期刊文献+

不完全性脊髓缺血损伤动物模型的建立及价值 被引量:2

Establishment of incomplete spinal cord ischemic injury rabbit models and their significance
原文传递
导出
摘要 目的探讨不完全性脊髓缺血损伤动物模型的建立方法,为不完全性脊髓缺血损伤机制研究提供理想的载体。方法24只新西兰大白兔按照随机数字表法分为对照组及3根组、4根组,每组8只。对照组用于排除麻醉和手术对运动诱发电位的影响;3根组、4根组分别结扎3根、4根腰动脉。各组麻醉后记录基线诱发电位,手术/结扎后30min、2d、7d记录诱发电位;麻醉清醒后、手术/结扎后2d、7d进行运动功能评分;手术/结扎后7d后取缺血中心区标本进行HE染色,镜下观察。结果3根组动物结扎后30min诱发电位波幅与对照组比较差异有统计学意义(P〈0.05),结扎后2d、7d与对照组比较差异无统计学意义(P〉0.051;4根组动物结扎后30min、2d、7d3个时间点诱发电位波幅与对照组比较差异均有统计学意义(P〈0.05)。3组动物手术/结扎后30min、2d、7d3个时间点的潜伏期与对照组比较差异均无统计学意义(P〉0.05)。各组动物运动功能评分结果与诱发电位波幅变化一致。结论结扎3根腰动脉可以造成可逆性不完全性脊髓缺血损伤,结扎4根腰动脉可以造成不可逆性不完全性脊髓缺血损伤。 Objective To explore the establishment of animal models of incomplete spinal cord ischemic injury to provide ideal carriers for researching the pathogenesis of incomplete spinal cord ischemic injury. Methods Twenty-four New Zealand rabbits were randomly divided into a control group (n=8) and 2 experimental groups (n=16); control group only underwent sham-operation without inducing spinal cord injury to exclude the influences of anesthesia and surgery on motor evoked potential (MEP); in the experimental groups, spinal cord ischemia injury models were established by the methods of selective ligation of segmental spinal artery from cranio-caudal direction. Baseline MEP after anesthetization were recorded, and the MEP 30 min, 2 and 7 d after vascular ligation were noted. Motor function was assessed after narcotic conscious, and 2 and 7 d after vascular ligation. The specimens 7 d after ligation were taken for HE staining. Results The amplitude of MEP in the experimental group having 3 lumbar artery ligation 30 minutes after ligation was significantly different as compared with that in the control group (P〈0.05); no significant differences on the amplitude of MEP were noted between these 2 groups 2 and 7 d after ligation (/〉〉0.05). Significant differences on the amplitude of MEP were noted between control group and experimental group having 4 lumbar artery ligation 30 min, and 2 and 7 d after ligation (P〈0.05). The latency of all these rabbits showed no significant difference 30 min, and 2 and 7 d after ligation (P〉0.05). The amplitude changes of MEP were accorded with the results of motor function scale. Conclusion Reversible incomplete spinal cord ischemia animal models can be established after 3 lumbar artery ligation; irreversible incomplete spinal cord ischemia animal models can be established after 4 lumbar artery ligation.
出处 《中华神经医学杂志》 CAS CSCD 北大核心 2011年第10期989-992,共4页 Chinese Journal of Neuromedicine
基金 福建省教育厅科技计划基金(JA08099)
关键词 脊髓损伤 动物模型 腰动脉 Spinal cord injury Animal model Lumbar
  • 相关文献

