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P D Spear

Publications and source records attributed to P D Spear.

At least 19 recordsLinked to original sources

Visual response properties of neurons in the LGN of normally reared and visually deprived macaque monkeys.

It is now well appreciated that parallel retino-geniculo-cortical pathways exist in the monkey as in the cat, the species in which parallel visual pathways were first and most thoroughly documented. What remains unclear is precisely how many separate pathways pass through the parvo- and magnocellular divisions of the macaque lateral geniculate nucleus (LGN), what relationships-homologous or otherwise-these pathways have to the cat's X, Y, and W pathways, and whether these are affected by visual deprivation. To address these issues of classification and trans-species comparison, we used achromatic stimuli to obtain an extensive set of quantitative measurements of receptive field properties in the parvo- and magnocellular laminae of the LGN of nine macaque monkeys: four normally reared and five monocularly deprived of vision by lid suture near the time of birth. In agreement with previous studies, we find that on average magnocellular neurons differ from parvocellular neurons by having shorter response latencies to optic chiasm stimulation, greater sensitivity to luminance contrast, and better temporal resolution. Magnocellular laminae are also distinguished by containing neurons that summate luminance over their receptive fields nonlinearly (Y cells) and whose temporal response phases decrease with increasing stimulus contrast (indicative of a contrast gain control mechanism). We found little evidence for major differences between magno- and parvocellular neurons on the basis of most spatial parameters except that at any eccentricity, the neurons with the smallest receptive field centers tended to be parvocellular. All parameters were distributed unimodally and continuously through the parvo- and magnocellular populations, giving no indications of subpopulations within each division. Monocular deprivation led to clear anatomical effects: cells in deprived-eye laminae were pale and shrunken compared with those in nondeprived eye laminae, and Cat-301 immunoreactivity in deprived laminae was essentially uniformly abolished. However, deprivation had only subtle effects on the response properties of LGN neurons. Neurons driven by the deprived eye in both magno- and parvocellular laminae had lower nonlinearity indices (i.e., summed signals across their receptive fields more linearly) and were somewhat less responsive. In magnocellular laminae driven by the deprived eye, neuronal response latencies to stimulation of the optic chiasm were slightly shorter than those in the nondeprived laminae, and receptive field surrounds were a bit stronger. No other response parameters were affected by deprivation, and there was no evidence for loss of a specific cell class as in the cat.

Animals↗

Functional plasticity in extrastriate visual cortex following neonatal visual cortex damage and monocular enucleation.

Neonatal lesions of primary visual cortex (areas 17, 18 and 19; VC) in cats lead to significant changes in the organization of visual pathways, including severe retrograde degeneration of retinal ganglion cells of the X/beta class. Cells in posteromedial lateral suprasylvian (PMLS) cortex display plasticity in that they develop normal receptive-field properties despite these changes, but they do not acquire the response properties of striate neurons that were damaged (e.g., high spatial-frequency tuning, low contrast threshold). One possibility is that the loss of X-pathway information, which is thought to underlie striate cortical properties in normal animals, precludes the acquisition of these responses by cells in remaining brain areas following neonatal VC damage. Previously, we have shown that monocular enucleation at the time of VC lesion prevents the X-/beta-cell loss in the remaining eye. The purpose of the present study was to determine whether this sparing of retinal X-cells leads to the development of striate-like response properties in PMLS cortex. We recorded the responses of PMLS neurons to visual stimuli to assess spatial-frequency tuning, spatial resolution, and contrast threshold. Results indicated that some PMLS cells in animals with a neonatal VC lesion and monocular enucleation displayed a preference for higher spatial frequencies, had higher spatial resolution, and had lower contrast thresholds than PMLS cells in cats with VC lesion alone. Taken together, these results suggest that preserving X-pathway input during this critical period leads to the addition of some X-like properties to PMLS visual responses.

Animals↗

Effects of aging on numbers and sizes of neurons in histochemically defined subregions of monkey striate cortex.

