A persistent postsynaptic modification mediates long-term potentiation in the hippocampus
Abstract
Long-term potentiation (LTP) is a long-lasting enhancement of synaptic transmission that can be induced by brief repetitive stimulation of excitatory pathways in the hippocampus. One of the most controversial points is whether the process underlying the enhanced synaptic transmission occurs pre- or postsynaptically. To examine this question, we have taken advantage of the novel physiological properties of excitatory synaptic transmission in the CA1 region of the hippocampus. Synaptically released glutamate activates both NMDA and non-NMDA receptors on pyramidal cells, resulting in an excitatory postsynaptic potential (EPSP) with two distinct components. A selective increase in the non-NMDA component of the EPSP was observed with LTP. This result suggests that the enhancement of synaptic transmission during LTP is caused by an increased sensitivity of the postsynaptic neuron to synaptically released glutamate.
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The AMPA, but not NMDA, component of EPSPs is affected by LTP.
“Consistently, the AMPA, but not NMDA, component of EPSPs is affected by LTP404142.”
From State-dependent diffusion of actin-depolymerizing factor/cofilin underlies the enlargement and shrinkage of dendritic spines (2016) · cites this paper as [40]
Cites
Intracellular injections of EGTA block induction of hippocampal long-term potentiation
Lynch, G., Larson, J., Kelso, S., Barrionuevo, G., & Schottler, F. (1983) · Nature · doi:10.1038/305719a0 · Cited by 1,116 · see citing works
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Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729 · see citing works
Self-citationNMDA receptor subunit diversity: impact on receptor properties, synaptic plasticity and disease
Paoletti, P., Bellone, C., & Zhou, Q. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3504 · Cited by 2,523 · see citing works
AMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588 · see citing works
Self-citationLiao, D., Hessler, N. A., & Malinow, R. (1995) · Nature · doi:10.1038/375400a0 · Cited by 1,365 · see citing works
AMPAR Removal Underlies Aβ-Induced Synaptic Depression and Dendritic Spine Loss
Hsieh, H., Boehm, J., Sato, C., Iwatsubo, T., Tomita, T., Sisodia, S., & Malinow, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.035 · Cited by 1,042 · see citing works
Engineering a memory with LTD and LTP
Nabavi, S., Fox, R., Proulx, C. D., Lin, J. Y., Tsien, R. Y., & Malinow, R. (2014) · Nature · doi:10.1038/nature13294 · Cited by 980 · see citing works
NMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms
Malenka, R. C., & Nicoll, R. A. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90197-t · Cited by 904 · see citing works
Self-citationThe role of the GluR2 subunit in AMPA receptor function and synaptic plasticity
Isaac, J. T. R., Ashby, M. C., & McBain, C. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.001 · Cited by 802 · see citing works
Fear conditioning induces a lasting potentiation of synaptic currents in vitro
McKernan, M. G., & Shinnick-Gallagher, P. (1997) · Nature · doi:10.1038/37605 · Cited by 771 · see citing works
Recycling Endosomes Supply AMPA Receptors for LTP
Park, M., Penick, E. C., Edwards, J. G., Kauer, J. A., & Ehlers, M. D. (2004) · Science · doi:10.1126/science.1102026 · Cited by 730 · see citing works
Self-citationGABAB autoreceptors regulate the induction of LTP
Davies, C. H., Starkey, S. J., Pozza, M. F., & Collingridge, G. L. (1991) · Nature · doi:10.1038/349609a0 · Cited by 615 · see citing works
Synaptic plasticity in the lateral amygdala: a cellular hypothesis of fear conditioning
Blair, H. T., Schafe, G. E., Bauer, E. P., Rodrigues, S. M., & LeDoux, J. E. (2001) · Learning & Memory · doi:10.1101/lm.30901 · Cited by 610 · see citing works
Is Heterosynaptic modulation essential for stabilizing hebbian plasiticity and memory
Bailey, C. H., Giustetto, M., Huang, Y.-Y., Hawkins, R. D., & Kandel, E. R. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036191 · Cited by 382 · see citing works
Encoding of contextual fear memory in hippocampal–amygdala circuit
