The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
NMDA Receptor Content of Synapses in Stratum Radiatum of the Hippocampal CA1 Area
Open accessAbstract
Glutamate receptors activated by NMDA (NMDARs) or AMPA (AMPARs) are clustered on dendritic spines of pyramidal cells. Both the AMPAR-mediated postsynaptic responses and the synaptic AMPAR immunoreactivity show a large intersynapse variability. Postsynaptic responses mediated by NMDARs show less variability. To assess the variability in NMDAR content and the extent of their coexistence with AMPARs in Schaffer collateral–commissural synapses of adult rat CA1 pyramidal cells, electron microscopic immunogold localization of receptors has been used. Immunoreactivity of NMDARs was detected in virtually all synapses on spines, but AMPARs were undetectable, on average, in 12% of synapses. A proportion of synapses had a very high AMPAR content relative to the mean content, resulting in a distribution more skewed toward larger values than that of NMDARs. The variability of synaptic NMDAR content [coefficient of variation (CV), 0.64–0.70] was much lower than that of the AMPAR content (CV, 1.17–1.45). Unlike the AMPAR content, the NMDAR content showed only a weak correlation with synapse size. As reported previously for AMPARs, the immunoreactivity of NMDARs was also associated with the spine apparatus within spines. The results demonstrate that the majority of the synapses made by CA3 pyramidal cells onto spines of CA1 pyramids express both NMDARs and AMPARs, but with variable ratios. A less-variable NMDAR content is accompanied by a wide variability of AMPAR content, indicating that the regulation of expression of the two receptors is not closely linked. These findings support reports that fast excitatory transmission at some of these synapses is mediated by activation mainly of NMDARs.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“NMDARs tend to be concentrated in the middle of the PSD with little overlap with AMPARs (253–255).”
From Synaptic memory and CaMKII (2023) · cites this paper as [254]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
The structure of the nervous system of the nematode Caenorhabditis elegans
White, J. G., Southgate, E., Thomson, J. N., & Brenner, S. (1986) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1986.0056 · Cited by 5,589
Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 3,535
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,478
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413
Berridge, M. J. (1998) · Neuron · doi:10.1016/s0896-6273(00)80510-3 · Cited by 2,200
The Fine Structure of the Nervous System.
Tennyson, V. M. (1970) · Archives of Neurology · doi:10.1001/archneur.1970.00480240094019 · Cited by 1,946
Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study.
Eg, G. (1959) · PubMed · Cited by 1,768
Principles and Techniques of Electron Microscopy
Mandal, A. K., Nordquist, J. A., & Hayat, M. A. (1981) · Transactions of the American Microscopical Society · doi:10.2307/3225561 · Cited by 1,439
Liao, D., Hessler, N. A., & Malinow, R. (1995) · Nature · doi:10.1038/375400a0 · Cited by 1,365
Research works printed but not linked: 1
- Somogyi P Nusser Z Roberts JDB Lujan R (1998b) Precision and variability in the placement of pre- and postsynaptic receptors in relation to neurotransmitter release sites. in Central synapses: quantal mechanisms and plasticity, Workshop IV, eds Faber DS Korn H Redman SJ Thompson SM Altman JS (Human Frontier Science Program, Strasbourg, France), pp 82–93.
Cited by
Sorted by citations
Structure and function of dendritic spines
Nimchinsky, E. A., Sabatini, B. L., & Svoboda, K. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.081501.160008 · Cited by 1,208
AMPA receptor trafficking at excitatory synapses
Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150
Transient and persistent dendritic spines in the neocortex in vivo
Holtmaat, A. J. G. D., Trachtenberg, J. T., Wilbrecht, L., Shepherd, G. M., Zhang, X., Knott, G. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.003 · Cited by 1,131
Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094
The Postsynaptic Architecture of Excitatory Synapses: A More Quantitative View
Sheng, M., & Hoogenraad, C. C. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.060805.160029 · Cited by 1,003
Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy.
