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静脉移植物的血管外支架置入术可降低血管内皮生长因子 A(VEGF-A)的表达,并在再内皮化后诱导内膜和中膜层中血管内皮生长因子受体 1(VEGFR-1)的显著下调。

Outside stenting of the vein graft decreases VEGF-A expression and induces significant down-regulation of VEGFR-1 in the intimal and medial layers after the re-endothelialization period.

机构信息

1st Department of Cardiac Surgery, Medical University of Silesia, Katowice, Poland.

出版信息

Med Sci Monit. 2010 Mar;16(3):BR89-96.

Abstract

BACKGROUND

Neointimal hyperplasia (NIH) in vein grafts implanted into the arterial system develops after re-endothelialization and is considered a significant risk factor of occlusion. Evidence suggests that VEGF-A expression with VEGFR-2 activation and/or VEGFR-1 down-regulation might be involved in inhibiting NIH formation. The aim was to assess whether a stented vein graft (SV) has an impact on VEGF-A and VEGFR-1 expression compared with non-stented vein grafts.

MATERIAL/METHODS: Twelve sheep received a radial vein with an outside stent (SV) and a radial vein (RV) transplanted into their carotid arteries. The covering of the luminal surface of the SV and RV grafts by endothelium was 98.3% and 96.3%, respectively, at 6 weeks. From the 6th to 12th weeks after transplantation, the time course of total VEGF-A expression and VEGFR-1 expression were evaluated separately for the intima and media.

RESULTS

VEGF-A and VEGFR-1 expression were significantly lower in the SV than in the RV group in the intima. In the media the SV grafts were associated with higher VEGF-A and VEGFR-1 expression at 6 and 8 weeks, but lower values were observed at weeks 10 and 12 compared with the RV grafts. Comparing the time courses of VEGF-A and VEGFR-1 expression in the intima and media with intimal/medial thickening in the SV and RV groups, negative correlations for the SV grafts were found.

CONCLUSIONS

These findings indicate that outside stenting of the vein graft decreases VEGF-A expression and induces significant down-regulation of VEGFR-1 in the intima and media after the re-endothelialization.

摘要

背景

在动脉系统中植入静脉移植物后,新生内膜增生(NIH)会在再内皮化后发生,被认为是闭塞的一个重要危险因素。有证据表明,VEGF-A 的表达与 VEGFR-2 的激活和/或 VEGFR-1 的下调可能参与了抑制 NIH 形成。本研究旨在评估支架置入的静脉移植物(SV)与非支架置入的静脉移植物相比,对 VEGF-A 和 VEGFR-1 表达的影响。

材料/方法:12 只绵羊接受了带外支架的桡静脉(SV)和桡静脉(RV)移植到颈动脉。6 周时,SV 和 RV 移植物的内腔表面内皮覆盖率分别为 98.3%和 96.3%。移植后第 6 至 12 周,分别评估了 SV 和 RV 移植物内膜和中膜的总 VEGF-A 表达和 VEGFR-1 表达的时程。

结果

SV 组的 VEGF-A 和 VEGFR-1 表达在内膜明显低于 RV 组。在中膜,SV 移植物在 6 周和 8 周时与 RV 移植物相比,VEGF-A 和 VEGFR-1 表达较高,但在 10 周和 12 周时表达较低。与 SV 和 RV 移植物的内膜和中膜 VEGF-A 和 VEGFR-1 表达的时间过程与内膜/中膜增厚进行比较,SV 移植物呈负相关。

结论

这些发现表明,静脉移植物的外支架置入可降低 VEGF-A 的表达,并在再内皮化后诱导内膜和中膜 VEGFR-1 的显著下调。

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