Miko M, Krepelka J, Mĕlka M, Vajdová D
Department of Microbiology and Biochemistry, Slovak Polytechnical University, Bratislava, Czechoslovakia.
Neoplasma. 1989;36(4):411-7.
Changes in ATP levels of both Ehrlich ascites carcinoma and P388 leukemia cells were evaluated after 2 h of incubation in the presence of different concentrations of benfluron (BF), 7-dihydrobenfluron (DBF) and N-oxide of benfluron (NOBF). Up to the concentration of 37.5 mumol/l, none of the substances significantly depressed the ATP levels. A more expressive decrease in ATP levels was noted only at concentrations of 75 mumol/l and higher. BF proved the most effective, less effective was DBF, while NOBF was practically without any effect. Of the remaining cytostatic drugs, Mitoxantrone, CCNU and Me-CCNU, in particular, proved efficient in depressing ATP level. The latter becomes depressed already after 15 min of incubation in the presence of the highest concentrations of benfluron and 7-dihydrobenfluron.
在不同浓度的苯氟隆(BF)、7-二氢苯氟隆(DBF)和苯氟隆N-氧化物(NOBF)存在的情况下孵育2小时后,评估了艾氏腹水癌细胞和P388白血病细胞的ATP水平变化。在浓度高达37.5μmol/L时,这些物质均未显著降低ATP水平。仅在浓度为75μmol/L及更高时,才观察到ATP水平有更明显的下降。BF被证明是最有效的,DBF效果稍差,而NOBF实际上没有任何效果。在其余的细胞毒性药物中,米托蒽醌、洛莫司汀和甲基洛莫司汀尤其被证明在降低ATP水平方面有效。在最高浓度的苯氟隆和7-二氢苯氟隆存在的情况下孵育15分钟后,ATP水平就开始下降。