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氨磷汀可保护血管免受电离辐射的影响。

Amifostine protects blood vessels from the effects of ionizing radiation.

作者信息

Giannopoulou Efstathia, Katsoris Panagiotis, Parthymou Anastasia, Kardamakis Dimitris, Papadimitriou Evangelia

机构信息

Laboratory of Molecular Pharmacology, Department of Pharmacy, University of Patras, GR 26504 Patras, Greece.

出版信息

Anticancer Res. 2002 Sep-Oct;22(5):2821-6.

Abstract

Amifostine (WR-2721) is a well-known radioprotective drug, selective for normal cells. The purpose of the present study was to define whether amifostine protects the vascular network from the effects of X-rays. We used the in vivo system of chicken embryo chorioallantoic membrane (CAM) as a model of angiogenesis. Amifostine reversed the early X-rays- induced decrease in the number of CAM blood vessels and reversed the early radiation-induced apoptosis of CAM cells. It also inhibited the increase in tyrosine nitration of actin and a-tubulin, which was observed 6 hours after CAM irradiation, when there was a significant decrease in non-protein SH groups. Furthermore, C6 rat glioma cells were inoculated on CAM and tumor growth, as well as tumor-induced angiogenesis, was estimated on haematoxylin-eosin-stained paraffin sections. Amifostine inhibited the post irradiation increase of C6 tumor-induced angiogenesis. These data suggest that amifostine protects CAM cells and blood vessels from the effects of X-rays, through mechanisms that do not depend solely on its free radical scavenging properties.

摘要

氨磷汀(WR - 2721)是一种著名的放射防护药物,对正常细胞具有选择性。本研究的目的是确定氨磷汀是否能保护血管网络免受X射线的影响。我们使用鸡胚绒毛尿囊膜(CAM)的体内系统作为血管生成模型。氨磷汀逆转了早期X射线诱导的CAM血管数量减少,并逆转了早期辐射诱导的CAM细胞凋亡。它还抑制了肌动蛋白和α - 微管蛋白酪氨酸硝化的增加,这种增加在CAM照射6小时后被观察到,此时非蛋白质巯基显著减少。此外,将C6大鼠胶质瘤细胞接种在CAM上,并在苏木精 - 伊红染色的石蜡切片上评估肿瘤生长以及肿瘤诱导的血管生成。氨磷汀抑制了照射后C6肿瘤诱导的血管生成增加。这些数据表明,氨磷汀通过不完全依赖其自由基清除特性的机制保护CAM细胞和血管免受X射线的影响。

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