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通过荧光激活细胞分选法测定热疗对阿霉素转运的调节作用。

Modulation of adriamycin transport by hyperthermia as measured by fluorescence-activated cell sorting.

作者信息

Rice G C, Hahn G M

机构信息

Department of Radiology, Stanford University, CA 94305.

出版信息

Cancer Chemother Pharmacol. 1987;20(3):183-7. doi: 10.1007/BF00570481.

Abstract

Heat-induced (45.5 degrees C) modification of adriamycin uptake and efflux were measured by flow cytometry in CHO cells in vitro. Administration of adriamycin with simultaneous 15-min or 30-min heat treatment increased drug uptake in a dose-dependent manner. Fluorescence-activated cell sorting showed that cytotoxicity to adriamycin was correlated with relative cellular concentration (fluorescence) for both unheated cells and those heated and simultaneously treated with adriamycin. However, if adriamycin administration followed the heat treatment, accumulation was significantly reduced, primarily as a result of decreased passive drug diffusion (rather than increased efflux) in the heated cells. Cells made heat-tolerant by prior heating also exhibited reduced adriamycin uptake 12 h later, and further heating did not increase uptake. Cell sorting experiments indicated that cytotoxicity of adriamycin was not necessarily correlated with intracellular drug levels when drug administration followed the heat treatment. Also, heat-sterilized cells exhibited a two-fold increase in adriamycin uptake over surviving cells, as assessed by simultaneous measurement of dansyl lysine and adriamycin content. These results indicate that sensitization to adriamycin by simultaneous heat treatment is probably due to increased drug uptake. The decreased sensitization observed when drug administration is followed by heating is probably the result of both decreased uptake and decreased drug DNA accessibility.

摘要

通过流式细胞术在体外测量了热诱导(45.5摄氏度)对阿霉素摄取和外排的影响,实验对象为CHO细胞。在给予阿霉素的同时进行15分钟或30分钟的热处理,药物摄取呈剂量依赖性增加。荧光激活细胞分选显示,对于未加热的细胞以及加热并同时用阿霉素处理的细胞,阿霉素的细胞毒性与相对细胞浓度(荧光)相关。然而,如果在热处理后给予阿霉素,药物蓄积会显著减少,这主要是由于加热细胞中被动药物扩散减少(而非外排增加)所致。预先加热而产生耐热性的细胞在12小时后阿霉素摄取也减少,进一步加热并未增加摄取。细胞分选实验表明,当在热处理后给予药物时,阿霉素的细胞毒性不一定与细胞内药物水平相关。此外,通过同时测量丹磺酰赖氨酸和阿霉素含量评估,经热灭菌的细胞相比存活细胞阿霉素摄取增加了两倍。这些结果表明,同时进行热处理使细胞对阿霉素敏感可能是由于药物摄取增加。在给药后进行加热时观察到的敏感性降低可能是摄取减少和药物与DNA可及性降低共同作用的结果。

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