Burdett D N, Shah R M
Department of Oral Biology, Faculty of Dentistry, University of British Columbia, Vancouver, Canada.
Anticancer Drugs. 1994 Jun;5(3):309-12. doi: 10.1097/00001813-199406000-00008.
Using dosages and a route of administration which resembled those used clinically in humans, the effects of vincristine on developing hamster embryos were evaluated. The results showed that the drug exerted a highly toxic effect in a dose-dependent manner; however, it exhibited only a sporadic teratogenic (gross malformation) effect. The data on DNA synthesis indicated involvement of internal organs and structures, which needs to be verified. Overall, the teratogenicity of the drug was more pronounced during pre-organogenesis than during the organogenesis period. It was suggested that, in contrast to the data reported in the literature, the different biological response to vincristine in hamster may relate to the use of the dose-route combination, and is potentially relevant to developmental and transplacental carcinogenesis studies.
使用与临床上用于人类的剂量和给药途径相似的方式,评估了长春新碱对发育中的仓鼠胚胎的影响。结果表明,该药物以剂量依赖性方式发挥高度毒性作用;然而,它仅表现出偶发的致畸(严重畸形)作用。关于DNA合成的数据表明内部器官和结构受到影响,这需要进一步验证。总体而言,该药物的致畸性在器官发生前期比器官发生期更为明显。有人提出,与文献报道的数据相反,仓鼠对长春新碱的不同生物学反应可能与剂量-途径组合的使用有关,并且可能与发育和经胎盘致癌研究相关。