BACKGROUND: In addition to its horizontal layers, primate striate cortex has a vertical modular organization. Among the vertical modules are histochemically defined areas of high and low cytochrome oxidase labeling in the supragranular layers, referred to, respectively, as blobs and interblobs. Cytochrome c oxidase (CO) blobs and interblobs differ in their inputs from the magnocellular and parvocellular visual pathways, their physiological properties, and many aspects of their neurochemistry. The present study investigated whether aging differentially affects neuron numbers or sizes in the supragranular blobs or interblobs. METHODS: The right hemisphere from three young adult (5.2-12.4 years) and four old (24.0-26.7 years) rhesus monkeys was used. Tangential sections through the central visual-field representation were stained for CO and counterstained with cresyl violet. Montages were constructed through cortical layers 2 and 3, and neuron counts and size measurements were made in blob and interblob regions using stereological procedures that yield unbiased estimates. Blob density also was calculated. RESULTS: CO blob density was 3.76/mm2 in young adults and 3.95/mm2 in old animals, a difference that was not statistically significant. Neuron soma sizes also did not differ significantly between young adult and old animals or between blob and interblob regions. In addition, neuron density was not significantly different between young adult and old animals. However, independent of age, neuron density was significantly higher in the center of interblobs (394,058 cells/mm3) than in the center of blobs (333,638/mm3). CONCLUSIONS: Our results and those of previous studies (Vincent et al. 1989. Anat. Rec. 223:329-341; Peters and Sethares. 1993. Anat. Rec. 236:721-729) suggest that aging has little or no effect on the densities or sizes of the different functional or morphological types of neurons that exist in the different cortical layers or in the different vertical modules marked by CO blobs and interblobs. These findings are consistent with the results of our previous anatomical and physiological studies of the rhesus monkey retina and lateral geniculate nucleus. These results suggest that the retinogenic-ulostriate pathways are relatively unaffected by aging in the rhesus monkey.

Aging↗

Plasticity following neonatal visual cortex damage in cats.

We have used the cat visual system as a model system to investigate how remaining areas of the brain are able to take over functions that are lost following brain damage and why neonates show better behavioral recovery than adults. Anatomical studies with both anterograde and retrograde tracing methods reveal an increased projection from retina through thalamus to the posteromedial lateral suprasylvian (PMLS) extrastriate visual area of cortex in the damaged hemisphere of cats with a neonatal visual cortex (areas 17, 18, and 19; VC) lesion. No such enhanced projection is seen after an adult lesion. In addition, single-cell neurophysiological studies indicate that physiological compensation is present in PMLS cortex after a neonatal VC lesion but not after an adult lesion. The physiological compensation replaces (or maintains) properties that are characteristic of PMLS neurons; there is little or no improvement to replace the superior spatial properties of striate cortex (or areas 18 or 19) neurons that were lost. Immunohistochemical studies of the possible roles of neuronal growth factors in the compensation indicate that low- and high-affinity receptors are present that would allow several neurotrophins to influence the normal retina throughout life. Furthermore, these receptors are upregulated transneuronally following neonatal VC damage and thus could play a role in lesion-induced changes in the retina and its central projections. Ongoing studies are continuing to examine the presence of neurotrophins and their receptors in the retina and brain during normal development and after VC damage. In addition, studies of the effects of administering neuronal growth factors are underway to determine whether compensation for VC damage can be improved in neonates or even be produced in adults.

Age Factors↗

Effects of aging on the primate visual system: spatial and temporal processing by lateral geniculate neurons in young adult and old rhesus monkeys.

1. Visual abilities decline during normal aging, and many of these declines are due to neural changes in the retina or central visual pathways. We have begun studies of the primate visual system to investigate the location and nature of these changes as well as to answer general questions about the effects of aging on neural function. We began with the dorsal lateral geniculate nucleus (LGN) because it is the main structure through which visual information passes on the way to cortex and because the parallel parvocellular and magnocellular pathways, which may be affected differently by aging, are anatomically distinct there. 2. Single-cell recordings were made in the LGN of young adult (5-16 yr) and old (25-28 yr) rhesus monkeys. We made quantitative measures of a wide variety of response properties for a large number of parvocellular (n = 257) and magnocellular (n = 113) neurons in the two groups of animals. As a result, in addition to studying the effects of aging, we were able to make quantitative comparisons between parvocellular and magnocellular neurons using larger samples than have been studied previously and for some properties that have not been studied before. 3. We found that magnocellular neurons have significantly higher maximal response rates and signal-to-noise ratios than parvocellular neurons. However, response latencies to visual stimulation were similar for neurons in the two types of layers. In agreement with previous studies, magnocellular neurons had higher maximal contrast sensitivity and higher contrast gain than parvocellular neurons. However, the sensitivity difference occurred because nearly all of the neurons with low sensitivities (< 10) were in the parvocellular layers, not because neurons in the magnocellular layers had the highest sensitivities. 4. Neurons with the smallest receptive-field centers, the highest spatial-frequency resolutions, and the highest optimal spatial frequencies were found in the parvocellular layers. However, the overall distributions of each of these properties overlapped substantially for neurons in the two types of layers, and the mean values were not significantly different. The mean high temporal-frequency cutoff was significantly higher for magnocellular than parvocellular neurons, but the difference was small (only 3 Hz), and it occurred because many parvocellular neurons had lower cutoffs than any seen in the magnocellular layers, not because magnocellular neurons had the highest temporal-frequency cutoffs. Parvocellular neurons also had narrower temporal-frequency tuning than magnocellular neurons. However, there was no significant difference in optimal temporal frequency.(ABSTRACT TRUNCATED AT 400 WORDS)

Aging↗

Effects of aging on the size, density, and number of rhesus monkey lateral geniculate neurons.

