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Disruption of experience-dependent synaptic modifications in striate cortex by infusion of an NMDA receptor antagonist
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To assess the possibility that NMDA receptors play a special role in visual cortical plasticity, the selective antagonist 2-amino-5- phosphonovaleric acid (APV) was continuously infused into the striate cortex of kittens as the visual environment was manipulated during the critical period. The cortex was studied using single-unit recording from sites between 3 and 6 mm from the infusion cannulae. One week of D,L-APV infusion coincident with monocular deprivation or “reverse suture” produced a concentration-dependent increase in the percentage of neurons that (1) lacked normal orientation selectivity and (2) were responsive to stimulation of the deprived eye. These effects outlasted the presence of the drug in the tissue. APV treatment also prevented the acquisition of selectivity and visual responsiveness that normally results from monocular visual experience after dark-rearing. Lasting effects of chronic APV infusion were not observed in adult striate cortex. The effects of APV on kitten striate cortex depended on the presence of the D stereoisomer as infusion of L-APV was without effect. Estimates of extracellular concentration using 3H-APV indicated that significant effects could be obtained with concentrations as low as 20 microM D,L-APV. Recordings from units during infusion indicated that visual responses were reduced by APV. Nonetheless, a normal percentage of visually responsive neurons was found at sites greater than or equal to 3 mm from the infusion cannula. There was no evidence that chronic APV infusion affected the sampling frequency of recorded neurons or disrupted cytoarchitecture at the sites further than 3 mm from the infusion cannula. Taken together, the data indicate that the effects of APV on kitten striate cortex are likely due specifically to the blockade of NMDA receptors. These data are considered in relation to several hypotheses concerning the role of NMDA receptors in the experience-dependent development of striate cortex.
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“Interestingly, the first phase of ODP requires NMDA receptor-dependent long-term depression (LTD)52.”
From Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex (2016) · cites this paper as [52]
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Citations
Cites
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302
Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,116
The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896
Excitatory Amino Acid Transmitters
Watkins, J. C., & Evans, R. H. (1981) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pa.21.040181.001121 · Cited by 2,497
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413
MacDermott, A. B., Mayer, M. L., Westbrook, G. L., Smith, S. J., & Barker, J. L. (1986) · Nature · doi:10.1038/321519a0 · Cited by 1,835
The physiology of excitatory amino acids in the vertebrate central nervous system
Mayer, M. L., & Westbrook, G. L. (1987) · Progress in Neurobiology · doi:10.1016/0301-0082(87)90011-6 · Cited by 1,711
Research works printed but not linked: 4
- Andersen, P. 0. (1987) Long-term potentiation: Outstanding prob- lems. In The Neural and Molecular Bases of Learning, J.-P. Changeux and M. Konishi, eds., pp 239-262, Wiley, New York.
- Berrv. R. L.. T. J. Tevler. and H. Taizhen (1988) Induction of LTP in%, primary ;isuaicoiex: Tetanus paramkters. 'Brain Res. (in press).
- Singer, W. (1979) Central core control of visual cortex functions. In The Neurosciences Fourth Study Program, F. 0. Schmitt and F. G. Worden, eds., pp. 1093-l 109, MIT Press, Cambridge, MA.
- Singer, W. (1987) Activity-dependent self-organization of synaptic connections as a substrate of learning. In The Neural and Molecular Bases of Learning, J.-P. Changeux and M. Konishi, eds., pp. 301- 336., Wiley, New York.
