Cited by 307Neuroscience and Neuropharmacology ResearchVisual perception and processing mechanismsNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.

The location and function of NMDA receptors in cat and kitten visual cortex

Open access

Fox, K, Sato, H, Daw, N·1989·The Journal of Neuroscience

DOI 10.1523/jneurosci.09-07-02443.1989PMC PMC6569778

Open this paper in CoChat — free account Open PDF

Abstract

The role of N-methyl-D-aspartate (NMDA) receptors in cat visual cortex was studied as a function of both layer and age by iontophoresis of the NMDA antagonist (D)-2-amino-5-phosphonovaleric acid (APV). Effects on both visual responses and spontaneous activity were observed. In superficial layers (II and III), D-APV reduced visual responses substantially at all ages. Iontophoresis of D-APV with 10 nA of ejecting current for 2–3 min was sufficient to reduce the response to approximately one third of control levels. The magnitude of the reduction did not vary with age. In granular and deep layers (IV, V, and VI), D-APV affected the visual response in young animals but only spontaneous activity in older animals. On average, visual responses were reduced to about half at 20–23 days of age and to about 75% at 4 weeks of age but in most cases were not significantly affected in adults. The rapid change in the functional effect of NMDA receptors over the third and fourth week in granular and deep layers suggests a role in development. There was a reasonable age correlation between the change in effect and the period of geniculocortical afferent segregation. Further experiments will be necessary to determine whether NMDA receptors are necessary for segregation to occur. The presence of an NMDA component to the visual response in the adult in layers II and III argues either that these layers retain some form of plasticity in the adult or that NMDA receptors play a role in the transmission of normal visual input to these layers.

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

Crossref · 10.1523/jneurosci.09-07-02443.1989

Cites

41 of 41 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.1003 · Cited by 2,628
Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413
COMPARISON OF THE EFFECTS OF UNILATERAL AND BILATERAL EYE CLOSURE ON CORTICAL UNIT RESPONSES IN KITTENS
Wiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1029 · Cited by 1,598
NMDA receptors - their role in long-term potentiation
Collingridge, G. L., & Bliss, T. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90175-5 · Cited by 1,178
The development of ocular dominance columns in normal and visually deprived monkeys
Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123
Long-term potentiation and NMDA receptors in rat visual cortex
Artola, A., & Singer, W. (1987) · Nature · doi:10.1038/330649a0 · Cited by 967
Blockade of "NMDA" Receptors Disrupts Experience-Dependent Plasticity of Kitten Striate Cortex
Kleinschmidt, A. K., Bear, M. F., & Singer, W. (1987) · Science · doi:10.1126/science.2443978 · Cited by 911
Anatomical organization of excitatory amino acid receptors and their pathways
Cotman, C. W., Monaghan, D. T., Ottersen, O. P., & Storm‐Mathisen, J. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90172-x · Cited by 875
Modulation of visual cortical plasticity by acetylcholine and noradrenaline
Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858
Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex
Stryker, M., & Harris, W. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-08-02117.1986 · Cited by 687

Show all 41 references

Research works printed but not linked: 1

Gilbert. C. D., and T. N. Wiesel (1981) Laminar specialisation and intracorticai connections in cat pnmaj visual cortex. In The Orga- nisation of the Cerebral Cortex. F. 0. Schmitt. F. G. Worden. G. Adelman,-and S. G. Dennis, eds., pp. 163-191, MIT Press, Cam- bridge, MA.

