Disruption of experience-dependent synaptic modifications in striate cortex by infusion of an NMDA receptor antagonist
Open accessAbstract
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.
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
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 first phase of ODP requires NMDA receptor-dependent long-term depression (LTD).
“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]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works
Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825 · see citing works
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,460 · see citing works
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 4,033 · see citing works
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 · see citing works
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896 · see citing works
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 · see citing works
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413 · see citing works
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 · see citing works
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 1,705 · see citing works
Wiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1029 · Cited by 1,598 · see citing works
Self-organization of orientation sensitive cells in the striate cortex
Malsburg, C. V. D. (1973) · Kybernetik · doi:10.1007/bf00288907 · Cited by 1,444 · see citing works
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
The Biochemistry of Memory: A New and Specific Hypothesis
LYNCH, G. S., & Baudry, M. (1984) · Science · doi:10.1126/science.6144182 · Cited by 1,045 · see citing works
Long-term potentiation and NMDA receptors in rat visual cortex
Artola, A., & Singer, W. (1987) · Nature · doi:10.1038/330649a0 · Cited by 966 · see citing works
Self-citationBlockade 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 906 · see citing works
Self-citationLong-term potentiation in the hippocampus involves activation of N-methyl-D-aspartate receptors
Harris, E. W., Ganong, A. H., & Cotman, C. W. (1984) · Brain Research · doi:10.1016/0006-8993(84)90275-0 · Cited by 903 · see citing works
Modulation of visual cortical plasticity by acetylcholine and noradrenaline
Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858 · see citing works
Self-citationPostsynaptic Calcium Is Sufficient for Potentiation of Hippocampal Synaptic Transmission
Malenka, R. C., Kauer, J. A., Zucker, R. S., & Nicoll, R. A. (1988) · Science · doi:10.1126/science.2845577 · Cited by 829 · see citing works
Foster, A. C., & Fagg, G. E. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90020-1 · Cited by 818 · see citing works
A Physiological Mechanism for Hebb's Postulate of Learning
Stent, G. S. (1973) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.70.4.997 · Cited by 710 · see citing works
Organization of visual pathways in normal and visually deprived cats.
Sherman, S. M., & Spear, P. D. (1982) · Physiological Reviews · doi:10.1152/physrev.1982.62.2.738 · Cited by 704 · see citing works
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 · see citing works
Synaptic enhancement in fascia dentata: Cooperativity among coactive afferents
McNaughton, B. L., Douglas, R. M., & Goddard, G. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90030-6 · Cited by 647 · see citing works
Hebbian synapses: biophysical mechanisms and algorithms.
Brown, T. H., Kairiss, E. W., & Keenan, C. L. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.002355 · Cited by 577 · see citing works
Hebbian synapses in hippocampus.
Kelso, S. R., Ganong, A. H., & Brown, T. H. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.14.5326 · Cited by 555 · see citing works
A Physiological Basis for a Theory of Synapse Modification
Bear, M. F., Cooper, L. N., & Ebner, F. F. (1987) · Science · doi:10.1126/science.3037696 · Cited by 528 · see citing works
Self-citationN-methyl-D-aspartate receptor antagonist desegregates eye-specific stripes.
Cline, H. T., Debski, E. A., & Constantine‐Paton, M. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.12.4342 · Cited by 523 · see citing works
Blakemore, C. B., & Sluyters, R. C. V. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010478 · Cited by 452 · see citing works
NMDA receptors in the visual cortex of young kittens are more effective than those of adult cats
Tsumoto, T., Hagihara, K., Sato, H., & Hata, Y. (1987) · Nature · doi:10.1038/327513a0 · Cited by 440 · see citing works
NMDA application potentiates synaptic transmission in the hippocampus
Kauer, J. A., Malenka, R. C., & Nicoll, R. A. (1988) · Nature · doi:10.1038/334250a0 · Cited by 423 · see citing works
Development of neuronal selectivity in primary visual cortex of cat.