Visual abilities decline during aging, and many of these declines are due to neural changes in the retina or brain. We have begun studies of the monkey visual system to investigate the location and nature of these changes as well as to answer general questions about the effects of aging on neural structure and function. We began with the dorsal lateral geniculate nucleus (LGN) because it is the main structure through which visual information passes on the way to cortex and because the parallel parvicellular and magnocellular pathways are most easily identified and studied in the LGN. In the present experiment, we determined the sizes, densities, and numbers of LGN neurons in young-adult (5 to 12.5 years) and old (23 to 27.5 years) rhesus monkeys. The measures were corrected for tissue shrinkage, and stereological procedures were used that yield unbiased estimates. In young-adult monkeys, neurons densities were lower in the magnocellular layers (about 14,000/mm3) than in the parvicellular layers (23,000/mm3). Neuron density increased about 28% from anterior to posterior in both types of layers. There was an average of approximately 1,267,000 neurons in the parvicellular layers and 148,000 neurons in the magnocellular layers; however, there was substantial variability (1.9-fold) among five brains studied. Aging produced a statistically significant decrease in neuron density in both the magnocellular (29% average decrease) and parvicellular (41% average decrease) layers. However, there was no significant loss of neurons. Rather, the density decrease was due to a small (nonsignificant) decrease in the number of neurons combined with a small (nonsignificant) increase in LGN volume. The increase in LGN volume was due to a significant increase in neuron soma-size and proportional increase in the volume of glial cells, blood vessels, and neuropil. These results, together with those of other studies, suggest that the effects of aging on the primate visual pathway from retina through striate cortex are relatively subtle. It is possible that the major neural changes occur more centrally. Alternatively, individual differences in the effect of aging may require much larger samples or prior screening to observe consistent changes.

Aging↗

Neural bases of visual deficits during aging.

Visual abilities decline during normal (non-pathological) aging. Many of these visual declines cannot be attributed to optical changes and must therefore be due to changes in the retina or central visual pathways. These include declines in visual acuity and spatial contrast sensitivity (especially under low luminance levels), suprathreshold contrast vision and contrast gain, temporal-frequency contrast sensitivity and resolution, spatial-temporal interactions, hyperacuity, binocular processing, and sensitivity to motion. Certain aspects of these vision deficits and comparisons with neurophysiological and lesion-behavior studies in monkeys suggest hypotheses about the nature and location (e.g. magnocellular vs parvocellular pathways, specific visual structures, and so on) of the neural deficits. Despite the well-documented psychophysical deficits, available anatomical studies in humans and monkeys suggest that aging has only relatively minor effects on the retino-geniculo-striate pathway. Retinal photoreceptor losses are relatively restricted to rods, and there is compensation among the remaining rods for those that are lost. Although some retinal ganglion cells appear to be lost, the loss is small relative to individual-to-individual variability. In addition, there appear to be no massive cell losses in the LGN or striate cortex. Physiological results in the monkey LGN suggest that the functional properties of LGN neurons, and therefore their retinal inputs, are not significantly affected by aging. Retinal pattern-evoked ERG studies in humans likewise suggest that the physiological properties of the retina are little affected by aging. Comparisons between pattern-evoked ERG and cortical evoked potentials in the same individuals suggest that some neural change occurs between the retina and striate cortex, but the location and nature of this change is not known. Thus, we are far from being able to answer the question, What are the neural bases of visual deficits during aging? There are several possible reasons for this: (1) The neurobiological methods that have been brought to bear on the question have been fairly limited. (2) Investigations of neural changes may not have been guided sufficiently by what is known about the psychophysical changes that occur with aging. (3) Existing studies may not have examined the correct locations in the visual system. (4) There is large individual-to-individual variability in the effects of aging and, with the small samples of individuals that typically are available in neural studies of aging, the variability could obscure detection of aging-related changes. Suggestions are offered for ways in which future research can solve these problems.(ABSTRACT TRUNCATED AT 400 WORDS)

Aging↗

How complete is physiological compensation in extrastriate cortex after visual cortex damage in kittens?

