The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
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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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
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Yoshida, A., Chen, K., Moritani, M., Yabuta, N. H., Nagase, Y., Takemura, M., & Shigenaga, Y. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970623)383:1 · Cited by 57
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Self-citationRoβner, S., Kumar, A., Kues, W. A., Witzemann, V., & Schliebs, R. (1993) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(93)90015-6 · 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
Toda, T., Hayakawa, I., Matsubayashi, Y., Tanaka, K., Ikenaka, K., Lu, Q., & Kawasaki, H. (2008) · Molecular and cellular neurosciences · doi:10.1016/j.mcn.2008.05.014 · Cited by 17
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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
Takebayashi, M., Kagaya, A., Uchitomi, Y., Yokota, N., Horiguchi, J., & Yamawaki, S. (1998) · Neurochemistry International · doi:10.1016/s0197-0186(97)00070-3 · Cited by 17
Udin, S. B., Scherer, W. J., & Constantine‐Paton, M. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90240-3 · Cited by 17
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Donahoe, J. W. (1997) · Advances in psychology · doi:10.1016/s0166-4115(97)80104-5 · Cited by 16
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Yang, B., Wang, Y., & Cynader, M. S. (1996) · Brain Research · doi:10.1016/0006-8993(96)00047-9 · Cited by 16
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Glazewski, S., Kossut, M. M., & Skangiel-Kramska, J. (1995) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(95)00051-h · Cited by 16
Huang, Z., Khaled, H. G., Kirschmann, M., Gobes, S. M. H., & Hahnloser, R. H. R. (2018) · eLife · doi:10.7554/elife.37571 · Cited by 16
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Kossut, M. M., & Singer, W. (1991) · Experimental Brain Research · doi:10.1007/bf00231735 · Cited by 15
Self-citationLiu, Y., Jia, W., Strosberg, A. D., & Cynader, M. S. (1993) · Brain Research · doi:10.1016/0006-8993(93)91162-l · Cited by 15
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Grant, S., & Keating, M. J. (1992) · Experimental Brain Research · doi:10.1007/bf00228254 · Cited by 15
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Self-citationNakamori, T., Sato, K., Kinoshita, M., Kanamatsu, T., Sakagami, H., Tanaka, K., & Ohki‐Hamazaki, H. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12954 · Cited by 14
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Smith, A. L., & Thompson, I. D. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00501.x · Cited by 14
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Chassy, P., & Gobet, F. R. (2010) · Cited by 14
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Johnson, G., & Bigge, C. F. (1991) · Annual reports in medicinal chemistry · doi:10.1016/s0065-7743(08)61189-6 · Cited by 14
Do NMDA Receptor Kinetics Regulate the End of Critical Periods of Plasticity?
Medina, A. E., Liao, D. S., Mower, A. F., & Ramoa, A. S. (2001) · Neuron · doi:10.1016/s0896-6273(01)00514-1 · Cited by 14
Doig, R. O., Santhakumar, S., Fehily, B., Raja, S., Solomon, T., Bartlett, C. A., Fitzgerald, M., & Hodgetts, S. I. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00085 · Cited by 13
Fox, K. D. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)62542-x · Cited by 13
Salami, M., Fathollahi, Y., Semnanian, S., & Atapour, N. (2000) · Neuroscience Research · doi:10.1016/s0168-0102(00)00187-5 · Cited by 13
Dolan, S., & Cahusac, P. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00375-s · Cited by 13
Shimegi, S., Fischer, Q. S., Yang, Y., Sato, H., & Daw, N. W. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00313.2003 · Cited by 13
Sato, H., Hata, Y., & Tsumoto, T. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00334-6 · Cited by 13
Thompson, R. F. (1992) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(92)90013-b · Cited by 13
Friedlander, M. J., FréAgnac, Y., & Burke, J. P. (1993) · Progress in Brain Research · doi:10.1016/s0079-6123(08)60370-2 · Cited by 16
Dunlop, S. A., Stirling, R. V., Rodger, J., Symonds, A. C. E., Bancroft, W. J., Tee, L. B. G., & Beazley, L. D. (2003) · Experimental Neurology · doi:10.1016/j.expneurol.2003.08.013 · Cited by 12
He, S., Shao, L.-R., Rittase, W. B., & Bausch, S. B. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.320 · Cited by 11
Höhmann, C. F., Wallace, S. A., Johnston, M. V., & Blue, M. E. (1998) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(98)00075-6 · Cited by 12
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Gunn, A. J., & Thoresen, M. (2006) · Neurotherapeutics · doi:10.1007/bf03207046 · Cited by 12
Patterning of the Somatosensory Maps with NMDA Receptors
Erzurumlu, R. S., & Iwasato, T. (2006) · Springer eBooks · doi:10.1007/978-0-387-38607-2_10 · Cited by 12
Kasamatsu, T., & Schmidt, E. (1997) · Brain Research Protocols · doi:10.1016/s1385-299x(96)00008-6 · Cited by 12
Dubroff, J. G., Stevens, R. T., Hitt, J. M., Maier, D. L., McCasland, J. S., & Hodge, C. J. (2005) · Somatosensory & Motor Research · doi:10.1080/08990220500084990 · Cited by 12
Appearance of glutamate-like immunoreactivity during retinal regeneration in the adult newt
Chiba, C. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01427-3 · Cited by 12
Developmental regulation of plasticity in cat somatosensory cortex
Juliano, S. L., Eslin, D. E., & Tommerdahl, M. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.4.1706 · Cited by 12
Gavornik, J. P., & Bear, M. F. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103019 · Cited by 11
Self-citationMower, G. D., & Chen, L. (2003) · Molecular Brain Research · doi:10.1016/j.molbrainres.2003.08.007 · Cited by 11
Faulkner, S. D., Vorobyov, V., & Sengpiel, F. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi059 · Cited by 11
Erzurumlu, R. S., & Guido, W. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)62547-9 · Cited by 11
Activation of NMDA Receptors Is Necessary for the Recovery of Cortical Binocularity
Krahe, T. E., & Medina, A. E. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00442.2009 · Cited by 10
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Huang, X. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.01.031 · Cited by 11
Developmental changes and ocular dominance plasticity in the visual cortex.