Cited by
Sorted by citations
Items 101–200 of 482
The formation of cooperative cell assemblies in the visual cortex
Singer, W. (1990) · Journal of Experimental Biology · doi:10.1242/jeb.153.1.177 · Cited by 123
Self-citationCooke, M. J., Wang, Y., Morshead, C. M., & Shoichet, M. S. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.04.032 · Cited by 118
Properties of vertebrate glutamate receptors: Calcium mobilization and desensitization
Zorumski, C. F., & Thio, L. L. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90020-f · Cited by 118
Cooke, S. F., & Bear, M. F. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0284 · Cited by 119
Self-citationKindling enhances sensitivity of CA3 hippocampal pyramidal cells to NMDA
Martin, D., McNamara, J., & Nadler, J. V. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-05-01928.1992 · Cited by 114
Diverse receptive fields in the lateral geniculate nucleus during thalamocortical development
Tavazoie, S. F., & Reid, R. C. (2000) · Nature Neuroscience · doi:10.1038/75786 · Cited by 113
Cell death in the developing vertebrate retina
Vecino, E., Hernández, M., & Garcı́a, M. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.041891ev · Cited by 113
Synaptic plasticity in visual cortex: comparison of theory with experiment
Clothiaux, E. E., Bear, M. F., & Cooper, L. N. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.5.1785 · Cited by 112
Self-citationBock, J., & Braun, K. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.5.2485 · Cited by 113
Erisir, A., & Harris, J. L. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05208.2003 · Cited by 111
Gordon, J. A., Cioffi, D., Silva, A. J., & Stryker, M. P. (1996) · Neuron · doi:10.1016/s0896-6273(00)80181-6 · Cited by 111
LTD-like molecular pathways in developmental synaptic pruning
Piochon, C., Kano, M., & Hansel, C. (2016) · Nature Neuroscience · doi:10.1038/nn.4389 · Cited by 118
Tissue plasminogen activator mediates reverse occlusion plasticity in visual cortex
Müller, C. M., & Griesinger, C. B. (1998) · Nature Neuroscience · doi:10.1038/248 · Cited by 109
Biological Basis of Emotions: Brain Systems and Brain Development
Chugani, H. T. (1998) · PEDIATRICS · doi:10.1542/peds.102.se1.1225 · Cited by 107
Cellular analogs of visual cortical epigenesis. I. Plasticity of orientation selectivity
Frégnac, Y., Shulz, D. E., Thorpe, S. J., & Bienenstock, E. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-04-01280.1992 · Cited by 106
Fox, K. D., Daw, N. W., Sato, H., & Czepita, D. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02672.1992 · Cited by 107
Developmental loss of miniature N -methyl- d -aspartate receptor currents in NR2A knockout mice
Townsend, M., Yoshii, A., Mishina, M., & Constantine‐Paton, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0335786100 · Cited by 107
Dudek, S. M., & Friedlander, M. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80136-1 · Cited by 106
Alkon, D. L., Amaral, D. G., Bear, M. F., Black, J., Carew, T. J., Cohen, N. J., Disterhoft, J. F., Eichenbaum, H., Golski, S., Gorman, L. K., et al. (1991) · Brain Research Reviews · doi:10.1016/0165-0173(91)90005-s · Cited by 212
Self-citationGabel, L. A., Won, S., Kawai, H. D., McKinney, M., Tartakoff, A. M., & Fallon, J. R. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2185-04.2004 · Cited by 103
Cruikshank, S. J., & Weinberger, N. M. (1996) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00015-x · Cited by 102
Receptive-field plasticity in the adult auditory cortex induced by Hebbian covariance
Cruikshank, S., & Weinberger, N. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00861.1996 · Cited by 98
Eye Opening Rapidly Induces Synaptic Potentiation and Refinement
Lü, W., & Constantine‐Paton, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.031 · Cited by 101
Localisation of amino acid neurotransmitters during postnatal development of the rat retina
Fletcher, E. L., & Kalloniatis, M. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970421)380:4 · Cited by 99
Glutamate as a Neurotransmitter
Mennerick, S. J., & Zorumski, C. F. (2012) · Wiley eBooks · doi:10.1002/9780470015902.a0000139.pub3 · Cited by 99
Activity-Dependent Regulation of NMDAR1 Immunoreactivity in the Developing Visual Cortex
Catalano, S. M., Chang, C. K., & Shatz, C. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08376.1997 · Cited by 98
Androgens modulate NMDA receptor-mediated EPSCs in the zebra finch song system.
