Ishikawa M, Takayanagi Y, Sasaki K
Department of Pharmacology and Toxicology, Tohoku College of Pharmacy, Sendai, Japan.
Pharmacol Toxicol. 1991 Jan;68(1):21-5. doi: 10.1111/j.1600-0773.1991.tb01202.x.
To reduce the side-effects and to enhance the antitumour activities of antitumour agents, we have been investigating their combined use with routine drugs. In the present study, we examined the effects of disulfiram (DSF) in combination with ifosfamide (IFX). DSF prevented IFX-induced bladder damage in a dose-dependent manner in tumour-free ddY mice when orally administered simultaneously with antitumour agent, but failed to diminish the acute lethal toxicity or leukocytotoxicity of IFX. Diethyldithiocarbamate (DDTC) prevented IFX-induced bladder damage when administered simultaneously with IFX or 1 to 5 hr afterwards. The antitumour activity of IFX in ddY-mice inoculated with Sarcoma 180 or in C57BL/6J mice inoculated with EL-4 leukaemia was not impaired when it was given simultaneously with DSF or 3 hr before DDTC. Thus, neither DSF nor DDTC impaired the antitumour effect of IFX and both diminished its adverse effects. The bladder protection of DSF and DDTC appeared resulted from adduct formation with acrolein and not from inhibition of the metabolic activation of IFX.
为了减少抗肿瘤药物的副作用并增强其抗肿瘤活性,我们一直在研究它们与常规药物的联合使用。在本研究中,我们检测了双硫仑(DSF)与异环磷酰胺(IFX)联合使用的效果。在无肿瘤的ddY小鼠中,当与抗肿瘤药物同时口服给药时,DSF以剂量依赖性方式预防了IFX诱导的膀胱损伤,但未能降低IFX的急性致死毒性或白细胞毒性。二乙基二硫代氨基甲酸盐(DDTC)在与IFX同时给药或之后1至5小时给药时,预防了IFX诱导的膀胱损伤。当与DSF同时给药或在DDTC给药前3小时给药时,IFX对接种肉瘤180的ddY小鼠或接种EL-4白血病的C57BL/6J小鼠的抗肿瘤活性并未受损。因此,DSF和DDTC均未损害IFX的抗肿瘤作用,且二者均降低了其不良反应。DSF和DDTC对膀胱的保护作用似乎是由与丙烯醛形成加合物所致,而非通过抑制IFX的代谢活化。