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The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Open accessAbstract
1. Kittens were visually deprived by suturing the lids of the right eye for various periods of time at different ages. Recordings were subsequently made from the striate cortex, and responses from the two eyes compared. As previously reported, monocular eye closure during the first few months of life causes a sharp decline in the number of cells that can be influenced by the previously closed eye. 2. Susceptibility to the effects of eye closure begins suddenly near the start of the fourth week, remains high until some time between the sixth and eighth weeks, and then declines, disappearing finally around the end of the third month. Monocular closure for over a year in an adult cat produces no detectable effects. 3. During the period of high susceptibility in the fourth and fifth weeks eye closure for as little as 3‐4 days leads to a sharp decline in the number of cells that can be driven from both eyes, as well as an over‐all decline in the relative influence of the previously closed eye. A 6‐day closure is enough to give a reduction in the number of cells that can be driven by the closed eye to a fraction of the normal. The physiological picture is similar to that following a 3‐month monocular deprivation from birth, in which the proportion of cells the eye can influence drops from 85 to about 7%. 4. Cells of the lateral geniculate receiving input from a deprived eye are noticeably smaller and paler to Nissl stain following 3 or 6 days' deprivation during the fourth week. 5. Following 3 months of monocular deprivation, opening the eye for up to 5 yr produces only a very limited recovery in the cortical physiology, and no obvious recovery of the geniculate atrophy, even though behaviourally there is some return of vision in the deprived eye. Closing the normal eye, though necessary for behavioural recovery, has no detectable effect on the cortical physiology. The amount of possible recovery in the striate cortex is probably no greater if the period of eye closure is limited to weeks, but after a 5‐week closure there is a definite enhancement of the recovery, even though it is far from complete.
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“It is noteworthy that critical periods for sensory plasticity occur in the same preadolescent period in which remodeling of connectivity occurs.34, 48, 49”
From A role for synaptic plasticity in the adolescent development of executive function (2013) · cites this paper as [48]
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“These sensitive windows are known as critical periods 35 , and constitute another major milestone in the development of brain circuits.”
From Developmental timing and critical windows for the treatment of psychiatric disorders (2016) · cites this paper as [35]
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Cites
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
Self-citationSINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.1003 · Cited by 2,628
Self-citationWiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1029 · Cited by 1,598
Self-citationBINOCULAR INTERACTION IN STRIATE CORTEX OF KITTENS REARED WITH ARTIFICIAL SQUINT
Hubel, D. H., & Wiesel, T. N. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1041 · Cited by 1,369
Self-citationWiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.978 · Cited by 1,291
Self-citationRECEPTIVE FIELDS OF CELLS IN STRIATE CORTEX OF VERY YOUNG, VISUALLY INEXPERIENCED KITTENS
Hubel, D. H., & Wiesel, T. N. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.994 · Cited by 1,113
Self-citationEXTENT OF RECOVERY FROM THE EFFECTS OF VISUAL DEPRIVATION IN KITTENS
Wiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1060 · Cited by 704
Self-citationApical dendritic spines of the visual cortex and light deprivation in the mouse
Valverde, P. (1967) · Experimental Brain Research · doi:10.1007/bf00237559 · Cited by 483
Consequences of monocular deprivation on visual behaviour in kittens
DEWS, P. B., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009023 · Cited by 266
Self-citationThe effect of visual deprivation on cortical neurons: A Golgi study
Globus, A., & Scheibel, A. B. (1967) · Experimental Neurology · doi:10.1016/0014-4886(67)90029-5 · Cited by 247
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Grossberg, S. (1976) · Biological Cybernetics · doi:10.1007/bf00344744 · Cited by 1,910
Wong‐Riley, M. T. T. (1979) · Brain Research · doi:10.1016/0006-8993(79)90728-5 · Cited by 1,853
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Barlow, H. B. (1972) · Perception · doi:10.1068/p010371 · Cited by 1,714
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Andersen, S. L. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(03)00005-8 · Cited by 1,503
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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
McDonald, J. W., & Johnston, M. V. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90011-c · Cited by 1,403
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Greenough, W. T., Black, J. E., & Wallace, C. S. (1987) · Child Development · doi:10.2307/1130197 · Cited by 1,398
