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Local Delivery of Vascular Endothelial Growth Factor Accelerates Reendothelialization and Attenuates Intimal Hyperplasia in Balloon-Injured Rat Carotid Artery

医学 内膜增生 再狭窄 新生内膜 气球 颈动脉 内膜 血管内皮生长因子 动脉 心脏病学 增殖细胞核抗原 生理盐水 血管平滑肌 内皮干细胞 增生 免疫染色 内皮 内科学 病理 支架 免疫组织化学 平滑肌 血管内皮生长因子受体 体外 生物 生物化学
作者
Takayuki Asahara,Christophe Bauters,Christopher M. Pastore,Marianne Kearney,Susan Rossow,Stuart Bunting,Napoleone Ferrara,James F. Symes,Jeffrey M. Isner
出处
期刊:Circulation [Lippincott Williams & Wilkins]
卷期号:91 (11): 2793-2801 被引量:440
标识
DOI:10.1161/01.cir.91.11.2793
摘要

Background Most strategies designed to reduce restenosis by the use of pharmacological or biological reagents involve direct inhibition of vascular smooth muscle cell (SMC) proliferation. Alternatively, SMC proliferation might be indirectly inhibited if reendothelialization could be specifically facilitated at sites of balloon-induced arterial injury. Accordingly, we investigated the hypothesis that application of an endothelial cell (EC)-specific mitogen to a freshly denuded intimal surface could accelerate reendothelialization and thereby attenuate intimal hyperplasia. Methods and Results The left carotid artery of 31 Sprague-Dawley rats was subjected to balloon injury, after which 16 rats were treated with a 30-minute incubation with 100 μg of vascular endothelial growth factor (VEGF), an EC-specific mitogen. Control animals (n=15) received a 30-minute incubation with 0.9% saline. At 2 weeks after balloon injury, carotid artery reendothelialization was markedly superior in the VEGF-treated group compared with the control group (14.59±1.12 versus 7.96±0.51 mm 2 , P <.0005). The extent of reendothelialization measured at 4 weeks after balloon injury remained superior for arteries treated with VEGF (18.04±0.90 mm 2 ) versus saline (13.42±0.84 mm 2 , P <.005). Neointimal thickening was correspondingly attenuated to a statistically significant degree in arteries treated with VEGF versus the control group at both the 2-week and 4-week time points. Immunostaining for proliferating cell nuclear antigen (PCNA) disclosed a threefold increase in PCNA-positive cells in the neointima of control arteries versus VEGF-treated arteries at 2 weeks after injury. Conclusions Application of VEGF, an EC-specific growth regulatory molecule, may be effectively used in vivo to promote reendothelialization and thereby indirectly attenuate neointimal thickening due to SMC proliferation.
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