Literature DB >> 3981230

Role of visual experience in activating critical period in cat visual cortex.

G D Mower, W G Christen.   

Abstract

Cats were reared in total darkness from birth until 4-5 mo of age (DR cats, n = 7) or with very brief visual experience (1 or 2 days) during an otherwise similar period of dark rearing [DR(1) cats, n = 3; DR(2) cats, n = 7]. Single-cell recordings were made in area 17 of visual cortex at the end of this rearing period and/or after a subsequent prolonged period of monocular deprivation. Control observations were made in normal cats (n = 3), cats reared with monocular deprivation from birth (n = 4), and cats monocularly deprived after being reared normally until 4 mo of age (n = 2). After rearing cats in total darkness, the majority of visual cortical cells were binocularly driven and the overall distribution of ocular dominance was not different from that of normal cats. Orientation-selective cells were very rare in dark-reared cats. Monocular deprivation imposed after dark rearing resulted in selective development of connections from the open eye. Most cells were responsive only to the open eye and the majority of these were orientation selective. These results were similar to, though less severe than, those found in cats reared with monocular deprivation from birth. Monocular deprivation imposed after 4 mo of normal rearing did not produce selective development of connections from the open eye in terms of either ocular dominance or orientation selectivity. In DR(1) cats visual cortical physiology was degraded in comparison to dark-reared cats after the rearing period. Most cells were binocularly driven but there was a higher frequency of unresponsive cells and a reduced frequency of orientation-selective cells. Subsequent monocular deprivation resulted in a further decrease in the number of binocularly driven cells and an increase in unresponsive cells. However, it did not produce a bias in favor of the open eye in terms of either ocular dominance or orientation selectivity. In DR(2) cats there was a high incidence of unresponsive cells and a marked loss of binocularly driven cells after the rearing period. Subsequent monocular deprivation failed to produce any significant changes.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 3981230     DOI: 10.1152/jn.1985.53.2.572

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  14 in total

1.  Dark rearing alters the development of GABAergic transmission in visual cortex.

Authors:  Bernardo Morales; Se-Young Choi; Alfredo Kirkwood
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

2.  The development and activity-dependent expression of aggrecan in the cat visual cortex.

Authors:  P C Kind; F Sengpiel; C J Beaver; A Crocker-Buque; G M Kelly; R T Matthews; D E Mitchell
Journal:  Cereb Cortex       Date:  2012-02-23       Impact factor: 5.357

3.  Effects of age and visual experience on [3H] MK801 binding to NMDA receptors in the kitten visual cortex.

Authors:  I J Reynolds; M F Bear
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

4.  Effects of transient and prolonged flashing light stimulation on the cytochrome oxidase module system in layer IV of the primary visual cortex of kittens.

Authors:  N S Merkul'eva; F N Makarov
Journal:  Neurosci Behav Physiol       Date:  2009-05-12

5.  A family of activity-dependent neuronal cell-surface chondroitin sulfate proteoglycans in cat visual cortex.

Authors:  C Lander; P Kind; M Maleski; S Hockfield
Journal:  J Neurosci       Date:  1997-03-15       Impact factor: 6.167

6.  The Newborn Individualized Developmental Care and Assessment Program (NIDCAP) with Kangaroo Mother Care (KMC): Comprehensive Care for Preterm Infants.

Authors:  Heidelise Als; Gloria B McAnulty
Journal:  Curr Womens Health Rev       Date:  2011-08

7.  Extended plasticity of visual cortex in dark-reared animals may result from prolonged expression of cpg15-like genes.

Authors:  Wei-Chung Allen Lee; Elly Nedivi
Journal:  J Neurosci       Date:  2002-03-01       Impact factor: 6.167

8.  Somatosensory and visual crossmodal plasticity in the anterior auditory field of early-deaf cats.

Authors:  M Alex Meredith; Stephen G Lomber
Journal:  Hear Res       Date:  2011-02-24       Impact factor: 3.208

9.  Plasticity of binocular visual connections in the frog, Xenopus laevis: reversibility of effects of early visual deprivation.

Authors:  M J Keating; E A Dawes; S Grant
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

10.  Factors influencing neurotrophic effects of electrical stimulation in the deafened developing auditory system.

Authors:  Patricia A Leake; Olga Stakhovskaya; Gary T Hradek; Alexander M Hetherington
Journal:  Hear Res       Date:  2008-06-07       Impact factor: 3.208

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