White, S. A., Livingston, F. S., & Mooney, R. D. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.5.2221 · Cited by 100
The Role of Nitric Oxide and NMDA Receptors in the Development of Motor Neuron Dendrites
Inglis, F. M., Furia, F., Zuckerman, K. E., Strittmatter, S. M., & Kalb, R. G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10493.1998 · Cited by 99
cAMP/Ca2+Response Element-Binding Protein Function Is Essential for Ocular Dominance Plasticity
Mower, A. F., Liao, D. S., Nestler, E. J., Neve, R. L., & Ramoa, A. S. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02237.2002 · Cited by 97
Essential role for a long-term depression mechanism in ocular dominance plasticity
Yoon, B.-J., Smith, G. B., Heynen, A. J., Neve, R. L., & Bear, M. F. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901305106 · Cited by 98
Self-citationGaluske, R. A. W., Kim, D., Castrén, E., Thoenen, H., & Singer, W. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01618.x · Cited by 93
Self-citationSynaptic Strength Modulation after Cortical Trauma: A Role in Epileptogenesis
Avramescu, S., & Timofeev, I. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0643-08.2008 · Cited by 91
Induction of a Neuronal Proteoglycan by the NMDA Receptor in the Developing Spinal Cord
Kalb, R. G., & Hockfield, S. J. (1990) · Science · doi:10.1126/science.2145629 · Cited by 91
Kaneko, M., Hanover, J. L., England, P. M., & Stryker, M. P. (2008) · Nature Neuroscience · doi:10.1038/nn2068 · Cited by 91
Rapid Hebbian axonal remodeling mediated by visual stimulation
Munz, M., Gobert, D., Schohl, A., Poquérusse, J., Podgorski, K., Spratt, P. W. E., & Ruthazer, E. S. (2014) · Science · doi:10.1126/science.1251593 · Cited by 90
Murphy, K. M., Beston, B. R., Boley, P. M., & Jones, D. G. (2005) · Developmental Psychobiology · doi:10.1002/dev.20053 · Cited by 90
Rapid Ocular Dominance Plasticity Requires Cortical but Not Geniculate Protein Synthesis
Taha, S. A., & Stryker, M. P. (2002) · Neuron · doi:10.1016/s0896-6273(02)00673-6 · Cited by 91
NMDA Receptor NR2 Subunit Dependence of the Slow Component of Magnesium Unblock
Clarke, R. J., & Johnson, J. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0577-06.2006 · Cited by 89
Functional Respiratory Rhythm Generating Networks in Neonatal Mice Lacking NMDAR1 Gene
Funk, G. D., Johnson, S. M., Smith, J. C., Dong, X.-W., Lai, J. H., & Feldman, J. L. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.3.1414 · Cited by 92
Neural organization of higher visual functions
Rolls, E. T. (1991) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(91)90090-t · Cited by 86
Ramoa, A. S., Mower, A. F., Liao, D. S., & Jafri, S. I. A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-12-04299.2001 · Cited by 82
Chen, L., Cooper, N. G. F., & Mower, G. D. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00076-0 · Cited by 87
Activity-dependent remodeling of connections in the mammalian visual system
Cramer, K. S. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80094-8 · Cited by 86
Cyclic AMP-dependent protein kinase mediates ocular dominance shifts in cat visual cortex
Beaver, C. J., Ji, Q., Fischer, Q. S., & Daw, N. W. (2001) · Nature Neuroscience · doi:10.1038/83985 · Cited by 85
Philpot, B. D., Weisberg, M. P., Ramos, M. S., Sawtell, N. B., Tang, Y., Tsien, J. Z., & Bear, M. F. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00136-8 · Cited by 85
Self-citationCrozier, R. A., Black, I. B., & Plummer, M. R. (1999) · Learning & Memory · doi:10.1101/lm.6.3.257 · Cited by 86
Mechanisms underlying human motor system plasticity
Boroojerdi, B., Ziemann, U., Chen, R. E., Bütefisch, C. M., & Cohen, L. G. (2001) · Muscle & Nerve · doi:10.1002/mus.1045 · Cited by 85
McKinney, R. A., Lüthi, A., Bandtlow, C. E., Gähwiler, B. H., & Thompson, S. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.20.11631 · Cited by 83
The AMPA Receptor Subunit GluR1 Regulates Dendritic Architecture of Motor Neurons
Inglis, F. M., Crockett, R., Korada, S., Abraham, W. C., Hollmann, M., & Kalb, R. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-08042.2002 · Cited by 82
Stereopsis After Congenital Monocular Cataract Extraction
Gregg, F. M., & Parks, M. M. (1992) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)71797-0 · Cited by 82
Proteolytic activity, synapse elimination, and the Hebb synapse
