Literature DB >> 625011

Effect of prior visual experience on cortical recovery from the effects of unilateral eyelid suture in kittens.

G G Blasdel, J D Pettigrew.   

Abstract

The reversibility of monocular deprivation was tested physiologically in twelve kittens which had received varying amounts of normal visual experience prior to unilateral eye closure. Recordings obtained from cells in cortical area 17 indicated that the effects of monocular deprivation are reversible in cats as old as 8 weeks if the animals have been allowed normal visual experience before eye closure.1. Four kittens had their right eyes closed at 3, 4, and 5 weeks of age. All animals were reverse sutured at about 8 weeks of age, and after 2 weeks forced usage of the deprived eye, each animal was tested physiologically for recovery. Single unit recordings revealed a consistent relation between the extent to which the effects of initial deprivation could reverse and the age of the animal at the time of this deprivation. Recordings from a fifth, 8 week old kitten, which had been monocularly deprived for 3 weeks, ensured that our shortest period of deprivation induces a severe deficit.2. Two kittens which were reared in the dark for 4 and 5 weeks before unilateral eye closure, failed to show substantial (greater than 20%) reversal when reverse lid-sutured at 8 weeks of age. This failure suggests that kittens having their eyes closed after normal experience show enhanced reversibility, at least in part, on account of their early experience and not necessarily because of shorter deprivation. A litter-mate of one of these kittens was allowed 9 days of normal vision after dark rearing and before lid suture. Recordings which were performed both before and after 6 days of reverse suture demonstrated a near total (85%) reversal in ocular dominance.3. Three animals, monocularly deprived after some normal experience, recovered substantial numbers of binocular cells after both eyes had been allowed to remain open. In one of these cats the effectiveness of monocular deprivation was confirmed physiologically before eye opening. These findings contrast with those of other workers who have failed to find many binocular cells in kittens that had been allowed to recover, with eye opening, from monocular deprivation which had lasted since birth.4. One kitten was reared for 2 weeks (3-5 weeks of age) with alternating monocular deprivation. Single unit recordings from this cat, which were made after four additional weeks of unilateral eye closure, revealed some cells which had resisted monocular deprivation and which responded strongly to stimulation of the deprived eye. Reverse suture in the same animal led to the recovery of many cells (36%), dominated by the initially deprived eye, but did not result in a reversal in ocular dominance.

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Year:  1978        PMID: 625011      PMCID: PMC1282512          DOI: 10.1113/jphysiol.1978.sp012169

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  26 in total

1.  Plasticity of ocular dominance columns in monkey striate cortex.

Authors:  D H Hubel; T N Wiesel; S LeVay
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1977-04-26       Impact factor: 6.237

2.  SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE.

Authors:  T N WIESEL; D H HUBEL
Journal:  J Neurophysiol       Date:  1963-11       Impact factor: 2.714

3.  Receptive fields, binocular interaction and functional architecture in the cat's visual cortex.

Authors:  D H HUBEL; T N WIESEL
Journal:  J Physiol       Date:  1962-01       Impact factor: 5.182

4.  The development of the kittens visual optics.

Authors:  F Thorn; M Gollender; P Erickson
Journal:  Vision Res       Date:  1976       Impact factor: 1.886

5.  Reversal of the physiological effects of monocular deprivation in the kitten's visual cortex.

Authors:  J A Movshon
Journal:  J Physiol       Date:  1976-09       Impact factor: 5.182

6.  The distribution of afferents representing the right and left eyes in the cat's visual cortex.

Authors:  C J Shatz; S Lindström; T N Wiesel
Journal:  Brain Res       Date:  1977-08-05       Impact factor: 3.252

7.  The effect of visual experience on the development of stimulus specificity by kitten cortical neurones.

Authors:  J D Pettigrew
Journal:  J Physiol       Date:  1974-02       Impact factor: 5.182

8.  Reversal of the physiological effects of monocular deprivation in kittens: further evidence for a sensitive period.

Authors:  C Blakemore; R C Van Sluyters
Journal:  J Physiol       Date:  1974-02       Impact factor: 5.182

9.  The period of susceptibility to the physiological effects of unilateral eye closure in kittens.

Authors:  D H Hubel; T N Wiesel
Journal:  J Physiol       Date:  1970-02       Impact factor: 5.182

10.  An improved method for plotting retinal landmarks and focusing the eyes.

Authors:  R Fernald; R Chase
Journal:  Vision Res       Date:  1971-01       Impact factor: 1.886

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  7 in total

Review 1.  A neurophysiological model for anomalous correspondence based on mechanisms of sensory fusion.

Authors:  J I Nelson
Journal:  Doc Ophthalmol       Date:  1981-03-31       Impact factor: 2.379

2.  Cumulative effect of brief daily periods of monocular vision on kitten striate cortex.

Authors:  C R Olson; R D Freeman
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

3.  A role for extraocular afferents in post-critical period reversal of monocular deprivation.

Authors:  D P Crewther; S G Crewther; J D Pettigrew
Journal:  J Physiol       Date:  1978-09       Impact factor: 5.182

4.  Rapid restoration of functional input to the visual cortex of the cat after brief monocular deprivation.

Authors:  C Blakemore; M J Hawken
Journal:  J Physiol       Date:  1982-06       Impact factor: 5.182

5.  The critical period for corpus callosum section to affect cortical binocularity.

Authors:  A J Elberger; E L Smith
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

6.  Synaptic and intrinsic homeostatic mechanisms cooperate to increase L2/3 pyramidal neuron excitability during a late phase of critical period plasticity.

Authors:  Mary E Lambo; Gina G Turrigiano
Journal:  J Neurosci       Date:  2013-05-15       Impact factor: 6.167

7.  Sparse coding can predict primary visual cortex receptive field changes induced by abnormal visual input.

Authors:  Jonathan J Hunt; Peter Dayan; Geoffrey J Goodhill
Journal:  PLoS Comput Biol       Date:  2013-05-09       Impact factor: 4.475

  7 in total

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