Cingolani, L. A., & Goda, Y. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2373 · Cited by 831
Signal-Processing Machines at the Postsynaptic Density
Kennedy, M. B. (2000) · Science · doi:10.1126/science.290.5492.750 · Cited by 788
Silent synapses and the emergence of a postsynaptic mechanism for LTP
Kerchner, G. A., & Nicoll, R. A. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2501 · Cited by 635
The Postsynaptic Organization of Synapses
Sheng, M., & Kim, E. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005678 · Cited by 603
Glutamate Receptor Exocytosis and Spine Enlargement during Chemically Induced Long-Term Potentiation
Kopec, C. D., Li, B., Wei, W., Boehm, J., & Malinow, R. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3918-05.2006 · Cited by 486
Role of ampa receptor endocytosis in synaptic plasticity
Carroll, R. C., Beattie, E. C., von Zastrow, M., & Malenka, R. C. (2001) · Nature Reviews Neuroscience · doi:10.1038/35072500 · Cited by 448
Differential activity-dependent regulation of the lateral mobilities of AMPA and NMDA receptors
Groc, L., Heine, M., Cognet, L., Brickley, K., Stephenson, F. A., Lounis, B., & Choquet, D. (2004) · Nature Neuroscience · doi:10.1038/nn1270 · Cited by 429
Self-citationUltrastructure of Synapses in the Mammalian BrainPreprint
Harris, K. M., & Weinberg, R. J. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005587 · Cited by 452
Glutamate and GABA receptor signalling in the developing brain
Luján, R., Shigemoto, R., & López‐Bendito, G. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.09.042 · Cited by 429
Release probability of hippocampal glutamatergic terminals scales with the size of the active zone
Holderith, N., Lorincz, A., Katona, G., Rózsa, B., Kulik, A., Watanabe, M., & Nusser, Z. (2012) · Nature Neuroscience · doi:10.1038/nn.3137 · Cited by 405
Ultrastructural Distribution of the α7 Nicotinic Acetylcholine Receptor Subunit in Rat Hippocampus
Fabian‐Fine, R., Skehel, P., Errington, M. L., Davies, H. A., Sher, E., Stewart, M. G., & Fine, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-20-07993.2001 · Cited by 364
Glutamate receptor dynamics in dendritic microdomains.
Newpher, T. M., & Ehlers, M. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.030 · Cited by 356
LTP leads to rapid surface expression of NMDA but not AMPA receptors in adult rat CA1
Grosshans, D. R., Clayton, D. A., Coultrap, S. J., & Browning, M. D. (2001) · Nature Neuroscience · doi:10.1038/nn779 · Cited by 362
Transcellular Nanoalignment of Synaptic Function
Biederer, T., Kaeser, P. S., & Blanpied, T. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.006 · Cited by 352
ORGANELLES AND TRAFFICKING MACHINERY FOR POSTSYNAPTIC PLASTICITY
Kennedy, M. J., & Ehlers, M. D. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112808 · Cited by 346
PDZ Domain Suppression of an ER Retention Signal in NMDA Receptor NR1 Splice Variants
Standley, S., Roche, K. W., McCallum, J. D., Sans, N., & Wenthold, R. J. (2000) · Neuron · doi:10.1016/s0896-6273(00)00161-6 · Cited by 352
Molecular aspects of glutamate dysregulation: implications for schizophrenia and its treatment
Konradi, C., & Heckers, S. (2003) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(02)00328-5 · Cited by 336
Chen, X., Levy, J. M., Hou, A., Winters, C., Azzam, R., Sousa, A. A., Leapman, R. D., Nicoll, R. A., & Reese, T. S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517045112 · Cited by 310
Laminar Organization of the NMDA Receptor Complex within the Postsynaptic Density
Valtschanoff, J. G., & Weinberg, R. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01211.2001 · Cited by 301
Diffusional trapping of GluR1 AMPA receptors by input-specific synaptic activity
Ehlers, M. D., Heine, M., Groc, L., Lee, M.-C., & Choquet, D. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.010 · Cited by 300
Changes in Synaptic Morphology Accompany Actin Signaling during LTP
