Fanciulli M, Gentile F P, Bruno T, Paggi M G, Benassi M, Floridi A
Laboratory for Cell Metabolism and Pharmacokinetics, Regina Elena Institute for Cancer Research, Rome, Italy.
Anticancer Drugs. 1992 Dec;3(6):615-21. doi: 10.1097/00001813-199212000-00009.
The effect of the combination of adriamycin (ADM) with the anti-inflammatory drug rhein (RH) on the membrane redox activity in human glioma cells was investigated. RH, although less effective than ADM, inhibits ferricyanide reduction by human glioma cells in a dose-dependent manner as well as ferricyanide-induced proton release. The inhibition of the plasma membrane redox system might represent a further mechanism by which RH, other than ATP depletion, affects cell survival. The analysis of the interaction between ADM and RH, performed with the isobolar method, demonstrates a strong synergic response, probably due to an effect on different sites of action. The synergism of the ADM-RH association allows us to achieve a pre-established extent of inhibition with ADM concentrations much lower than with ADM alone. RH might, therefore, represent a very useful tool to improve the therapeutic index of ADM and to lower its general toxicity.
研究了阿霉素(ADM)与抗炎药物大黄酸(RH)联合使用对人胶质瘤细胞膜氧化还原活性的影响。RH虽然不如ADM有效,但能以剂量依赖的方式抑制人胶质瘤细胞对铁氰化物的还原以及铁氰化物诱导的质子释放。质膜氧化还原系统的抑制可能是RH除了ATP耗竭之外影响细胞存活的另一种机制。用等效线法分析ADM和RH之间的相互作用,结果显示出强烈的协同反应,这可能是由于对不同作用位点的影响。ADM与RH联合使用的协同作用使我们能够在ADM浓度远低于单独使用ADM时达到预先设定的抑制程度。因此,RH可能是提高ADM治疗指数并降低其总体毒性的非常有用的工具。