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The effect of dark rearing on the time course of the critical period in cat visual cortex
Abstract
The effects of dark rearing on the time course of the postnatal critical period for monocular deprivation (MD) in visual cortex were determined in cats who experienced 2 days of MD at various postnatal ages. In normal development, plasticity (susceptibility to MD) was very low at 3 weeks, rose sharply at 6 weeks, and gradually declined over the next 10 weeks. This developmental profile was dramatically altered by dark rearing which slowed the entire time course of the critical period. In dark reared cats, plasticity rose steadily over the first 12 weeks, and was maintained at 16 weeks. There was a crossover of the two profiles of the critical period such that at young ages (6 weeks) normal cats were more plastic than dark reared cats while at later ages (after 9 weeks) dark reared cats were more plastic. A second experiment indicated that dark rearing slowed down the progression of the critical period even after it had been initiated by a period of normal vision. MD produced substantial effects after the normal critical period in cats who were reared normally for the first 6-8 weeks of life and then placed in darkness until 5 months of age. The results are discussed in terms of a simple model of the accelerating effect of visual input and the decelerating effect of total darkness on the time course of the critical period.
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“Furthermore, dark-rearing from birth delays the maturation of PNNs and prolongs the critical period for ocular dominance plasticity (Pizzorusso et al., 2002; Mower, 1991; Lander et al., 1997).”
From Light reintroduction after dark exposure reactivates plasticity in adults via perisynaptic activation of MMP-9 (2017) · cites this paper as Mower, 1991
Citations
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
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
SINGLE-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
Plasticity of ocular dominance columns in monkey striate cortex
Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,629
The development of ocular dominance columns in normal and visually deprived monkeys
Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123
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
Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.
Shatz, C. J., & Stryker, M. P. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012421 · Cited by 691
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
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
Pettigrew, J. D. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010469 · Cited by 389
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Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
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Huang, Z. J., Kirkwood, A., Pizzorusso, T., Porciatti, V., Morales, B., Bear, M. F., Maffei, L., & Tonegawa, S. (1999) · Cell · doi:10.1016/s0092-8674(00)81509-3 · Cited by 1,198
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McGee, A. W., Yang, Y., Fischer, Q. S., Daw, N. W., & Strittmatter, S. M. (2005) · Science · doi:10.1126/science.1114362 · Cited by 643
Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity
Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649
Sugiyama, S., Di Nardo, A. A., Aizawa, S., Matsuo, I., Volovitch, M., Prochiantz, A., & Hensch, T. K. (2008) · Cell · doi:10.1016/j.cell.2008.05.054 · Cited by 491
Face perception in monkeys reared with no exposure to faces
Sugita, Y. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706079105 · Cited by 465
Kirkwood, A., Lee, H., & Bear, M. F. (1995) · Nature · doi:10.1038/375328a0 · Cited by 430
Philpot, B. D., Sekhar, A. K., Shouval, H., & Bear, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00187-8 · Cited by 440
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Quinlan, 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
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Reducing Intracortical Inhibition in the Adult Visual Cortex Promotes Ocular Dominance Plasticity
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Visual Stimulation Is Required for Refinement of ON and OFF Pathways in Postnatal Retina
Tian, N., & Copenhagen, D. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00389-1 · Cited by 304
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Daw, N. W. (1998) · Archives of Ophthalmology · doi:10.1001/archopht.116.4.502 · Cited by 293
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Scheetz, A. J., & Constantine‐Paton, M. (1994) · The FASEB Journal · doi:10.1096/fasebj.8.10.8050674 · Cited by 284
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Als, H., & McAnulty, G. B. (2011) · Current Women s Health Reviews · doi:10.2174/157340411796355216 · Cited by 241
Critical Period Plasticity Matches Binocular Orientation Preference in the Visual Cortex
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Gianfranceschi, L., Siciliano, R., Walls, J., Morales, B., Kirkwood, A., Huang, Z. J., Tonegawa, S., & Maffei, L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1934836100 · Cited by 201
Lander, C., Kind, P., Maleski, M., & Hockfield, S. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-06-01928.1997 · Cited by 195