Chen, L. Y., Rex, C. S., Casale, M. S., Gall, C. M., & Lynch, G. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0164-07.2007 · Cited by 296
Synaptopodin-deficient mice lack a spine apparatus and show deficits in synaptic plasticity
Deller, T., Körte, M., Chabanis, S., Drakew, A., Schwegler, H., Stefani, G. G., Zúñiga, A., Schwarz, K., Bonhoeffer, T., Zeller, R., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1832384100 · Cited by 291
NMDA Receptor Subunit-Dependent [Ca2+] Signaling in Individual Hippocampal Dendritic Spines
Sobczyk, A., Scheuß, V., & Svoboda, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1221-05.2005 · Cited by 294
Rapid functional maturation of nascent dendritic spines
Zito, K., Scheuss, V., Knott, G., Hill, T., & Svoboda, K. (2009) · Neuron · doi:10.1016/j.neuron.2008.10.054 · Cited by 272
Distinct Localization of P2X Receptors at Excitatory Postsynaptic Specializations
Rubio, M. E., & Soto, F. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00641.2001 · Cited by 267
Structural Synaptic Modifications Associated with Hippocampal LTP and Behavioral Learning
Geinisman, Y. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.952 · Cited by 262
A Unified Model of the Presynaptic and Postsynaptic Changes During LTP at CA1 Synapses
Lisman, J., & Raghavachari, S. (2006) · Science's STKE · doi:10.1126/stke.3562006re11 · Cited by 241
Long-term potentiation: outstanding questions and attempted synthesis
Lisman, J. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1242 · Cited by 240
Molecular anatomy of the postsynaptic density.
Okabe, S. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.01.006 · Cited by 225
The Number of Glutamate Receptors Opened by Synaptic Stimulation in Single Hippocampal Spines
Nimchinsky, E. A., Yasuda, R., Oertner, T. G., & Svoboda, K. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5066-03.2004 · Cited by 219
Contribution of cytoskeleton to the internalization of AMPA receptors
Zhou, Q., Xiao, M., & Nicoll, R. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.3.1261 · Cited by 233
Different modes of hippocampal plasticity in response to estrogen in young and aged female rats
Adams, M. M., Shah, R. A., Janssen, W. G. M., & Morrison, J. H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.141215898 · Cited by 225
Emerging roles of GluN3-containing NMDA receptors in the CNS
Pérez-Otaño, I., Larsen, R. S., & Wesseling, J. F. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.92 · Cited by 214
Petersen, J. D., Chen, X., Vinadé, L., Döṣemeci, A., Lisman, J. E., & Reese, T. S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11270.2003 · Cited by 212
Endocytosis and synaptic removal of NR3A-containing NMDA receptors by PACSIN1/syndapin1
Pérez‐Otaño, I., Luján, R., Tavalin, S. J., Plomann, M., Modregger, J., Liu, X., Jones, E. G., Heinemann, S. F., Lo, D. C., & Ehlers, M. (2006) · Nature Neuroscience · doi:10.1038/nn1680 · Cited by 218
Clark, B. A., & Cull-Candy, S. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-11-04428.2002 · Cited by 207
Nicholson, D. A., Yoshida, R., Berry, R. W., Gallagher, M., & Geinisman, Y. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1725-04.2004 · Cited by 204
Extrasynaptic and synaptic NMDA receptors form stable and uniform pools in rat hippocampal slices
Harris, A. Z., & Pettit, D. L. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.137679 · Cited by 202
From the stochasticity of molecular processes to the variability of synaptic transmission
Ribrault, C., Sekimoto, K., & Triller, A. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3025 · Cited by 198
NR2B-Containing Receptors Mediate Cross Talk among Hippocampal Synapses
Scimemi, A., Fine, A., Kullmann, D. M., & Rusakov, D. A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0364-04.2004 · Cited by 198
