Isochronic transplantation of neonatal grafts in the visual cortex of cats: responsiveness, ocular dominance and specificity of cortical cells to visual stimulation

1991 ◽  
Vol 87 (1) ◽  
Author(s):  
U. Yinon ◽  
S. Gelerstein
Keyword(s):  
Visual Cortex ◽  
Visual Stimulation ◽  
Ocular Dominance ◽  
Cortical Cells

Postnatal development of functional properties of visual cortical cells in rats with excitotoxic lesions of basal forebrain cholinergic neurons

1997 ◽  
Vol 14 (1) ◽  
pp. 111-123 ◽  
Author(s):  
Rosita Siciliano ◽  
Gigliola Fontanesi ◽  
Fiorella Casamenti ◽  
Nicoletta Berardi ◽  
Paola Bagnoli ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Postnatal Development ◽  
Functional Properties ◽  
Basal Forebrain ◽  
Critical Period ◽  
Ocular Dominance ◽  
Cholinergic Neurons ◽  
Field Size ◽  
Cortical Cells ◽  
Visual Cortical

AbstractIn the rat, visual cortical cells develop their functional properties during a period termed as critical period, which is included between eye opening, i.e.˘postnatal day (PD) 15, and PD40. The present investigation was aimed at studying the influence of cortical cholinergic afferents from the basal forebrain (BF) on the development of functional properties of visual cortical neurons. At PD15, rats were unilaterally deprived of the cholinergic input to the visual cortex by stereotaxic injections of quisqualic acid in BF cholinergic nuclei projecting to the visual cortex. Cortical cell functional properties, such as ocular dominance, orientation selectivity, receptive-field size, and cell responsiveness were then assessed by extracellular recordings in the visual cortex ipsilateral to the lesioned BF both during the critical period (PD30) and after its end (PD45). After the recording session, the rats were sacrificed and the extent of both cholinergic lesion in BF and cholinergic depletion in the visual cortex was determined. Our results show that lesion of BF cholinergic nuclei transiently alters the ocular dominance of visual cortical cells while it does not affect the other functional properties tested. In particular, in lesioned animals recorded during the critical period, a higher percentage of visual cortical cells was driven by the contralateral eye with respect to normal animals. After the end of the critical period, the ocular dominance distribution of animals with cholinergic deafferentation was not significantly different from that of controls. Our results suggest the possibility that lesions of BF cholinergic neurons performed during postnatal development only transiently interfere with cortical competitive processes.

Unilateral photoreceptor rescue can improve the ability of the opposite, untreated, eye to drive cortical cells in a retinal degeneration model

2005 ◽  
Vol 22 (1) ◽  
pp. 37-43 ◽  
Author(s):  
S.V. GIRMAN ◽  
R.D. LUND
Keyword(s):  
Cell Transplantation ◽  
Royal College ◽  
Visual Stimulation ◽  
Ocular Dominance ◽  
Photoreceptor Degeneration ◽  
Cortical Cells ◽  
Cortical Responses ◽  
Visual Cortical ◽  
Postsynaptic Mechanism ◽  
Stimulation Of

In the Royal College of Surgeons, rat photoreceptor degeneration occurs over the first several months of life, causing deterioration of visual cortical responsiveness seen as greater numbers of cells being nonresponsive to visual stimulation, poor tuning of those cells that do respond, and an overall tendency for domination by the contralateral visual input. If the progress of degeneration in one eye is slowed by intraretinal cell transplantation, cortical responses to stimulation of the remaining, untreated, eye are much stronger, better tuned and histograms of ocular dominance resemble more those in normal rats. This suggests that the rescued eye is able to enhance performance in the untreated eye by some form of postsynaptic mechanism.