Daw, N. W., & Beaver, C. J. (2001) · The Keio Journal of Medicine · doi:10.2302/kjm.50.192 · Cited by 10
Orientation Selectivity Is Reduced by Monocular Deprivation in Combination With PKA Inhibitors
Beaver, C. J., Fischer, Q. S., Ji, Q., & Daw, N. W. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.4.1933 · Cited by 10
Long-Term Potentiation and Memory
(2012) · Springer eBooks · doi:10.1007/springerreference_169302 · Cited by 10
Ocular dominance plasticity: Molecular mechanisms revisited
Kasamatsu, T., & Imamura, K. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.25001 · Cited by 10
Cao, Y., Fajardo, D. S., Guerrero‐Given, D., Samuel, M. A., Ohtsuka, T., Boye, S. L., Kamasawa, N., & Martemyanov, K. A. (2022) · Current Biology · doi:10.1016/j.cub.2022.09.016 · Cited by 9
Li, P., Prasad, S., Mitchell, D. E., Hachisuka, A., Sawada, J.-I., Alhousseini, A., & Gu, Q. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi109 · Cited by 9
Self-citationCai, S., Fischer, Q. S., He, Y. H., Zhang, L., Liu, H., Daw, N. W., & Yang, Y. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180162 · Cited by 8
Nakadate, K., Imamura, K., & Watanabe, Y. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00224-3 · Cited by 9
Experience-dependent development of NMDAR1 subunit expression in the lateral geniculate nucleus
Fava, M., Duffy, K. R., & Murphy, K. M. (1999) · Visual Neuroscience · doi:10.1017/s0952523899164162 · Cited by 9
Tanaka, S., & Miyashita, M. (2009) · Neural Computation · doi:10.1162/neco.2009.04-08-752 · Cited by 8
Quantitative behavioural phenotyping to investigate anaesthesia induced neurobehavioural impairment
Nambyiah, P., & Brown, A. E. (2021) · Scientific Reports · doi:10.1038/s41598-021-98405-x · Cited by 7
Experience dependent plasticity of higher visual cortical areas in the mouse
Craddock, R., Vasalauskaite, A., Ranson, A., & Sengpiel, F. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad203 · Cited by 9
Age and Visual Experience-dependent Expression of NMDAR1 Splice Variants in Rat Retina
Manta, G. A., Spathis, A. D., Taraviras, S. L., Kouvelas, E. D., & Mitsacos, A. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0467-5 · Cited by 8
Synaptic Mechanisms of Activity-Dependent Remodeling in Visual Cortex during Monocular Deprivation
Rittenhouse, C. D., & Majewska, A. K. (2009) · Journal of Experimental Neuroscience · doi:10.4137/jen.s2559 · Cited by 9
Kobayashi, M., Imamura, K., Kaub, P. A., Nakadate, K., & Watanabe, Y. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00033-0 · Cited by 8
Langdon, R. B., & Sur, M. (1992) · Brain Research · doi:10.1016/0006-8993(92)90403-v · Cited by 8
Cuppini, R., Ambrogini, P., & Sartini, S. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00506-x · Cited by 8
Using Osmotic Minipumps for Intracranial Delivery of Amino Acids and Peptides
White, J. D., & Schwartz, M. W. (1994) · Methods in neurosciences · doi:10.1016/b978-0-12-185291-7.50017-5 · Cited by 8
Characterization of the N-methyl-d-aspartate (NMDA) receptor in the embryonic chick brain
Jacobsson, S. O. P., Hedin, H. L. M., Sellström, Å., & Fowler, C. J. (1998) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/pl00005217 · Cited by 8
Cellular mechanisms of visual cortical plasticity: a game of cat and mouse.Preprint
Gordon, J. A. (1997) · Learning & Memory · doi:10.1101/lm.4.3.245 · Cited by 8
Chronic effects of NMDA and APV on tectal output in Xenopus laevis
Scherer, W. J., & Udin, S. B. (1991) · Visual Neuroscience · doi:10.1017/s0952523800010567 · Cited by 8
Lee, C., Joo, K., Kim, M., Rhie, D., & Jang, H. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23604 · Cited by 7
Synchronous Oscillations and Memory Formation ☆
Singer, W. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21027-4 · Cited by 7
Self-citation
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.
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 ›
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