Ackerman N B, Makohon S
Surg Gynecol Obstet. 1981 Mar;152(3):262-7.
The effects of cooling and freezing temperatures on vascular perfusion in solitary Walker carcinosarcomas implanted in the liver were studied in Sprague-Dawley rats. With cooling to above freezing temperatures, perfusion with Microfil decreased significantly in both the encircling tumor plexus as well as in the internal tumor circulation. Freezing and thawing produced acute, significant increases of arterial perfusion in encircling and internal tumor circulations. Tumor vascular permeability, as measured by an Evans blue extraction method, increased tremendously as a result of freezing and thawing. Significant rises in permeability were observed at five minutes to 24 hours, with peak activity at six hours. The tumor circulation appeared to respond to the insult of freezing and thawing in a manner similar to that of normal blood vessels, whereas results of previous studies have shown different reactions to chemical vasoactive agents. The acute increases of perfusion and permeability in the tumors as a result of freezing and thawing could be useful as a means of improving the concentration of antitumor agents.
在斯普拉格-道利大鼠中,研究了冷却和冷冻温度对植入肝脏的单个沃克癌肉瘤血管灌注的影响。冷却至高于冰点温度时,环绕肿瘤丛以及肿瘤内部循环中的微丝灌注均显著减少。冷冻和解冻使环绕肿瘤和肿瘤内部循环中的动脉灌注急剧显著增加。通过伊文思蓝提取法测量,肿瘤血管通透性因冷冻和解冻而大幅增加。在5分钟至24小时观察到通透性显著升高,6小时时活性达到峰值。肿瘤循环对冷冻和解冻损伤的反应方式似乎与正常血管相似,而先前研究结果显示对化学血管活性药物有不同反应。冷冻和解冻导致肿瘤灌注和通透性的急性增加,可用作提高抗肿瘤药物浓度的一种手段。