Effect of the Group II Metabotropic Glutamate Agonist, 2R,4R-APDC, Varies With Age, Layer, and Visual Experience in the Visual Cortex

1999 ◽  
Vol 82 (1) ◽  
pp. 86-93 ◽  
Author(s):  
C. J. Beaver ◽  
Q.-H. Ji ◽  
N. W. Daw
Keyword(s):  
Visual Cortex ◽  
Metabotropic Glutamate Receptors ◽  
Visual Stimulation ◽  
Ocular Dominance ◽  
Visual Response ◽  
Single Neurons ◽  
Metabotropic Glutamate ◽  
Layer 4 ◽  
Group Ii ◽  
Dark Rearing

Group II metabotropic glutamate receptors (mGluR 2/3) are distributed differentially across the layers of cat visual cortex, and this distribution varies with age. At 3–4 wk, mGluR 2/3 receptor immunoreactivity is present in all layers. By 6–8 wk of age, it is still present in extragranular layers (2, 3, 5, and 6) but has disappeared from layer 4, and dark-rearing postpones the disappearance of Group II receptors from layer 4. We examined the physiological effects of Group II activation, to see if these effects varied similarly. The responses of single neurons in cat primary visual cortex were recorded to visual stimulation, then the effect of iontophoresis of 2R,4R-4 aminopyrrolidine-2,4-decarboxylate (2R,4R-APDC), a Group II specific agonist, was observed in animals between 3 wk and adulthood. The effect of 2R,4R-APDC was generally suppressive, reducing both the visual response and spontaneous activity of single neurons. The developmental changes were in agreement with the immunohistochemical results: 2R,4R-APDC had effects on cells in all layers in animals of 3–4 wk but not in layer 4 of animals >6 wk old. Moreover, the effect of 2R,4R-APDC was reduced in the cortex of older animals (>22 wk). Dark-rearing animals to 47–54 days maintained the effects of 2R,4R-APDC in layer 4. The disappearance of Group II mGluRs from layer 4 between 3 and 6 wk of age is correlated with the segregation of ocular dominance columns in that layer, raising the possibility that mGluRs 2/3 are involved in this process.

scholarly journals A Theory of the Visual Motion Coding in the Primary Visual Cortex

1996 ◽  
Vol 8 (4) ◽  
pp. 705-730 ◽  
Author(s):  
Zhaoping Li
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Visual Motion ◽  
Ocular Dominance ◽  
Phase Relationship ◽  
Field Size ◽  
Color Channel ◽  
Cortical Cells ◽  
Motion Direction ◽  
Motion Coding

This paper demonstrates that much of visual motion coding in the primary visual cortex can be understood from a theory of efficient motion coding in a multiscale representation. The theory predicts that cortical cells can have a spectrum of directional indices, be tuned to different directions of motion, and have spatiotemporally separable or inseparable receptive fields (RF). The predictions also include the following correlations between motion coding and spatial, chromatic, and stereo codings: the preferred speed is greater when the cell receptive field size is larger, the color channel prefers lower speed than the luminance channel, and both the optimal speeds and the preferred directions of motion can be different for inputs from different eyes to the same neuron. These predictions agree with experimental observations. In addition, this theory makes predictions that have not been experimentally investigated systematically and provides a testing ground for an efficient multiscale coding framework. These predictions are as follows: (1) if nearby cortical cells of a given preferred orientation and scale prefer opposite directions of motion and have a quadrature RF phase relationship with each other, then they will have the same directional index, (2) a single neuron can have different optimal motion speeds for opposite motion directions of monocular stimuli, and (3) a neuron's ocular dominance may change with motion direction if the neuron prefers opposite directions for inputs from different eyes.

