癌变·畸变·突变 ›› 1999, Vol. 11 ›› Issue (3): 128-131.doi: 10.3969/j.issn.1004-616x.1999.03.008

• 论著 • 上一篇    下一篇

用Ames 法和致畸试验研究醋氨己酸锌的遗传毒性

马明福1  李练兵1  曾维三1  徐小丽1  王治乔2   

  1. 1重庆市计划生育科学研究所 重庆 400020   2 军事医学科学院毒物药物研究所 北京 100850
  • 收稿日期:1998-09-29 修回日期:1999-03-01 出版日期:1999-05-30 发布日期:1999-05-30

STUDY ON THE GENOTOXICITY OF ZINC ACEXAMATIE BY THE AMES TEST AND TERATOGENIC TEST

Ma Mingfu1 , Li Lianbing1 , Zeng Weishan1 , Xu xiaoli1 , Wang Zhiqiao2   

  1. 1Chongqing Family Planning Scientif ic Research , Chongqing  400020 , 2 Instit ute of Pharmacology and Toxicology , Academy of Military Medical Sciences , Beijing  100850
  • Received:1998-09-29 Revised:1999-03-01 Online:1999-05-30 Published:1999-05-30

摘要: 用Ames 试验和致畸试验对醋氨己酸锌进行了致突变和致畸作用研究。结果表明醋氨己酸锌在Ames 试验的TA97 、TA98 、TA100 和TA102 4 个标准菌株±S9mix条件下,1 - 5000μg/ 皿6 个剂量的标准平皿掺入试验中,未诱发各菌株阳性突变反应。小鼠致畸试验32179mg/ kg·bw、262134mg/ kg·bw 和524167mg/ kg·bw 剂量组,在母鼠妊娠期6 - 15d p. o 给药,各剂量组活胎率与溶剂对照组比较,无显著差异( P > 0105) 。对胎鼠外观、骨骼和内脏无致畸作用。但524167mg/ kg·bw 组对妊娠母鼠体重、胎鼠体重和尾长有影响,显示一定的母体和胚胎毒性。

关键词: 醋氨己酸锌, 突变, 致畸作用

Abstract: This paper reported the research result s of mutagenicity and teratogenicity effect of zinc acexamatie.The result showed that zinc acexamatie with doses level (1 - 5000μg/ plate) did not induce positive mutations of st rains TA97 、TA98 、TA100 and TA102 with or without S9mix in Ames test . It was divided into three groups of Zinc acexamatic received (po) dosages of 32. 97mg/ kg. body weight , 262. 34mg/ kg. body weight , 524. 67mg/ kg.body weight on the 6th to 15th day of gestation mouse respectively in the teratogenic test . The f requency of live fetuses of each dose group were no significant difference as compared with solvent cont rol group. It did not cause deformity of the fetus appearances , bone and internal organs. But there were significant differences between solvent cont rol group and 524. 67mg/ kg group in the growth of body weight in gestation of mouse , body weight and tail length in fetus. The result showed that zinc acexamatie possess maternal toxicity and embryotoxicity.

Key words: zinc acexamatie, mutation, teratogenic effect s