Liu, Y., Fields, R. D., Fitzgerald, S., Festoff, B. W., & Nelson, P. G. (1994) · Journal of Neurobiology · doi:10.1002/neu.480250312 · Cited by 82
Kwon, Y. W., & Gurney, M. E. (1996) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199604)29:4 · Cited by 44
NR2 subunit‐dependence of NMDA receptor channel block by external Mg2+
Qian, A., Buller, A. L., & Johnson, J. W. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.076737 · Cited by 81
Huber, K. M., Sawtell, N. B., & Bear, M. F. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00001.1998 · Cited by 80
Self-citationPostnatal Development of Glutamate Receptor-Mediated Responses in the Neostriatum
Colwell, C. S., Cepeda, C., Crawford, C. A., & Levine, M. S. (1998) · Developmental Neuroscience · doi:10.1159/000017310 · Cited by 79
Newly Learned Auditory Responses Mediated by NMDA Receptors in the Owl Inferior Colliculus
Feldman, D. E., Brainard, M. S., & Knudsen, E. I. (1996) · Science · doi:10.1126/science.271.5248.525 · Cited by 79
Rosier, A. M., Arckens, L., Demeulemeester, H. G., Orban, G. A., Eysel, U. T., Wu, Y. ‐., & Vandesande, F. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903590309 · Cited by 79
Zhang, L., & Warren, R. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.01025.2001 · Cited by 75
A Role For Glial Cells in Activity-Dependent Central Nervous Plasticity? Review and Hypothesis
Müller, C. M. (1992) · International review of neurobiology · doi:10.1016/s0074-7742(08)60099-9 · Cited by 77
McEwen, B. S., Cameron, H. A., Chao, H. M., Gould, E., Magariños, A. M., Watanabe, Y., & Woolley, C. S. (1993) · Cellular and Molecular Neurobiology · doi:10.1007/bf00711583 · Cited by 73
Liao, D. S., Krahe, T. E., Prusky, G. T., Medina, A. E., & Ramoa, A. S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00266.2004 · Cited by 73
Developmental Changes in Intracellular Calcium Regulation in Rat Cerebral Cortex during Hypoxia
Bickler, P. E., Gallego, S. M., & Hansen, B. M. (1993) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1993.103 · Cited by 73
Ernst, A. F., Wu, H. H., El‐Fakahany, E. E., & McLoon, S. C. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00229.1999 · Cited by 73
Injection of MK-801 affects ocular dominance shifts more than visual activity.
Daw, N., Gordon, B., Fox, K., Flavin, H., Kirsch, J., Beaver, C., Ji, Q.-H., Reid, S. N. M., & Czepita, D. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.1.204 · Cited by 80
Plasticity of the visual cortex and treatment of amblyopia
Sengpiel, F. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.063 · Cited by 72
Babikian, T., Prins, M. L., Cai, Y., Barkhoudarian, G., Hartonian, I., Hovda, D. A., & Giza, C. C. (2010) · Developmental Neuroscience · doi:10.1159/000320667 · Cited by 74
Regulation of NMDA receptor subunit mRNA expression in the rat brain during postnatal development
Riva, M. A., Tascedda, F., Molteni, R., & Racagni, G. (1994) · Molecular Brain Research · doi:10.1016/0169-328x(94)90155-4 · Cited by 72
Daw, M. I., Scott, H. L., & Isaac, J. T. R. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.01.001 · Cited by 70
Hess, G., Jacobs, K. M., & Donoghue, J. P. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90226-7 · Cited by 70
Schnupp, J. W. H., King, A. J., Smith, A. L., & Thompson, I. D. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-02-01516.1995 · Cited by 71
Cell delivery to the central nervous system
Shoichet, M. S., & Winn, S. R. (2000) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(00)00055-7 · Cited by 70
Experience-Dependent Development of Spinal Motor Neurons
Inglis, F. M., Zuckerman, K. E., & Kalb, R. G. (2000) · Neuron · doi:10.1016/s0896-6273(00)81164-2 · Cited by 68
Aoki, C. J., & Kabak, S. (1992) · Visual Neuroscience · doi:10.1017/s0952523800002832 · Cited by 68
Segregation of geniculocortical afferents during the critical period: a role for subplate neurons
Ghosh, A., & Shatz, C. J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03862.1994 · Cited by 66
Aoki, C. J., Kojima, N., Sabaliauskas, N. A., Shah, L. N., Ahmed, T. H., Oakford, J., Ahmed, T., Yamazaki, H., Hanamura, K., & Shirao, T. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22137 · Cited by 66
Renger, J. J., Hartman, K. N., Tsuchimoto, Y., Yokoi, M., Nakanishi, S., & Hensch, T. K. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022618799 · Cited by 66
