中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2010年
7期
972-975
,共4页
徐云强%冯世庆%王沛%马信龙%宁广智%班德翔%王希山
徐雲彊%馮世慶%王沛%馬信龍%寧廣智%班德翔%王希山
서운강%풍세경%왕패%마신룡%저엄지%반덕상%왕희산
脊髓损伤%再生%雪旺细胞%软骨素酶%细胞移植
脊髓損傷%再生%雪旺細胞%軟骨素酶%細胞移植
척수손상%재생%설왕세포%연골소매%세포이식
Spinal cord injury%Regeneration%Schwann cells%Chondroitinase%Cell transplantation
目的 观察软骨素酶联合雪旺细胞移植在治疗急性脊髓损伤中的作用.方法 Wistar大鼠80只,制作T10节段急性脊髓损伤模型(致伤力10g×4cm).随机分成4组:对照组、雪旺细胞移植组、硫酸软骨素酶治疗组和联合治疗组.采用脊髓运动功能评分(BBB法,总分21)、神经电生理(SEP&MEP)检查和生物素葡聚糖胺(BDA)神经示踪及标本NF-200免疫组织化学染色等比较各组疗效.结果 4周后BBB评分实验组较对照组明显提高,各组间差异有统计学意义(P<0.05)(12周时4组分别为9.11±1.41、11.22±1.59、11.77±1.76和14.22±1.92).术后4周起,神经电生理检查实验组动物较对照组差异有统计学意义(P<0.05),12周时4组MEP的波幅分别恢复至术前的28.8%、44.9%、49.0%和56.8%.BDA示踪显示联合组较对照组有较多的神经纤维穿过损伤部位.NF-200免疫组织化学染色吸光度(A)比较各组间差异有统计学意义(P<0.05),3个实验组纵切片A值与对照组的比值为1.44、1.55和2.78.结论 联合应用软骨素酶和雪旺细胞移植来治疗脊髓损伤,起到协同作用,效果好于单一方法,能明显促进脊髓损伤后的轴突再生和肢体功能恢复.
目的 觀察軟骨素酶聯閤雪旺細胞移植在治療急性脊髓損傷中的作用.方法 Wistar大鼠80隻,製作T10節段急性脊髓損傷模型(緻傷力10g×4cm).隨機分成4組:對照組、雪旺細胞移植組、硫痠軟骨素酶治療組和聯閤治療組.採用脊髓運動功能評分(BBB法,總分21)、神經電生理(SEP&MEP)檢查和生物素葡聚糖胺(BDA)神經示蹤及標本NF-200免疫組織化學染色等比較各組療效.結果 4週後BBB評分實驗組較對照組明顯提高,各組間差異有統計學意義(P<0.05)(12週時4組分彆為9.11±1.41、11.22±1.59、11.77±1.76和14.22±1.92).術後4週起,神經電生理檢查實驗組動物較對照組差異有統計學意義(P<0.05),12週時4組MEP的波幅分彆恢複至術前的28.8%、44.9%、49.0%和56.8%.BDA示蹤顯示聯閤組較對照組有較多的神經纖維穿過損傷部位.NF-200免疫組織化學染色吸光度(A)比較各組間差異有統計學意義(P<0.05),3箇實驗組縱切片A值與對照組的比值為1.44、1.55和2.78.結論 聯閤應用軟骨素酶和雪旺細胞移植來治療脊髓損傷,起到協同作用,效果好于單一方法,能明顯促進脊髓損傷後的軸突再生和肢體功能恢複.
목적 관찰연골소매연합설왕세포이식재치료급성척수손상중적작용.방법 Wistar대서80지,제작T10절단급성척수손상모형(치상력10g×4cm).수궤분성4조:대조조、설왕세포이식조、류산연골소매치료조화연합치료조.채용척수운동공능평분(BBB법,총분21)、신경전생리(SEP&MEP)검사화생물소포취당알(BDA)신경시종급표본NF-200면역조직화학염색등비교각조료효.결과 4주후BBB평분실험조교대조조명현제고,각조간차이유통계학의의(P<0.05)(12주시4조분별위9.11±1.41、11.22±1.59、11.77±1.76화14.22±1.92).술후4주기,신경전생리검사실험조동물교대조조차이유통계학의의(P<0.05),12주시4조MEP적파폭분별회복지술전적28.8%、44.9%、49.0%화56.8%.BDA시종현시연합조교대조조유교다적신경섬유천과손상부위.NF-200면역조직화학염색흡광도(A)비교각조간차이유통계학의의(P<0.05),3개실험조종절편A치여대조조적비치위1.44、1.55화2.78.결론 연합응용연골소매화설왕세포이식래치료척수손상,기도협동작용,효과호우단일방법,능명현촉진척수손상후적축돌재생화지체공능회복.
Objective To investigate the effect of the combination of chondroitinase and Schwann cells (SCs) transplantation after spinal cord injury (SCI) in adult rats. Methods Eighty adult Wistar rats were divided into four groups; the control group (A), the Schwann cells transplantation group ( B), the chondroitinase ABC(ChABC) group (C) and the SCs transplantation plus chondroitinase ABC group (D). The thoracic T10 spinal cord injury model was made by Impactor model II manual (10g×4 cm). After SCI, the rats in group B received SCs transplantation in injured sites, those in group C received ChABC treatment, and those in group D received the combined treatment. The rats in group A only received blank saline and medium. The locomotor functions were evaluated according to the BBB score scale (total 21), and the neuroelectrophysiological changes (SEP&MEP) were examined by electromyographic machine. Twelve weeks after SCI, biotinylated dextran amine (BDA) was injected into the cerebral cortex to trace the corticospinal tracts. Two weeks after the tracing, the animals were killed and the spinal cord frozen sections were made. The tissue sections were processed with Cy3 fluorescence stain, HE stain and anti NF-200 immuohistological stain. Results From 4 weeks after SCI, the rats in groups B, C and D had obviously higher BBB scores than in control group (P<0.05) , and BBB scores in group D was the highest. The scores in groups A, B, C and D were 9. 11 ±1.41, 11.22 ±1.59, 11.77 ±1.76 and 14. 22 ± 1. 92 respectively 12 weeks later. In electromyographic examination (SEP&MEP) , the rats in groups B, C and D gained better recovery than group A (P <0. 05), and group D was the best. At the week 12, the MEP wave recovery rate was 28. 8% , 44. 9% , 49. 0% and 56. 8% in groups A, B, C and D respectively. In BDA tracing slides, some axons could cross the injured sites in group D. There was significant difference in anti-NF-200 stain area among four groups (P<0.05). The absorbance ( A) ratio between groups B, D, D and group A was 1.44, 1. 55 and 2. 78, respectively. Conclusion Combined therapy with ChABC and SCs transplantation can promote axonal regeneration and function recovery after SCI.