The Ross Laboratory for Studies in Neural Birth Defects, Department of Medical Neurobiology, Institute for Medical Research-Israel-Canada, The Hebrew University-Hadassah Medical School, Box 12272, 91120 Jerusalem, Israel.
Behav Brain Res. 2009 Dec 28;205(2):499-504. doi: 10.1016/j.bbr.2009.08.006. Epub 2009 Aug 12.
Identifying the mechanisms underlying the adverse effects of developmental neurotoxicants enables the design of therapies that can potentially reverse neurobehavioral deficits in adulthood. We administered chlorpyrifos (CPF), a model organophosphate pesticide to pregnant mice and identified visuospatial deficits in adult offspring using performance in the Morris maze. We then evaluated two strategies to reverse the effects, nicotine administration and transplantation of neural stem cells. Daily administration of nicotine prior to behavioral testing did not alter maze performance by itself, but completely reversed the deficits evoked by prenatal CPF exposure. Similarly, control animals grafted with neural stem cells in adolescence did not show any alterations in behavioral performance as adults, but the grafts completely reversed the effects of prenatal CPF treatment. This study thus provides a model for the development and application of both pharmacologic and cell-based therapies to offset the effects of neurobehavioral teratogens.
确定发育神经毒物不良影响的机制使我们能够设计出潜在的治疗方法,以逆转成年期的神经行为缺陷。我们给怀孕的老鼠施用了毒死蜱(CPF),一种典型的有机磷杀虫剂,并通过在 Morris 水迷宫中的表现来确定成年后代的视觉空间缺陷。然后,我们评估了两种逆转效果的策略,尼古丁给药和神经干细胞移植。在行为测试前每天给予尼古丁本身并不会改变迷宫表现,但完全逆转了产前 CPF 暴露引起的缺陷。同样,在青春期移植神经干细胞的对照动物在成年后没有表现出任何行为表现的改变,但移植完全逆转了产前 CPF 处理的影响。因此,这项研究为开发和应用药物和细胞治疗方法来抵消神经行为致畸物的影响提供了一个模型。