Frégnac, Y., & Imbert, M. (1984) · Physiological Reviews · doi:10.1152/physrev.1984.64.1.325 · Cited by 336 · see citing works
The location and function of NMDA receptors in cat and kitten visual cortex
Fox, K., Sato, H., & Daw, N. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-07-02443.1989 · Cited by 307 · see citing works
Dingledine, R. J. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014899 · Cited by 282 · see citing works
Reiter, H. O., & Stryker, M. P. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.10.3623 · Cited by 266 · see citing works
A cellular analogue of visual cortical plasticity
Frégnac, Y., Shulz, D. E., Thorpe, S. J., & Bienenstock, E. (1988) · Nature · doi:10.1038/333367a0 · Cited by 248 · see citing works
From basic network principles to neural architecture: emergence of orientation-selective cells.
Linsker, R. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.21.8390 · Cited by 244 · see citing works
Changes in the circuitry of the kitten visual cortex are gated by postsynaptic activity
Rauschecker, J. P., & Singer, W. (1979) · Nature · doi:10.1038/280058a0 · Cited by 183 · see citing works
Self-citationVisual responses in adult cat visual cortex depend on N-methyl-D-aspartate receptors.
Miller, K. D., Chapman, B., & Stryker, M. P. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.13.5183 · Cited by 181 · see citing works
Long-term potentiation of synaptic transmission in kitten visual cortex
Komatsu, Y., Fujii, K., Maeda, J. E. M. S., Sakaguchi, H., & Toyama, K. (1988) · Journal of Neurophysiology · doi:10.1152/jn.1988.59.1.124 · Cited by 144 · see citing works
Gu, Q., Bear, M. F., & Singer, W. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90183-1 · Cited by 144 · see citing works
Self-citationWigström, H., & Gustafsson, B. (1985) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1985.tb07621.x · Cited by 134 · see citing works
A critical period for long-term potentiation in the developing rat visual cortex
Perkins, A. T., & Teyler, T. J. (1988) · Brain Research · doi:10.1016/0006-8993(88)91478-3 · Cited by 117 · see citing works
Cooper, L. N. (1973) · Elsevier eBooks · doi:10.1016/b978-0-12-460350-9.50043-6 · Cited by 113 · see citing works
Cortical activity blockade prevents ocular dominance plasticity in the kitten visual cortex
Reiter, H. O., Waitzman, D. M., & Stryker, M. P. (1986) · Experimental Brain Research · doi:10.1007/bf00243841 · Cited by 108 · see citing works
Ramoa, A. S., Paradiso, M. A., & Freeman, R. D. (1988) · Experimental Brain Research · doi:10.1007/bf00248220 · Cited by 105 · see citing works
Excitatory amino acid transmitters in neuronal circuits of the cat visual cortex
Tsumoto, T., Masui, H., & Sato, H. (1986) · Journal of Neurophysiology · doi:10.1152/jn.1986.55.3.469 · Cited by 96 · see citing works
Kasamatsu, T., Itakura, T., & JONSSON, G. (1981) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)32615-7 · Cited by 76 · see citing works
Disruption of cortical activity prevents ocular dominance changes in monocularly deprived kittens
Shaw, C., & Cynader, M. (1984) · Nature · doi:10.1038/308731a0 · Cited by 74 · see citing works
The effect of monocular exposure to temporal contrasts on ocular dominance in kittens
Singer, W., Rauschecker, J. P., & Werth, R. (1977) · Brain Research · doi:10.1016/0006-8993(77)90832-0 · Cited by 53 · see citing works
Self-citationParadiso, M. A., Bear, M. F., & Daniels, J. D. (1983) · Experimental Brain Research · doi:10.1007/bf00237878 · Cited by 46 · see citing works
Self-citationLong-lasting physiological effects of bath applied N-methyl-d-aspartate
Thibault, O., Joly, M., Müller, D., Schottler, F., Dudek, S. M., & LYNCH, G. S. (1989) · Brain Research · doi:10.1016/0006-8993(89)91553-9 · Cited by 45 · see citing works
Responsivity of normal kitten striate cortex deteriorates after brief binocular deprivation.
