Department of Psychology, University of Delaware, Newark, Delaware 19716, USA.
Dev Psychobiol. 2010 Sep;52(6):583-91. doi: 10.1002/dev.20465.
Long-Evans rats were trained on spatial delayed alteration (SDA) in a T-maze following medial prefrontal cortical (mPFC) infusions of different doses of the noncompetitive NMDA-receptor antagonist, MK-801 (.125 microl; .25 microl; or .25 microlsaline, bilaterally), on postnatal day (PND) 19, 26, or 33. Pups trained on PND 19 showed almost no learning of SDA, regardless of drug condition (including saline). On PND 26, both doses of MK-801 significantly and equivalently prevented SDA learning, with performance during the final three training blocks remaining near chance levels, in contrast with 85% correct performance in the saline control group. On PND 33, substantial SDA learning was evident regardless of dose, although a modest impairment appeared in mid-training at both doses. These findings confirm previous reports of mPFC involvement in the early postnatal ontogeny of SDA and suggest a developmentally transient role of mPFC NMDA-receptor function in this task.
长爪沙鼠在接受内侧前额叶皮质(mPFC)双侧不同剂量非竞争性 NMDA 受体拮抗剂 MK-801(0.125 微升;0.25 微升;或 0.25 微升生理盐水)注射后,于出生后第 19、26 或 33 天在 T 迷宫中接受空间延迟改变(SDA)训练。在 PND19 接受训练的幼鼠几乎没有 SDA 的学习,无论药物条件如何(包括生理盐水)。在 PND26 时,MK-801 的两种剂量均显著且等效地阻止了 SDA 的学习,与生理盐水对照组 85%的正确表现相比,在最后三个训练块中的表现仍接近机会水平。在 PND33 时,无论剂量如何,都可以明显地进行 SDA 学习,尽管在两种剂量下,在训练中期都出现了适度的障碍。这些发现证实了之前关于 mPFC 参与 SDA 早期产后发育的报告,并表明 mPFC NMDA 受体功能在该任务中的发育性暂态作用。