宋玉成, 夏薇, 江金花, 王庆端. 盐酸千金藤素逆转EAC/ADR细胞多药耐药性的作用及其机制J. 药学学报, 2005, 40(3): 204-207.
引用本文: 宋玉成, 夏薇, 江金花, 王庆端. 盐酸千金藤素逆转EAC/ADR细胞多药耐药性的作用及其机制J. 药学学报, 2005, 40(3): 204-207.
SONG Yu-cheng, XIA Wei, JIANG Jin-hua, WANG Qing-duan. Reversal of multidrug resistance in drug-resistant cell line EAC/ADR by cepharanthine hydrochloride and its mechanismJ. Acta Pharmaceutica Sinica, 2005, 40(3): 204-207.
Citation: SONG Yu-cheng, XIA Wei, JIANG Jin-hua, WANG Qing-duan. Reversal of multidrug resistance in drug-resistant cell line EAC/ADR by cepharanthine hydrochloride and its mechanismJ. Acta Pharmaceutica Sinica, 2005, 40(3): 204-207.

盐酸千金藤素逆转EAC/ADR细胞多药耐药性的作用及其机制

Reversal of multidrug resistance in drug-resistant cell line EAC/ADR by cepharanthine hydrochloride and its mechanism

  • 摘要: 目的研究盐酸千金藤素对艾氏腹水癌耐药细胞株EAC/ADR多药耐药性的逆转作用及其与核因子κB(NF-κB)的关系,探讨其作用机制。方法MTT法、小鼠移植瘤模型实验观察盐酸千金藤素体外和体内逆转细胞多药耐药性的作用; Dot-ELISA法检测细胞核NF-κB水平及药物作用后的变化。结果盐酸千金藤素体外能逆转EAC/ADR细胞的耐药性,逆转倍数为13倍;体内能延长荷瘤小鼠的生存时间,生命延长率为75.37%;并能降低EAC/ADR细胞中NF-κB的持续性活性及化疗药物对其的激活。结论盐酸千金藤素具有逆转多药耐药性的作用,其机制可能与抑制NF-κB的活性有关。

     

    Abstract: AimTo investigate the correlation between reversal effect of cepharanthine hydrochloride (CH) on multidrug resistance (MDR) in drug-resistant cell line EAC/ADR and the nuclear transcription factor-κB (NF-κB). MethodsCytotoxicity was determined by the tetrazolium (MTT) assay in vitro. An EAC/ADR cell homograft model was established to investigate the effect of CH on reversing MDR in vivo. The constitutive activity and activation of NF-κB by drugs were measured by Dot-Enzyme-linked Immune Sorbent Assay (Dot-ELISA). ResultsCH was shown to potentiate the cytotoxicity of ADR, a 13- fold reversal effect of resistance was achieved in vitro. In mice bearing EAC/ADR cell homografts, CH was found to prolong the survival time of animals bearing tumor. Increase in life span over control was 75.37%. In addition, the constitutive activity of NF-κB and activation of NF-κB by chemotherapy were lowered by CH. ConclusionThe findings suggest that CH is able to reverse drug resistance and its mechanism may be related to suppressing the constitutive activity and activation of NF-κB by drugs.

     

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