Previous studies indicate that neurons in the cat's posteromedial lateral suprasylvian (PMLS) visual area of cortex show physiological compensation after neonatal but not adult damage to areas 17, 18, and 19 of the visual cortex (collectively, VC). Thus, VC damage in adults produces a loss of direction selectivity and a decrease in response to the ipsilateral eye among PMLS cells, but these changes are not seen in adult cats that received VC damage as kittens. This represents compensation for early VC damage in the sense that PMLS neurons develop properties they would have had if there had been no brain damage. However, this is only a partial compensation for the effects of VC damage. A full compensation would involve development of properties of the VC cells that were removed in the damage. The present study investigated whether this type of compensation occurs for detailed spatial- and temporal-frequency processing. Single-cell recordings were made in PMLS cortex of adult cats that had received a VC lesion on the day of birth or at 8 weeks of age. Responses to sine-wave gratings that varied in spatial frequency, contrast, and temporal frequency were assessed quantitatively. We found that the spatial- and temporal-frequency processing of PMLS cells in adult cats that had neonatal VC damage were not significantly different from PMLS cells in normal cats. Therefore, there was no evidence that PMLS cells can compensate for VC damage by developing properties that are better than normal and like those of the striate cortex cells that were damaged. We also assessed the effects of long-term VC damage in adult cats to determine whether the normal properties seen in cats with neonatal VC damage represent a compensation for abnormalities in PMLS cortex present after adult damage. In a previous study, we found that acute VC damage in adult cats has small but reliable effects on maximal response amplitude, maximal contrast sensitivity, and spatial resolution (Guido et al. 1990b). In the present study, we found that long-term VC damage in adult cats does not increase these abnormalities as a result of secondary degenerative changes. In fact, the minor abnormalities that were present after an acute VC lesion were virtually absent following a long-term adult lesion, perhaps because they were due to transient traumatic effects. Therefore, there was little evidence for abnormalities in spatial- or temporal-frequency processing following long-term adult VC damage for which PMLS cells might show compensation following long-term neonatal damage.(ABSTRACT TRUNCATED AT 400 WORDS)

Aging↗

Binocular processing in the cat's dorsal lateral geniculate nucleus. III. Spatial frequency, orientation, and direction sensitivity of nondominant-eye influences.

The present experiments examined the extent to which binocular processing in the cat's dorsal lateral geniculate nucleus (LGN) depends upon the spatial frequency, orientation, and direction of movement of stimuli presented to the nondominant eye. In Experiment 1, we tested the effects of varying these stimulus parameters on the responses of LGN cells to nondominant-eye stimulation. Sixteen of 34 cells tested had statistically significant responses to the nondominant eye and, in agreement with a previous study (Guido et al. 1989), the responsive cells were spatial-frequency sensitive. However, there was little evidence for orientation or direction sensitivity in responses to the nondominant eye: changes in discharge with changes in stimulus orientation and direction were small and were statistically significant in only nine of the cells. In Experiment 2, we tested the effects of varying spatial frequency, orientation, and direction of movement of stimuli presented to the nondominant eye on its ability to influence responses to the dominant eye (i.e., on binocular interactions). The dominant eye was stimulated with the optimal spatial frequency for the cell being tested. For 22 of 45 cells tested, nondominant-eye stimulation had a statistically significant effect on the response to the dominant eye. Fourteen of these cells showed band-pass spatial-frequency sensitivity in the nondominant-eye influence, and eight showed low-pass spatial-frequency sensitivity. However, only 11 of the cells had statistically significant variations in their binocular interactions that depended on the orientation or direction of stimuli presented to the nondominant eye. Furthermore, even for those cells, the effect of varying orientation and direction was only about half as strong as the effect of varying spatial frequency. We conclude that binocular processing in the LGN, including responses to the nondominant eye and nondominant-eye influences on responses to the dominant eye, are affected significantly by the spatial frequency of the nondominant-eye stimulus and relatively little by stimulus orientation or direction of movement. The significance of these findings for understanding the functions of LGN binocular processing is discussed.

Analysis of Variance↗

Binocular interactions in the cat's dorsal lateral geniculate nucleus, II: Effects on dominant-eye spatial-frequency and contrast processing.

