Marret S, Gressens P, Van-Maele-Fabry G, Picard J, Evrard P
Service de Médecine Néonatale, Centre Hospitalier Universitaire de Rouen, France.
Brain Res. 1997 Oct 31;773(1-2):213-6. doi: 10.1016/s0006-8993(97)00938-4.
In toto mouse embryos were cultivated at embryonic day 8.5 for 26 h with 105, 310 or 620 microM caffeine; 105-310 microM correspond to concentrations transferred by the placenta of heavy caffeine consumers. Failure of neural tube closure, excessive proliferation of neuroepithelial cells and premature evagination of telencephalic vesicles were present in 50% of treated embryos. When reaching the embryonic neural tube before neuronal migration, caffeine regionally modifies the schedule and/or rate of neural cell proliferation.
将整个小鼠胚胎在胚胎第8.5天用105、310或620微摩尔咖啡因培养26小时;105 - 310微摩尔对应重度咖啡因消费者胎盘转运的浓度。50%的处理胚胎出现神经管闭合失败、神经上皮细胞过度增殖和端脑泡过早外翻。在神经元迁移之前到达胚胎神经管时,咖啡因会局部改变神经细胞增殖的时间表和/或速率。