首页> 外文会议>Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy III >Morphological changes of tumor microvasculature following photodynamic therapy
【24h】

Morphological changes of tumor microvasculature following photodynamic therapy

机译:光动力治疗后肿瘤微血管的形态学变化

获取原文
获取原文并翻译 | 示例

摘要

Abstract: In this study, the effect of PDT on tumor microvasculature was studied by light and electron microscope. Walker-256 tumors, implanted subcutaneously in rats, were exposed to 200J/cm$+2$/ 630nm light, 24h after injection of PsD-007 at dose of 15mg/kg of body weight. Animals were killed and tumors were removed at time 0, 1/2, 1, 2, 6, 12 and 24h after treatment. The tumors with PDT displayed progressive injury to both microvasculature and tumor cells. Pathological changes such as swelling or vacuolization of mitochondria in endothelial cells could be seen immediately following PDT. At 6h post PDT, the injury to endothelial cells became more severe. Microthrombosis, diffuse hemorrhage and perivascular tumor cell mecrosis are also noted. By 12-24h after PDT, complete destruction of microvessels and obvious tumor cell mecrosis were observed. Untreated tumors or light only or drug only didn't show these changes. The results indicated that disruption of tumor microvasculature may be an important mechanism of action of PDT. !9
机译:摘要:本研究通过光镜和电镜研究了PDT对肿瘤微血管的影响。在以15mg / kg体重的剂量注射PsD-007后24小时,将在大鼠皮下植入的Walker-256肿瘤暴露于200J / cm $ + 2 $ / 630nm的光下。在治疗后的0、1 / 2、1、2、6、12和24小时处死动物并切除肿瘤。 PDT肿瘤对微脉管系统和肿瘤细胞均表现出进行性损伤。 PDT后可立即观察到病理变化,例如内皮细胞中线粒体的肿胀或空泡。 PDT后6小时,对内皮细胞的伤害变得更加严重。还注意到微血栓形成,弥漫性出血和血管周肿瘤细胞坏死。在PDT后12-24h,观察到微血管完全破坏和明显的肿瘤细胞坏死。未经治疗的肿瘤或仅光照或仅药物未显示这些变化。结果表明,破坏肿瘤微脉管系统可能是PDT的重要作用机制。 !9

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号