH有效、安全,脱蛋白骨联合VEGF165基因治疗为骨坏死的修复提供了理论基础。 Objective To explore a new method for early avascular necrosis of the femoral head ( AVNFH) therapy. Methods Sixty-nine New Zealand adult rabbits with a mean weight of 2.8 kg after AVNFH establishment were randomly divided into 3 groups. In group 1, the deproteinized bone (DPB) combined with the recombinant plasmid pcDNA3.1/VEGF165 was implanted in the drilled channel of the necrotic femoral head. In group 2, only DPB was implanted. In group 3, only channel was drilled without DPB or plasmid implantation. Femoral head specimens were obtained at 3 d, 1, 2, 4 and 8 weeks after operation. The expression of vascular endothelial growth factor (VEGF) and the security of this manipulation were examined by RT-PCR, Western blotting and immunohistochemical techniques. X-ray examined bone formation generally. Angiogenesis and repair of the femoral head were observed by histological and histomorphometric analysis. Results In group 1, the expression.of VEGF was detected in the femoral head implanted by DPB-VEGF compound. The expression of VEGF165 mRNA and protein reached the maximum in 1 week after implantation and lasted more than 3 weeks, but none of them were detected in distant organs. The femoral head implanted by DPB-VEGF compound showed a significant difference in vascularization at 2 and 4 weeks and a significant difference in bone formation at 2, 4 and 8 weeks after operation from those in other groups on histomorphometric analysis (P 〈 0.01 ). Conclusion The transfection of the VEGF165 gene enhances local angiogenesis in early stage and DPB-VEGF compound improves bone formation. VEGF gene therapy on rabbit AVNFH is effective and secure. The deproteinized bone combined with VEGF gene provides a potential method for therapy of osteonecrosis.
出处 《第三军医大学学报》 CAS CSCD 北大核心 2006年第3期215-219,共5页 Journal of Third Military Medical University
基金 重庆市卫生局资助项目(002010)~~
关键词 脱蛋白骨 血管内皮生长因子 基因治疗 股骨头缺血坏死 deproteinized bone vascular endothelial growth factor gene therapy avascular necrosis of the femoral head
  • 相关文献

参考文献6

二级参考文献16

  • 1丁真奇,谭富生,吴祖尧,曹本珍,蒋电明.四种移植材料修复兔颅骨缺损的比较研究[J].中华创伤杂志,1994,10(6):261-263. 被引量:61
  • 2傅荣,杨志明.骨膜成骨细胞培养与生物活性陶瓷复合的实验研究[J].中国修复重建外科杂志,1996,10(4):197-201. 被引量:22
  • 3Lin F H,Biomaterials,1999年,20卷,5期,475页
  • 4Egol KA, Jazrawi LM, DeWal H, et al. Orthopaedic manifestations of systemic lupus erythematosus. Bull Hosp Jt Dis 2001; 60 ( 1 ): 29 - 34
  • 5Sakai H, Okuda H, Yajima H, et al. Steroid-induced osteonecrosis of the femoral condyle in a pediatric patient with nephrotic syndrome. Am J Knee Surg 2002;15(1): 41-3
  • 6Berczi C, Asztalos L, Kincses Z, et al. Comparison of calcium and alfacalcidol supplement in the prevention of osteopenia after kidney transplantation. Osteoporos Int 2003; 14(5): 412 - 7
  • 7Arico M, Boccalatte MF, Silvestri D, et al. Osteonecrosis: An emerging complication of intensive chemotherapy for childhood acute lymphoblastic leukemia. Haematologica 2003;88(7): 747 -53
  • 8Korompilias AV, Gilkeson GS, Seaber AV, et al. Hemorrhage and thrombus formation in early experimental osteonecrosis. Clin Orthop 2001;(386): 11 -8
  • 9Matsui M, Saito S, Ohzono K, et al. Experimental steroid-induced osteonecrosis in adult rabbits with hypersensitivity vasculitis. Clin Orthop 1992; (277): 61 - 72
  • 10Nakata K, Masuhara K, Nakamura N, et al. Inducible osteonecrosis in a rabbit serum sickness model: deposition of immune complexes in bone marrow. Bone 1996; 18(6): 609 - 15

共引文献139

同被引文献18

  • 1孟纯阳,安洪,蒋电明,李玉宝.网孔纳米羟基磷灰石/聚酰胺人工骨修复兔桡骨缺损[J].中华创伤杂志,2005,21(3):187-191. 被引量:61
  • 2孟纯阳,安洪,蒋电明,高鹏飞.纳米羟基磷灰石/聚酰胺的细胞相容性研究[J].中华创伤骨科杂志,2005,7(8):749-752. 被引量:19
  • 3孟纯阳,安洪,蒋电明.新型纳米骨关节修复重建材料的生物活性及近期对机体钙磷代谢的影响[J].中国骨与关节损伤杂志,2005,20(10):682-684. 被引量:25
  • 4胡志明,王海彬,周明乾,姚新生,马骊,王小宁.激素性股骨头坏死股骨头微血管的变化[J].南方医科大学学报,2006,26(6):785-787. 被引量:13
  • 5Jie Wei, Yubao Li, Yi He. Processing properties of nano apatite--polyamide biocomposites[J]. Journal of materials Science, 2005,40:793-796.
  • 6Jie Wei,Yubao Li,W eiqun Chen,el al. A study on nano--composite Of hydr0xyapatite and polyamide[J]. Journal of materials Seienee, 2003,38 : 3303-3306.
  • 7Alex L,Joseph F,James JH. biostructural augmentation for the treatmerit of osteonecrosis: rationale, technique, and case exam- ple[J]. Journal of the Southern Orthopaedic Association, 2002,11(3) :167-171.
  • 8Wang CJ, Wang FS, Ko JY, Huang HY, Chen CJ, Sun YC, Yang YJ. Extracorporeal shock wave therapy shows regenera- tion in hip necrosis[J].Rheumatol 2008 ; 47 : 543-546.
  • 9Ramachandran M, Ward K, Brown RR, Munns CF,Cowell CT, Little DG. Intravenous bisphosphonate therapy for traumatic os- teoneerosis of the femoral head in adolescents[J]. J Bone Joint Surg Am 2007 ,89 :1727-1734.
  • 10Disch AC, Matziolis G, Perka C. The management of necrosis-associated and idiopathic bone-marrow oedema of the proximal femur by intravenous iloprost[J].J Bone Joint Surg Br 2005 ,87 : 560-564.

引证文献2

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