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H Sherk

Publications and source records attributed to H Sherk.

9 recordsLinked to original sources
PubMed1992

Retinotopic order is surprisingly good within cell columns in the cat's lateral suprasylvian cortex.

The retinotopic map in the striate-recipient region of the cat's lateral suprasylvian cortex (referred to here as the lateral suprasylvian area (LS)) has generally been described as quite disorderly. The disorder is commonly attributed to receptive field scatter within cell columns, reflecting the very large size of receptive fields. However, scatter within columns has never been investigated. In the experiments reported here, we examined the receptive field scatter of cells in columns, and also the scatter of a limited sample of their afferents arising from areas 17 and 18. To measure post-synaptic receptive field scatter, electrode penetrations were made parallel to columns in LS, with the electrode approaching from the medial side, traversing the suprasylvian gyrus and emerging into the suprasylvian sulcus. In all 13 such penetrations, receptive fields were clustered together despite their large size. Their centers were scattered over a region that occupied on average less than 20% of the largest field in the column. In contrast, in columns in areas 17 and 18 receptive field centers reportedly are dispersed over regions about equal to the largest of the fields (Hubel and Wiesel 1962, 1965, 1974). The scatter of afferents' receptive fields was assessed anatomically by measuring the overlap between patches of different anterograde tracers in LS. These patches represented terminal labeling from two adjacent or overlapping tracer injections in area 17. While a large degree of overlap would be predicted if afferents have substantial scatter, we found the overlap to be small unless the two injection sites themselves were highly overlapping. Scatter in afferents' receptive fields was measured more directly by physiological recording. In previous experiments, cells in LS were silenced by the local injection of kainic acid, and responses were recorded from axon terminals arising from areas 17 and 18 (Sherk 1989). We examined the receptive field scatter in three penetrations made approximately normal to the cortical surface. Scatter was modest, much less than predicted by the size of post-synaptic receptive fields. Because the degree of receptive field scatter for postsynaptic cells in LS was similar to that of inputs from areas 17 and 18, the scatter of these inputs might be entirely responsible for that seen postsynaptically. Postsynaptic receptive field scatter, on the other hand, was too small to explain the reported disorder in the map in LS.

Animals↗
PubMed1992

Flattening the cerebral cortex by computer.

A computer program was developed for unfolding the cerebral cortex so that it could be viewed as a 2-dimensional surface. Input to the program consisted of tissue sections cut in a standard plane of section. Each section was represented by one line, which corresponded to a contour line in the flattened map. From these data, the computer constructed a 3-dimensional surface representation, which it then flattened. Because the cerebral cortex has considerable intrinsic curvature, flattening required that some regions be expanded and others shrunken. These changes occurred as a natural consequence of local decisions made by the computer as it laid down successive contours. The user could intervene during both surfacing and flattening in order to shape the developing map. The program has been used to generate 37 flattened maps from various regions of cat cortex, and 1 from monkey cortex. The local topography of cortical features such as gyri, sulci, architectonic boundaries, and patches of transported tracer, appeared to be conserved fairly faithfully. Areal distortion was also modest, with an average change in surface area of only 12%.

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PubMed1979

A comparison of visual-response properties in cat's parabigeminal nucleus and superior colliculus.

1. The visual-response properties of single cells in the cat's superior colliculus and parabigeminal nucleus were compared. In the colliculus, 151 cells (restricted to the upper layer) were studied, and in the parabigeminal nucleus, 134 cells. 2. Response characteristics in the two structures were similar in many respects: among these were receptive-field size, ocular dominance, and lack of specificity for stimulus shape and contrast (light versus dark). 3. Quantitatively, there were some significant differences between the two populations of cells. Parabigeminal neurons tended to respond more brisky and reliably, while being less selective for those stimulus parameters tested (size, velocity, and direction of movement). Spontaneous activity was much higher in the parabigeminal nucleus than in the colliculus. Finally, parabigeminal cell responses to stationary stimuli were somewhat brisker than those of tectal cells. 4. These data suggest that a physiologically distinct population of tectal cells sends input to the parabigeminal nucleus, probably with some convergence on individual cells.

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PubMed1979

Connections and visual-field mapping in cat's tectoparabigeminal circuit.

