[LAMINAR LOCATION OF NEURONS PROVIDING INTERHEMISPHERIC CONNECTIONS IN THE VISUAL CORTEX IN CATS WITH IMPAIRMENTS OF BINOCULAR VISION].

The distributio of cells in the visual cortical layers of intact cats (n=7) and cats with experimentally induced strabismus (n=10) and monocular deprivation (n=5) was studied after microiontophoretic injection of horseradish peroxidase into the ocular-dominance columns in areas 17, 18 and the transition zone 17/18. It was found that in cats with impaired binocular vision, the callosal cells were located deeper in layers of I/II, and higher - in layer IV, as compared to those in intact cats. Also in cats with impaired binocular vision, the proportion of callosal cells in layer IV was increased, while in layers II/III it was reduced as compared to intact cats. The most pronounced changes were noted in monocular deprived animals. These findings suggest an important role of sensory input in the formation of the callosal neurons layer distribution.

[The influence of strabismus and monocular deprivation on the size of callosal cells in cortical areas 17 and 18 of the cat].

To reveal the changes in visual cortex structure following impaired early binocular experience, the size (somatic area) of callosal cells in areas 17, 18 ofmonocularly deprived and convergent strabismic cats was measured. Horseradish peroxidase was injected into the single ocular dominance columns of areas 17, 18 and the transition zone 17/18. In both groups of impaired cats the mean size of callosal cells in area 17 was increased in comparison to intact cats. In area 18, the similar difference was found in monocularly deprived cats only. It was shown that the differences in the mean sizes of cells are due to the increase of the number of large cells. In strabismic cats, the portion of large cells (soma > 200 mkm2) in area 17 was 58% and in area 18 was 8%. The relative share of large cells in areas 17 and 18 of monocularly deprived cats was similar (28 and 26 % correspondingly). These data show that early binocular vision impairments may lead to the changes in cytoarchitecture of cortical layers where the interhemispheric connections originate.

[The size of cells providing interhemispheric and intrahemispheric connections in the visual cortex of binocular vision-impaired cats].

The size (somatic area) of 658 cells located in layers 2/3 of cortical areas 17, 18 of both hemispheres in intact monocularly deprived and bilateral strabismic cats was measured. These cells were retrogradely labelled after injections of horseradish peroxidase into ocular dominance columns in areas 17, 18. In all groups of cats, the mean somatic area of callosal cells was significantly larger than the mean somatic area of intrahemispheric cells. It was found that the mean somatic area of callosal cells was increased by 26.6% in monocularly deprived cats and by 20.2% in strabismic cats in relation to the mean somatic area of callosal cells in intact cats. In addition, the mean somatic area of intrahemispheric cells in monocularly deprived cats was indistinguishable from the mean somatic area of intrahemispheric cells in strabismic cats and in intact cats. It is concluded that early binocular vision impairments produce enlargement of callosal cells' size in the visual cortex.

Effects of divergent strabismus on the horizontal connections of neurons in the cat visual cortex.

Neuron connections of eye dominance columns in the visual cortex were studied in kittens at age 5-6 months with experimental strabismus induced on days 13-16 of life (by tenotomy of the medial ocular muscle). A photographic method was used to assess the angle between the visual axes of the eyes. The operated oculomotor muscle was found to undergo partial reattachment to the eyeball. In some kittens, the operated eye returned to the normal position, while others showed persisting deviation of the eyes by 5-15 degrees. Loss of the binocular properties of cortical neurons have been demonstrated in such animals (Sireteanu et al., 1993). Differences were seen in the extents of connections of cortical eye dominance columns between these groups of cats. Elimination of diplopia and non-correspondence of the two retinal images in kittens of these groups is suggested to be mediated by different mechanisms: alternation of the eyes on fixation or suppression of the activity of the deviant eye.

[The influence of divergent strabismus on horizontal neuronal connections in the cat visual cortex].

We have investigated the neuronal connections of ocular dominance columns in the visual cortex of 5- 6-month-old divergent strabismic cats. Strabismus was induced by tenotomy of medial rectus muscle at the age of 13-16 postnatal days. The angle between visual axes of the eyes was assessed using photographic technique. It was found that severed ocular muscle partially reattaches to the eye globe. In some animals the deviated eye has returned to normal position, in the others the residual eye deviation was 5-15 degrees. The loss of cortical binocularity for such animals is well known [Sireteanu et al., 1993]. The differences in the length of cortical neuronal connections of ocular dominance columns were revealed between these groups of animals. In our opinion, in these animal groups different mechanisms are used to prevent diplopic vision and incongruence of two retinal images: one is alternating fixation and other--suppression of deviated eye activity.

