Inhibition of Long-Term Potentiation by NMDA-Mediated Nitric Oxide Release
- 28 August 1992
- journal article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 257 (5074) , 1273-1276
- https://doi.org/10.1126/science.1519065
Abstract
Activation of N -methyl-D-aspartate (NMDA) receptors before tetanic stimulation blocks long-term potentiation (LTP) in the CA1 region of the hippocampus. This NMDA-mediated inhibition of LTP can be reversed by the nitric oxide (NO) inhibitors L- N G -monomethyl-arginine or hemoglobin and mimicked by sodium nitroprusside. These results indicate that the timing of NO release relative to high-frequency activation of CA1 synapses may be an important determinant of LTP generation and suggest that NO may play a positive or negative modulatory role in LTP depending on prior events at the tetanized synapse and the ambient concentration of excitatory amino acids.Keywords
This publication has 31 references indexed in Scilit:
- The role of nitric oxide in hippocampal long-term potentiationNeuron, 1992
- The Influence of Prior Synaptic Activity on the Induction of Long-Term PotentiationScience, 1992
- Postsynaptic contribution to long-term potentiation revealed by the analysis of miniature synaptic currentsNature, 1992
- Nitric oxide synthase protein and mRNA are discretely localized in neuronal populations of the mammalian CNS together with NADPH diaphoraseNeuron, 1991
- Long‐term enhancement of CA1 synaptic transmission is due to increased quantal size, not quantal contentHippocampus, 1991
- Postsynaptic factors control the duration of synaptic enhancement in area CA1 of the hippocampusNeuron, 1991
- Localization of nitric oxide synthase indicating a neural role for nitric oxideNature, 1990
- Presynaptic enhancement shown by whole-cell recordings of long-term potentiation in hippocampal slicesNature, 1990
- L-arginine is the physiological precursor for the formation of nitric oxide in endothelium-dependent relaxationBiochemical and Biophysical Research Communications, 1988
- Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factorNature, 1987