Determination of absolute protein numbers in single synapses by a GFP-based calibration technique
Sugiyama, Y., Kawabata, I., Sobue, K., & Okabe, S. (2005) · Nature Methods · doi:10.1038/nmeth783 · Cited by 189
Nicholson, D. A., Trana, R. E., Katz, Y., Kath, W. L., Spruston, N., & Geinisman, Y. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.022 · Cited by 196
Regulation of synaptic transmission and plasticity by neuronal nicotinic acetylcholine receptors
McKay, B. E., Placzek, A. N., & Dani, J. A. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.07.001 · Cited by 181
Köhr, G., Jensen, V., Koester, H. J., Mihaljević, A. L., Utvik, J. K., Kvello, A., Ottersen, O. P., Seeburg, P. H., Sprengel, R., & Hvalby, Ø. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-34-10791.2003 · Cited by 183
Opposing mechanisms mediate morphine- and cocaine-induced generation of silent synapses
Graziane, N., Sun, S., Wright, W. J., Jang, D., Liu, Z., Huang, Y. H., Nestler, E. J., Wang, Y. T., Schlüter, O. M., & Dong, Y. (2016) · Nature Neuroscience · doi:10.1038/nn.4313 · Cited by 174
A Monte Carlo Model Reveals Independent Signaling at Central Glutamatergic Synapses
Franks, K. M., Bartol, T. M., & B, T. J. S. A. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)75248-x · Cited by 176
Synapse Distribution Suggests a Two-Stage Model of Dendritic Integration in CA1 Pyramidal Neurons
Katz, Y., Menon, V., Nicholson, D. A., Geinisman, Y., Kath, W. L., & Spruston, N. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.023 · Cited by 168
Willems, J., de Jong, A. P. H., Scheefhals, N., Mertens, E. J., Catsburg, L. A. E., Poorthuis, R. B., de Winter, F., Verhaagen, J., Meye, F. J., & MacGillavry, H. D. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000665 · Cited by 176
Influence of the NR3A subunit on NMDA receptor functions
Henson, M. A., Roberts, A. C., Pérez‐Otaño, I., & Philpot, B. D. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.01.004 · Cited by 195
Ganeshina, O., Berry, R. W., Petralia, R. S., Nicholson, D. A., & Geinisman, Y. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10950 · Cited by 165
Norrholm, S. D., & Ouimet, C. C. (2001) · Synapse · doi:10.1002/syn.10006 · Cited by 169
Aging, spatial learning, and total synapse number in the rat CA1 stratum radiatum
Geinisman, Y., Ganeshina, O., Yoshida, R., Berry, R. W., Disterhoft, J. F., & Gallagher, M. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.12.001 · Cited by 166
Functional organization of postsynaptic glutamate receptors
Scheefhals, N., & MacGillavry, H. D. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.05.002 · Cited by 166
NR2B tyrosine phosphorylation modulates fear learning as well as amygdaloid synaptic plasticity
Nakazawa, T., Komai, S., Watabe, A. M., Kiyama, Y., Fukaya, M., Arima‐Yoshida, F., Horai, R., Sudo, K., Ebine, K., Delawary, M., et al. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601156 · Cited by 149
Evidence That Long-Term Potentiation Occurs within Individual Hippocampal Synapses during Learning
Fedulov, V., Rex, C. S., Simmons, D. A., Palmer, L. C., Gall, C. M., & LYNCH, G. S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2003-07.2007 · Cited by 152
Distribution of Kainate Receptor Subunits at Hippocampal Mossy Fiber Synapses
Darstein, M., Petralia, R. S., Swanson, G. T., Wenthold, R. J., & Heinemann, S. F. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-22-08013.2003 · Cited by 148
Maturation of EPSCs and Intrinsic Membrane Properties Enhances Precision at a Cerebellar Synapse
Cathala, L., Brickley, S. G., Cull-Candy, S. G., & Farrant, M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-14-06074.2003 · Cited by 149
Asymmetry of Glia near Central Synapses Favors Presynaptically Directed Glutamate Escape
Lehre, K. P., & Rusakov, D. A. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)75154-0 · Cited by 152
Determining the Neurotransmitter Concentration Profile at Active Synapses