Interhemisphere connections of eye dominance columns in the cat visual cortex in conditions of impaired binocular vision.

Data from studies of interhemisphere connections in fields 17 and 18 of cats reared in conditions of impaired binocular vision (monocular deprivation, uni- and bilateral strabismus) are presented. Monosynaptic connections between neurons were studied by microiontophoretic application of horseradish peroxidase into cortical eye dominance columns and the distributions of retrograde labeled callosal cells were analyzed. Spatial asymmetry and eye-specific interhemisphere neuron connections persisted in conditions of monocular deprivation and strabismus. Quantitative changes in connections were less marked in monocular deprivation than strabismus. In cats with impaired binocular vision, as in intact animals, the widths of callosal-receiving zones were greater than the widths of the callosal cell zones, which is evidence for the non-reciprocity of interhemisphere connections in cortical areas distant from the projection of the vertical meridian. Morphofunctional differences between cells mediating connections in the opposite directions are proposed.

[Interhemispheric connections of ocular-dominance columns in cats with binocular vision impairment].

We have investigated the interhemispheric connections of areas 17 and 18 in cats with impaired binocular vision (monocular deprivation, uni- and bilateral strabismus). Monosynaptic neuronal connections were studied using microionophoretic injections of horseradish peroxidase in the single cortical columns and analsys of spatial distribution of retrogradely labelled callosal cells was performed. In the cases of monocular deprivation and strabismus, the spatial asymmetry and eye-specificity of interhemispheric connections are retained. Quantitative changes of connections are more pronounced in strabismic cats. In cats with binocular vision impairments, as well as in control ones, the width of callosal-recipient zone is larger than of the callosal cells zone. This may indicate that interhemispheric connections are non-reciprocal in the areas of cortex that are more distant from the projection of vertical meridian of visual field. We expect that there should be morpho-functional in the cells that are providing connections in opposite directions.

Neuronal connections of eye-dominance columns in the cat cerebral cortex after monocular deprivation.

Plastic changes in intrahemisphere neuronal connections of the eye-dominance columns of cortical fields 17 and 18 were studied in monocularly deprived cats. The methodology consisted of microintophoretic administration of horseradish peroxidase into cortical columns and three-dimensional reconstruction of the areas of retrograde labeled cells. The eye dominance of columns was established, as were their coordinates in the projection of the visual field. In field 17, the horizontal connections of columns receiving inputs from the non-deprived eye via the crossed-over visual tracts were longer than the connections of the "non-crossed" columns of this eye and were longer than in normal conditions; the connections of the columns of the deprived eye were significantly reduced. Changes in the spatial organization of horizontal connections in field 17 were seen for the columns of the non-deprived eye (areas of labeled cells were rounder and the density of labeled cells in these areas were non-uniform). The longest horizontal connections in deprived cats were no longer than the lengths of these connections in cats with strabismus. It is suggested that the axon length of cells giving rise to the horizontal connections of cortical columns has a limit which is independent of visual stimulation during the critical period of development of the visual system.

[Neuronal connections of ocular dominance columns in the cortex of monocularly deprived cats].

We have investigated the developmental changes of intrahemispheric neuronal connections of the areas 17 & 18 ocular dominance columns in monocularly deprived cats. Single cortical columns were microiontophoretically injected with horseradish peroxidase and 3D reconstruction of retrogradely labelled cells' region was done. Ocular dominance of injected columns and their coordinates in the visual field map were determined. In area 17 it was shown that for non-deprived eye the connections of columns that are driven via the crossed pathways were longer than connections of columns driven via uncrossed ones, and in both cases they were longer than connections in intact cats. The connections of deprived eye columns are significantly reduced. We have observed some changes in the spatial organization of long-range connections in area 17 for columns driven by the non-deprived eye (more rounded shape of regions of labeled cells, non-uniform distribution of cells within it). Maximal length of such connections did not exceed the length of connections in strabismic cats. We speculate that the length of cell axons providing for the horizontal connections of cortical columns has some intrinsic limit that does not depend on visual stimulation during the critical period of development.

Interhemisphere connections of the visual cortex in cats with bilateral strabismus.

The distribution of retrograde labeled callosal cells after microiontophoretic application of horseradish peroxidase into individual cortical columns in fields 17 and 18 was studied in cats reared with bilateral strabismus (with an angle of eye deviation of 10-35 degrees ). The area containing labeled cells was located asymmetrically in relation to the position of the injected column in the opposite hemisphere. Some of the cells were located in those parts of the transitional zone between fields 17 and 18 whose retinotopic coordinates corresponded to the column coordinates (as in intact cats). Other labeled cells were located in fields 17 and 18 and were grouped into clusters located at distances of about 1000 microm from the marginal clusters of the transitional zone. The locations of labeled cells in the lateral geniculate body showed that most columns receive inputs from the ipsilateral eye. Evidence for eye specificity of these monosynaptic interhemisphere connections is presented. The functional significance of changes in these connections in bilateral strabismus is discussed.