Physiological effects of unequal alternating monocular exposure

1983 ◽  
Vol 49 (3) ◽  
pp. 804-818 ◽  
Author(s):  
D. G. Tieman ◽  
M. A. McCall ◽  
H. V. Hirsch
Keyword(s):  
Visual Cortex ◽  
Receptive Field ◽  
Single Cells ◽  
Ocular Dominance ◽  
Receptive Fields ◽  
Dorsal Lateral Geniculate Nucleus ◽  
Cortical Cells ◽  
Receptive Field Properties ◽  
Binocular Competition ◽  
Almost All

1. In order to investigate the effects of an imbalance in stimulation to the eyes without the confounding influence of continuous deprivation of one eye, we reared cats with unequal alternating monocular exposure (AME) and, for comparison, cats with equal AME. We recorded extracellularly from single cells in area 17 of visual cortex. 2. For unequal AME cats, a majority of the cells that were visually responsive were dominated by the eye that had received more patterned visual experience. The percentage of cells dominated by the more experienced eye was greater with a large imbalance in stimulation to the two eyes (AME 8/1, 77%) than with a small imbalance (AME 8/4, 62%). 3. For both equal AME cats and unequal AME cats, we obtained evidence for differences in cells activated by the contralateral and by the ipsilateral afferents. a) In equal AME cats receiving only 1 h of exposure per day, we obtained a greater dominance by the contralateral eye (60%) than in equal AME cats receiving 8 h of exposure per day (42%). b) Although a large imbalance in stimulation (AME 8/1) resulted in a shift in ocular dominance in both cortical hemispheres, a moderate imbalance (AME 8/4) resulted in a smaller shift, which was apparent only in the hemisphere ipsilateral to the less-experienced eye. 4. The percentage of cortical cells responsive to each eye was uniform throughout the depth of cortex. Thus, for the unequal AME cats, cells activated by the less-experienced eye were no more frequent in layer IV of visual cortex than in the infragranular and supragranular layers. 5. Although almost all cells recorded from AME cats had relatively normal receptive-field properties, three receptive-field properties of cells in unequal AME cats showed an effect of the rearing. In each case cells dominated by the less-experienced eye and recorded in the cortical hemisphere ipsilateral to it showed the largest changes. These cells a) were more poorly tuned, b) had lower cutoff velocities, and c) had smaller receptive fields. 6. It is suggested that cortical cells that putatively receive Y-cell afferents from the dorsal lateral geniculate nucleus (LGNd) are more affected by an imbalance in stimulation than are cortical cells that putatively receive X-cell afferents. Thus, the decrease in mean receptive-field area and cutoff velocity for the cells dominated by the less-experienced eye is suggested to be due to a greater shift in ocular dominance by the cortical cells receiving Y-cell afferents from the LGNd. 7. The interaction between binocular competition and deprivation of pattern vision may contribute to differences between monocularly deprived cats and unequal AME cats.

Physiological studies of visual cortex reorganization following cortical deafferentation in neonatal cats

1995 ◽  
Vol 73 (9) ◽  
pp. 1378-1388 ◽  
Author(s):  
U. Yinon ◽  
R. Shemesh ◽  
H. Arda ◽  
M. Rosner ◽  
P. P. Jaros
Keyword(s):  
Visual Cortex ◽  
Ocular Dominance ◽  
Medial Part ◽  
Middle Zone ◽  
Cortical Cells ◽  
Unit Recording ◽  
Functional Reorganization ◽  
Physiological Studies ◽  
Made In

Whether restoration takes place in the visual cortex of neonates was physiologically studied in cortical cells of cats following their deafferentation. Deafferentation was performed by a parasagittal incision made in the visual cortex, separating the medial part of it from the thalamocortical and other visual fibers. Responsiveness (percentage of responsive cells) in the middle zone (the middle sector along the cortical incision) of the deafferented region was 82.5%, compared with 91.7% in the afferented (lateral to the incision) region (p = 0.5). In comparison, the responsiveness level was 32.3 and 81.3% (p < 0.05) in the respective zones of the similarly deafferented adult controls. The ocular dominance distribution and binocularity were almost normal in the deafferented region of the neonatally operated cats, whereas binocularity was remarkably diminished in the adult controls. Recovery was also found in the specificity of the cells to orientation and direction in the neonatally operated cats, but not in the adult-operated cats. Thus, functional reorganization of the columnar organizations takes place in the neonatally deafferented but not in the adult-operated cats.Key words: visual cortex, neonatal cats, deafferentation, unit recording, responsiveness.

