Nagaoka S, Kawasaki S, Sasaki K, Nakanishi T
Jpn J Cancer Res. 1986 Feb;77(2):205-11.
The intracellular uptake, retention and cytotoxic effect of adriamycin (ADR) were investigated by a flow cytometry technique with NIH 3T3 cells. The intracellular uptake and cytotoxic effect of ADR increased as a function of exposure time and external drug concentration at 37 degrees. A good correlation was found between eventual survival and intracellular ADR uptake. The intracellular uptake and cytotoxic effect of ADR increased with increasing temperature and were shown to be functions of both incubation time and temperature. The intracellular uptake and cytotoxic effect of ADR were increased even at 39 degrees and 41 degrees, temperatures which had no effect on the viability of cells. The combination of hyperthermia (43 degrees) and ADR showed a synergistic effect. It was found that the cytotoxic effects of ADR in combination with various levels of hyperthermia were stronger than those which would be predicted from the intracellular ADR uptake at 37 degrees. The degree of enhancement was temperature-dependent. Since the efflux of intracellular ADR was the same with or without hyperthermia, the increased intracellular ADR uptake caused by elevated temperature was considered to result from an increase in influx.
采用流式细胞术,以NIH 3T3细胞为研究对象,对阿霉素(ADR)的细胞内摄取、滞留及细胞毒性作用进行了研究。在37℃时,ADR的细胞内摄取及细胞毒性作用随暴露时间和外部药物浓度的增加而增强。最终存活率与细胞内ADR摄取之间存在良好的相关性。ADR的细胞内摄取及细胞毒性作用随温度升高而增强,且表现为孵育时间和温度的函数。即使在39℃和41℃时,ADR的细胞内摄取及细胞毒性作用也会增强,而这两个温度对细胞活力并无影响。热疗(43℃)与ADR联合使用显示出协同效应。研究发现,ADR与不同程度热疗联合使用时的细胞毒性作用,强于根据37℃时细胞内ADR摄取量所预测的效果。增强程度与温度有关。由于无论有无热疗,细胞内ADR的外排情况相同,因此认为温度升高导致细胞内ADR摄取增加是由内流增加所致。