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[致畸实验中的CT作用模式]

[ct-Mode of Action in the Teratogenic Experiment].

作者信息

Hafen P, Kreybig T V

出版信息

Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1975;83(1):31-55. doi: 10.1007/BF00284400.

Abstract

The doses of 10 and 20 mg/kg N-methyl-N-nitrosourea which were teratogenetically effective after a single dose were distributed over 12,24, 48, and 96 hrs during the embryonic developmental phase of the rat. It turned out that the effects were enormously increased when both doses were given in ten single doses during 12 hrs. The number of fetuses that had died down during gestation was increased considerably, the surviving fetuses bore, without exception, the marks of extreme malformations, as, for example, big haemorrhagic cysts instead of the mandible and the tongue. The distribution of the doses over 24 hrs showed, as far as quantity is concerned, comparable teratogenic effects, which, however, during the time of treatment varied in quality according to the variation of the critical sensitivity of the developmental phase. The distribution over even longer periods of time gradually weakened the effect. There were also some other symptoms that became manifest. So it can be said that N-methyl-N-nitrosourea is according to its teratogenic effects also a typical ct-poison (Druckrey) with the maximum of cumulation after distributing the dose over 12 hrs of the gestation.

摘要

单次给药具有致畸作用的10毫克/千克和20毫克/千克N-甲基-N-亚硝基脲剂量,在大鼠胚胎发育阶段于12、24、48和96小时内进行给药。结果发现,当在12小时内分十次给予这两种剂量时,致畸作用大大增强。孕期死亡的胎儿数量大幅增加,存活的胎儿无一例外都带有严重畸形的痕迹,例如,没有下颌和舌头,取而代之的是大的出血性囊肿。就数量而言,在24小时内给药显示出相当的致畸作用,然而,在治疗期间,根据发育阶段临界敏感性的变化,致畸作用在质量上有所不同。在更长时间内给药会逐渐减弱这种作用。还出现了一些其他明显的症状。因此可以说,就其致畸作用而言,N-甲基-N-亚硝基脲也是一种典型的细胞毒剂(德鲁克里),在妊娠12小时内给药后累积作用最强。

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