Scimemi, A., & Beato, M. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8087-7 · Cited by 151
Zheng, K., Scimemi, A., & Rusakov, D. A. (2008) · Biophysical Journal · doi:10.1529/biophysj.108.129874 · Cited by 146
Molecular heterogeneity of central synapses: afferent and target regulation
Craig, A. M., & Boudin, H. (2001) · Nature Neuroscience · doi:10.1038/88388 · Cited by 142
A Morphological Correlate of Synaptic Scaling in Visual Cortex
Wallace, W., & Bear, M. F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1110-04.2004 · Cited by 141
Mismatched Appositions of Presynaptic and Postsynaptic Components in Isolated Hippocampal Neurons
Rao, A., Cha, E. M., & Craig, A. M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08344.2000 · Cited by 139
Spine microdomains for postsynaptic signaling and plasticity
Newpher, T. M., & Ehlers, M. D. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.02.004 · Cited by 140
Adams, M. M., Fink, S. E., Janssen, W. G. M., Shah, R. A., & Morrison, J. H. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20148 · Cited by 137
Presynaptic NMDARs in the Hippocampus Facilitate Transmitter Release at Theta Frequency
McGuinness, L., Taylor, C. J., Taylor, R. D. T., Yau, C., Langenhan, T., Hart, M. L., Christian, H., Tynan, P. W., Donnelly, P., & Emptage, N. J. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.023 · Cited by 138
Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126
Nyíri, G., Stephenson, F. A., Freund, T. F., & Somogyi, P. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00157-x · Cited by 127
Self-citationUnipolar brush cells form a glutamatergic projection system within the mouse cerebellar cortex
Nunzi, M. G., Birnstiel, S., Bhattacharyya, B. J., Slater, N. T., & Mugnaini, E. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1180 · Cited by 120
Spatial organization of cofilin in dendritic spines
Rácz, B., & Weinberg, R. J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.11.025 · Cited by 125
Trans-Endocytosis via Spinules in Adult Rat Hippocampus
Špaček, J., & Harris, K. M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0287-04.2004 · Cited by 124
A role for the spine apparatus in LTP and spatial learning
Jedlička, P., Vlachos, A., Schwarzacher, S. W., & Deller, T. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.033 · Cited by 122
Secretory Outposts for the Local Processing of Membrane Cargo in Neuronal Dendrites
Hanus, C., & Ehlers, M. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00775.x · Cited by 117
Spine loss and other dendritic abnormalities in epilepsy
Swann, J. W., Al‐Noori, S., Jiang, M., & Lee, C. L. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 268
Nanoscale co-organization and coactivation of AMPAR, NMDAR, and mGluR at excitatory synapses
Goncalves, J., Bartol, T. M., Camus, C., Levet, F., Menegolla, A. P., Sejnowski, T. J., Sibarita, J.-B., Vivaudou, M., Choquet, D., & Hosy, E. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1922563117 · Cited by 112
Ganeshina, O., Berry, R. W., Petralia, R. S., Nicholson, D. A., & Geinisman, Y. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.02.025 · Cited by 111
Postsynaptic silent synapses: evidence and mechanisms
Isaac, J. T. R. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(03)00229-6 · Cited by 113
Activity-Dependent Plasticity of the NMDA-Receptor Fractional Ca2+ Current
Sobczyk, A., & Svoboda, K. (2007) · Neuron · doi:10.1016/j.neuron.2006.11.016 · Cited by 111
AMPA amd NMDA receptors: similarities and differences in their synaptic distribution
Nusser, Z. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00086-6 · Cited by 108
Pickard, L., Noël, J., Duckworth, J. K., Fitzjohn, S. M., Henley, J. M., Collingridge, G. L., & Molnár, E. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00127-7 · Cited by 109
The Role of Perisynaptic Glial Sheaths in Glutamate Spillover and Extracellular Ca2+ Depletion
