» Articles » PMID: 5498493

The Period of Susceptibility to the Physiological Effects of Unilateral Eye Closure in Kittens

Overview
Journal J Physiol
Specialty Physiology
Date 1970 Feb 1
PMID 5498493
Citations 701
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

An anti-Hebbian model for binocular visual plasticity and its attentional modulation.

Chen Z, Cai Y Commun Biol. 2025; 8(1):418.

PMID: 40075123 PMC: 11903768. DOI: 10.1038/s42003-025-07833-2.


Neuron-to-glia and glia-to-glia signaling directs critical period experience-dependent synapse pruning.

Nelson N, Miller V, Broadie K Front Cell Dev Biol. 2025; 13:1540052.

PMID: 40040788 PMC: 11876149. DOI: 10.3389/fcell.2025.1540052.


Three systems of circuit formation: assembly, updating and tuning.

Barabasi D, Ferreira Castro A, Engert F Nat Rev Neurosci. 2025; .

PMID: 39994473 DOI: 10.1038/s41583-025-00910-9.


Glia control experience-dependent plasticity in an olfactory critical period.

Leier H, Foden A, Jindal D, Wilkov A, Van der Linden Costello P, Vanderzalm P Elife. 2025; 13.

PMID: 39883485 PMC: 11781797. DOI: 10.7554/eLife.100989.


Single-cell synaptome mapping: its technical basis and applications in critical period plasticity research.

Uchigashima M, Mikuni T Front Neural Circuits. 2024; 18:1523614.

PMID: 39726910 PMC: 11670323. DOI: 10.3389/fncir.2024.1523614.


References
1.
Wiesel T, Hubel D . Comparison of the effects of unilateral and bilateral eye closure on cortical unit responses in kittens. J Neurophysiol. 1965; 28(6):1029-40. DOI: 10.1152/jn.1965.28.6.1029. View

2.
Hubel D, Wiesel T . Binocular interaction in striate cortex of kittens reared with artificial squint. J Neurophysiol. 1965; 28(6):1041-59. DOI: 10.1152/jn.1965.28.6.1041. View

3.
Wiesel T, Hubel D . Extent of recovery from the effects of visual deprivation in kittens. J Neurophysiol. 1965; 28(6):1060-72. DOI: 10.1152/jn.1965.28.6.1060. View

4.
Valverde F . Apical dendritic spines of the visual cortex and light deprivation in the mouse. Exp Brain Res. 1967; 3(4):337-52. DOI: 10.1007/BF00237559. View

5.
Globus A, SCHEIBEL A . The effect of visual deprivation on cortical neurons: a Golgi study. Exp Neurol. 1967; 19(3):331-45. DOI: 10.1016/0014-4886(67)90029-5. View