Related Experiment Videos
A nitric oxide synthase inhibitor impairs memory storage in mice
1Laboratorio de Neurofarmacologia de Procesos de Memoria, Catedra de Farmacologia, Facultad de Farmacia y Bioquimica, Universidad de Buenos Aires, Junin 9560, Buenos Aires, RA-1113, Argentina.
Neurobiology of Learning and Memory
|May 1, 1996
Summary
Nitric oxide synthase inhibition by L-NAME impairs memory retention in mice. This memory impairment is linked to the L-arginine/nitric oxide pathway
Area of Science:
- Neuroscience
- Pharmacology
- Molecular Biology
Background:
- Nitric oxide (NO) is a signaling molecule implicated in various physiological processes, including synaptic plasticity and memory.
- Inhibitors of nitric oxide synthase (NOS) have been used to investigate the role of NO in cognitive functions.
Purpose of the Study:
- To investigate the role of the L-arginine/nitric oxide pathway in the consolidation of inhibitory avoidance memory.
- To determine if post-training administration of a NOS inhibitor affects memory retention.
Main Methods:
- Male Swiss mice were trained on a one-trial step-through inhibitory shock-avoidance task.
- Post-training administration of NG-nitro-L-arginine methyl ester (L-NAME), a competitive NOS inhibitor, or its inactive enantiomer D-NAME.
- Assessment of memory retention 48 hours post-training by measuring retention latencies.
- Administration of L-arginine or D-arginine to assess the specificity of L-NAME effects.
Main Results:
- Posttraining L-NAME administration dose-dependently impaired memory retention, evidenced by reduced latencies.
- The D-enantiomer (D-NAME) did not affect memory retention, indicating stereospecificity.
- L-NAME's effects were time-dependent, suggesting an impact on memory consolidation or storage.
- The memory impairment induced by L-NAME was reversed by co-administration of L-arginine but not D-arginine.
Conclusions:
- The L-arginine/nitric oxide pathway plays a crucial role in the storage of inhibitory avoidance memory in mice.
- Inhibition of NOS post-training disrupts memory consolidation, highlighting NO's involvement in this process.
- These findings support the hypothesis that NO signaling is essential for certain forms of memory formation.