中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2013年
3期
609-611
,共3页
张雁儒%尚燕%刘宏建%周明武%王义生
張雁儒%尚燕%劉宏建%週明武%王義生
장안유%상연%류굉건%주명무%왕의생
脱细胞%异体神经%坐骨神经缺损%神经修复
脫細胞%異體神經%坐骨神經缺損%神經脩複
탈세포%이체신경%좌골신경결손%신경수복
Acellular%Allogeneic nerve%Sciatic nerve defects%Nerve regeneration
目的 观察化学脱细胞异体神经对大鼠坐骨神经缺损的修复效果.方法 成年雄性SD大鼠23只,其中5只取其双侧坐骨神经用于制备脱细胞异体神经,剩余18只随机分为自体神经移植组(A组)和脱细胞异体神经移植组(B组).所有实验动物均建立左侧坐骨神经1 cm缺损模型,暴露右侧坐骨神经作为正常对照.术后分4、8、12周3个时间点分批进行大体观察,检测坐骨神经功能指数(SFI);术后12周,行肌电图,苏木素-伊红(HE)染色,神经丝蛋白200免疫组织化学和免疫荧光检测.结果 术后两组大鼠伤口愈合良好,移植神经的吻合口光滑且无膨大;各时间点的SFI检测结果(A组-83.7、-63.25、-48.6;B组-86.58、-70.69、-57.43),A组均优于B组,但差异无统计学意义(P>0.05);术后12周,A组小腿三头肌湿重恢复率[A组(66.16±19.58)%,B组(45.20±17.17)%]和峰-峰波幅[A组(8.10±2.74) mV,B组5.34±2.67)mV]大于B组,且差异有统计学意义(P<0.05);术后12周,潜伏期[A组(1.80±0.35) ms,B组1.95 ±0.44)ms]和神经传导速度[A组(27.76±9.84)m/s,B组(22.12±5.98) m/s],A组结果均高于B组,但差异无统计学意义(P>0.05);苏木素-伊红(HE)染色和免疫组织化学观察B组新生的神经纤维与A组差异无统计学意义(P>0.05).结论 化学脱细异体神经与自体神经比较,对坐骨神经缺损的修复效果接近.
目的 觀察化學脫細胞異體神經對大鼠坐骨神經缺損的脩複效果.方法 成年雄性SD大鼠23隻,其中5隻取其雙側坐骨神經用于製備脫細胞異體神經,剩餘18隻隨機分為自體神經移植組(A組)和脫細胞異體神經移植組(B組).所有實驗動物均建立左側坐骨神經1 cm缺損模型,暴露右側坐骨神經作為正常對照.術後分4、8、12週3箇時間點分批進行大體觀察,檢測坐骨神經功能指數(SFI);術後12週,行肌電圖,囌木素-伊紅(HE)染色,神經絲蛋白200免疫組織化學和免疫熒光檢測.結果 術後兩組大鼠傷口愈閤良好,移植神經的吻閤口光滑且無膨大;各時間點的SFI檢測結果(A組-83.7、-63.25、-48.6;B組-86.58、-70.69、-57.43),A組均優于B組,但差異無統計學意義(P>0.05);術後12週,A組小腿三頭肌濕重恢複率[A組(66.16±19.58)%,B組(45.20±17.17)%]和峰-峰波幅[A組(8.10±2.74) mV,B組5.34±2.67)mV]大于B組,且差異有統計學意義(P<0.05);術後12週,潛伏期[A組(1.80±0.35) ms,B組1.95 ±0.44)ms]和神經傳導速度[A組(27.76±9.84)m/s,B組(22.12±5.98) m/s],A組結果均高于B組,但差異無統計學意義(P>0.05);囌木素-伊紅(HE)染色和免疫組織化學觀察B組新生的神經纖維與A組差異無統計學意義(P>0.05).結論 化學脫細異體神經與自體神經比較,對坐骨神經缺損的脩複效果接近.
목적 관찰화학탈세포이체신경대대서좌골신경결손적수복효과.방법 성년웅성SD대서23지,기중5지취기쌍측좌골신경용우제비탈세포이체신경,잉여18지수궤분위자체신경이식조(A조)화탈세포이체신경이식조(B조).소유실험동물균건립좌측좌골신경1 cm결손모형,폭로우측좌골신경작위정상대조.술후분4、8、12주3개시간점분비진행대체관찰,검측좌골신경공능지수(SFI);술후12주,행기전도,소목소-이홍(HE)염색,신경사단백200면역조직화학화면역형광검측.결과 술후량조대서상구유합량호,이식신경적문합구광활차무팽대;각시간점적SFI검측결과(A조-83.7、-63.25、-48.6;B조-86.58、-70.69、-57.43),A조균우우B조,단차이무통계학의의(P>0.05);술후12주,A조소퇴삼두기습중회복솔[A조(66.16±19.58)%,B조(45.20±17.17)%]화봉-봉파폭[A조(8.10±2.74) mV,B조5.34±2.67)mV]대우B조,차차이유통계학의의(P<0.05);술후12주,잠복기[A조(1.80±0.35) ms,B조1.95 ±0.44)ms]화신경전도속도[A조(27.76±9.84)m/s,B조(22.12±5.98) m/s],A조결과균고우B조,단차이무통계학의의(P>0.05);소목소-이홍(HE)염색화면역조직화학관찰B조신생적신경섬유여A조차이무통계학의의(P>0.05).결론 화학탈세이체신경여자체신경비교,대좌골신경결손적수복효과접근.
Objective To investigate the effect of chemical extracted acellular nerve on sciatic nerve defects of SD rats.Methods Twenty-three adult male SD rats were selected.The sciatic nerves were harvested from five of them to prepare acellular nerves.The remaining 18 rats were divided into two groups:autologous nerve graft (group A),and chemical extracted acellular nerve graft (group B).All of the experimental animals were used to establish the left sciatic nerve 1-cm long defect models,and the right sciatic nerves were exposed as the controls.At 4th,8th,and 12th week after operation,the sciatic functional index (SFI) was calculated.At 12th week after operation,hematoxylin and eosin (HE) staining,electrophysiology,immanohistochemistry and tissue immunofluorescence were done.Results All the incisions healed well after surgery.The anastomotic stomata in transplanting nerves were smooth and not swollen.SFI at different time points in group A (-83.7,-63.25,-48.6) was higher than that in group B (-86.58,-70.69,-57.43),but the difference was not statistically significant (P > 0.05).At 12th week after operation,the wet weight recovery rate of triceps surae muscles [group A:(66.16 ± 19.58)%,group B:(45.20 ± 17.17)%] and amplitude [(group A:(8.10 ±2.74) mV,group B:(5.34 ±2.67) mV] were higher in group A than in group B,with the difference being significant (P < 0.05).The compound muscle action potential [group A:(1.80 ± 0.35) ms,group B:(1.95 ± 0.44) ms] and conduction velocities [group A:(27.76 ± 9.84) m/s,group B:(22.12 ± 5.98) m/s] had no significant difference between two groups (P > 0.05).HE staining and immunohistochemistry revealed that regenerated nerve fibers showed no significant difference between two groups.Conclusion Chemical extracted acellular nerve and autologous nerve exhibited the similar effects on sciatic nerve defects of SD rats.