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Tian, N., & Copenhagen, D. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00470-6 · Cited by 156
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Hofer, S. B., Mrsic‐Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.06.007 · Cited by 142
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Fox, K. D., & Daw, N. W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90136-a · Cited by 127
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Coleman, J. E., Nahmani, M., Gavornik, J. P., Haslinger, R., Heynen, A. J., Erişir, A., & Bear, M. F. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1248-10.2010 · Cited by 102
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Shieh, P. B., & Ghosh, A. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199910)41:1 · Cited by 160
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Murase, S., Lantz, C. L., & Quinlan, E. M. (2017) · eLife · doi:10.7554/elife.27345 · Cited by 87
Chen, L., Cooper, N. G. F., & Mower, G. D. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00076-0 · Cited by 87
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Gordon, K. A., Wong, D. D. E., Valero, J., Jewell, S., Yoo, P., & Papsin, B. C. (2011) · Brain Topography · doi:10.1007/s10548-011-0181-2 · Cited by 87
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Achille, A., Rovere, M., & Soatto, S. (2018) · Cited by 74
Visual Acuity Development and Plasticity in the Absence of Sensory Experience
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Wang, B., Feng, L., Liu, M., Liu, X., & Cang, J. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.023 · Cited by 72
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Lee, W.-C. A., & Nedivi, E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01807.2002 · Cited by 72
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Shaw, C. A., Lanius, R. A., & van den Doel, K. (1994) · Brain Research Reviews · doi:10.1016/0165-0173(94)90014-0 · Cited by 65
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Daw, N. W. (1995) · Springer eBooks · doi:10.1007/978-1-4757-6940-1_12 · Cited by 64
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Tropea, D., Capsoni, S., Tongiorgi, E., Giannotta, S., Cattaneo, A., & Domenici, L. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01436.x · Cited by 63
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Reid, S. N. M., Daw, N. W., Gregory, D. S., & Flavin, H. J. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-23-07619.1996 · Cited by 54
Zhou, X., Nagarajan, N., Mossop, B. J., & Merzenich, M. M. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.01.026 · Cited by 53
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Bear, M. F. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)62541-8 · Cited by 53
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Aamodt, S. M., Nordeen, E. J., & Nordeen, K. W. (1995) · Journal of Neurobiology · doi:10.1002/neu.480270108 · Cited by 50
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Nordeen, K. W., & Nordeen, E. J. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1298.018 · Cited by 46
Chen, G., Rasch, M. J., Wang, R., & Zhang, X.-H. (2015) · Scientific Reports · doi:10.1038/srep17847 · Cited by 45
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Woodard, K. A., & Pollak, S. D. (2020) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2020.05.004 · Cited by 50
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Hogsden, J. L., & Dringenberg, H. C. (2009) · Brain Research · doi:10.1016/j.brainres.2009.06.001 · Cited by 40
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Kind, P. C., Kelly, G. M., Fryer, H. J. L., Blakemore, C. B., & Hockfield, S. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-04-01471.1997 · Cited by 34
Miskolczi, C., Halász, J., & Mikics, É. (2018) · Pediatric Research · doi:10.1038/s41390-018-0205-7 · Cited by 38
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Hogan, D., Roffwarg, H. P., & Shaffery, J. P. (2001) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2001.00270.x · Cited by 33
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Metadata
- Authors
- Mower, G. D.
- Affiliations
- Boston Children's Hospital (US)
- Corresponding author
- Mower, George D.
- Venue
- Developmental Brain Research
- Publisher
- Elsevier BV
- Published
- 1991-02
- Volume
- 58
- Issue
- 2
- Pages
- 151-158
- ISSN
- 0165-3806 (ISSN-L)
- OpenAlex
- W1977850041
- Cited by
- 220
- References
- 31
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 3 · 2023: 1 · 2022: 8 · 2021: 2 · 2020: 3 · 2019: 7 · 2018: 10 · 2017: 6 · 2016: 4 · 2015: 5 · 2014: 9 · 2013: 11 · 2012: 5
- FWCI
- 1.87
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Developmental Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (7r01ns025216-05)
- National Institute of Neurological Disorders and Stroke (NS 25216)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD06276)
- 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
- dark rearing, critical period, monocular deprivation, visual cortex, cortical plasticity, postnatal development, cats, visual development
- MeSH terms
- Animals, Animals, Newborn, Cats, Darkness, Reference Values, Sensory Deprivation, Time Factors, Visual Cortex
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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