Rusakov, D. A. (2001) · Biophysical Journal · doi:10.1016/s0006-3495(01)75846-8 · Cited by 106
Sindreu, C. B. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.8.823 · Cited by 103
The substrates of memory: Defects, treatments, and enhancement
LYNCH, G. S., Rex, C. S., Chen, L. Y., & Gall, C. M. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.082 · Cited by 103
Rash, J. E., Davidson, K. G. V., Kamasawa, N., Yasumura, T., Kamasawa, M., Zhang, C., Michaels, R., Restrepo, D., Ottersen, O. P., Olson, C. O., et al. (2005) · Journal of Neurocytology · doi:10.1007/s11068-005-8360-2 · Cited by 102
Computational reconstitution of spine calcium transients from individual proteins
Bartol, T. M., Keller, D. X., Kinney, J. P., Bajaj, C., Harris, K. M., B, T. J. S. A., & Kennedy, M. B. (2015) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2015.00017 · Cited by 98
Alterations in CA1 hippocampal synapses in a mouse model of fragile X syndrome
Jawaid, S., Kidd, G. J., Wang, J., Swetlik, C., Dutta, R., & Trapp, B. D. (2017) · Glia · doi:10.1002/glia.23284 · Cited by 93
Dalby, N. O., & Módy, I. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00118.2003 · Cited by 98
Differential expression of NMDA and AMPA receptor subunits in rat dorsal and ventral hippocampus
Pandis, C., Sotiriou, E., Kouvaras, E., Asprodini, E., Papatheodoropoulos, C., & Angelatou, F. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.003 · Cited by 95
Zhang, J., & Diamond, J. S. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21089 · Cited by 94
Ikegaya, Y., Kim, J.-A., Baba, M., Iwatsubo, T., Nishiyama, N., & Matsuki, N. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.22.4083 · Cited by 88
Synaptic Strength of Individual Spines Correlates with Bound Ca 2+ –Calmodulin-Dependent Kinase II
Asrican, B., Lisman, J. E., & Otmakhov, N. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3587-07.2007 · Cited by 85
Levy, R. B., & Aoki, C. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-05001.2002 · Cited by 86
Orefice, L. L., Waterhouse, E. G., Partridge, J. G., Lalchandani, R. R., Vicini, S., & Xu, B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0012-13.2013 · Cited by 87
NMDA Receptors in Hippocampal GABAergic Synapses and Their Role in Nitric Oxide Signaling
Szabadits, E., Cserép, C., Szőnyi, A., Fukazawa, Y., Shigemoto, R., Watanabe, M., Itohara, S., Freund, T. F., & Nyíri, G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5938-10.2011 · Cited by 81
Yamasaki, M., Fukaya, M., Yamazaki, M., Azechi, H., Natsume, R., Abe, M., Sakimura, K., & Watanabe, M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-15.2016 · Cited by 43
Metadata
- Authors
- Racca, C., Stephenson, F. A., Streit, P., Roberts, J. D. B., & Somogyi, P.
- Affiliations
- University of Oxford (GB)
- University of London (GB)
- University of Zurich (CH)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2000-04-01
- Volume
- 20
- Issue
- 7
- Pages
- 2512-2522
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6772245
- OpenAlex
- W2144874949
- Cited by
- 304
- References
- 59
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 14 · 2023: 7 · 2022: 9 · 2021: 8 · 2020: 10 · 2019: 8 · 2018: 9 · 2017: 5 · 2016: 10 · 2015: 10 · 2014: 6 · 2013: 6 · 2012: 14
- FWCI
- 8.02
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- National Institutes of Health
- National Institute on Deafness and Other Communication Disorders
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- NMDA receptor, AMPA receptors, Schaffer collateral synapses, CA1 pyramidal neurons, CA3 pyramidal cells, dendritic spines, spine apparatus, synapse size, hippocampus
- MeSH terms
- Animals, Cell Line, Dendrites, Humans, Immunohistochemistry, Synapses, Receptors, N-Methyl-D-Aspartate, Rats, Wistar, Pyramidal Cells, Receptors, AMPA, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review