Fischer, Q. S., Beaver, C. J., Yang, Y., Rao, Y., Jakobsdóttir, K. B., Storm, D. R., McKnight, G. S., & Daw, N. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2409-04.2004 · Cited by 65
Protein kinase C and receptor kinase gene expression in olfactory receptor neurons
Bruch, R. C., Kang, J., Moore, M. L., & Medler, K. F. (1997) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199710)33:4 · Cited by 17
Cramer, K. S., & Sur, M. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(96)00188-5 · Cited by 64
The NMDA antagonist memantine impairs classical eyeblink conditioning in humans
Schugens, M. M., Egerter, R., Daum, I., Schepelmann, K., Klockgether, T., & Löschmann, P. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)13452-8 · Cited by 64
Mechanisms of Plasticity in the Visual Cortex
Daw, N. W. (1995) · Springer eBooks · doi:10.1007/978-1-4757-6940-1_12 · Cited by 64
Turi, G. (2003) · Florence Research (University of Florence) · Cited by 69
Adolescent Health and the Environment
Golub, M. S. (2000) · Environmental Health Perspectives · doi:10.1289/ehp.00108355 · Cited by 61
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
Activity-dependent development of spinal cord motor neurons
Kalb, R. G., & Hockfield, S. J. (1992) · Brain Research Reviews · doi:10.1016/0165-0173(92)90020-m · Cited by 63
Mouse vision as a gateway for understanding how experience shapes neural circuits
Priebe, N. J., & McGee, A. W. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00123 · Cited by 68
Cramer, K. S., Moore, C., & Sur, M. (1995) · The Journal of comparative neurology · doi:10.1002/cne.903530211 · Cited by 62
Domenici, L., Cellerino, A., & Maffei, L. (1993) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1993.0004 · Cited by 60
Medina, A. E., Krahe, T. E., & Ramoa, A. S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00714.2004 · Cited by 59
The role of afferent activity in the maintenance of primate neocortical function
Jones, E. G. (1990) · Journal of Experimental Biology · doi:10.1242/jeb.153.1.155 · Cited by 57
Lin, S., & Constantine‐Paton, M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03725.1998 · Cited by 58
Sleep and developmental plasticity
Frank, M. G. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00014-4 · 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
Glanzman, D. (1994) · Journal of Neurobiology · doi:10.1002/neu.480250608 · Cited by 57
Neonatal Alcohol Exposure Induces Long-Lasting Impairment of Visual Cortical Plasticity in Ferrets
Medina, A. E., Krahe, T. E., Coppola, D. M., & Ramoa, A. S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10002.2003 · Cited by 54
Vutskits, L. (2012) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e31826a1178 · Cited by 54
Jt, F. (1991) · Journal of Pediatric Ophthalmology & Strabismus · doi:10.3928/0191-3913-19910701-03 · Cited by 53
Activation of muscarinic receptors modulates NMDA receptor-mediated responses in auditory cortex
Aramakis, V. B., Bandrowski, A. E., & Ashe, J. H. (1997) · Experimental Brain Research · doi:10.1007/pl00005601 · Cited by 53
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
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Metadata
- Authors
- Bear, M., Kleinschmidt, A., Gu, Q., & Singer, W.
- Affiliations
- Max Planck Institute for Brain Research (DE)
- ORCID
- Kleinschmidt, A
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1990-03-01
- Volume
- 10
- Issue
- 3
- Pages
- 909-925
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6570130
- OpenAlex
- W2134646026
- Cited by
- 488
- References
- 61
- Citations by year
- 2025: 1 · 2024: 4 · 2023: 4 · 2022: 3 · 2021: 6 · 2020: 6 · 2019: 5 · 2018: 3 · 2017: 5 · 2016: 3 · 2015: 5 · 2014: 6 · 2013: 6 · 2012: 10
- FWCI
- 11.20
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Alfred P. Sloan Foundation
- Office of Naval Research
- 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, primary visual cortex, visual cortical plasticity, critical period, monocular deprivation, orientation selectivity, dark rearing, APV, kitten visual development
- MeSH terms
- Animals, Cats, Photic Stimulation, Sensory Deprivation, Synapses, Vision, Ocular, Visual Cortex, Vision, Monocular, 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.
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