Horsman M R, Winther J
Department of Experimental Clinical Oncology, Danish Cancer Society, Aarhus, Denmark.
Acta Oncol. 1989;28(5):693-7. doi: 10.3109/02841868909092295.
Results from experimental tumours suggest that the mechanism of action of photodynamic therapy (PDT) involves both a direct killing of tumour cells, and a secondary effect resulting from vascular damage. We have investigated the possible vascular changes induced by PDT in an intraocular retinoblastoma-like rat tumour model using the 86RbCl extraction procedure. Light irradiation (90 J/cm2; 633 nm; 30 min) of intraocular tumours 24 h after an intraperitoneal injection of 5 mg/kg Photofrin II produced an increase in the tumour uptake of 86RbCl during the treatment period. However, 24 h later these values had decreased to 25% of that normally found in control animals. These effects were observed in both the tumour material and associated normal eye tissue, but not in PDT treated normal eyes without tumours. The results confirm that the vasculature of this eye tumour model is a target for some of the PDT effects.
实验性肿瘤的结果表明,光动力疗法(PDT)的作用机制既涉及对肿瘤细胞的直接杀伤,也涉及血管损伤导致的继发效应。我们使用86RbCl提取程序,在眼内视网膜母细胞瘤样大鼠肿瘤模型中研究了PDT可能引起的血管变化。腹腔注射5mg/kg的二血卟啉醚(Photofrin II)24小时后,对眼内肿瘤进行光照射(90 J/cm2;633nm;30分钟),在治疗期间肿瘤对86RbCl的摄取增加。然而,24小时后,这些值降至正常对照动物的25%。在肿瘤组织和相关的正常眼组织中均观察到了这些效应,但在未患肿瘤且接受PDT治疗的正常眼中未观察到。结果证实,该眼肿瘤模型的脉管系统是PDT部分效应的靶点。