Sorted by citations

Items 101–200 of 307

Cellular analogs of visual cortical epigenesis. II. Plasticity of binocular integration
Shulz, D. E., & Frégnac, Y. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-04-01301.1992 · Cited by 62
The promise of layer-specific neuroimaging for testing predictive coding theories of psychosis
Haarsma, J., Kok, P., & Browning, M. D. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.10.009 · Cited by 61
Neurochemical organization of the macaque striate cortex: Correlation of cytochrome oxidase with Na+K+ATPase, NADPH-diaphorase, nitric oxide synthase, and N-methyl-d-aspartate receptor subunit 1
Wong‐Riley, M. T. T., Anderson, B. D., Liebl, W., & Huang, Z. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00432-6 · Cited by 63
Chapter 11 Intracortical processes regulating the integration of sensory information
Ebner, F. F., & Armstrong‐James, M. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)63172-6 · Cited by 63
Effects of the novel NMDA antagonist, NPC 12626, on long-term potentiation, learning and memory
Walker, D. L., & Gold, P. E. (1991) · Brain Research · doi:10.1016/0006-8993(91)90460-d · Cited by 63
Histochemical localization of synaptic zinc in the developing cat visual cortex
Dyck, R. H., Beaulieu, C., & Cynader, M. S. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903290105 · Cited by 62
NMDA and non-NMDA glutamate receptors in auditory transmission in the barn owl inferior colliculus
Feldman, D. E., & Knudsen, E. I. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05939.1994 · Cited by 62
Thalamocortical NMDA conductances and intracortical inhibition can explain cortical temporal tuning
Krukowski, A. E., & Miller, K. D. (2001) · Nature Neuroscience · doi:10.1038/86084 · Cited by 61
Adrenergic regulation of visuocortical plasticity: a role of the locus coeruleus system
Kasamatsu, T. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63837-6 · Cited by 62
Adult thalamocortical transmission involves both NMDA and non-NMDA receptors
Gil, Z., & Amitai, Y. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.4.2547 · Cited by 60
D-Cycloserine: Agonist turned antagonist
Lanthorn, T. H. (1994) · Amino Acids · doi:10.1007/bf00813745 · Cited by 60
The contributions of NMDA, non-NMDA, and GABA receptors to postsynaptic responses in neurons of the optic tectum
Hickmott, P., & Constantine‐Paton, M. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-10-04339.1993 · Cited by 60
Kainate receptor modification in the fetal guinea pig brain during hypoxia
Mishra, O. P., Kubin, J. A., McGowan, J. E., & Delivoria‐Papadopoulos, M. (1995) · Neurochemical Research · doi:10.1007/bf00995380 · Cited by 58
NMDA, AMPA, and benzodiazepine binding site changes in Alzheimer's disease visual cortex
Carlson, M. D., Penney, J. B., & Young, A. B. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90120-z · Cited by 58
Distribution and developmental change in [3H]MK‐801 binding within zebra finch song nuclei
Aamodt, S. M., Kozlowski, M. R., Nordeen, E. J., & Nordeen, K. W. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230806 · Cited by 58
Contrast adaptation and excitatory amino acid receptors in cat striate cortex
McLean, J., & Palmer, L. A. (1996) · Visual Neuroscience · doi:10.1017/s0952523800007720 · Cited by 57
Cellular localization and laminar distribution of NMDAR1 mRNA in the rat cerebral cortex
Conti, F., Minelli, A., Molnar, M., & Brecha, N. C. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903430406 · Cited by 57
The Nature and Plasticity of Sensory Processing within Adult Rat Barrel Cortex
Armstrong‐James, M. (1995) · Cerebral cortex · doi:10.1007/978-1-4757-9616-2_8 · Cited by 56
Specific Roles of NMDA and AMPA Receptors in Direction-Selective and Spatial Phase-Selective Responses in Visual Cortex
Rivadulla, C., Sharma, J., & Sur, M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01710.2001 · Cited by 55
NMDA receptors participate differentially in two different synaptic inputs in neurons of the zebra finch robust nucleus of the archistriatum in vitro
Kubota, M., & Saito, N. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90002-b · Cited by 54
Laminar distribution of NMDA receptors in cat and monkey visual cortex visualized by [3H]‐MK‐801 binding
Rosier, A. M., Arckens, L., Orban, G. A., & Vandesande, F. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903350307 · Cited by 50
Chapter 14 Nmda-receptor-dependent synaptic plasticity in the visual cortex
Bear, M. F. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)62541-8 · Cited by 53