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Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300
Adolescence as a sensitive period of brain development
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BLAKEMORE, C., & COOPER, G. F. (1970) · Nature · doi:10.1038/228477a0 · Cited by 1,005
Postnatal development of the visual cortex and the influence of environment
Wiesel, T. N. (1982) · Nature · doi:10.1038/299583a0 · Cited by 978
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A critical window for cooperation and competition among developing retinotectal synapses
Zhang, L. I., Tao, H. W., Holt, C. E., Harris, W. A., & Poo, M. (1998) · Nature · doi:10.1038/25665 · Cited by 911
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Gordon, J. A., & Stryker, M. P. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03274.1996 · Cited by 856
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der Loos, H. V., & Woolsey, T. A. (1973) · Science · doi:10.1126/science.179.4071.395 · Cited by 819
Elimination of synapses in the developing nervous system
Purves, D., & Lichtman, J. W. (1980) · Science · doi:10.1126/science.7414326 · Cited by 808
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
Synaptogenesis in human visual cortex—evidence for synapse elimination during normal development
Huttenlocher, P. R., de Courten, C., Garey, L. J., & Van der Loos, H. (1982) · Neuroscience Letters · doi:10.1016/0304-3940(82)90379-2 · Cited by 745
Sydnor, V. J., Larsen, B., Bassett, D. S., Alexander‐Bloch, A. F., Fair, D. A., Liston, C. M., Mackey, A. P., Milham, M. P., Pines, A. R., Roalf, D. R., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.06.016 · Cited by 750
Inhibitory threshold for critical-period activation in primary visual cortex
Fagiolini, M., & Hensch, T. K. (2000) · Nature · doi:10.1038/35004582 · Cited by 716
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Stent, G. S. (1973) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.70.4.997 · Cited by 710
Identification of a Signaling Pathway Involved in Calcium Regulation of BDNF Expression
Shieh, P. B., Hu, S.-C., Bobb, K., Timmusk, T., & Ghosh, A. (1998) · Neuron · doi:10.1016/s0896-6273(00)81011-9 · Cited by 693
Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.
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Innate and environmental factors in the development of the kitten's visual cortex.
Blakemore, C. B., & Sluyters, R. C. V. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp010995 · Cited by 679
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LeVay, S., Stryker, M. P., & Shatz, C. J. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901790113 · Cited by 658
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Tottenham, N. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.068.2009 · Cited by 651
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Yap, E.-L., & Greenberg, M. E. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.013 · Cited by 706
Hughes, A. (1977) · Handbook of sensory physiology · doi:10.1007/978-3-642-66468-7_11 · Cited by 592
Removing brakes on adult brain plasticity: From molecular to behavioral interventions
Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589
Do children really recover better? Neurobehavioural plasticity after early brain insult
Anderson, V. A., Spencer‐Smith, M. M., & WOOD, A. G. (2011) · Brain · doi:10.1093/brain/awr103 · Cited by 643
Critical periods for experience-dependent synaptic scaling in visual cortex
Desai, N. S., Cudmore, R. H., Nelson, S. B., & Turrigiano, G. G. (2002) · Nature Neuroscience · doi:10.1038/nn878 · Cited by 582
The role of visual experience in the development of columns in cat visual cortex
Crair, M. C., Gillespie, D. C., & Stryker, M. P. (1998) · Science · doi:10.1126/science.279.5350.566 · Cited by 578
Rapid Remodeling of Axonal Arbors in the Visual Cortex
Antonini, A., & Stryker, M. P. (1993) · Science · doi:10.1126/science.8511592 · Cited by 559
Regulation of Class I MHC Gene Expression in the Developing and Mature CNS by Neural Activity
Corriveau, R. A., Huh, G. S., & Shatz, C. J. (1998) · Neuron · doi:10.1016/s0896-6273(00)80562-0 · Cited by 548
Retinal waves and visual system development
Wong, R. O. L. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.29 · Cited by 544
Pattern of dendritic branching in occipital cortex of rats reared in complex environments
Greenough, W. T., & Volkmar, F. R. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90090-3 · Cited by 536
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
MOTOR REORGANIZATION AFTER UPPER LIMB AMPUTATION IN MAN
Cohen, L. G., Bandinelli, S., FINDLEY, T. W., & Hallett, M. (1991) · Brain · doi:10.1093/brain/114.1.615 · Cited by 525
Sleep Enhances Plasticity in the Developing Visual Cortex
Frank, M. G., Issa, N. P., & Stryker, M. P. (2001) · Neuron · doi:10.1016/s0896-6273(01)00279-3 · Cited by 523
The development of synapses in the visual system of the cat
Cragg, B. G. (1975) · Journal of Comparative Neurology · doi:10.1002/cne.901600202 · Cited by 520
Neuromodulatory transmitter systems in the cortex and their role in cortical plasticity
Gu, Q. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00026-x · Cited by 518
Light regulates expression of brain-derived neurotrophic factor mRNA in rat visual cortex.
