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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >THE EFFECT OF HYPERTHERMIA AND VERAPAMIL ON MELPHALAN CYTOTOXICITY AND TRANSPORT IN MULTIDRUG-RESISTANT CHINESE HAMSTER OVARY CELLS
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THE EFFECT OF HYPERTHERMIA AND VERAPAMIL ON MELPHALAN CYTOTOXICITY AND TRANSPORT IN MULTIDRUG-RESISTANT CHINESE HAMSTER OVARY CELLS

机译:高温和维拉帕米对多药耐药中国仓鼠卵巢细胞中甲酚的细胞毒性和运输的影响

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The effect of both hyperthermia and verapamil on cytotoxicity and transport of melphalan was studied in a pleiotropic drug-resistant Chinese hamster ovary cell line (CH(R)C5) and in the drug-sensitive parent line (AuxB1). The CH(R)C5 cell line was selected for resistance to colchicine but is also cross-resistant to other drugs including melphalan. Verapamil(10 mu M) increased melphalan cytotoxicity in drug-resistant cells but not in drug-sensitive cells. Hyperthermia (40 to 45 degrees C) increased melphalan cytotoxicity in both cell lines. In drug-resistant but not drug-sensitive cells, melphalan cytotoxicity was increased further when verapamil was combined with hyperthermia (40 to 45 degrees C). The increased cytotoxicity caused by verapamil in drug-resistant cells was accompanied by alterations in membrane permeability to melphalan. The cellular uptake of melphalan after 15 min increased in the presence of verapamil (7 to 30 mu M) at 37 and 42 degrees C. When verapamil (10 mu M) was present, the rate of efflux of melphalan from (CHCS)-C-R cells decreased by almost 40% at 37 degrees C, The rate of efflux was increased at 42 degrees C relative to 37 degrees C, but with verapamil the rate decreased to that obtained at 37 degrees C in CH(R)C5 cells, In drug-sensitive cells, verapamil (less than or equal to 50 mu M) did not affect either uptake or efflux of melphalan. These findings suggest that verapamil could be beneficial by increasing the effectiveness of melphalan in the elimination of multidrug-resistant cells. The combination of hyperthermia and verapamil could be especially advantageous by increasing melphalan cytotoxicity in a localized target region. (C) 1995 by Radiation Research Society [References: 54]
机译:在多效耐药的中国仓鼠卵巢细胞系(CH(R)C5)和对药物敏感的亲本系(AuxB1)中,研究了高温和维拉帕米对马法兰的细胞毒性和转运的影响。选择CH(R)C5细胞系对秋水仙碱有抗性,但对包括马法兰的其他药物也有交叉抗性。维拉帕米(10μM)增加了耐药性细胞中马法兰的细胞毒性,但对药敏性细胞却没有。热疗(40至45摄氏度)在两种细胞系中均增加了美法仑的细胞毒性。在抗药性而不是药敏性细胞中,当维拉帕米与热疗(40至45摄氏度)联合使用时,美法仑的细胞毒性进一步增加。维拉帕米在耐药细胞中引起的细胞毒性增加,伴随着对美法仑的膜通透性改变。在37和42摄氏度下在存在维拉帕米(7至30μM)的情况下,15分钟后细胞对马法兰的吸收增加。当存在维拉帕米(10μM)时,(CHCS)-CR中马法兰的流出速率在37摄氏度下,细胞减少了近40%。在42摄氏度下相对于37摄氏度,外排率增加了,但是在使用维拉帕米的情况下,CH(R)C5细胞的外排率降低到了37摄氏度下的外排率。灵敏的维拉帕米(小于或等于50μM)细胞既不影响美法仑的摄取或流出。这些发现表明,维拉帕米可能通过提高美法仑在消除多药耐药细胞中的有效性而受益。热疗和维拉帕米的组合可通过增加局部靶区域中的马法兰的细胞毒性而特别有利。 (C)1995年,由放射研究学会[参考文献:54]

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