Kim, W. B., & Cho, J.-H. (2020) · Nature Communications · doi:10.1038/s41467-020-15121-2 · Cited by 289 · see citing works
The impact of postsynaptic calcium on synaptic transmission — its role in long-term potentiation
Malenka, R. C., Kauer, J. A., Perkel, D. J., & Nicoll, R. A. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90094-5 · Cited by 275 · see citing works
Self-citationPhotoinactivation of native AMPA receptors reveals their real-time trafficking
Adesnik, H., Nicoll, R. A., & England, P. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.11.030 · Cited by 234 · see citing works
Self-citationHippocampal Interneurons Express a Novel Form of Synaptic Plasticity
McMahon, L. L., & Kauer, J. A. (1997) · Neuron · doi:10.1016/s0896-6273(00)80269-x · Cited by 182 · see citing works
Self-citationPoncer, J. C., Esteban, J. A., & Malinow, R. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-11-04406.2002 · Cited by 177 · see citing works
Lamsa, K., Heeroma, J. H., & Kullmann, D. M. (2005) · Nature Neuroscience · doi:10.1038/nn1486 · Cited by 158 · see citing works
Huang, C. S., Shi, S.-H., Ule, J., Ruggiu, M., Barker, L. A., Darnell, R. B., Jan, Y. N., & Jan, L. Y. (2005) · Cell · doi:10.1016/j.cell.2005.07.033 · Cited by 157 · see citing works
Leon, J., Moreno, A. J., Garay, B. I., Chalkley, R. J., Burlingame, A. L., Wang, D., & Dubal, D. B. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.07.024 · Cited by 123 · see citing works
Pathway-Selective Adjustment of Prefrontal-Amygdala Transmission during Fear Encoding
Arruda-Carvalho, M., & Clem, R. L. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2664-14.2014 · Cited by 127 · see citing works
Approaches and Limitations in the Investigation of Synaptic Transmission and Plasticity
Glasgow, S. D., McPhedrain, R., Madranges, J. F., Kennedy, T. E., & Ruthazer, E. S. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00020 · Cited by 100 · see citing works
Shors, T. J., & Thompson, R. F. (1992) · Synapse · doi:10.1002/syn.890110311 · Cited by 88 · see citing works
Noguchi, J., Hayama, T., Watanabe, S., Ucar, H., Yagishita, S., Takahashi, N., & Kasai, H. (2016) · Scientific Reports · doi:10.1038/srep32897 · Cited by 60 · see citing works
Procedural Learning and the Development and Stability of Character
Grigsby, J., & Hartlaub, G. H. (1994) · Perceptual and Motor Skills · doi:10.2466/pms.1994.79.1.355 · Cited by 38 · see citing works
Le, A. A., Quintanilla, J., Amani, M., Piomelli, D., Lynch, G., & Gall, C. M. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105565 · Cited by 22 · see citing works
Asztely, F., Hanse, E., Wigström, H., & Gustafsson, B. (1992) · Synapse · doi:10.1002/syn.890110409 · Cited by 18 · see citing works
Hippocampal synaptic plasticity and NMDA receptors: a role in information storage?
MORRIS, R. G. M., DAVIS, S., & BUTCHER, S. P. (1991) · Behavioural and Neural Aspects of Learning and Memory · doi:10.1093/acprof:oso/9780198521983.003.0011 · Cited by 15 · see citing works
- Authors
- Kauer, J. A., Malenka, R. C., & Nicoll, R. A.
- Affiliations
- University of California, San Francisco (US)
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1988-12
- Volume
- 1
- Issue
- 10
- Pages
- 911-917
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2157365188
- Cited by
- 497
- References
- 1
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 8 · 2023: 8 · 2022: 7 · 2021: 12 · 2020: 6 · 2019: 5 · 2018: 6 · 2017: 8 · 2016: 6 · 2015: 4 · 2014: 8 · 2013: 13 · 2012: 7
- FWCI
- 13.97
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs
- National Institutes of Health (MH00437, MH38256, NS24205)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Keywords
- long-term potentiation, hippocampus, CA1 region, non-NMDA receptors, NMDA receptor, excitatory postsynaptic potentials, glutamate sensitivity, synaptic transmission, pyramidal neurons
- MeSH terms
- Animals, Aspartic Acid, Glutamates, Hippocampus, Membrane Potentials, Synaptic Transmission, Quinoxalines, Synapses, Receptors, N-Methyl-D-Aspartate, N-Methylaspartate, Receptors, Neurotransmitter, 6-Cyano-7-nitroquinoxaline-2,3-dione, Rats
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