Disrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatum

• DOI: 10.1073/pnas.0601758103
• Publication Date: 2006-10-03T00:37:21Z
• Authors: Mai T. Dang; Fumiaki Yokoi; Henry H. Yin; David M. Lovinger; Yanyan Wang; Yuqing Li
• Keywords: Mice, Knockout; 0303 health sciences; Neuronal Plasticity; Long-Term Potentiation; Receptors, N-Methyl-D-Aspartate; Basal Ganglia; Corpus Striatum; Mice; 03 medical and health sciences; Synapses; Animals; Learning; RGS Proteins

Much research has implicated the striatum in motor learning, but the underlying mechanisms have not been identified. Although NMDA receptor (NMDAR)-dependent long-term potentiation has been observed in the striatum, its involvement in motor learning remains unclear. To examine the role of striatal NMDAR in motor learning, we created striatum-specific NMDAR1 subunit knockout mice, analyzed the striatal anatomy and neuronal morphology of these mice, evaluated their performance on well established motor tasks, and performed electrophysiological recordings to assay striatal NMDAR function and long-term synaptic plasticity. Our results show that deleting the NMDAR1 subunit of the NMDAR specifically in the striatum, which virtually abolished NMDAR-mediated currents, resulted in only small changes in striatal neuronal morphology but severely impaired motor learning and disrupted dorsal striatal long-term potentiation and ventral striatal long-term depression.