Retinal activity regulates developmental switches in functional properties and ifenprodil sensitivity of NMDA receptors in the lateral geniculate nucleus
Ramoa, A. S., & Prusky, G. T. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00061-8 · Cited by 52
Experience-dependent plasticity mechanisms for neural rehabilitation in somatosensory cortex
Fox, K. D. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0252 · Cited by 53
Self-citation
Expression of two forms of glutamic acid decarboxylase (GAD67 and GAD65) during postnatal development of cat visual cortex
Guo, Y. H., Kaplan, I. V., Cooper, N. G. F., & Mower, G. D. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)81789-0 · Cited by 51
Laminar and cellular distribution of AMPA, kainate, and NMDA receptor subunits in monkey sensory-motor cortex
Mu�oz, A., Woods, T. M., & Jones, E. G. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990517)407:4 · Cited by 52
Glutamate-induced increases in intracellular Ca2+ in cultured frog tectal cells mediated by direct activation of NMDA receptor channels
ClineP, H. T., & Tsien, R. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90361-3 · Cited by 50
Early isolation from conspecific song does not affect the normal developmental decline of N‐methyl‐ D ‐aspartate receptor binding in an avian song nucleus
Aamodt, S. M., Nordeen, E. J., & Nordeen, K. W. (1995) · Journal of Neurobiology · doi:10.1002/neu.480270108 · Cited by 50
Binocular competition in the control of geniculate cell size depends upon visual cortical N-methyl-D-aspartate receptor activation.
Bear, M. F., & Colman, H. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.23.9246 · Cited by 48
Expression of N-methyl- d-aspartate glutamate receptor subunits in the prefrontal cortex of the rat
Rudolf, G., Cronin, C. A., Landwehrmeyer, G. B., Standaert, D. G., Penney, J., & Young, A. B. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00048-6 · Cited by 49
Pathogenic Role of Glutamate in Hyperthermia‐Induced Seizures
Morimoto, T., Nagao, H., Yoshimatsu, M., Yoshida, K., & Matsuda, H. (1993) · Epilepsia · doi:10.1111/j.1528-1157.1993.tb02585.x · Cited by 48
Quantitative localization of NMDAR1 receptor subunit immunoreactivity in inferotemporal and prefrontal association cortices of monkey and human
Huntley, G. W., Vickers, J. C., & Morrison, J. H. (1997) · Brain Research · doi:10.1016/s0006-8993(96)00847-5 · Cited by 47
Visual–Procedural Memory Consolidation during Sleep Blocked by Glutamatergic Receptor Antagonists
Gais, S., Rasch, B., Wagner, U., & Born, J. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5374-07.2008 · Cited by 47
LTP and LTD vary with layer in rodent visual cortex
Daw, N. W., Rao, Y., Wang, X., Fischer, Q. S., & Yang, Y. (2004) · Vision Research · doi:10.1016/j.visres.2004.09.004 · Cited by 49
Self-citation
Chapter 17 GABA mediated inhibitory processes in the function of the geniculo-striate system
Sillito, A. M. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)63622-5 · Cited by 47
Cortisol reduces plasticity in the kitten visual cortex
Daw, N. W., Sato, H., Fox, K. D., Carmichael, S. T., & Gingerich, R. L. (1991) · Journal of Neurobiology · doi:10.1002/neu.480220206 · Cited by 46
Self-citation
Evidence for excitatory amino acid neurotransmitters in the geniculo-cortical pathway and local projections within rat primary visual cortex
Johnson, R. R., & Burkhalter, A. (1992) · Experimental Brain Research · doi:10.1007/bf00228997 · Cited by 46
The effect of age on binding of MK-801 in the cat visual cortex
Gordon, B., Daw, N. W., & Parkinson, D. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90190-t · Cited by 43
Self-citation
Regulation of N-methyl-d-aspartate (NMDA) receptor function during the rearrangement of developing neuronal connections
Hofer, M., & Constantine‐Paton, M. (1994) · Progress in brain research · doi:10.1016/s0079-6123(08)60546-4 · Cited by 43
Intrinsic and Thalamic Excitatory Inputs Onto Songbird LMAN Neurons Differ in Their Pharmacological and Temporal Properties
Boettiger, C. A., & Doupe, A. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.5.2615 · Cited by 41
Excitatory Amino Acid Receptors Participate in Synaptic Transmission of Visual Responses in the Superficial Layers of the Cat Superior Colliculus
Binns, K. E., & Salt, T. E. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00257.x · Cited by 40
Co‐regulation of ocular dominance plasticity and NMDA receptor subunit expression in glutamic acid decarboxylase‐65 knock‐out mice
Kanold, P. O., Kim, Y. A., GrandPré, T., & Shatz, C. J. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.171215 · Cited by 40
