摘要
本研究运用小鼠骨髓细胞微核心试验评价叶绿素的衍生物——叶绿酸铜纳(ChlorophyllinSodium—CopperSalt,CHL)抑制间接诱变剂环磷酰胺(Cyclophosphamide,CP)的诱变作用。实验根据小鼠给予CHL和CP的时间,设计4种不同程序,以此探索CHL抗诱变作用的机理.实验结果表明,CHL本身无诱变作用,但对CP诱导微核作用有明显的抑制。同时也提示CHL对CP的抗诱变作用可能至少有2种机理。Theinvivomousebone-marrowPCEmicronucleustochecktheantimutagenicpotentialsofchlorophyllin(CHL)onmutationinducedbycyclophosphamide(CP)wascar-riedout.InordertoexplosethepossiblemechanismofantimutageniceffectofCHL.Thedif-ferenttreatmentschedulesintheadministrationofCHLandofCPtomiceweredesigned.Theresult?
The in vivo mouse bone-marrow PCE
micronucleus to check the antimutagenicpotentials of chlorophyllin(CHL)on mutation induced by
cyclophosphamide(CP)was car-ried out.In order to explose the possible mechanism of
antimutagenic effect of CHL. The dif-ferent treatment schedules in the administration of CHL and
of CP to mice were designed.The results indicated that CHL itself is not a mutagen,but showed
significant inhibitory ef-fect against CP in inducing micronuclei. There should at least two
mechanisms involved in theantimutagenic effect of CHL to CP.
出处
《癌变.畸变.突变》
CAS
CSCD
1995年第1期34-38,共5页
Carcinogenesis,Teratogenesis & Mutagenesis
关键词
叶绿酸铜钠
抗诱变作用
药理
chlorophyllin,
cyclophosphamide, antimutagenic effect, micronucleus test.