Castrén, E., Zafra, F., Thoenen, H., & Lindholm, D. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.20.9444 · Cited by 513
Essential fatty acids in visual and brain development
Uauy, R. D., Hoffman, D. R., Peirano, P. D., Birch, D. G., & Birch, E. E. (2001) · Lipids · doi:10.1007/s11745-001-0798-1 · Cited by 497
Cognitive Response Profile of the Human Fusiform Face Area as Determined by MEG
Halgren, E. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.1.69 · Cited by 490
Bear, M., Kleinschmidt, A., Gu, Q., & Singer, W. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-03-00909.1990 · Cited by 488
A Positron Emission Tomographic Study of Auditory Localization in the Congenitally Blind
Weeks, R., Horwitz, B., Aziz‐Sultan, M. A., Tian, B., Wessinger, C. M., Cohen, L. G., Hallett, M., & Rauschecker, J. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02664.2000 · Cited by 491
NMDA Receptor-Dependent Ocular Dominance Plasticity in Adult Visual Cortex
Sawtell, N. B., Frenkel, M. Y., Philpot, B. D., Nakazawa, K., Tonegawa, S., & Bear, M. F. (2003) · Neuron · doi:10.1016/s0896-6273(03)00323-4 · Cited by 482
Perry, B. D. (2002) · Brain and Mind · doi:10.1023/a:1016557824657 · Cited by 480
How do sensitive periods arise and what are they for?
Bateson, P. (1979) · Animal Behaviour · doi:10.1016/0003-3472(79)90184-2 · Cited by 473
The induction of acetylcholine synthesis in primary cultures of dissociated rat sympathetic neurons
Patterson, P. H., & Chun, L. L. Y. (1977) · Developmental Biology · doi:10.1016/0012-1606(77)90269-x · Cited by 467
Blakemore, C. B., & Sluyters, R. C. V. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010478 · Cited by 452
Eluvathingal, T. J., Chugani, H. T., Behen, M. E., Juhász, C., Muzik, O., Maqbool, M., Chugani, D. C., & Makki, M. (2006) · Pediatrics · doi:10.1542/peds.2005-1727 · Cited by 451
A role for synaptic plasticity in the adolescent development of executive function
Selemon, L. D. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.7 · Cited by 439
“It is noteworthy that critical periods for sensory plasticity occur in the same preadolescent period in which remodeling of connectivity occurs.(34,48,49)”
BackgroundPerceptual learning in Vision Research
Sagi, D. (2010) · Vision Research · doi:10.1016/j.visres.2010.10.019 · Cited by 461
Kasamatsu, T., & Pettigrew, J. D. (1976) · Science · doi:10.1126/science.959850 · Cited by 432
Holmes, J. M., & Clarke, M. W. (2006) · The Lancet · doi:10.1016/s0140-6736(06)68581-4 · Cited by 425
Kirkwood, A., Lee, H., & Bear, M. F. (1995) · Nature · doi:10.1038/375328a0 · Cited by 430
Multiple sensitive periods in human visual development: Evidence from visually deprived children
Lewis, T. L., & Maurer, D. M. (2005) · Developmental Psychobiology · doi:10.1002/dev.20055 · Cited by 447
The topography and variability of the primary visual cortex in man
Stensaas, S. S., Eddington, D. K., & Dobelle, W. H. (1974) · Journal of neurosurgery · doi:10.3171/jns.1974.40.6.0747 · Cited by 420
Nutrition in Brain Development and Aging: Role of Essential Fatty Acids
Uauy, R. D., & Dangour, A. D. (2006) · Nutrition Reviews · doi:10.1301/nr.2006.may.s24-s33 · Cited by 426
Mechanisms Of Cognitive Development
Siegler, R. S. (1989) · Annual Review of Psychology · doi:10.1146/annurev.ps.40.020189.002033 · Cited by 416
Selective reconfiguration of layer 4 visual cortical circuitry by visual deprivation
Maffei, A., Nelson, S. B., & Turrigiano, G. G. (2004) · Nature Neuroscience · doi:10.1038/nn1351 · Cited by 415
Binocular depth perception and the cerebral cortex
Parker, A. J. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2131 · Cited by 406
Critical-Period Plasticity in the Visual Cortex
Levelt, C. N., & Hübener, M. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113813 · Cited by 402
Hierarchical and parallel mechanisms in the organization of visual cortex
