Rose G P, Dewar A J, Moffett B J, Stratford I J
Clin Toxicol. 1981 Dec;18(12):1411-26. doi: 10.3109/15563658108990350.
We have obtained biochemical evidence that misonidazole when administered in large doses to rats produces a sparse dying-back peripheral neuropathy and degenerative changes in the trigeminal ganglia and cerebellum. In our experience these neurotoxic effects of misonidazole cannot be detected reliably by the use of simple behavioural and functional tests, e.g., inclined plane and narrowing bridge tests (Rose and Dewar, unpublished results). Therefore, these methods would be of limited use in the neurotoxicity screening of misonidazole analogues. On the other hand, the biochemical approach provides a convenient quantitative method which could be used as the basis for comparing the neurotoxicity of other candidate radiosensitizing drugs.
我们已获得生化证据,即大剂量给大鼠施用米索硝唑会导致稀疏的逆行性周围神经病变以及三叉神经节和小脑中的退行性变化。根据我们的经验,通过简单的行为和功能测试,如斜面和窄桥测试(罗斯和杜瓦尔,未发表的结果),无法可靠地检测到米索硝唑的这些神经毒性作用。因此,这些方法在米索硝唑类似物的神经毒性筛查中的用途有限。另一方面,生化方法提供了一种便捷的定量方法,可作为比较其他候选放射增敏药物神经毒性的基础。