Lee Sung Hak, Kang Jung Won, Lin Tao, Lee Jae Eun, Jin Dong Il
Department of Animal Science & Biotechnology, Chungnam National University, Daejeon 305-764, Republic of Korea.
Biomed Res Int. 2013;2013:726478. doi: 10.1155/2013/726478. Epub 2013 Nov 14.
The zebrafish model is an attractive candidate for screening of developmental toxicity during early drug development. Antiepileptic drugs (AEDs) arouse concern for the risk of teratogenicity, but the data are limited. In this study, we evaluated the teratogenic potential of seven AEDs (carbamazepine (CBZ), ethosuximide (ETX), valproic acid (VPN), lamotrigine (LMT), lacosamide (LCM), levetiracetam (LVT), and topiramate (TPM)) in the zebrafish model. Zebrafish embryos were exposed to AEDs from initiation of gastrula (5.25 hours post-fertilization (hpf)) to termination of hatching (72 hpf) which mimic the mammalian teratogenic experimental design. The lethality and teratogenic index (TI) of AEDs were determined and the TI values of each drug were compared with the US FDA human pregnancy categories. Zebrafish model was useful screening model for teratogenic potential of antiepilepsy drugs and was in concordance with in vivo mammalian data and human clinical data.
斑马鱼模型是早期药物开发过程中筛选发育毒性的一个有吸引力的候选模型。抗癫痫药物(AEDs)引发了对致畸风险的关注,但相关数据有限。在本研究中,我们评估了七种抗癫痫药物(卡马西平(CBZ)、乙琥胺(ETX)、丙戊酸(VPN)、拉莫三嗪(LMT)、拉科酰胺(LCM)、左乙拉西坦(LVT)和托吡酯(TPM))在斑马鱼模型中的致畸潜力。斑马鱼胚胎从原肠胚起始(受精后5.25小时(hpf))到孵化结束(72 hpf)暴露于抗癫痫药物中,这模拟了哺乳动物致畸实验设计。测定了抗癫痫药物的致死率和致畸指数(TI),并将每种药物的TI值与美国食品药品监督管理局(US FDA)的人类妊娠分类进行了比较。斑马鱼模型是筛选抗癫痫药物致畸潜力的有用模型,并且与体内哺乳动物数据和人类临床数据一致。