Stone, J., Dreher, B., & Leventhal, A. G. (1979) · Brain Research Reviews · doi:10.1016/0165-0173(79)90010-9 · Cited by 402
Activity-dependent homeostatic specification of transmitter expression in embryonic neurons
Borodinsky, L. N., Root, C. M., Cronin, J. A., Sann, S. B., Gu, X., & Spitzer, N. C. (2004) · Nature · doi:10.1038/nature02518 · Cited by 396
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
Pettigrew, J. D. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010469 · Cited by 389
Steele, C. J., Bailey, J. A., Zatorre, R. J., & Penhune, V. B. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3578-12.2013 · Cited by 388
Gilbert, C. D. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.2.467 · Cited by 383
The Value of Dimensional Models of Early Experience: Thinking Clearly About Concepts and Categories
McLaughlin, K. A., Sheridan, M. A., Humphreys, K. L., Belsky, J., & Ellis, B. J. (2021) · Perspectives on Psychological Science · doi:10.1177/1745691621992346 · Cited by 418
Sensitive periods in development: Structural characteristics and causal interpretations.
Bornstein, M. H. (1989) · Psychological Bulletin · doi:10.1037/0033-2909.105.2.179 · Cited by 377
Developmental timing and critical windows for the treatment of psychiatric disorders
Marín, O. (2016) · Nature Medicine · doi:10.1038/nm.4225 · Cited by 374
Spatial Relationships among Three Columnar Systems in Cat Area 17
Hübener, M., Shoham, D., Grinvald, A., & Bonhoeffer, T. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09270.1997 · Cited by 372
Structural and functional recovery from early monocular deprivation in adult rats
Pizzorusso, T., Medini, P., Landi, S., Baldini, S., Berardi, N., & Maffei, L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602657103 · Cited by 367
National Outcomes of Cataract Extraction
Javitt, J. C., Street, D. A., Tielsch, J. M., Wang, Q., Kolb, M. M., Schein, O. P., Sommer, A. H., Bergner, M., Steinberg, E. P., Steinberg, E. P., et al. (1994) · Ophthalmology · doi:10.1016/s0161-6420(13)31251-2 · Cited by 365
Barlow, H. B. (1981) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1981.0022 · Cited by 364
Restoration of visual cortical plasticity by local microperfusion of norepinephrine
Kasamatsu, T., Pettigrew, J. D., & Ary, M. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901850110 · Cited by 363
Ellis, B. J., Sheridan, M. A., Belsky, J., & McLaughlin, K. A. (2022) · Development and Psychopathology · doi:10.1017/s0954579421001838 · Cited by 397
A psychobiological theory of attachment
Kraemer, G. W. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00069752 · Cited by 359
Neurogenesis of the cat's primary visual cortex
Luskin, M. B., & Shatz, C. J. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420409 · Cited by 344
The Lens: Development, Proteins, Metabolism and Cataract
Harding, J. J., & Crabbe, M. J. C. (1984) · Elsevier eBooks · doi:10.1016/b978-0-12-206921-5.50008-8 · Cited by 343
Metadata
- Authors
- Hubel, D. H., & Wiesel, T. N.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 1970-02
- Volume
- 206
- Issue
- 2
- Pages
- 419-436
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- PMC
- PMC1348655
- OpenAlex
- W2104220712
- Cited by
- 3,030
- References
- 14
- Citations by year
- 2026: 44 · 2025: 56 · 2024: 66 · 2023: 53 · 2022: 61 · 2021: 60 · 2020: 67 · 2019: 67 · 2018: 69 · 2017: 77 · 2016: 69 · 2015: 83 · 2014: 70 · 2013: 85 · 2012: 87
- FWCI
- 30.69
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Keywords
- monocular deprivation, eyelid closure, kittens, primary visual cortex, lateral geniculate nucleus, visual development, critical period, cortical plasticity, visual recovery, binocular vision
- MeSH terms
- Age Factors, Animals, Cats
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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