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慢性低灌注对大鼠脑白质血管生成与血脑屏障的影响 被引量:8

Effect of Chronic Cerebral Hypoperfusion on Angiogenesis and Blood-brain Barrier in White Matter
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摘要 目的:观察慢性低灌注状态下大鼠脑白质区域血管生成及血脑屏障破坏状况及其可能联系。方法:96只大鼠随机分为假手术组、缺血1周组、缺血2周组、缺血4周组各24只,缺血组大鼠结扎双侧颈总动脉构建慢性低灌注模型,假手术组不结扎。在相应时间点检测各组大鼠脑白质区域微血管密度、血管内皮细胞生长因子(VEGF)m RNA表达水平及伊文思蓝(EB)静脉注射后脑组织内EB浓度。结果:各缺血组白质区域血管网密度较假手术组高(P<0.01),血管密度在缺血2周组中达高峰。各缺血组VEGF m RNA表达水平均较假手术组增高(P<0.05),缺血2周及缺血4周组的VEGF m RNA表达水平较缺血1周组降低(P<0.05)。各缺血组EB浓度均较假手术组增高(P<0.01),缺血2周及缺血4周组EB浓度较缺血1周组增高(P<0.05)。结论:慢性低灌注状态可诱导VEGF表达、促进血管生成,这种血管生成可能参与脑白质区域血脑屏障破坏机制。 Objective:To explore angiogenesis and blood-brain barrier (BBB) disruption under chronic cerebral hypoperfusion status in white matter areas. Methods: Ninty-six male Wistar rats were divided into groups of sham-operated, ischemia 1 week, ischemia 2 weeks and ischemia 4 weeks (n=24 in each group). Permanent, bilater- al common carotid artery occlusion was used to induce hypoperfusion in forebrain of the rats, and the sham- operated group was not ligated. Capillary density was used to assess the angiogenic level. Quantitative measurement of Evans Blue was used to assess the BBB function. Reverse transcription polymerase chain reaction (RT-PCR) was used to evaluate the expression of vascular endothelial growth factor (VEGF) mRNA. Results: The vessel density in the white matter of the ischemia groups were increased than that of the sham-ope/ated group (P〈0.01), and the vessel density of the ischemia 2 weeks group was highest. The VEGF mRNA expression of the ischemia groups was higher than that in the sham-operated group (P〈0.05), and the VEGF mRNA expression in the ischemia 2, 4 weeks groups were decreased compared with that in the ischemia 1 week group (P〈0.05). The Evans Blue concentrations of the ischemia groups were increased in comparison with that in the sham-operated group (P〈0.05), and the Evans Blue concentrations in the ischemia 2, 4 weeks groups were higher than that in the ischemia 1 week group (P〈0.05). Conclusion: Chronic cerebral hypoperfusion can induce angiogenesis which may contribute to BBB disruption in white matter areas.
出处 《神经损伤与功能重建》 2016年第1期9-11,共3页 Neural Injury and Functional Reconstruction
关键词 脑缺血 血脑屏障 血管生成 白质损害 brain ischemia blood-brain barrier angiogenesis white matter impairment
作者简介 通讯作者林琅plexor@163.com
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参考文献15

  • 1Thomas T, Miners S, Love S. Post-mortem assessment of hypoperfusion of cerebral cortex in Alzheimer's disease and vascular dementia [J]. Brain, 2015, 138: 1059-1069.
  • 2Kandiah N, Goh O, Mak E, et al. Carotid stenosis: a risk factor for cere- bral white-matter disease[J]. J Stroke Cerebrovasc Dis, 2014, 23: 136-139.
  • 3Schreiber S, Bueche CZ, Garz C, et al. Blood brain barrier breakdown as the starting point of cerebral small vessel disease? - New insights from a rat model[J]. Exp Transl Stroke Med, 2013, 5: 4.
  • 4Yang Y, Rosenberg GA. Blood-brain barrier breakdown in acute and chronic cerebrovascular disease[J]. Stroke, 2011,42: 3323-3328.
  • 5Easton AS. Regulation of permeability across the blood-brain barrier[J]. Adv Exp Med Biol, 2012, 763: 1-19.
  • 6Chapouly C, Tadesse Argaw A, Horng S, et al. Astrocytic TYMP and VEGFA drive blood-brain barrier opening in inflammatory central nervous system lesions[J]. Brain, 2015, 138: 1548-1567.
  • 7Tsipis CP, Sun X, Xu K, et al. Hypoxia-induced angiogenesis and capil- lary density determination[J]. Methods Mol Biol, 2014, 1135: 69-80.
  • 8Gurol ME. Cerebral hypoperfusion and white matter disease in healthy elderly and patients with Alzheimer's disease [J]. Eur J Neurol, 2013, 20: 214-215.
  • 9Bridges LR, Andoh J, Lawrence AJ, et al. Blood-brain barrier dysfunc- tion and cerebral small vessel disease (arteriolosclerosis) in brains of older people[J]. J Neuropathol Exp Neurol, 2014, 73: 1026-1033.
  • 10Bai Y, Zhu X, Chao J, et al. Pericytes Contribute to the Disruption of the Cerebral Endothelial Barrier via Increasing VEGF Expression: Implica- tions for Stroke[J]. PLoS One, 2015, 10: e0124362.

二级参考文献23

  • 1Rikitake Y, Kim HH, Huang Z, et al. Inhibition of Rho kinase (ROCK) leads to increased cerebral blood flow and stroke protection. Stroke, 2005,36:2251-2257.
  • 2Shibuya M, Hirai S,Seto M, et al. Effects of fasudil in acute ischemic stroke: results of a prospective placebo-controlled double-blind trial. J Neurol Sci, 2005,238 : 31-39.
  • 3van der Flier WM, van Straaten EC, Barkhof F, et al. Small vessel disease and general cognitive function in nondisabled elderly:the LADIS study. Stroke,2005,36:2116-2120.
  • 4Baezner G, Blahak C, Poggesi A, et al. Association of gait and balance disorders with age-related white matter changes: the LADIS study. Neurology, 2008,70: 935-942.
  • 5Komaki S, Nagayama H, Ohgami H, et al. Prospective study of major depressive disorder with white matter hyperintensity. Comparison of patients with and without lacunar infarction. Eur Arch Psychiatry Clin Neurosci, 2008,288 : 160-164.
  • 6Poggesi A, Pracucci G, Chabriat H, et al. Urinary complaints in nondisahled elderly people with age-related white matter changes: the Leukoaraiosis And DISability (LADIS) Study. J Am Geriatr Soc,2008,56:1638-1643.
  • 7Inzitari D, Simoni M, Pracucci G, et al. Risk of rapid global functional decline in elderly patients with severe cerebral agerelated white matter changes: the LADIS study. Arch Intern Med,2007,167:81-88.
  • 8lkram MA, Vernooii MW, Vrooman HA, et al. Brain tissue volumes and small vessel disease in relation to the risk of mortality. Neurobiol Aging, 2009,30 : 450-456.
  • 9Bokura H, Kobayashi S, Yamaguchi S, et al. Silent brain infarction and subcortical white matter lesions increase the risk of stroke and mortality: a prospective cohort study. J Stroke Cerebrovasc Dis, 2006,15 : 57-63.
  • 10Murray AD, Staff RT, Shenkin SD, et al. Brain white matter hyperintensities : relative importance of vascular risk factors in nondemented elderly people. Radiology, 2005,237: 251-257.

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