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

1985 ◽  
Vol 53 (2) ◽  
pp. 572-589 ◽  
Author(s):  
G. D. Mower ◽  
W. G. Christen
Keyword(s):  
Visual Cortex ◽  
Visual Experience ◽  
Ocular Dominance ◽  
Orientation Selectivity ◽  
Monocular Deprivation ◽  
Total Darkness ◽  
Cortical Cells ◽  
Visual Cortical ◽  
Dark Rearing ◽  
Made In

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)

Cholinergic and noradrenergic afferents influence the functional properties of the postnatal visual cortex in rats

1999 ◽  
Vol 16 (6) ◽  
pp. 1015-1028 ◽  
Author(s):  
ROSITA SICILIANO ◽  
FRANCESCO FORNAI ◽  
IRENE BONACCORSI ◽  
LUCIANO DOMENICI ◽  
PAOLA BAGNOLI
Keyword(s):  
Visual Cortex ◽  
Functional Properties ◽  
Cortical Neurons ◽  
Developmental Plasticity ◽  
Signal To Noise Ratio ◽  
Ocular Dominance ◽  
Field Size ◽  
Cortical Cells ◽  
Visual Cortical ◽  
Na Depletion

Based on previous evidence that acetylcholine (ACh) and noradrenaline (NA) play a permissive role in developmental plasticity in the kitten visual cortex, we reinvestigated this topic in the postnatal visual cortex of rats with normal vision. In rats, the functional properties of visual cortical cells develop gradually between the second and the sixth postnatal week (Fagiolini et al., 1994). Cortical cholinergic depletion, by basal forebrain (BF) lesions at postnatal day (PD) 15 (eye opening), leads to a transient disturbance in the distribution of ocular dominance (Siciliano et al., 1997). In the present study, we investigated the development of visual cortical response properties following cytotoxic lesions of the locus coeruleus (LC) alone or in combination with lesions of cholinergic BF. The main result is that early NA depletion impairs the orientation selectivity of cortical neurons, causes a slight increase of their receptive-field size, and reduces the signal-to-noise ratio of cell responses. Similar effects are obtained following NA depletion in adult animals, although the effects of adult noradrenergic deafferentation are significantly more severe than those obtained after early NA depletion. Additional cholinergic depletion causes an additional transient change in ocular-dominance distribution similarly to that obtained after cholinergic deafferentation alone. Comparisons between depletion of NA on the one hand and depletion of both NA and ACh on the other suggest that the effects of combined deafferentation on the functional properties studied result from simple linear addition of the effects of depleting each afferent system alone.

scholarly journals Synaptic Mechanisms of Activity-Dependent Remodeling in Visual Cortex during Monocular Deprivation

2009 ◽  
Vol 2 ◽  
pp. JEN.S2559 ◽  
Author(s):  
Cynthia D. Rittenhouse ◽  
Ania K Majewska
Keyword(s):  
Visual Cortex ◽  
Critical Period ◽  
Ocular Dominance ◽  
Monocular Deprivation ◽  
Neuronal Structure ◽  
Cortical Cells ◽  
Dependent Plasticity ◽  
Cortical Synapses ◽  
Activity Dependent ◽  
Synaptic Mechanisms

It has long been appreciated that in the visual cortex, particularly within a postnatal critical period for experience-dependent plasticity, the closure of one eye results in a shift in the responsiveness of cortical cells toward the experienced eye. While the functional aspects of this ocular dominance shift have been studied for many decades, their cortical substrates and synaptic mechanisms remain elusive. Nonetheless, it is becoming increasingly clear that ocular dominance plasticity is a complex phenomenon that appears to have an early and a late component. Early during monocular deprivation, deprived eye cortical synapses depress, while later during the deprivation open eye synapses potentiate. Here we review current literature on the cortical mechanisms of activity-dependent plasticity in the visual system during the critical period. These studies shed light on the role of activity in shaping neuronal structure and function in general and can lead to insights regarding how learning is acquired and maintained at the neuronal level during normal and pathological brain development.

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