中国寄生虫学与寄生虫病杂志 ›› 1988, Vol. 6 ›› Issue (4): 272-274.

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小鼠微核试验检测咯萘啶、氯喹、阿的平、伯氨喹、呋喃嘧酮与苯硫脲嗪的诱变性

邵葆若,徐月琴   

  1. 中国预防医学科学院寄生虫病研究所
  • 收稿日期:2017-01-10 修回日期:2017-01-10 出版日期:1988-11-30 发布日期:2017-01-10

THE MOUSE MICRONECLEUS TEST FOR MUTAGENICITY OF PYRONARIDINE, CHLOROQUINE, QUINACRINE, PRIMAQUINE, FURAPYRIMIDONE AND PHENTHIOUREZINE

  • Received:2017-01-10 Revised:2017-01-10 Online:1988-11-30 Published:2017-01-10

摘要: 昆明远交系小鼠(♂)分别ig抗疟药咯萘啶、氯喹、阿的平、伯氨喹与抗丝虫药呋喃嘧酮、苯硫脲嗪,大剂量为≥LD_(50)。药后24h作股骨骨髓细胞涂片,Giemsa染色。各服药组小鼠的多染红细胞微核率均4(?),示该6药的小鼠微核试验检测无诱变性。

关键词: 诱变性, 呋喃嘧酮, 阿的平, 试验检测, 咯萘啶, 苯硫脲, 小鼠, 伯氨喹, 细胞微核率, 微核试验

Abstract: Four antimalarials, pyronaridine, chloroquine, quinacrine, primaquine, and two an-tifilarials, furapyrimidone, phenthiourezine (I) were administered to groups of Kunming hybrid male mice at ≥LD50 doses. Giemsa stained bone marrow cell smears of the mice were made 24 h after administration and the micronulceated polychromatic erythrocytes pel 1000 polychromatic erythrocytes (MNPCE % ) were counted. The MNPCE %?of each mouse in the six drug groups was 4‰, within the range of the controls, 1.3±1.6‰ (X ± SD), indicating that the six drugs were negative in micronucleus test, having no Structural chromosome damage or damage to the spindle apparatus.