中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2014年
6期
1369-1371
,共3页
王正锋%王瑞华%刘献志%张水军
王正鋒%王瑞華%劉獻誌%張水軍
왕정봉%왕서화%류헌지%장수군
脊髓缺血性损伤%模型,动物%小鼠%长期存活
脊髓缺血性損傷%模型,動物%小鼠%長期存活
척수결혈성손상%모형,동물%소서%장기존활
Spinal cord ischemia%Model,animal%Mouse%Long-term survival
目的 制备模仿胸腹主动脉瘤术后脊髓缺血性损伤且长期存活的小鼠模型.方法 夹闭胸主动脉8、10、12 min,假手术组为对照组,术中测定脊髓表面血流量,多时间点测定小鼠后肢运动功能,术后7d观察小鼠脊髓切片,术后4周分析小鼠生存曲线.应用SPSS 17.0软件进行数据分析.结果 胸主动脉夹闭术中小鼠脊髓表面血流量降低到基础水平的(7.2±3.5)%.对照组小鼠后肢运动功能无障碍且脊髓切片正常,各手术组小鼠术后1h时后肢运动功能障碍最严重.夹闭8 min可以引起后肢运动功能障碍,但2周后BBB评分恢复,与对照组比较差异有统计学意义(P>0.05),夹闭10 min可以引起持续到4周的后肢功能障碍(BBB评分和Roterod运动评分,与对照组比较差异有统计学意义(P<0.01)和运动神经元死亡(脊髓前脚存活神经元数目与对照组比较,差异有统计学意义(P<0.01),且小鼠能够长期存活(中位生存期为24.7 d,与夹闭8 min组比较,差异无统计学意义(P>0.05),夹闭12 min虽然可以引起严重的后肢运动功能障碍和神经元死亡,但长期存活的可能性小(中位生存期为14.7 d,与夹闭8、10 min组比较,差异有统计学意义(P<0.01).结论 通过夹闭胸主动脉制备小鼠脊髓缺血模型,10 min为最佳夹闭时间,得到的动物模型可以长期存活,有利于研究脊髓缺血损伤长时间内的动态变化.
目的 製備模倣胸腹主動脈瘤術後脊髓缺血性損傷且長期存活的小鼠模型.方法 夾閉胸主動脈8、10、12 min,假手術組為對照組,術中測定脊髓錶麵血流量,多時間點測定小鼠後肢運動功能,術後7d觀察小鼠脊髓切片,術後4週分析小鼠生存麯線.應用SPSS 17.0軟件進行數據分析.結果 胸主動脈夾閉術中小鼠脊髓錶麵血流量降低到基礎水平的(7.2±3.5)%.對照組小鼠後肢運動功能無障礙且脊髓切片正常,各手術組小鼠術後1h時後肢運動功能障礙最嚴重.夾閉8 min可以引起後肢運動功能障礙,但2週後BBB評分恢複,與對照組比較差異有統計學意義(P>0.05),夾閉10 min可以引起持續到4週的後肢功能障礙(BBB評分和Roterod運動評分,與對照組比較差異有統計學意義(P<0.01)和運動神經元死亡(脊髓前腳存活神經元數目與對照組比較,差異有統計學意義(P<0.01),且小鼠能夠長期存活(中位生存期為24.7 d,與夾閉8 min組比較,差異無統計學意義(P>0.05),夾閉12 min雖然可以引起嚴重的後肢運動功能障礙和神經元死亡,但長期存活的可能性小(中位生存期為14.7 d,與夾閉8、10 min組比較,差異有統計學意義(P<0.01).結論 通過夾閉胸主動脈製備小鼠脊髓缺血模型,10 min為最佳夾閉時間,得到的動物模型可以長期存活,有利于研究脊髓缺血損傷長時間內的動態變化.
목적 제비모방흉복주동맥류술후척수결혈성손상차장기존활적소서모형.방법 협폐흉주동맥8、10、12 min,가수술조위대조조,술중측정척수표면혈류량,다시간점측정소서후지운동공능,술후7d관찰소서척수절편,술후4주분석소서생존곡선.응용SPSS 17.0연건진행수거분석.결과 흉주동맥협폐술중소서척수표면혈류량강저도기출수평적(7.2±3.5)%.대조조소서후지운동공능무장애차척수절편정상,각수술조소서술후1h시후지운동공능장애최엄중.협폐8 min가이인기후지운동공능장애,단2주후BBB평분회복,여대조조비교차이유통계학의의(P>0.05),협폐10 min가이인기지속도4주적후지공능장애(BBB평분화Roterod운동평분,여대조조비교차이유통계학의의(P<0.01)화운동신경원사망(척수전각존활신경원수목여대조조비교,차이유통계학의의(P<0.01),차소서능구장기존활(중위생존기위24.7 d,여협폐8 min조비교,차이무통계학의의(P>0.05),협폐12 min수연가이인기엄중적후지운동공능장애화신경원사망,단장기존활적가능성소(중위생존기위14.7 d,여협폐8、10 min조비교,차이유통계학의의(P<0.01).결론 통과협폐흉주동맥제비소서척수결혈모형,10 min위최가협폐시간,득도적동물모형가이장기존활,유리우연구척수결혈손상장시간내적동태변화.
Objective To develop long-term survival spinal cord ischemia model mimicking the injury from the surgery of thoracoabdominal aneurysm in mice.Methods Thoracic aorta was clamped for 8,10 and 12 min via left lateral thoracotomy.The mice subject to sham operation served as control group.The lumbar spinal cord blood flow was measured during thoracic aorta cross-clamping.Hind limbs movement function was evaluated before and 1 h,1,3,5,7 days,and 2,4 weeks post-injury.The slices of the spinal cord were observed and survival neurons in the ventral horn were evaluated at 7th day post-injury.Survival curve was analyzed at 4th week post-injury in mice.The data were statistically analyzed using SPSS 17.0 software.Results The blood flow was reduced to (7.2 ± 3.5) % of the baseline after crossclamping the thoracic aorta.There was no hind limbs movement functional deficit,and histological staining of the spinal cord ischemia slices was normal in the control group.There was a most serious hind limbs movement functional deficit at 1 st h post-injury.The duration of 8 min cross-clamping could result in movement functional deficit,but open field Basso Beattie Bresnahan (BBB) score recovered at 2nd week postinjury (P > 0.05 vs.control group).The duration of 10 min cross-clamping could result in continuous and stable hind limbs movement functional deficit at 4th week (P <0.01 vs.control group for open field BBB score and latency to fall from Rota rod) and neuronal cell death (P < 0.01 vs.control group for the ventral horn neurons).Most importantly,the mice had a long term survival in 10 min group (the median survival period was 24.7 days,P >0.05 vs.8 min group).The duration of 12 min cross-clamping could result in less probability of long-term survival (the median survival period was 14.7 days,P <0.01 vs.8 min group and 10 min group),although it could result in serious hind limbs movement functional deficit.Conclusion Ten min was the best duration for mice spinal cord ischemia model through thoracic aorta cross-clamping.This kind of model can be used to study the dynamic changes of spinal cord ischemia because of the animals' long-term survival.