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WR-2721对环磷酰胺诱导的小鼠微核的抑制作用。

Suppressing effect of WR-2721 on micronuclei induced by cyclophosphamide in mice.

作者信息

Czyzewska A, Mazur L

机构信息

Department of Animal Physiology, Jagiellonian University, Cracow, Poland.

出版信息

Teratog Carcinog Mutagen. 1995;15(3):109-14. doi: 10.1002/tcm.1770150303.

Abstract

The effect of WR-2721 against cyclophosphamide-induced clastogenicity was studied using the in vivo micronucleus assay. The frequency of micronuclei in polychromatic erythrocytes in the peripheral blood of mice treated with WR-2721 and cyclophosphamide (CP), each of the compounds at a dose of 200 mg/kg body weight, was evaluated during the 15-day period. The suppressing effect of WR-2721, given 30 min prior to cyclophosphamide administration, on micronuclei induced by the alkylating agent was demonstrated. The number of micronuclei was increased on day 1 after CP application and declined thereafter with the frequency of micronucleated polychromatic erythrocytes remaining lower in WR-2721 pre-treated mice. The modulatory effect of WR-2721 on the clastogenic activity of cyclophosphamide in the erythropoietic system by the mouse micronucleus test was shown.

摘要

使用体内微核试验研究了WR-2721对环磷酰胺诱导的致断裂性的影响。在15天的时间段内,评估了以200mg/kg体重剂量的WR-2721和环磷酰胺(CP)处理的小鼠外周血中多染性红细胞的微核频率。结果表明,在给予环磷酰胺前30分钟给予WR-2721,对烷化剂诱导的微核有抑制作用。环磷酰胺给药后第1天微核数量增加,此后下降,WR-2721预处理的小鼠中多染性红细胞微核化频率保持较低。通过小鼠微核试验显示了WR-2721对环磷酰胺在红细胞生成系统中的致断裂活性的调节作用。

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