Pharmacological Specialization of Learned Auditory Responses in the Inferior Colliculus of the Barn Owl
Feldman, D. E., & Knudsen, E. I. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-08-03073.1998 · Cited by 39
Selective alterations in glutamate receptor subtypes after unilateral orbital enucleation
Chalmers, D. T., & McCulloch, J. (1991) · Brain Research · doi:10.1016/0006-8993(91)90515-w · Cited by 39
Neurotransmitters as Neurotrophic Factors
Leslie, F. M. (1993) · Elsevier eBooks · doi:10.1016/b978-0-08-057132-4.50024-1 · Cited by 39
Developmental alterations in NMDA receptor-mediated [Ca2+]i elevation in substantia gelatinosa neurons of neonatal rat spinal cord
Hori, Y., & Kanda, K. (1994) · Developmental Brain Research · doi:10.1016/0165-3806(94)90098-1 · Cited by 37
Regulation of NMDA Receptor mRNA During Visual Map Formation and After Receptor Blockade
Hofer, M., Prusky, G. T., & Constantine‐Paton, M. (1994) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1994.62062300.x · Cited by 38
Thalamocortical and corticocortical excitatory postsynaptic potentials mediated by excitatory amino acid receptors in the cat motor cortexin vivo
Salt, T. E., Meier, C. L., Seno, N., Krucker, T., & Herrling, P. L. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00357-b · Cited by 38
Learning-related changes in hippocampal field potentials
Moser, E. I. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00051-8 · Cited by 40
Efferent connectivity of the hippocampal formation of the zebra finch (Taenopygia guttata): An anterograde pathway tracing study usingPhaseolus vulgaris leucoagglutinin
Sz�kely, A. D., & Krebs, J. R. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960429)368:2 · Cited by 115
Gestational 2,3,7,8-tetrachlorodibenzo-p-dioxin exposure effects on sensory cortex function
Hood, D. B., Woods, L., Brown, L. A., Johnson, S., & Ebner, F. F. (2006) · NeuroToxicology · doi:10.1016/j.neuro.2006.05.022 · Cited by 36
Layer Variations of Long-Term Depression in Rat Visual Cortex
Rao, Y., & Daw, N. W. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00298.2004 · Cited by 36
Self-citation
Optical recording of epileptiform voltage changes in the neocortical slice
Albowitz, B., Kuhnt, U., & Ehrenreich, L. (1990) · Experimental Brain Research · doi:10.1007/bf00228113 · Cited by 36
Contribution of quisqualate/ kainate and NMDA receptors to excitatory synaptic transmission in the rat's visual cortex
Nishigori, A., Tsumoto, T., & Kimura, F. (1990) · Visual Neuroscience · doi:10.1017/s0952523800000754 · Cited by 35
Contribution of GABAergic Inhibition to Receptive Field Structures of Monkey Inferior Temporal Neurons
Wang, Y. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.1.62 · Cited by 34
Transient and long-lasting effects of iontophoretically administered norepinephrine on somatosensory cortical neurons in halothane-anesthetized cats
Warren, R. A., & Dykes, R. W. (1996) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y95-225 · Cited by 33
Prolonged NMDA-Mediated Responses, Altered Ifenprodil Sensitivity, and Epileptiform-Like Events in the Malformed Hippocampus of Methylazoxymethanol Exposed Rats
Calcagnotto, M. E., & Baraban, S. C. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01155.2004 · Cited by 32
The Cortical Neuron as an Electrophysiological Unit
Gutnick, M. J., & Crill, W. E. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0003 · Cited by 32
Effects of age and visual experience on [3H] MK801 binding to NMDA receptors in the kitten visual cortex
Reynolds, I. J., & Bear, M. F. (1991) · Experimental Brain Research · doi:10.1007/bf00231745 · Cited by 32
Distinct Laminar Requirements for NMDA Receptors in Experience-Dependent Visual Cortical Plasticity
Fong, M., Finnie, P. S. B., Kim, T.-K., Thomazeau, A., Kaplan, E. S., Cooke, S. F., & Bear, M. F. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz260 · Cited by 29
Development of voltage-dependent and ligand-gated channels in excitable membranes
Spitzer, N. C. (1994) · Progress in brain research · doi:10.1016/s0079-6123(08)60538-5 · Cited by 32
Neurochemical organization of the primate visual cortex
Morrison, J. H., Hof, P. R., & Huntley, G. W. (1998) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(98)80004-3 · Cited by 31
Localization of the calcium/calmodulin-dependent protein phosphatase, calcineurin, in the hindbrain and spinal cord of the rat
Strack, S., Wadzinski, B. E., & Ebner, F. F. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961104)375:1 · Cited by 35
Roles of N-methyl-d-aspartate receptors in ocular dominance plasticity in developing visual cortex: re-evaluation
