冼励坚, 李永强, 刘然义, 曹弃元, 孙健. 油菜素内酯对CCRF-VCR1000细胞多药抗药性的逆转作用及其机制的初步探讨J. 药学学报, 2005, 40(2): 117-121.
引用本文: 冼励坚, 李永强, 刘然义, 曹弃元, 孙健. 油菜素内酯对CCRF-VCR1000细胞多药抗药性的逆转作用及其机制的初步探讨J. 药学学报, 2005, 40(2): 117-121.
XIAN Li-jian, LI Yong-qiang, LIU Ran-yi, CAO Qi-yuan, SUN Jian. Reversing effect of brassinolide on multidrug resistance of CCRF-VCR1000 cells and a preliminary investigation on its mechanismsJ. Acta Pharmaceutica Sinica, 2005, 40(2): 117-121.
Citation: XIAN Li-jian, LI Yong-qiang, LIU Ran-yi, CAO Qi-yuan, SUN Jian. Reversing effect of brassinolide on multidrug resistance of CCRF-VCR1000 cells and a preliminary investigation on its mechanismsJ. Acta Pharmaceutica Sinica, 2005, 40(2): 117-121.

油菜素内酯对CCRF-VCR1000细胞多药抗药性的逆转作用及其机制的初步探讨

Reversing effect of brassinolide on multidrug resistance of CCRF-VCR1000 cells and a preliminary investigation on its mechanisms

  • 摘要: 目的了解油菜素内酯(BR)对多药抗药性细胞CCRF-VCR1000耐药性的逆转及机理。方法MTT法测定耐药因子及逆转倍数;罗丹明法测定药物积累;Sulliven方法测定拓扑异构酶II催化活性;Western blotting方法检测p53蛋白表达。结果CCRF-VCR1000细胞对阿霉素、VP-16和VCR分别呈153.1,55.9和8 123.1倍耐药。BR在不具细胞毒的浓度下(0.001-10.00 μg·mL-1)使耐药性逆转4.4-11.6倍;并使耐药细胞药物积累改善;过度表达的p53回复到敏感细胞水平。结论在无细胞毒浓度下,BR能逆转CCRF-VCR1000的耐药性;抑制P糖蛋白对药物的外排。下调异常表达的p53蛋白可能是其逆转机制之一。

     

    Abstract: AimTo investigate the effect of brassinolide, a plant growth modulator, on multidrug resistance (MDR) of human T lymphoblastoid cell line CCRF-VCR 1000 which was obtained by progressively addition of vincristine (VCR) to sensitive CCRF-CEM cells, and to explore preliminarily the mechanism of reversing action. MethodsMTT method was used to detect the resistant factor of resistant cell line and the reversing fold after addition of brassinolide. The intracellular accumulation of rhodamine 123, a fluorescent dye transported by P-glycoprotein was detected by flow cytometry, the catalytic activity of topoisomerase II was assessed by Sulliven method to find the effect of brassinolide on resistance. The protein expression of p53 was measured using Western blotting in the sensitive cells and resistant cells to explore the effect of brassinolide. ResultsThe resistant factors of CCRF-VCR cells on adriamycin, VP-16 and VCR are respectively as 153.1, 55.9 and 8 123.1 folds comparing to the sensitive cell line CCRF-CEM. After treatment of brassinolide under the concentration of 0.001-10.0 μg·mL-1, the resistance of CCRF-VCR was reversed partly with the reversing folds respectively as 4.4-11.6. The intracellular accumulation of rhodamine 123 was significantly reduced in the resistant cells. After treatment of brassinolide, the accumulation increased, the level of fluorescent dye was situated between resistant cells and sensitive cells. No alteration of the catalytic activity of topoisomerase II was found among three groups. The level of protein expression of p53 in resistant cells was higher than that of sensitive cells. After brassinolide treatment, the expression of p53 in CCRF-VCR cells restored to the level of sensitive cells. ConclusionBrassinolide could effectively reverse the resistance of CCRF-VCR cells by inhibiting the effusion of drug transported by P-glucoprotein. To down regulate the abnormal expression of p53 maybe one of the mechanisms of reversing MDR for brassinolide.

     

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