期刊名称:Journal of Clinical Biochemistry and Nutrition
印刷版ISSN:0912-0009
电子版ISSN:1880-5086
出版年度:1986
卷号:1
期号:2
页码:171-179
DOI:10.3164/jcbn.1.171
出版社:The Society for Free Radical Research Japan
摘要:We studied the cytotoxicity of cyclophosphamide following the administration of phenobarbital or chloral hydrate to nude mice bearing human tumor xenografts. Cyclophosphamide, 60mg/kg, was injected intraperitoneally once a week for four weeks. The antitumor efficacy of cyclophosphamide was not altered by pretreatment with phenobarbital, but was significantly increased by pretreatment with chloral hydrate. In a parallel study, we measured the concentration of blood NBP-alkylating metabolites in nude mice after administration of cyclophosphamide, 60mg/kg. The AUC (area under blood decay curve) values of NBP-alkylating metabolites were 299±39, 270±13, and 521±57nmol eq nor-mustard ml-1·h in the controls, phenobarbital-pretreated, and chloral hydrate-pretreated groups, respectively. In contrast, Cmax (maximal concentration) values did not show any significant differences among these three groups. An increase in the AUC value of NBP-alkylating metabolites might have led to the stimulation of cytotoxicity of cyclophosphamide in the chloral hydrate-pretreated group. These results indicate that cyclophosphamide possesses AUC-dependent cytotoxicity against human tumor.