伊维菌素增强阿霉素诱导的耐药小鼠白血病细胞凋亡

S. Furusawa, H. Shibata, Hiromi Nishimura, S. Nemoto, M. Takayanagi, Y. Takayanagi, K. Sasaki
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引用次数: 10

摘要

在阿霉素耐药小鼠P388白血病细胞中,观察伊维菌素存在和不存在情况下,阿霉素对细胞凋亡和细胞周期的影响。伊维菌素(2 μM)增加了多药耐药小鼠白血病P388细胞对阿霉素的敏感性,显著增加了耐药细胞的凋亡和阿霉素在细胞内的积累,但对亲本细胞无影响。利用荧光电位探针3,3 ' -二己基-草炭菁,我们发现伊维菌素诱导耐药细胞的质膜电位增加。伊维菌素还增强了耐药细胞中阿霉素诱导的细胞周期G2/M阻断。伊维菌素可能通过与p -糖蛋白或改变的耐多药细胞膜的其他组分直接相互作用来逆转耐药。
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Potentiation of Doxorubicin-Induced Apoptosis of Resistant Mouse Leukaemia Cells by Ivermectin
The apoptosis and cell cycle effect of doxorubicin were evaluated in the presence and absence of ivermectin in mouse doxorubicin-resistant P388 leukaemia cells. Ivermectin (2 μM) increased the sensitivity to doxorubicin of multidrug resistant (MDR) mouse leukemic P388 cells and significantly enhanced the apoptosis and intracellular accumulation of doxorubicin in resistant cells, but had no effect on parent cells. Using the fluorescent potential probe, 3,3′-dihexyl-oxacarbocyanine, we found that ivermectin induced a plasma membrane potential increase in resistant cells. Ivermectin also enhanced doxorubicin-induced G2/M blockade of the cell cycle in resistant cells. It is possible that ivermectin could reverse resistance by direct interaction with the P-glycoprotein or other components of the altered MDR cell membrane.
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