Giannopoulou Efstathia, Katsoris Panagiotis, Parthymou Anastasia, Kardamakis Dimitris, Papadimitriou Evangelia
Laboratory of Molecular Pharmacology, Department of Pharmacy, University of Patras, GR 26504 Patras, Greece.
Anticancer Res. 2002 Sep-Oct;22(5):2821-6.
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.
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。