癌变·畸变·突变 ›› 2005, Vol. 17 ›› Issue (6): 367-369.doi: 10.3969/j.issn.1004-616x.2005.06.013

• 论著 • 上一篇    下一篇

环磷酰胺剂量、取样时间对小鼠骨髓微核率的影响

肖 凯;李宏霞   

  1. 四川大学华西医院国家成都中药安全性评价中心
  • 收稿日期:2004-10-10 修回日期:2005-04-28 出版日期:2005-11-30 发布日期:2005-11-30
  • 通讯作者: 李宏霞

Effects of Cyclophosphamide Dose and Sampling Time on Mouse Micronucleus Frequency in Bone Marrow

XIAO Kai; LI Hong-xia   

  1. National Chengdu Center for Safety Evaluation of Traditional Chinese Medicine, West China Hospital, Sichuan University
  • Received:2004-10-10 Revised:2005-04-28 Online:2005-11-30 Published:2005-11-30
  • Contact: LI Hong-xia

摘要: 背景与目的: 观察NIH小鼠在给予不同剂量环磷酰胺(Cyclophosphamide, CP)后不同取样时间点的骨髓嗜多染红细胞(Polychromatic erythrocytes, PCE)微核率的变化。 材料与方法: 小鼠一次性腹腔注射CP 40、80 mg/kg后,于18 、24 、48 h取胸骨骨髓涂片,Giemsa染色,计数1 000 个PCE中含有微核的细胞数(微核率)及200 个红细胞中PCE与正染红细胞(Normochromatic erythrocytes, NCE)的比值。 结果: 小鼠在给予40 mg/kg和80 mg/kg CP后的骨髓微核率随取样时间的变化趋势是一致的,给药后一段时间逐渐升高,24 h达高峰,之后又逐渐下降。给药组各时间点的微核率与对照组相比差异均有统计学意义,而给药组PCE与NCE比值与对照组的比较差异均无统计学意义,提示小鼠一次腹腔注射40 mg/kg和80 mg/kg CP后对骨髓细胞无明显抑制作用。80 mg/kg CP剂量组各时间点上的微核率显著高于40 mg/kg 剂量组,表现出明显的剂量_反应关系。 结论: 在本实验室条件下,40 mg/kg和80 mg/kg CP均可致小鼠骨髓嗜多染红细胞的微核率显著增加,具有剂量_反应关系。在一次性腹腔注射环磷酰胺后24 h观察所得微核率最高。故认为环磷酰胺可用作微核试验的阳性对照,剂量范围为40~80 mg/kg,给药后24 h取材最佳。

关键词: 微核率, 环磷酰胺, 嗜多染红细胞, 骨髓

Abstract: BACKGROUND & AIM: To evaluate the effects of different doses of cyclophosphamide (CP) and sampling time on mouse micronucleus frequency in bone marrow. MATERIAL AND METHODS: Young adult NIH mice were treated with a sigle dose of CP(40 or 80 mg/kg) by intraperitoneal injection. The micronucleus freqyuency in bone marrow polychromatic erythrocytes (PCE) at different sampling time 18 , 24 , 48 h after treatment was evaluated. RESULTS: Our data showed: ① The changing trends of the micronucleus frequencies in PCE in the two groups receiving 40 mg/kg and 80 mg/kg of CP were the same at different sampling times. The peak time of the micronucleus incidence was at 24 h after treatment. ② The ratios of PCE to NCE of the two treated groups were not significantly different from the control group. This indicated that the mice bone marrow cells were not suppressed by one CP of 40 or 80 mg/kg by intraperitoneal injection. ③ The micronucleus frequency in PCE of 40 mg/kg was significantly different from that of 80 mg/kg, showing a dose_response relationship. CONCLUSION: CP can be used as a positive control of micronucleus test. The dose range of 40~80 mg/kg was fine, and the optimal sampling time is at 24 h after treatment.

Key words: micronucleus frequency, cyclophosphamide, polychromatic erythrocyte, bone marrow