Changes in the structure of neuronal connections in the visual cortex of cats with experimentally induced bilateral strabismus.

The spatial distribution of neuronal connections in cortical field 17 was studied in cats with experimentally induced bilateral convergent strabismus on postnatal days 10-14. Horseradish peroxidase was applied microiontophoretically to individual columns of neurons in fields 17 and 18 and retrograde-labeled cells were identified in both hemispheres. Increases and decreases in the extent of intra-hemisphere connections were seen in the mediolateral direction (projections of the horizontal meridian of the visual field). Most columns showed increases in inter-hemisphere connections in this same direction, which may support the more reliable unification of the two visual hemifields. In addition, some columns showed increases in intra-and inter-hemisphere connections in the rostrocaudal direction (projections of the vertical meridian). Thus, bilateral strabismus induced during the critical period of development leads to changes in the structure of both intra-hemisphere and inter-hemisphere connections of individual cortical columns in fields 17 and 18.

[Interhemispheric connections in the visual cortex of cats reared with bilateral strabismus].

We have determined the spatial distribution of retrograde labelled callosal cells after microiontophoretic horseradish peroxidase injections into the single cortical columns of area 17, 18 in cats reared with bilateral convergent strabismus. The obtained strabismus angle was in the range 10-35 degrees. The zone of labelled cells was located asymmetrically in respect to location of injected column in opposite hemisphere. Some cells were revealed in the transition zone 17/18 and their retinotopic coordinates corresponded to the injected column, as was shown in intact cats. Other labelled cells were located in areas 17, 18, in clusters approximately in 1000 mkm from marginal clusters of transition zone. Analysis of labeling in lateral geniculate nucleus has shown that most of the injected columns were driven by ipsilateral eye. The data obtained may be interpreted as evidence of eye-specificity of monosynaptic callosal connections. The functional role in such connections changes in cats with bilateral strabismus is discussed.

Neuronal connection of the cortex and reconstruction of the visual space.

The distributions of retrograde labeled cells in fields 17 and 18 and the fields 17/18 transitional zone were studied in both hemispheres of cats after microiontophoretic administration of horseradish peroxidase into individual cortical columns in fields 17, 18, 19, and 21a. The clustered organization of the internal connections of the cortical fields, the asymmetrical locations of labeled callosal cells relative to the injected columns, and the defined distribution of labeled cells in layers A of the lateral geniculate body suggested that eye-specific neuronal connections support "binding" of the visual hemifields separately for each eye. Application of marker to columns in fields 19 or 21a demonstrated disparate inputs from fields 17 and 18 and the fields 17/18 transitional zone. It is suggested that these connections may support the extraction of loci and stereoscopic boundaries located in the central sectors of the visual space.

[Changes of the structure of neuronal connections in visual cortex of cats with experimentally induced bilateral strabismus].

The spatial distribution of neuronal connections in cortical area 17 in cats with bilateral convergent strabismus, surgically induced on postnatal days 10-14, was investigated. Single cortical columns of areas 17 and 18 were microiontophoretically injected with horseradish peroxidase and retrogradely labeled cells in both hemispheres were detected. The intrahemispheric connections in area 17 along the mediolateral direction (the projection of visual field horizontal meridian) were found to be either dilated or reduced. For most columns, the interhemispheric connections in this direction were increased, which may provide for more reliable unification of two visual hemifields. Moreover, the extension of intra- and interhemispheric connections in rostrocaudal direction (along the visual field vertical meridian projection) was detected in some cortical columns. Thus bilateral strabismus induced during the developmental critical period, modifies the structure of both of intra- and inter-hemispheric spatial neuronal connections of individual cortical columns in areas 17 and 18.

[Interhemispheric connections of areas 17 and 18 in the cortical columns of cats with unilateral strabismus]. / Mezhpolusharnye sviazi korkovykh kolonok polei 17 i 18 u koshek s unilateral'nym kosoglaziem.

The interhemispheric connections of areas 17 and 18 of the cerebral cortex were investigated in cats with experimental unilateral strabismus. Single cortical columns were microiontophoretically injected with horseradish peroxidase, and retrogradelly labeled cells were demonstrated in the opposite brain hemisphere. After tracer injection in area 18 columns, the labeled callosal cells were located in area 17/18 transitional zone, similar to what was found in normal cats. However, in some cases the expansion of the region of callosally labeled cells distribution, was found. It is proposed that the extent of the region of callosally-connected cells may vary depending on whether the cells receive their input from intact or strabismic eye.

