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在小鼠胚胎上测试的两种神经otropic药物(氟哌啶醇和右吗拉胺)的致畸潜力。

Teratogenic potential of two neurotropic drugs, haloperidol and dextromoramide, tested on mouse embryos.

作者信息

Jurand A, Martin L V

机构信息

Department of Genetics, University of Edinburgh, Scotland.

出版信息

Teratology. 1990 Jul;42(1):45-54. doi: 10.1002/tera.1420420107.

Abstract

Potential teratogenic activity of two neurotropic drugs, haloperidol and dextromoramide tartrate, was tested by using the mouse embryo experimental model. Like numerous other drugs of this class these two are also embryotoxic. After treatment 1 hour into the 9th gestation day they induce the neurotropic syndrome of malformations comprising exencephaly, craniorachischisis, kinking of the spinal cord, brachyury, and dilation of the fourth brain ventricle. In addition, dextromoramide tartrate was found to induce one more, so far unknown, neural tube defect, namely the ectopia of the neural tube. Delay of treatment by 1 or 2 hours tends to displace the location of the neural tube defects along the length of the neural axis towards the anterior and posterior directions. Even after accumulating these results at relatively high doses, it is difficult to estimate human reproductive risks from this animal data for human therapeutic doses.

摘要

利用小鼠胚胎实验模型测试了两种嗜神经药物(氟哌啶醇和酒石酸右吗拉胺)的潜在致畸活性。与该类众多其他药物一样,这两种药物也具有胚胎毒性。在妊娠第9天治疗1小时后,它们会诱发包括无脑畸形、脊柱裂、脊髓扭结、短尾、第四脑室扩张在内的嗜神经畸形综合征。此外,还发现酒石酸右吗拉胺会诱发另一种迄今未知的神经管缺陷,即神经管异位。治疗延迟1或2小时往往会使神经管缺陷的位置沿神经轴长度向前和向后方向移位。即使在相对高剂量下积累了这些结果,也很难根据这些动物数据估计人类治疗剂量对人类生殖的风险。

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