Freeman, R. D., Mallach, R., & Hartley, S. (1981) · Journal of Neurophysiology · doi:10.1152/jn.1981.45.6.1074 · Cited by 43 · see citing works
Hebbian Synapses: Biophysical Mechanisms And Algorithms
Brown, T. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.13.1.475 · Cited by 33 · see citing works
Evidence for a threshold in experience-dependent long-term changes of kitten visual cortex
Greuel, J. M., Luhmann, H. J., & Singer, W. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90203-3 · Cited by 30 · see citing works
Self-citationRauschecker, J. P., & Singer, W. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90196-1 · Cited by 13 · see citing works
Self-citationDingledine, R. (2021) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/xy8p-n016 · Cited by 13 · see citing works
A Possible Organization of Animal Memory and Learning
Cooper, L. N. (1995) · World Scientific series in 20th century physics · doi:10.1142/9789812795885_0002 · Cited by 10 · see citing works
Greuel, J. M., Luhmann, H. J., & Singer, W. (1988) · Springer eBooks · doi:10.1007/978-1-4757-9610-0_40 · Cited by 8 · see citing works
Self-citationOntogenetic Self-Organization and Learning
Singer, W. (1992) · doi:10.1093/oso/9780195077124.003.0012 · Cited by 8 · see citing works
Self-citationThe stability of 6-hydroxydopamine under minipump conditions
Haycock, D. A., & Bear, M. F. (1984) · Experimental Brain Research · doi:10.1007/bf00237455 · Cited by 6 · see citing works
Self-citation
Flagged first, then by citations
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
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968 · see citing works
Self-citationSynaptic Activity and the Construction of Cortical Circuits
Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048 · see citing works
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323 · see citing works
CORTICAL PLASTICITY: From Synapses to Maps
Buonomano, D. V., & Merzenich, M. M. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.149 · Cited by 2,083 · see citing works
Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,001 · see citing works
Neurotrophins and Neuronal Plasticity
Thoenen, H. (1995) · Science · doi:10.1126/science.270.5236.593 · Cited by 1,927 · see citing works
Developmental mechanisms that generate precise patterns of neuronal connectivity
Goodman, C. S., & Shatz, C. J. (1993) · Cell · doi:10.1016/s0092-8674(05)80030-3 · Cited by 1,425 · see citing works
Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300 · see citing works
Artola, A., Bröcher, S., & Singer, W. (1990) · Nature · doi:10.1038/347069a0 · Cited by 880 · see citing works
Self-citationThe time course of learning a visual skill
Karni, A., & Sagi, D. (1993) · Nature · doi:10.1038/365250a0 · Cited by 792 · see citing works
Impulse activity and the patterning of connections during cns development
Shatz, C. J. (1990) · Neuron · doi:10.1016/0896-6273(90)90333-b · Cited by 766 · see citing works
Synaptic mechanisms for plasticity in neocortex
Feldman, D. E. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135516 · Cited by 704 · see citing works
Woolley, C. S., & McEwen, B. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07680.1994 · Cited by 679 · see citing works
Development and plasticity of cortical processing architectures
Singer, W. (1995) · Science · doi:10.1126/science.270.5237.758 · Cited by 669 · see citing works
Self-citationDevelopment and plasticity of the primary visual cortex
Espinosa, J. S., & Stryker, M. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.009 · Cited by 672 · see citing works
NR2A Subunit Expression Shortens NMDA Receptor Synaptic Currents in Developing Neocortex
Flint, A. C., Maisch, U. S., Weishaupt, J. H., Kriegstein, A. R., & Monyer, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02469.1997 · Cited by 615 · see citing works
Yuste, R., & Katz, L. C. (1991) · Neuron · doi:10.1016/0896-6273(91)90243-s · Cited by 591 · see citing works
Michaelis, E. K. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00055-5 · Cited by 576 · see citing works
Rapid, experience-dependent expression of synaptic NMDA receptors in visual cortex in vivo
Quinlan, E., Philpot, B. D., Huganir, R., & Bear, M. (1999) · Nature Neuroscience · doi:10.1038/7263 · Cited by 614 · see citing works
Self-citationMayford, M. R., Wang, J., Kandel, E. R., & O’Dell, T. J. (1995) · Cell · doi:10.1016/0092-8674(95)90009-8 · Cited by 525 · see citing works
Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex
Sipe, G. O., Lowery, Tremblay, M.-È., Kelly, E. A., Lamantia, C. E., & Majewska, A. K. (2016) · Nature Communications · doi:10.1038/ncomms10905 · Cited by 512 · see citing works
Critical periods during sensory development
Berardi, N., Pizzorusso, T., & Maffei, L. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)00047-1 · Cited by 490 · see citing works
Li, Y., Erzurumlu, R. S., Chen, C., Jhaveri, S., & Tonegawa, S. (1994) · Cell · doi:10.1016/0092-8674(94)90108-2 · Cited by 469 · see citing works
Role of NO Production in NMDA Receptor-Mediated Neurotransmitter Release in Cerebral Cortex
Montague, P. R., Gancayco, C. D., Winn, M. J., Marchase, R. B., & Friedlander, M. J. (1994) · Science · doi:10.1126/science.7508638 · Cited by 466 · see citing works
Developmental switch in the expression of NMDA receptors occurs in vivo and in vitro
Williams, K. L., Russell, S. L., Shen, Y. M., & Molinoff, P. B. (1993) · Neuron · doi:10.1016/0896-6273(93)90317-k · Cited by 456 · see citing works
Sucher, N. J., Akbarian, S., Chi, C.-L., Leclerc, C., Awobuluyi, M., Deitcher, D. L., Wu, M., Yuan, J., Jones, E. G., & Lipton, S. A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06509.1995 · Cited by 420 · see citing works
Mechanisms of Deafferentation-Induced Plasticity in Human Motor Cortex
Ziemann, U., Hallett, M., & Cohen, L. G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-17-07000.1998 · Cited by 406 · see citing works
The development of topography in the visual cortex: a review of models
Swindale, N. V. (1996) · Network Computation in Neural Systems · doi:10.1088/0954-898x/7/2/002 · Cited by 393 · see citing works
The BCM theory of synapse modification at 30: interaction of theory with experiment
Cooper, L. N., & Bear, M. F. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3353 · Cited by 395 · see citing works
Self-citationQuinlan, E. M., Olstein, D. H., & Bear, M. F. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12876 · Cited by 382 · see citing works
Self-citationEyre, J. A., Miller, S. N., Clowry, G. J., Conway, E., & Watts, C. (2000) · Brain · doi:10.1093/brain/123.1.51 · Cited by 345 · see citing works
Roles of NMDA receptor activity and nitric oxide production in brain development
Contestabile, A. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(00)00018-7 · Cited by 338 · see citing works
Postsynaptic control of plasticity in developing somatosensory cortex
Schlaggar, B. L., Fox, K. D., & O'Leary, D. M. (1993) · Nature · doi:10.1038/364623a0 · Cited by 339 · see citing works
Long-term potentiation and long-term depression in the neocortex
Tsumoto, T. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90011-3 · Cited by 327 · see citing works
N-methyl-D-aspartate receptor antagonists disrupt the formation of a mammalian neural map.
Simon, D. K., Prusky, G. T., O'Leary, D. D. M., & Constantine‐Paton, M. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.22.10593 · Cited by 320 · see citing works
Liu, X.-B., Murray, K. D., & Jones, E. G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2476-04.2004 · Cited by 316 · see citing works
Molecular mechanism for loss of visual cortical responsiveness following brief monocular deprivation
Heynen, A. J., Yoon, B.-J., Liu, C.-H., Chung, H. J., Huganir, R. L., & Bear, M. F. (2003) · Nature Neuroscience · doi:10.1038/nn1100 · Cited by 305 · see citing works
Self-citationAstrocytes Assemble Thalamocortical Synapses by Bridging NRX1α and NL1 via Hevin
Singh, S. K., Stogsdill, J. A., Pulimood, N. S., Dingsdale, H., Kim, Y. H., Pilaz, L., Kim, I. H., Manhães, A. C., Rodrigues, W. D. S., Pamukcu, A., et al. (2016) · Cell · doi:10.1016/j.cell.2015.11.034 · Cited by 311 · see citing works
Rabacchi, S. A., Bailly, Y. J. R., Delhaye‐Bouchaud, N., & Mariani, J. (1992) · Science · doi:10.1126/science.1352066 · Cited by 308 · see citing works
NMDA receptors and memory encoding
Morris, R. G. M. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.014 · Cited by 295 · see citing works
Molecular basis of plasticity in the visual cortex
Berardi, N., Pizzorusso, T., Ratto, G. M., & Maffei, L. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00168-1 · Cited by 284 · see citing works
Homosynaptic long-term depression in the visual cortex
Kirkwood, A., & Bear, M. F. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-05-03404.1994 · Cited by 286 · see citing works
Self-citationLerea, L. S., & McNamara, J. O. (1993) · Neuron · doi:10.1016/0896-6273(93)90239-n · Cited by 284 · see citing works
Acceleration of Visual System Development by Environmental Enrichment
Cancedda, L., Putignano, E., Sale, A., Viegi, A., Berardi, N., & Maffei, L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0845-04.2004 · Cited by 278 · see citing works
Disruption of retinogeniculate afferent segregation by antagonists to NMDA receptors
Hahm, J., Langdon, R. B., & Sur, M. (1991) · Nature · doi:10.1038/351568a0 · Cited by 270 · see citing works
Visual Deprivation Reactivates Rapid Ocular Dominance Plasticity in Adult Visual Cortex
He, H., Hodos, W., & Quinlan, E. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5554-05.2006 · Cited by 263 · see citing works
Aoki, C. J., Venkatesan, C., Go, C. G., Mong, J., & Dawson, T. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05202.1994 · Cited by 255 · see citing works
Maffei, L., Berardi, N., Domenici, L., Parisi, V, & Pizzorusso, T. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04651.1992 · Cited by 252 · see citing works
Kawashima, T., Okuno, H., Nonaka, M., Adachi-Morishima, A., Yagishita-Kyo, N., Okamura, M., Takemoto‐Kimura, S., Worley, P. F., & Bito, H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806518106 · Cited by 251 · see citing works
Involvement of Subplate Neurons in the Formation of Ocular Dominance Columns
Ghosh, A., & Shatz, C. J. (1992) · Science · doi:10.1126/science.1542795 · Cited by 249 · see citing works
Kanold, P. O., & Shatz, C. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.008 · Cited by 245 · see citing works
Gunn, A. J., & Thoresen, M. (2006) · NeuroRx · doi:10.1016/j.nurx.2006.01.007 · Cited by 245 · see citing works
Mechanisms of sleep-dependent consolidation of cortical plasticity
Aton, S. J., Seibt, J., Dumoulin, M., Jha, S. K., Steinmetz, N., Coleman, T., Naidoo, N., & Frank, M. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.007 · Cited by 244 · see citing works
The critical period for ocular dominance plasticity in the Ferret's visual cortex
Issa, N. P., Trachtenberg, J. T., Chapman, B., Zahs, K. R., & Stryker, M. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-16-06965.1999 · Cited by 243 · see citing works
Enhanced Excitability of the Human Visual Cortex Induced by Short-term Light Deprivation
Boroojerdi, B. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.5.529 · Cited by 238 · see citing works
Monocular deprivation induces homosynaptic long-term depression in visual cortex
Rittenhouse, C. D., Shouval, H. Z., Paradiso, M. A., & Bear, M. F. (1999) · Nature · doi:10.1038/16922 · Cited by 228 · see citing works
Self-citationCritical Period Mechanisms in Developing Visual Cortex
Hensch, T. K. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)69008-4 · Cited by 226 · see citing works
Tropea, D., Kreiman, G., Lyckman, A., Mukherjee, S., Yu, H., Horng, S., & Sur, M. (2006) · Nature Neuroscience · doi:10.1038/nn1689 · Cited by 226 · see citing works
Bröcher, S., Artola, A., & Singer, W. (1992) · Brain Research · doi:10.1016/0006-8993(92)90110-u · Cited by 272 · see citing works
Self-citationMolecular basis for induction of ocular dominance plasticity
Bear, M. F., & Rittenhouse, C. D. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199910)41:1 · Cited by 99 · see citing works
An Oral Vaccine Against NMDAR1 with Efficacy in Experimental Stroke and Epilepsy
During, M. J., Symes, C. W., Lawlor, P. A., Lin, J. Y., Dunning, J., Fitzsimons, H. L., Poulsen, D. J., Leone, P., Xu, R., Dicker, B. L., et al. (2000) · Science · doi:10.1126/science.287.5457.1453 · Cited by 218 · see citing works
Neuronal activity during development: permissive or instructive?
Crair, M. C. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80011-7 · Cited by 203 · see citing works
Long-term retention of learning-induced receptive-field plasticity in the auditory cortex.
Weinberger, N. M., Javid, R., & Lepan, B. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.6.2394 · Cited by 198 · see citing works
Synapse elimination accompanies functional plasticity in hippocampal neurons
Bastrikova, N., Gardner, G. A., Reece, J. M., Jeromin, A., & Dudek, S. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800027105 · Cited by 195 · see citing works
Behavioral consequences of abnormal cortical development: insights into developmental disabilities
Berger-Sweeney, J. E. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(96)02251-6 · Cited by 190 · see citing works
The predictive brain: temporal coincidence and temporal order in synaptic learning mechanisms.Preprint
Montague, P. R., & Sejnowski, T. J. (1994) · Learning & Memory · doi:10.1101/lm.1.1.1 · Cited by 185 · see citing works
Recent advances in quantitative colocalization analysis: Focus on neuroscience
Zinchuk, V. S., & Grossenbacher‐Zinchuk, O. (2009) · Progress in Histochemistry and Cytochemistry · doi:10.1016/j.proghi.2009.03.001 · Cited by 184 · see citing works
Torasdotter, M., METSIS, M. L., Henriksson, B. G., Winblad, B. G., & Mohammed, A. H. S. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00142-3 · Cited by 184 · see citing works
Lu, H., Gonzalez, E., & Crair, M. C. (2001) · Neuron · doi:10.1016/s0896-6273(01)00501-3 · Cited by 180 · see citing works
Regulation of motor neuron dendrite growth by NMDA receptor activation
Kalb, R. G. (1994) · Development · doi:10.1242/dev.120.11.3063 · Cited by 177 · see citing works
Involvement of Serotonin in Developmental Plasticity of Kitten Visual Cortex
Gu, Q., & Singer, W. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01104.x · Cited by 173 · see citing works
Self-citationYang, E. J., Ahn, Y. S., & Chung, K. C. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104091200 · Cited by 172 · see citing works
Dumas, T. C. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.08.002 · Cited by 169 · see citing works
Roe, A. W., Pallas, S. L., Kwon, Y. H., & Sur, M. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-09-03651.1992 · Cited by 169 · see citing works
Lisman, J. E. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0260 · Cited by 165 · see citing works
Enriched environment and acceleration of visual system development
Sale, A., Putignano, E., Cancedda, L., Landi, S., Cirulli, F., Berardi, N., & Maffei, L. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.07.008 · Cited by 164 · see citing works
Extracellular Matrix and Visual Cortical Plasticity
Berardi, N., Pizzorusso, T., & Maffei, L. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.008 · Cited by 163 · see citing works
Wells, D. G., Dong, X., Quinlan, E., Huang, Y.-S., Bear, M., Richter, J., & Fallon, J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09541.2001 · Cited by 176 · see citing works
Self-citationLoss of Arc renders the visual cortex impervious to the effects of sensory experience or deprivation
McCurry, C. L., Shepherd, J. D., Tropea, D., Wang, K. H., Bear, M. F., & Sur, M. (2010) · Nature Neuroscience · doi:10.1038/nn.2508 · Cited by 159 · see citing works
Self-citationKato, N., Artola, A., & Singer, W. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90153-a · Cited by 156 · see citing works
Self-citationSpatial Signaling in the Development and Function of Neural Connections
Montague, P. R., Gally, J. A., & Edelman, G. M. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.3.199 · Cited by 150 · see citing works
Roberts, E. B., & Ramoa, A. S. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.5.2587 · Cited by 150 · see citing works
Lambo, M. E., & Turrigiano, G. G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4502-12.2013 · Cited by 132 · see citing works
Gu, Q., Bear, M. F., & Singer, W. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90183-1 · Cited by 144 · see citing works
Self-citationThe role of astrocyte‐mediated plasticity in neural circuit development and function
Perez-Catalan, N. A., Doe, C. Q., & Ackerman, S. D. (2021) · Neural Development · doi:10.1186/s13064-020-00151-9 · Cited by 137 · see citing works
Moore, A. N., Waxham, M. N., & Dash, P. K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.24.14214 · Cited by 144 · see citing works
Gu, Q., & Singer, W. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00514.x · Cited by 137 · see citing works
Self-citationImpaired Sensory Processing as a Basis for Object-Recognition Deficits in Schizophrenia
Doniger, G. M., Silipo, G. S., Rabinowicz, E. F., Snodgrass, J. G., & Javitt, D. C. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.11.1818 · Cited by 137 · see citing works
Roberts, E. B., Meredith, M. A., & Ramoa, A. S. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1021 · Cited by 135 · see citing works
Synapse Elimination in the Central Nervous System: Functional Significance and Cellular Mechanisms
Lohof, A. M., Delhaye‐Bouchaud, N., & Mariani, J. (1996) · Reviews in the Neurosciences · doi:10.1515/revneuro.1996.7.2.85 · Cited by 135 · see citing works
Activity-regulated genes as mediators of neural circuit plasticity
Leslie, J. H., & Nedivi, E. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.05.002 · Cited by 133 · see citing works
Corner, M. A., van Pelt, J., Wolters, P. S., Baker, R. E., & Nuytinck, R. H. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00062-8 · Cited by 132 · see citing works
Excitatory amino acids in epilepsy and potential novel therapies
Meldrum, B. S. (1992) · Epilepsy Research · doi:10.1016/0920-1211(92)90040-z · Cited by 133 · see citing works
A Role for Nitric Oxide in the Development of the Ferret Retinogeniculate Projection
Cramer, K. S., Angelucci, A., Hahm, J., Bogdanov, M. B., & Sur, M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-07995.1996 · Cited by 130 · see citing works
The Formation of Cooperative Cell Assemblies in the Visual Cortex
Singer, W. (1991) · Springer series in synergetics · doi:10.1007/978-3-642-84301-3_8 · Cited by 130 · see citing works
Self-citationDo NMDA receptors have a critical function in visual cortical plasticity?
Fox, K. D., & Daw, N. W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90136-a · Cited by 127 · see citing works
Datwani, A., Iwasato, T., Itohara, S., & Erzurumlu, R. S. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1195 · Cited by 124 · see citing works
Visual input induces long-term potentiation of developing retinotectal synapses
Zhang, L. I., Tao, H. W., & Poo, M. (2000) · Nature Neuroscience · doi:10.1038/76665 · Cited by 124 · see citing works
Shi, J., Aamodt, S. M., & Constantine‐Paton, M. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06264.1997 · Cited by 122 · see citing works
THE ACTION OF NEUROTROPHINS IN THE DEVELOPMENT AND PLASTICITY OF THE VISUAL CORTEX
Cellerino, A., & Maffei, L. (1996) · Progress in Neurobiology · doi:10.1016/0301-0082(96)00008-1 · Cited by 122 · see citing works
- 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.
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