中国组织工程研究与临床康复
中國組織工程研究與臨床康複
중국조직공정연구여림상강복
JOURNAL OF CLINICAL REHABILITATIVE TISSUE ENGINEERING RESEARCH
2008年
53期
10425-10429
,共5页
张春礼%徐虎%范宏斌%郑佳鹏%陈戎波
張春禮%徐虎%範宏斌%鄭佳鵬%陳戎波
장춘례%서호%범굉빈%정가붕%진융파
前交叉韧带,损伤%腱,移植%成纤维细胞生长因子,碱性%血管生成
前交扠韌帶,損傷%腱,移植%成纖維細胞生長因子,堿性%血管生成
전교차인대,손상%건,이식%성섬유세포생장인자,감성%혈관생성
背景:以往实验已证实碱性成纤维细胞生长因子在体内外均有促新生血管形成的作用.冻干法可以减低移植物的抗原性,经冻干处理后的移植物保存时间长并且运输方便,更容易商品化.冻干肌腱补充活性细胞生长因子有望加速新血管的牛成.目的:拟验证碱性成纤维细胞生长因子促进冻干肌腱移植重建前交叉韧带后早期血管的生成作用.设计、时间及地点:对照观察动物实验,于2006-06/20017-06在解放军第四军医大学西京医院骨科研究所完成.材料:选用健康成年家犬14只.方法:取2只犬,无菌手术取其双下肢伸趾长肌腱16条,冻干处理后供实验用.将其余12只犬左、右侧膝关节分别移植单纯冻干肌腱和复合100 u g/L碱性成纤维细胞生长因子后冻干肌腱重建前交叉韧带.主要观察指标:分别于移植后1, 2,3,4,5,6 周取材,每次取2只.进行苏木精-伊红染色,通过图像分析仪定性观察新生血管的生成情况.结果:复合碱性成纤维细胞生长因子冻干肌腱组移植后两三周出现新生血管,四五周达到高峰;单纯冻干肌腱组移植后四五周出现新生血管.复合碱性成纤维细胞生长因子冻干肌腱组新血管长入肌腱的时间先于对照组,深度深于对照组.结论:复合100 u g/L碱性成纤维细胞生长因子的冻干肌腱移植重建前交叉韧带后,在新血管形成的时间及长入肌腱的深度方面均优于单纯冻干肌腱.
揹景:以往實驗已證實堿性成纖維細胞生長因子在體內外均有促新生血管形成的作用.凍榦法可以減低移植物的抗原性,經凍榦處理後的移植物保存時間長併且運輸方便,更容易商品化.凍榦肌腱補充活性細胞生長因子有望加速新血管的牛成.目的:擬驗證堿性成纖維細胞生長因子促進凍榦肌腱移植重建前交扠韌帶後早期血管的生成作用.設計、時間及地點:對照觀察動物實驗,于2006-06/20017-06在解放軍第四軍醫大學西京醫院骨科研究所完成.材料:選用健康成年傢犬14隻.方法:取2隻犬,無菌手術取其雙下肢伸趾長肌腱16條,凍榦處理後供實驗用.將其餘12隻犬左、右側膝關節分彆移植單純凍榦肌腱和複閤100 u g/L堿性成纖維細胞生長因子後凍榦肌腱重建前交扠韌帶.主要觀察指標:分彆于移植後1, 2,3,4,5,6 週取材,每次取2隻.進行囌木精-伊紅染色,通過圖像分析儀定性觀察新生血管的生成情況.結果:複閤堿性成纖維細胞生長因子凍榦肌腱組移植後兩三週齣現新生血管,四五週達到高峰;單純凍榦肌腱組移植後四五週齣現新生血管.複閤堿性成纖維細胞生長因子凍榦肌腱組新血管長入肌腱的時間先于對照組,深度深于對照組.結論:複閤100 u g/L堿性成纖維細胞生長因子的凍榦肌腱移植重建前交扠韌帶後,在新血管形成的時間及長入肌腱的深度方麵均優于單純凍榦肌腱.
배경:이왕실험이증실감성성섬유세포생장인자재체내외균유촉신생혈관형성적작용.동간법가이감저이식물적항원성,경동간처리후적이식물보존시간장병차운수방편,경용역상품화.동간기건보충활성세포생장인자유망가속신혈관적우성.목적:의험증감성성섬유세포생장인자촉진동간기건이식중건전교차인대후조기혈관적생성작용.설계、시간급지점:대조관찰동물실험,우2006-06/20017-06재해방군제사군의대학서경의원골과연구소완성.재료:선용건강성년가견14지.방법:취2지견,무균수술취기쌍하지신지장기건16조,동간처리후공실험용.장기여12지견좌、우측슬관절분별이식단순동간기건화복합100 u g/L감성성섬유세포생장인자후동간기건중건전교차인대.주요관찰지표:분별우이식후1, 2,3,4,5,6 주취재,매차취2지.진행소목정-이홍염색,통과도상분석의정성관찰신생혈관적생성정황.결과:복합감성성섬유세포생장인자동간기건조이식후량삼주출현신생혈관,사오주체도고봉;단순동간기건조이식후사오주출현신생혈관.복합감성성섬유세포생장인자동간기건조신혈관장입기건적시간선우대조조,심도심우대조조.결론:복합100 u g/L감성성섬유세포생장인자적동간기건이식중건전교차인대후,재신혈관형성적시간급장입기건적심도방면균우우단순동간기건.
BACKGROUND: Based on previous studies, the combination of basic fibroblast growth factor (bFGF) with graft may accelerate the procedure of vascular invasion of anterior cruciate ligament (ACL) graft. The antigenicity of graft could be inhibited by the destruction of major histolocompatibility complex (MHC) through the treatment of allogenous tendon by freeze. The freeze. dried tendon showed advantages including prolonged storage time. availability for transport and possibility of commercial application. There is no experimental and clinical study on the graft substance of bFGF combined tendon in ACL reconstruction in animal model so far. OBJECTIVE: To observe histologically the effect of exogenous application or bFGF combined to freeze-dried tendon on angiogenic enhancement in early ACL reconstruction. DESIGN, TIME AND SETTING: Controlled animal study, which was performed in the Department of Orthopeadics, Xijing Hospital. Fourth Military Medical University of Chinese PLA between June 2006 and June 2007.MATERIALS: Fourteen dogs were used in the experiment. METHODS: Extensor digitorum longus tendon was harvested from the rest 2 dogs and treated by freeze-dry as graft for other experimental dogs. bFGF(100 u g/L)was combined to freeze-dried tendon and then transplanted into one side knee to substitute the original ACL. While only freeze-dried tendon was used in the transplantation at the other side as control. MAIN OUTCOME MEASURES: Twelve of them were randomly divided into 6 groups according to the 6 time points,i,e.,1,2,3,4,5,6 weeks after surgery(2 dogs in each group).The histological observation with HE staining was done under microscope to mainly observe the angiogenesis in the transplanted ACL. RESULTS: Neovascularization occurred at the 2nd to 3rd weeks and reached the peak at the 4th to 5th weeks postoperatively at the experimental sides. By contrast. The neovascularization occurred at the 4th to 5th weeks postoperatively at the control sides. Neovascularization in the combined group was longer and deeper than that in the control group. CONCLUSION: The time of neovascular formation and the depth of vascular penetration into the tendon in the group of bFGF combined to freeze-dried tendon are superior to those in the control group.