Harrigan M R, Ennis S R, Sullivan S E, Keep R F
Department of Neurosurgery, University of Michigan Health System, Ann Arbor 48109, USA.
Acta Neurochir (Wien). 2003 Jan;145(1):49-53. doi: 10.1007/s00701-002-1035-1.
Therapeutic cerebral angiogenesis, utilizing angiogenic factors to enhance collateral vessel formation within the central nervous system, is a potential method for cerebral revascularization. A prior dose-response study determined that intracerebroventricular infusion of vascular endothelial growth factor (VEGF) increases vascular density with minimal associated brain edema at a concentration of 5 microg/ml. The purpose of this study was to assess effects of intracerebroventricular infusion of VEGF (5 microg/ml) on cerebral blood flow, infarct volume, and brain edema after ischemia.
Recombinant human VEGF(165) was infused into the right lateral ventricle of rats with an osmotic minipump at a rate of 1 microl/hr for 7 days. Control animals received vehicle only. Ischemia was produced by transient (2 hours) middle cerebral artery occlusion (MCAO). After MCAO, cerebral blood flow was determined with the indicator fractionation technique: infarct volume was assessed with 2,3,5-triphenlytetrazolium chloride staining, and brain edema was determined by measuring brain water content.
Cerebral blood flow was not significantly different in animals treated with VEGF compared to controls. There was a significant reduction in total infarct volume after temporary MCAO in VEGF-treated animals compared to controls (163+/-37 mm(3) vs. 309+/-54 mm(3), P<0.05). Brain water content after transient MCAO was also significantly reduced in VEGF-treated animals compared to controls (80.9+/-0.7% vs. 83.3+/-0.6%, P<0.05).
Intracerebroventricular infusion of VEGF(165) (5 microg/ml) decreases infarct volume and brain edema after temporary MCAO without a significant increase in cerebral blood flow. These results indicate that VEGF may have a direct neuroprotective effect in cerebral ischemia.
治疗性脑内血管生成,即利用血管生成因子增强中枢神经系统内的侧支血管形成,是一种脑血运重建的潜在方法。先前的剂量反应研究表明,脑室内注入血管内皮生长因子(VEGF),在浓度为5微克/毫升时可增加血管密度,且相关脑水肿最小。本研究的目的是评估脑室内注入VEGF(5微克/毫升)对缺血后脑血流量、梗死体积和脑水肿的影响。
将重组人VEGF(165)用渗透微型泵以1微升/小时的速度注入大鼠右侧脑室,持续7天。对照动物仅接受赋形剂。通过短暂(2小时)大脑中动脉闭塞(MCAO)产生缺血。MCAO后,用指示剂分级技术测定脑血流量;用2,3,5-三苯基氯化四氮唑染色评估梗死体积,通过测量脑含水量确定脑水肿情况。
与对照组相比,接受VEGF治疗的动物脑血流量无显著差异。与对照组相比,VEGF治疗的动物在短暂MCAO后总梗死体积显著减小(163±37立方毫米对309±54立方毫米,P<0.05)。与对照组相比,VEGF治疗的动物在短暂MCAO后脑含水量也显著降低(80.9±0.7%对83.3±0.6%,P<0.05)。
脑室内注入VEGF(165)(5微克/毫升)可减少短暂MCAO后的梗死体积和脑水肿,而脑血流量无显著增加。这些结果表明,VEGF在脑缺血中可能具有直接的神经保护作用。