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血管内皮生长因子促进周细胞覆盖脑毛细血管,改善随后局灶性脑缺血期间的脑血流,并保护代谢半影区。

Vascular endothelial growth factor promotes pericyte coverage of brain capillaries, improves cerebral blood flow during subsequent focal cerebral ischemia, and preserves the metabolic penumbra.

机构信息

Department of Neurology, University Hospital Essen, Hufelandstrasse 55, D-45122 Essen, Germany.

出版信息

Stroke. 2013 Jun;44(6):1690-7. doi: 10.1161/STROKEAHA.111.000240. Epub 2013 Apr 30.

Abstract

BACKGROUND AND PURPOSE

Therapeutic angiogenesis aims at improving cerebral blood flow by amplification of vascular sprouting, thus promoting tissue survival under conditions of subsequent ischemia. It remains unknown whether induced angiogenesis leads to the formation of functional vessels that indeed result in hemodynamic improvements. Observations of hemodynamic steal phenomena and disturbed neurovascular integrity after vascular endothelial growth factor delivery questioned the concept of therapeutic angiogenesis.

METHODS

Mice were treated with recombinant human vascular endothelial growth factor (0.02 μg/d; intracerebroventricular) for 3 to 21 days and subsequently exposed to 90-minute middle cerebral artery occlusion. Angiogenesis, histological brain injury, IgG extravasation, cerebral blood flow, protein synthesis and energy state, and pericyte coverage on brain capillaries were evaluated in a multiparametric approach combining histochemical, autoradiographic, and regional bioluminescence techniques.

RESULTS

Vascular endothelial growth factor increased brain capillary density within 10 days and reduced infarct volume and inflammation after subsequent middle cerebral artery occlusion, and, when delivered for prolonged periods of 21 days, enhanced postischemic blood-brain barrier integrity. Increased cerebral blood flow was noted in ischemic brain areas exhibiting enhanced angiogenesis and was associated with preservation of the metabolic penumbra, defined as brain tissue in which protein synthesis has been suppressed but ATP preserved. Vascular endothelial growth factor enhanced pericyte coverage of brain endothelial cells via mechanisms involving increased N-cadherin expression on cerebral microvessels.

CONCLUSIONS

That cerebral blood flow is increased during subsequent ischemic episodes, leading to the stabilization of cerebral energy state, fosters hope that by promoting new vessel formation brain tissue survival may be improved.

摘要

背景与目的

治疗性血管生成旨在通过促进血管发芽来改善脑血流,从而在随后发生缺血的情况下促进组织存活。目前尚不清楚诱导的血管生成是否会导致形成功能性血管,从而真正改善血液动力学。血管内皮生长因子(VEGF)给药后观察到的血液动力学盗血现象和神经血管完整性受损,使治疗性血管生成的概念受到质疑。

方法

通过重组人血管内皮生长因子(0.02 μg/d;侧脑室)治疗小鼠 3 至 21 天,然后暴露于 90 分钟大脑中动脉闭塞。通过联合组织化学、放射自显影和区域生物发光技术的多参数方法评估血管生成、脑损伤组织学、IgG 外渗、脑血流、蛋白质合成和能量状态以及脑毛细血管周细胞覆盖。

结果

VEGF 在 10 天内增加了脑毛细血管密度,并减少了随后大脑中动脉闭塞后的梗死体积和炎症,并且当持续给药 21 天以上时,增强了缺血后血脑屏障的完整性。在表现出增强的血管生成的缺血脑区中观察到脑血流量增加,并且与代谢边缘区的保存相关,该区域定义为蛋白质合成受到抑制但 ATP 保留的脑组织。VEGF 通过涉及脑微血管上 N-钙粘蛋白表达增加的机制增强了周细胞对脑内皮细胞的覆盖。

结论

在随后的缺血发作期间脑血流增加,导致脑能量状态稳定,这使人们希望通过促进新血管形成来改善脑组织存活。

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