Kremkau F W
Br J Cancer Suppl. 1982 Mar;5:226-32.
Studies on the effects of ultrasound on several solid tumours in experimental animals have indicated that tumour growth rates can be reduced. These data are generally consistent with a thermal mechanism of action. Application of combined ultrasound and X-irradiation have shown that with some experimental animal tumours the radiation dose required to locally control 50% of the tumours can be reduced by ultrasound. These results were also consistent with a thermal mechanism of action hypothesis. Fractionated X-irradiation was not enhanced as much as single dose. Pulsing the ultrasound with the same time-average intensity resulted in the same radiosensitivity enhancement. The combined effects of ultrasound and cancer chemotherapy drugs have been studied in mouse leukaemia. The treatment was applied in vitro with cells in suspension. Subsequent to treatment, the cells were inoculated into host mice and survival was monitored. Cytotoxic action of 5 of 10 drugs studied was enhanced by ultrasound. A thermal mechanism of action apparently was not involved. Cavitation in the suspension probably played a role in the cytotoxic enhancement. Experimental data are consistent with the concept that ultrasound causes rapidly reversible cell damage which, in the presence of cytotoxic drugs, is not so readily reversed and results in significant loss of lethal potential of the malignant cells to the host.
对实验动物身上几种实体瘤的超声效应研究表明,肿瘤生长速率可以降低。这些数据总体上与热作用机制相符。联合应用超声和X射线照射显示,对于一些实验动物肿瘤,超声可降低局部控制50%肿瘤所需的辐射剂量。这些结果也与热作用机制假说相符。分次X射线照射的增强效果不如单次剂量。以相同的时间平均强度对超声进行脉冲处理,可产生相同的放射敏感性增强效果。超声与癌症化疗药物的联合效应已在小鼠白血病中进行了研究。该处理在体外对悬浮细胞进行。处理后,将细胞接种到宿主小鼠体内并监测存活率。所研究的10种药物中有5种的细胞毒性作用因超声而增强。显然不涉及热作用机制。悬浮液中的空化作用可能在细胞毒性增强中发挥了作用。实验数据与以下概念一致:超声会导致细胞快速可逆性损伤,在存在细胞毒性药物的情况下,这种损伤不易逆转,并导致恶性细胞对宿主的致死潜能显著丧失。