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胰岛素对大鼠急性脊髓损伤保护作用的实验研究-07.2

阅读: 时间: 2007-2-13 15:42:00

吴星火  聂宇  杨述华  王晶  夏天  杨操

 (华中科技大学同济医学院附属协和医院骨科  武汉 430022)

    目的:探讨胰岛素对大鼠急性脊髓损伤的保护作用及其效果。方法:采用改良Allen WD 法建立大鼠急性脊髓损伤模型。60SD大鼠随机分为损伤对照组和胰岛素治疗组,术后8 h, 1, 3, 7,14 d检测大鼠脊髓损伤后运动诱发电位(MEP)的潜伏期及波幅;采用原位末端标记(TUNEL)观察脊髓细胞凋亡;采用激光多普勒血流仪(LDF) 监测了胰岛素对伤段脊髓SCBF 量的影响。结果:术后各时相胰岛素组MEP潜伏期与对照组相比无明显差异,MEP波幅较对照组明显增高(P<0.05);胰岛素治疗组TUNEL 阳性细胞的数目明显少于损伤对照组(P<0.05);两组脊髓血流量(SCBF)均明显下降,但对照组下降更明显。结论:初步研究表明胰岛素能改善脊髓血流量、抑制神经细胞的凋亡、减轻神经功能缺失,对急性脊髓损伤有保护作用。

关键词  胰岛素;脊髓损伤;大鼠;实验研究

中图分类号:R965.1

文献标识码:A

文章编号:1008-049X200702-0122-03

 

Experimental Study of the Neuroprotective Effect of Insulin to Acute Spinal Cord Injury in Rats

Wu XinghuoNie YuYang ShuhuaWang JingXia TianYang CaoDepartment of OrthopedicsUnion HospitalTongji Medical College of Huazhong University of Science and TechnologyWuhan 430022China)

ABSTRACT  ObjectiveTo study the protective effect of insulin to acute spinal cord injury in ratsMethodAcute spinal cord injury model in rats was built by modified Allen WDSixty healthy adult Sprague-Dawley rats were randomly divided into two groupscontrol group and insulin groupThe  latency and amplitude of MEPMotion Evoked Potentialwere analyzed at 8 h1 d3 d7d14 d postoperatively n=6 in each time point were analyzedApoptosis neurons were labeled with TUNEL dyeingThe spinal cord blood flowSCBFwas recorded by laserDoppler flowmetryResultThere were no changes in the latencies of MEPs in both groupsand the mean amplitudes of MEPs were higher in insulin groups than in control groupsThe number of TUNEL staining positive cells in the insulin group was less than in control groupP<0.05)。And SCBF decreased in both groupsespecially in control groupConclusionThe study indicated that insulin could improve SCBFinhibit neurocyte apoptosispalliate loss of neural functionwhich might protect injured spinal cord

KEY WORDS  InsulinSpinal cord injuryRatExperimental study

作者简介:吴星火,男,博士在读,主要从事骨组织工程的研究。

E-mailwuxinghuo@163.com

作者简介:杨述华,教授,博士生导师,主要从事骨与关节疾病研究。

Tel:(02785726196

 

参   考   文   献

1 Sekhon LH,Fehlings MG.Epidemiology,demographics,and pathophysiology of acute spinal cord injury[J].Spine,2001,26(Suppl):2-12

2 Wozniak M,Rydzewski B,Baker SP,et al.The cellular and physiological actions of insulin in the central nervous system[J]. Neurochem Int,1993,22(1):1-10

3 张子印,吕国蔚.脊髓损伤模型与再生实验研究[J].中华神经外科杂志,1991,7(2):149-151

4 García-Alías G,Verdú E,Forés J,et al.Functional characterization of photochemical graded spinal cord injury in the rat[J]. J Neurotrauma,2003,20(5):501-510

5 Zhao WQ,Alkon DL.Role of insulin and insulin receptor in learning and memory[J]. Mol Cell Endocrinol,2001,177 (1-2):125-134

6 Morrisey K,Evans RA,Wakefield L,et al. Translational regulation of renal proximal tubular epithelial cell transforming growth factor-beta1 generation by insulin[J]. Am J Pathol,2001,159(5):1905-1915

7 Aikawa R,Nawano M,Gu Y,et al.Insulin prevents cardiomyocytes from oxidative stressinduced apoptosis through activation of PI3 kinase/AktJ[J].Circulation,2000,102(23):2873-2879

8 Wrathall JR,Teng YD,Choiniere D. Amelioration of functional deficits from spinal cord trauma with systemically administered NBQX,an antagonist of non-N-methyl-D aspartate receptors[J]. Exp Neurol,1996,137(1):119-126

9 Liu XZ,Xu XM,Hu R,et al. Neuronal and glial apoptosis after traumatic spinal cord injury[J]. J Neurosci,1997,17(14):5395-5406

10 Tator CH,Koyanagi I. Vascular Mechanisms in the pathophysiology of human spinal cord injury[J]. J Neurosurg,1997,86(3):483-492

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