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改变膜脂成分和普鲁卡因对腹水肿瘤细胞热杀伤的影响。

Effect of altered membrane lipid composition and procaine on hyperthermic killing of ascites tumor cells.

作者信息

Hidvégi E J, Yatvin M B, Dennis W H, Hidvégi E

出版信息

Oncology. 1980;37(5):360-3. doi: 10.1159/000225470.

Abstract

The influence of membrane fluidity on hyperthermic cell killing has been investigated in ascites tumor cells. Membrane lipid composition of P388 ascites tumor cells were modified by feeding host animals with diets containing either unsaturated fatty acids (UFA) or saturated fatty acids (SFA). Both kinds of ascites were heat treated in vitro at 37, 42 or 43.5 degrees C for 30 or 60 min. The cell killing effect of hyperthermia was tested by transplantation of cells into recipient mice and survival examined. While at 37 and 42 degrees C for 1 h, there was no difference in cell killing of the two types of ascites, elevating the temperature to 43.5 degrees C the survival was significantly longer on transplantation of ascites of UFA diet. This effect was potentiated by membrane-fluidizing drugs. On the addition of 1 mM procaine during 1 h treatment at 43.5 degrees C, the ascites of SFA diet killed 80% of mice, while the ascites of UFA diet left all the mice alive at least for 3 months. Scanning electron-microscopic observations of the treated cells was performed in parallel and showed close correspondence with the results of survival studies. In conclusion, the increase of membrane fluidity by incorporating more of UFA or by the addition of membrane-fluidizing drugs or especially by the combination of both, the sensitivity of cells to heat enhanced. These experiments support the hypothesis that membranes are a target for hyperthermia.

摘要

在腹水肿瘤细胞中研究了膜流动性对热疗细胞杀伤的影响。通过给宿主动物喂食含有不饱和脂肪酸(UFA)或饱和脂肪酸(SFA)的饮食来改变P388腹水肿瘤细胞的膜脂质组成。两种腹水在体外分别于37、42或43.5℃热处理30或60分钟。通过将细胞移植到受体小鼠中并检查存活率来测试热疗的细胞杀伤效果。在37和42℃处理1小时时,两种腹水的细胞杀伤没有差异,但将温度升至43.5℃时,喂食UFA饮食的腹水移植后存活率显著延长。这种效果被膜流化药物增强。在43.5℃处理1小时期间添加1 mM普鲁卡因,喂食SFA饮食的腹水使80%的小鼠死亡,而喂食UFA饮食的腹水使所有小鼠至少存活3个月。同时对处理后的细胞进行扫描电子显微镜观察,结果与存活研究结果密切相关。总之,通过加入更多的UFA或添加膜流化药物,特别是两者结合增加膜流动性,细胞对热的敏感性增强。这些实验支持了膜是热疗靶点的假说。

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