Kasamatsu, T., Imamura, K., Mataga, N., Hartveit, E., Heggelund, U., & Heggelund, P. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00222-4 · Cited by 30
Morphology of identified corticospinal cells in the rat following motor cortex injury: absence of use-dependent change
Prusky, G. T., & Whishaw, I. Q. (1996) · Brain Research · doi:10.1016/0006-8993(95)01347-4 · Cited by 30
Functions of Local Circuits in Neocortex: Synchrony and Laminae
Connors, B. W., & Amitai, Y. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0009 · Cited by 30
Atypical visual and somatosensory adaptation in schizophrenia-spectrum disorders
Andrade, G. N., Butler, J. S., Peters, G. A., Molholm, S., & Foxe, J. J. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.63 · Cited by 29
Unique Properties of NMDA Receptors Enhance Synaptic Excitation of Radiatum Giant Cells in Rat Hippocampus
Kirson, E. D., & Yaari, Y. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-13-04844.2000 · Cited by 29
Chronic application of NMDA decreases the NMDA sensitivity of the evoked tectal potential in the frog
Debski, E. A., Cline, H., McDonald, J., & Constantine‐Paton, M. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-09-02947.1991 · Cited by 28
A Model for the Action of NMDA Conductances in the Visual Cortex
Fox, K. D., & Daw, N. W. (1992) · Neural Computation · doi:10.1162/neco.1992.4.1.59 · Cited by 27
Self-citation
Experimental Down-Regulation of the NMDA Channel Associated With Synapse Pruning
Hickmott, P. W., & Constantine‐Paton, M. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.1096 · Cited by 27
Dynamics of spiking neurons: between homogeneity and synchrony
Rangan, A. V., & Young, L.-S. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0429-1 · Cited by 25
l-Threo-3,4-Dihydroxyphenylserine enhanced ocular dominance plasticity in adult cats
Mataga, N., Imamura, K., & Watanabe, Y. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90352-8 · Cited by 26
Transient Synaptic Potentiation in the Visual Cortex. I. Cellular Mechanisms
Harsanyi, K., & Friedlander, M. J. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.3.1269 · Cited by 25
Optical Imaging of Epileptiform Events in Visual Cortex in Response to Patterned Photic Stimulation
Schwartz, T. H. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg076 · Cited by 25
NMDA Receptor Antagonist Ketamine Impairs Feature Integration in Visual Perception
Meuwese, J. D. I., van Loon, A. M., Scholte, H. S., Lirk, P. B., Vulink, N. C. C., Hollmann, M. W., & Lamme, V. A. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079326 · Cited by 26
Laminar differences in plasticity in area 17 following retinal lesions in kittens or adult cats
Waleszczyk, W. J., Wang, C., Young, J. M., Burke, W. J., Calford, M. B., & Dreher, B. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02674.x · Cited by 24
Involvement of NMDA and Non-NMDA Receptors in the Neuronal Responses of the Primary Motor Cortex to Input from the Supplementary Motor Area and Somatosensory Cortex: Studies of Task-Performing Monkeys.
Shima, K., & Tanji, J. (1998) · The Japanese Journal of Physiology · doi:10.2170/jjphysiol.48.275 · Cited by 24
Inhibitory Inputs to Hippocampal Interneurons Are Reorganized in Lis1 Mutant Mice
Jones, D. L., & Baraban, S. C. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00392.2009 · Cited by 24
Developmental changes in NMDA receptor-mediated visual activity in the rat superior colliculus, and the effect of dark rearing
Binns, K. E., & Salt, T. E. (1998) · Experimental Brain Research · doi:10.1007/s002210050407 · Cited by 24
NMDA and non-NMDA receptors mediate taste afferent inputs to cortical taste neurons in rats
Otawa, S., Takagi, K., & Ogawa, H. (1995) · Experimental Brain Research · doi:10.1007/bf00231062 · Cited by 23
A Model of Color Vision Based on Cortical Reentry
Wray, J., & Edelman, G. M. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.5.701 · Cited by 23
Modification of NMDA receptor by in vitro lipid peroxidation in fetal guinea pig brain
Goel, R., Mishra, O. P., Razdan, B., & Delivoria‐Papadopoulos, M. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90024-f · Cited by 23
The modification of NMDA receptors by visual experience in the rat retina is age dependent
Xue, J., & Cooper, N. G. F. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00141-3 · Cited by 22
SI Neuron Response Variability Is Stimulus Tuned and NMDA Receptor Dependent
Whitsel, B. L., Favorov, O. V., Delemos, K. A., Lee, C.-J., Tommerdahl, M., Essick, G. K., & Nakhle, B. M. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.6.2988 · Cited by 22