参考文献9

二级参考文献40

  • 1曲静,张洪涛,杨惠林.兔腰动脉阻断建立脊髓缺血再灌注动物模型的实验研究[J].中国临床康复,2004,8(20):4006-4007. 被引量:6
  • 2Judson JA, Cant BR, Shaw MA. Early prediction of outcome from cerebral trauma by somatosensory evoked potentials [J]. Cri Care Med, 1990, 18(4): 363-368.
  • 3Pohlmann-Eden B, Dingethal K, Bender HJ, et al. How reliable is the predictive vlaue of SEP (somatosensory evoked potentials) patterns in severe brain damage with special regard to the bilateral loss of cortical responses?[J]. Intensive Care Med, 1997, 23(3): 301-308.
  • 4Schwarz S, Schwab S, Aschoff A, et al. Favorable recovery from bilateral loss of somatosensory evoked potentials [J]. Crit Care Med, 1999, 27(1): 182-187.
  • 5Amantini A, Gripp A, Fossi S, et al. Predicion of 'awakening'and outcome in prolonged acute coma from severe traumatic brain injury:evidence for validity of short latency SEPs [J]. Clin Neurophysiol, 2005, 116(1): 229-235.
  • 6Leocani L,Martinelli V,Natali-Sora MG,et al.Somatosensory evoked potentials and sensory involvement in multiple sclerosis:comparison with clinical findings and quantitative sensory tests[J].Mult Scler,2003,9(3):275-279.
  • 7Bromm B.Lorenz J.Neurophysiohigical evaluation of pain[J].Electroencephalogr Clin Neurophysiol,1998,107(2):227-253.
  • 8Katsarava Z,Ayzenberg I,Sack F,et al.A novel method of eliciting pain-related potentials by transcutancous electrical stimulation[J].Headache,2006,46(10):1511-1517.
  • 9Arondt-Nielsen L,Chen ACN.Lasers and other thermal stimulators for activation of skin nociceptors in humans[J].Neurophysiol Clin,2003,33(6):259-268.
  • 10Towell AD,Purves AM,Boyd SG.CO《,2》 laser activation of nociceptive and non-nociceptive thermal afferents from hairy and glabrous skin[J].Pain,1996,66 (1):79-86.

共引文献842

同被引文献29

  • 1朱广友,郑崇达,沈彦,王少华.阴部神经诱发电位研究[J].法医学杂志,1993,9(3):117-121. 被引量:2
  • 2管玉龙,刘锋,董培青,万彩红,杨璟.脊髓缺血损伤动物模型的建立[J].中国体外循环杂志,2006,4(1):46-48. 被引量:7
  • 3Iwamoto S,Higashi A,Ueno T,et al.Protective effect of sivelestat Sodium hydrate (ONO-5046) on ischemic spinal cord injury[J].Interact Cardiovasc Thorac Surg,2009,8(6): 606-609.
  • 4Feezor RJ,Martin TD,Hess PJ,et al.Extent of aortic coverage and incidence of spinal cord ischemia after thoracic endovascular aneurysm repair[J].Ann Thorac Surg,2008,86(6): 1809-1814.
  • 5Zivin JA,DeGirolami U.Spinal cord infarction: a highly reproducible stroke model[J].Stroke,1980,11(2): 200-202.
  • 6Herlambang B,Orihashi K,Mizukami T,et al.New method for absolute spinal cord ischemia protection in rabbits[J].J VASC SURG,2011,54(4): 1109-1116.
  • 7Kim J,Hwang J,Huh J,et al.Acute normovolemic hemodilution can aggravate neurological injury after spinal cord ischemia in rats[J].Anesth Analg,2012,114(6): 1285-1291.
  • 8Wang Z,Yang W,Britz GW,et al.Development of a simplified spinal cord ischemia model in mice[J].J Neurosci Methods,2010,189(2): 246-251.
  • 9Kakimoto M,Kawaguchi M,Sakamoto T,et al.Evaluation of rapid ischemic preconditioning in a rabbit model of spinal cord ischemia[J].Anesthesiology,2003,99(5): 1112-1117.
  • 10Hori M,Aoki S,Oishi H,et al.Utility of time-resolved three-dimensional magnetic resonance digital subtraction angiography without contrast material for assessment of intracranial dural arterio-venous fistula[J].Acta Radiol,2011,52(7): 808-812.

引证文献2

二级引证文献12

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