Furusawa S, Fujimura T, Sasaki K, Takayanagi Y
Chem Pharm Bull (Tokyo). 1989 Dec;37(12):3420-2. doi: 10.1248/cpb.37.3420.
The effects of chlordiazepoxide, diazepam and oxazepam on the lethal toxicity and metabolic activation of ifosfamide were investigated in mice. Ifosfamide was administered 24 h after the final injection of chlordiazepoxide, diazepam or oxazepam (100 mg/kg/d for 3 d, i.p.). The prior administration of chlordiazepoxide, diazepam or oxazepam enhanced the toxicity of ifosfamide (778 mg/kg, i.p.) during observation for 6 d after the administration of ifosfamide. In chlordiazepoxide-, diazepam- or oxazepam-treated mice, a higher concentration of active metabolite in the plasma after the administration of ifosfamide (200 or 600 mg/kg, i.p.) was observed as compared with that in mice treated with ifosfamide alone. On the other hand, chlordizepoxide, diazepam or oxazepam markedly enhanced the activity of ifosfamide oxidase in the liver microsomes. These results suggest that the potentiation of ifosfamide toxicity is due to stimulation of the metabolic activation of ifosfamide by chlordizepoxide, diazepam and oxazepam.
在小鼠中研究了氯氮卓、地西泮和奥沙西泮对异环磷酰胺的致死毒性和代谢活化的影响。在最后一次注射氯氮卓、地西泮或奥沙西泮(100毫克/千克/天,连续3天,腹腔注射)24小时后给予异环磷酰胺。在给予异环磷酰胺后6天的观察期内,预先给予氯氮卓、地西泮或奥沙西泮可增强异环磷酰胺(778毫克/千克,腹腔注射)的毒性。与仅用异环磷酰胺处理的小鼠相比,在用氯氮卓、地西泮或奥沙西泮处理的小鼠中,给予异环磷酰胺(200或600毫克/千克,腹腔注射)后血浆中活性代谢物的浓度更高。另一方面,氯氮卓、地西泮或奥沙西泮显著增强了肝微粒体中异环磷酰胺氧化酶的活性。这些结果表明,异环磷酰胺毒性的增强是由于氯氮卓、地西泮和奥沙西泮刺激了异环磷酰胺的代谢活化。