Effect of the Group II Metabotropic Glutamate Agonist, 2R,4R-APDC, Varies With Age, Layer, and Visual Experience in the Visual Cortex
Beaver, C. J., Ji, Q.-H., & Daw, N. W. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.1.86 · Cited by 22
Self-citation
Role of NMDA receptors in the propagation of excitation in rat visual cortex as studied by optical imaging
Fukuda, M., Hata, Y., Ohshima, M., & Tsumoto, T. (1998) · Neuroscience Research · doi:10.1016/s0168-0102(98)00018-2 · Cited by 20
NMDA receptors in sensory information processing
Nelson, S. B., & Sur, M. (1992) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(92)90184-m · Cited by 20
Hyaluronic acid based extracellular matrix regulates surface expression of GluN2B containing NMDA receptors
Schweitzer, B., Singh, J., Fejtova, A., Groc, L., Heine, M., & Frischknecht, R. (2017) · Scientific Reports · doi:10.1038/s41598-017-07003-3 · Cited by 19
Neural strategies for learning during sensitive periods of development
Bottjer, S. W. (2002) · Journal of Comparative Physiology A · doi:10.1007/s00359-002-0356-0 · Cited by 18
Role of Immediate Early Gene Expression in Cortical Morphogenesis and Plasticity
Andreasson, K. I., & Kaufmann, W. E. (2002) · Results and problems in cell differentiation · doi:10.1007/978-3-540-46006-0_6 · Cited by 19
Endogenous NMDA-Receptor Activation Regulates Glutamate Release in Cultured Spinal Neurons
Robert, A., Black, J. A., & Waxman, S. G. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.196 · Cited by 18
Postnatal development of NMDA receptor-mediated synaptic transmission in cat visual cortex
Iwakiri, M., & Komatsu, Y. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90087-q · Cited by 19
Involvement of Nerve Growth Factor in Visual Cortex Plasticity
Gu, Q. (1995) · Reviews in the Neurosciences · doi:10.1515/revneuro.1995.6.4.329 · Cited by 19
Long-lasting enhancement of sound discrimination ability after sound exposure in rats
Sakai, M., Kudoh, M., & Shibuki, K. (1999) · Neuroscience Research · doi:10.1016/s0168-0102(98)00118-7 · Cited by 19
NMDA receptors in layers II and III of rat cerebral cortex
Currie, S. N., Wang, X. F., & Daw, N. W. (1994) · Brain Research · doi:10.1016/0006-8993(94)90801-x · Cited by 18
Self-citation
Enhanced responses to NMDA receptor activation in the developing cat caudate nucleus
Siviy, S. M., Buchwald, N. A., & Levine, M. S. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90437-x · Cited by 18
Immunocytochemical Characterization of AMPA-Selective Glutamate Receptor Subunits: Laminar and Compartmental Distribution in Macaque Striate Cortex
Carder, R. K. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-09-03352.1997 · Cited by 18
Sensory activity differentially modulates N-methyl-d-aspartate receptor subunits 2A and 2B in cortical layers
Corson, J. A., Nahmani, M., Lubarsky, K., Badr, N., Wright, C., & Erişir, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.07.016 · Cited by 20
Chronic mild acidosis specifically reduces functional expression of N-methyl-d-aspartate receptors and increases long-term survival in primary cultures of cerebellar granule cells
Leahy, J. C., Chen, Q., & Vallano, M. L. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90543-6 · Cited by 17

Authors: Fox, K., Sato, H., & Daw, N.
Affiliations: Washington University in St. Louis (US)
ORCID: Fox, K
Sato, H
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 1989-07-01
Volume: 9
Issue: 7
Pages: 2443-2454
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.09-07-02443.1989
PMC: PMC6569778
OpenAlex: W2166938907
Cited by: 307
References: 41
Citations by year: 2025: 1 · 2024: 1 · 2023: 1 · 2022: 1 · 2020: 2 · 2019: 1 · 2017: 2 · 2016: 1 · 2015: 1 · 2014: 1 · 2013: 5 · 2012: 4
FWCI: 9.22
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 184 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Eye Institute (EY-00053)
National Institute of Neurological Disorders and Stroke (NS18070)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: NMDA receptor, visual cortex, kitten development, D-APV, visual responses, spontaneous activity, cortical layers, synaptic plasticity, cats
MeSH terms: Aging, Animals, Cats, Dose-Response Relationship, Drug, Neurons, Tissue Distribution, Valine, Visual Cortex, 2-Amino-5-phosphonovalerate, Receptors, N-Methyl-D-Aspartate, Receptors, Neurotransmitter

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

The location and function of NMDA receptors in cat and kitten visual cortex

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks