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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.
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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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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
Wiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1029 · Cited by 1,598
Self-organization of orientation sensitive cells in the striate cortex
Malsburg, C. V. D. (1973) · Kybernetik · doi:10.1007/bf00288907 · Cited by 1,444
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
The Biochemistry of Memory: A New and Specific Hypothesis
LYNCH, G. S., & Baudry, M. (1984) · Science · doi:10.1126/science.6144182 · Cited by 1,041
Long-term potentiation and NMDA receptors in rat visual cortex
Artola, A., & Singer, W. (1987) · Nature · doi:10.1038/330649a0 · Cited by 967
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 911
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 905
Modulation of visual cortical plasticity by acetylcholine and noradrenaline
Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858
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
Foster, A. C., & Fagg, G. E. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90020-1 · Cited by 818
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
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
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
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
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
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
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
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 525
Blakemore, C. B., & Sluyters, R. C. V. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010478 · Cited by 452
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
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
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
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
Dingledine, R. J. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014899 · Cited by 288
Reiter, H. O., & Stryker, M. P. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.10.3623 · Cited by 266
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
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
Visual 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
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 177
Self-citationLong-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
Gu, Q., Bear, M. F., & Singer, W. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90183-1 · Cited by 144
Self-citationWigström, H., & Gustafsson, B. (1985) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1985.tb07621.x · Cited by 134
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
Cooper, L. N. (1973) · Elsevier eBooks · doi:10.1016/b978-0-12-460350-9.50043-6 · Cited by 111
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
Ramoa, A. S., Paradiso, M. A., & Freeman, R. D. (1988) · Experimental Brain Research · doi:10.1007/bf00248220 · Cited by 105
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
Kasamatsu, T., Itakura, T., & JONSSON, G. (1981) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)32615-7 · Cited by 76
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
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
Self-citationParadiso, M. A., Bear, M. F., & Daniels, J. D. (1983) · Experimental Brain Research · doi:10.1007/bf00237878 · Cited by 46
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
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
Hebbian Synapses: Biophysical Mechanisms And Algorithms
Brown, T. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.13.1.475 · Cited by 33
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
Self-citationRauschecker, J. P., & Singer, W. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90196-1 · Cited by 13
Self-citationDingledine, R. (2021) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/xy8p-n016 · Cited by 13
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
Greuel, J. M., Luhmann, H. J., & Singer, W. (1988) · Springer eBooks · doi:10.1007/978-1-4757-9610-0_40 · Cited by 8
Self-citationOntogenetic Self-Organization and Learning
Singer, W. (1992) · doi:10.1093/oso/9780195077124.003.0012 · Cited by 8
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
Self-citation
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
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
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
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
Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,074
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
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