1. The aim of these experiments was to analyze the organization of the reciprocal connections between the cat's superior colliculus and parabigeminal nucleus. Both physiological and anatomical techniques were employed. 2. A population of cells in the superficial gray and upper optic layers of the colliculus was labeled retrogradely by horseradish peroxidase injections into the parabigeminal nucleus. No other sources of input to the nucleus were found in the brain stem or diencephalon. 3. A map of the visual field within the parabigeminal nucleus was reconstructed by plotting visual receptive fields at 350 parabigeminal sites with microelectrodes. The map resembled that found in the colliculus, although it was considerably less orderly. The entire contralateral visual field was represented and, in addition, roughly the central 40 degrees of the ipsilateral hemifield was included; futhermore, the expansion of the central visual field was similar to that of the tectal map. 4. The return parabigeminal projections to the caudal parts of the two colliculi, representing the contralateral hemifields, were in register with the tectal visual-field maps. In contrast, the parabigeminal pathways to the anterior segments of the two colliculi, representing part of the ipsilateral visual fields, were not clearly topographic. The projection to this part of the contralateral colliculus showed little order, while that to the ipsilateral colliculus was extremely sparse. 5. A single site in the colliculus can be the target of axons from nonhomologous locations in the two parabigeminal nuclei; so that both parabigeminal inputs are in register with the tectal map.

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PubMed1978

Area 18 cell responses in cat during reversible inactivation of area 17.

1. A region of area 17 in the cat was temporarily inactivated by cooling, and cells in a topographically corresponding part of area 18 were studied during the blockage of area 17 input. 2. The responses of most area 18 cells were markedly reduced by cooling area 17 and recovered on rewarming primary visual cortex. 3. The selectivity of area 18 cells for oriented stimuli was not affected by inactivating area 17. These cells also, in general, retained their selectivities for the direction of stimulus movement and for the sign of contrast (light or dark) of a moving edge in the absence of input from area 17. 4. There was a greater decrease, on the average, of area 18 cell responses to slowly moving stimuli than to rapidly moving stimuli when area 17 was cooled; however, the exact pattern of change varied considerably from cell to cell. 5. These results suggest that cells in area 18 are to some degree dependent on input from area 17 for their responses, but to a large extent are independent in their selectivity for those stimulus parameters (orientation, direction of movement, sign of contrast) studied.

Animals↗
PubMed1978

Physiological consequences for the cat's visual cortex of effectively restricting early visual experience with oriented contours.

1. The early visual experience of nine cats was restricted to viewing horizontal or vertical lines inside opaque goggles. 2. When the kittens were 3-4 mo old, extracellular recordings were made in the primary visual cortex. To obtain a representative sample of cortical cells, units were studied at regularly spaced intervals along the course of electrode penetrations traveling oblique to the cortical surface. An automated assessment of preferred orientation using a computer-driven optical display was employed, and during the recording session the experimenters did not know which orientation(s) each animal had viewed in early life. 3. In the cats that viewed horizontal lines with one eye and vertical lines with the other during rearing, two major findings of previous workers (14) were confirmed. First, a majority of units were not selective for orientation. Second, units with preferred orientations near vertical tended to be activated exclusively by the eye that had viewed vertical, and likewise for horizontal. 4. In cats that viewed lines of the same orientation with both eyes during rearing, a substantially smaller proportion of units were selective for orientation; the preferred orientations of these units also tended to match the orientation to which the cats had been exposed. 5. Portions of some electrode penetrations showed an orderly arrangement of cells according to preferred orientation similar to that seen in normal cats, but with regions over which only nonselective cells were found. Many penetrations appeared less orderly. 6. The results are consistent with a role for early visual experience in maintaining the responsiveness and innate selectivity of cortical neurons, although they cannot entirely rule out the possibility that experience may alter or determine the preferred orientation of some cells.

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PubMed1976

Quantitative study of cortical orientation selectivity in visually inexperienced kitten.

1. Extracellular recordings were made from single units in the visual cortices of six kittens deprived of experience with pattern vision by binocular lid suture. 2. Selectivity for stimulus orientation was quantitatively assessed in 98 units; 90 responded selectively to the orientation of a moving bar stimulus, the remainder responding nonselectively or too poorly to classify. Cells in these visually inexperienced kittens were similar in their degree of selectivity for orientation to cells tested in adult cats. However, responses tended to be weaker and somewhat more erratic. 3. About half the cells in this simple responded to both directions of stimulus motion at the optimal orientation. Most of those responding to only one direction of motion were considered orientation rather than direction selective because they responded more strongly or more selectively to a moving bar than to a moving spot. 4. Cells appeared to be organized within the cortex in a pattern similar to that found in adult cats, with cells in one column selective for the same orientation, and adjacent column having similar preferred orientations. 5. It is concluded that selectivity for stimulus orientation in the cat's visual cortex is innately determined.

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PubMed1975

Modification of cortical orientation selectivity in the cat by restricted visual experience: a reexamination.

Recent reports have stated that the orientation selectivity of cells in the cat's visual cortex can be biased by limiting the early visual environment to stripes of one orientation. Data obtained from seven kittens using systematic and quantitative sampling of preferred orientation, together with a blind procedure, do not show a bias toward the orientation presented in one type of restricted rearing environment.

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