Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4344251 | Neuroscience Letters | 2012 | 4 Pages |
Using a combination of electrophysiological recordings, behavioral tests and local pharmacological administration in hippocampus, we investigated in the present study the effects of nitric oxide (NO) synthase inhibitor N-nitro-l-arginine methyl ester (l-NAME) on the behavioral long-term potentiation (LTP) and maze learning performance in freely moving rats. The results showed as follows: (1) intrahippocampal l-NAME administration led to a defect in maze learning performance of the animals; (2) l-NAME treatment also substantially impaired the induction of the behavioral LTP in perforant pathway to dentate gyrus (PP-DG) pathway induced by maze learning task, while it had no significant effects on basic synaptic transmission in PP-DG pathway; Collectively, these results indicate that NO synthesis may be critical for the behavioral LTP in PP-DG pathway and maze learning performance.
► Behavioral LTP is a LTP model that is induced by maze learning performance. ► l-NAME, an NO synthesis inhibitor, impairs both maze learning and behavioral LTP. ► NO synthesis may be critical for behavioral LTP in freely moving animals.