Structure of internal interneuronal connections in field 17 of the cat cerebral cortex.

The spatial distribution of horizontal internal connections in field 17 of the cat cortex was studied after microiontophoretic application of horseradish peroxidase to individual cortical columns. Cluster analysis of the distribution of labeled cells in the superficial layers in the tangential plane of the cortex was performed. Field 17 included 7 +/- 1 clusters of up to five cells. Clusters were distributed into two layers, separated by 1.2 +/- 0.3 mm. The distance between the centers of the clusters forming rows was 0.8 +/- 0.3 mm. The spatial characteristics of the grouping of cells sending axons into the cortical column were compared with published data based on optical visualization of the activity of neurons in orientational and eye-dominant columns of the visual cortex. It is suggested that columns in field 17 are associated with 6-8 hypercolumns, though only with a single type of neuron within these hypercolumns, in terms of eye dominance and orientational preference.

Afferent connections of fields 17 and 18 of the cat cerebral cortex formed by neurons of the dorsal lateral geniculate body.

Horseradish peroxidase (HRP) was applied microiontophoretically to nine individual columns in fields 17 and six columns in field 18 of the cat cerebral cortex. Most labeled cells in the dorsal lateral geniculate body were identified in layer A. The ratio of number of labeled cells in layer A to the number of labeled cells in layer A1 was assessed (the A/A1 ratio). Application of HRP to columns in field 17 yielded A/A1 ratios of 0.5 to 2.5; application to field 18 gave ratios ranging from 0.2 to 0.9. This suggests that the fields studied here contained columns which were afferent in relation to the ipsilateral eye and the contralateral eye.

Structure of reciprocal connections of visual cortical fields 17 and 18 in the cat.

Microiontophoretic application of horseradish peroxidase to individual columns in fields 17 and 18 of the cat cortex was used to identify the distribution by area and layer of retrograde labeled cells in both fields. After application of marker to fields 17 or 18, the area of labeled cells in field 17 (in the tangential plane) was extended and orientated along the projection of the horizontal meridian of the field of vision. The area of labeled cells in field 18 in these cases was orientated along the projections of the vertical meridian. Similar differences in the organization of the connections of fields 17 and 18 were seen in the projection zone of the central 10 degrees of the field of vision at different elevations. Thus, the spatial distributions of internal and external connections in each field coincide and their orientations in fields 17 and 18 are mutually perpendicular. It is suggested that field 17 performs the more detailed analysis of information on the horizontal components of an image and communicates this to field 18, while field 18 is responsible for the more detailed analysis of information about the vertical components of the same image, communicating this to field 17.

[The structure of internal intraneuronal connections in the area 17 of the cat cerebral cortex]. / Struktura vnutrennikh mezhneironnykh sviazei polia 17 kory bol'shogo mozga koshki.

Spatial distribution of horizontal intrinsic neuronal connections in area 17 of cat cerebral cortex was studied following HRP microion tophoretic injections into the single cortical columns. Cluster analysis of labelled cell distribution in superficial layers was performed in the tangential cortical plane. Area 17 was found to contain 7 +/- 1 clusters each consisting of 1-5 cells. Clusters were arranged in two rows, separated by a distance of 1.2 +/- 0.3 mm. The distance between the centers of the clusters that form the rows was equal to 0.8 +/- 0.3 mm. The spatial characteristics of cell clusters sending axons to cortical column, found in this study, were compared with the known data on the optical imaging of the activity of neurons of orientation and ocular dominance columns of visual cortex. It is suggested that area 17 cortical column receives inputs from cells of 6-8 hypercolumns that have similar ocular dominance and orientation preference.

[Afferent connections of columns of area 17 and 18 of the cerebral cortex formed by neurons of dorsal lateral geniculate bodies in cats]. / Afferentnye sviazi kolonok polei 17 i 18 kory bol'shogo mozga koshki, formiruemye neironami dorsal'nogo naruzhnogo kolenchatogo tela.

Horseradish peroxidase (HRP) was injected microiontophoretically into nine single area 17 columns and six area 18 columns of the cat's cerebral cortex. Within the dorsal lateral geniculate nucleus most of the labelled cells were found in the laminae A. The ratio of HRP-labelled cells in lamina A to those in lamina Al (A/A1) was estimated. After injection of HRP in area 17 columns this ratio varied from 0.5 to 2.5, while after HRP injection into area 18 columns it varied from 0.2 to 0.9. These data may indicate that in the areas studied contain the columns that receive afferents from both ipsilateral and contralateral eyes.