The present study tested the hypothesis that nondominant-eye influences on lateral geniculate nucleus (LGN) neurons affect the processing of spatial and contrast information from the dominant eye. To do this, we determined the effects of stimulating the nondominant eye at its optimal spatial frequency on the responses of LGN cells to sine-wave gratings of different spatial frequency and contrast presented to the dominant eye. Detailed testing was carried out on 49 cells that had statistically significant responses to stimulation of the nondominant eye alone. Spatial-frequency response functions to nondominant-eye stimulation indicated that the responses were spatially tuned, as reported previously (Guido et al., 1989). Optimal spatial frequencies through the nondominant eye were significantly correlated with the optimal spatial frequencies through the dominant eye (r = 0.54; P less than 0.0001), and the optimal spatial frequencies were fairly similar for the two eyes. Nondominant-eye stimulation changed the maximal amplitude of the fundamental (F1) response to dominant-eye stimulation for only about 45% (22 of 49) of the cells that responded to nondominant-eye stimulation alone. The response vs. contrast function through the dominant eye was altered for 73% of the cells (51% independent of spatial frequency). Three types of effects were observed: a change in the initial slope of the response vs. contrast function (contrast gain), a change in the response amplitude at which saturation occurred, or an overall change in response at all contrasts. The incidence of these changes was similar for X and Y cells in LGN layers A, A1, and C (only four W cells were tested). Nondominant-eye stimulation had little or no effect on the sizes or sensitivities of the receptive-field centers or surrounds for the dominant eye. In addition, nondominant-eye stimulation had little or no effect on optimal spatial frequency, spatial resolution, or the bandwidth of spatial-frequency contrast sensitivity curves for the dominant eye. Possible functions of binocular interactions in the LGN are considered. The present results suggest a role in interocular contrast-gain control. Interocular contrast differences can occur before the acquisition of binocular fusion, when the two eyes are viewing different aspects of a visual stimulus. Psychophysical and physiological studies suggest that an interocular mechanism exists to maintain relatively constant binocular interactions despite differences in interocular contrast. The present results suggest that at least part of this mechanism occurs in the LGN.

Animals↗

Thalamic projections to the lateral suprasylvian visual area in cats with neonatal or adult visual cortex damage.

Previous transneuronal anterograde tracing studies have shown that the retino-thalamic pathway to the posteromedial lateral suprasylvian (PMLS) visual area of cortex is heavier than normal in adult cats that received neonatal damage to visual cortical areas 17, 18, and 19. In contrast, the strength of this projection does not appear to differ from that in normal animals in cats that experienced visual cortex damage as adults. In the present study, we used retrograde tracing methods to identify the thalamic cells that project to the PMLS cortex in adult cats that had received a lesion of visual cortex during infancy or adulthood. In five kittens, a unilateral visual cortex lesion was made on the day of birth, and horseradish peroxidase (HRP) was injected into the PMLS cortex of both hemispheres when the animals were 10.5 to 13 months old. For comparison, HRP was injected bilaterally into the PMLS cortex of three cats 6.5 to 13.5 months after they received a similar unilateral visual cortex lesion as adults. In cats with a neonatal lesion, retrograde labeling was found in the large neurons that survive in the otherwise degenerated layers A and A1 of the lateral geniculate nucleus (LGN) ipsilateral to the lesion. Retrograde labeling of A-layer neurons was not seen in the undamaged hemisphere of these animals or in either hemisphere of animals that had received a lesion as adults. As in normal adult cats, retrograde labeling also was present in the C layers of the LGN, the medial interlaminar nucleus, the posterior nucleus of Rioch, the lateral posterior nucleus, and the pulvinar nucleus ipsilateral to a neonatal or adult lesion. Quantitative estimates indicate that the number of labeled cells is much larger than normal in the C layers of the LGN ipsilateral to a neonatal visual cortex lesion. Thus the results indicate that the heavier than normal projection from the thalamus to PMLS cortex that exists in adult cats after neonatal visual cortex damage arises, at least in part, from surviving LGN neurons in the A and C layers of the LGN. Although several thalamic nuclei, as well as the C layers of the LGN, continue to project to PMLS cortex after an adult visual cortex lesion, these projections appear not to be affected significantly by the lesion.

Aging↗

Development of the projections from the dorsal lateral geniculate nucleus to the lateral suprasylvian visual area of cortex in the cat.

In the study reported in the preceding paper, we used retrograde labeling methods to show that the enhanced projection from the thalamus to the posteromedial lateral suprasylvian (PMLS) visual area of cortex that is present in adult cats following neonatal visual cortex damage arises at least partly from surviving neurons in the dorsal lateral geniculate nucleus (LGN). In the C layers of the LGN, many more cells than normal are retrogradely labeled by horseradish peroxidase (HRP) injected into PMLS cortex ipsilateral to a visual cortex lesion. In addition, retrogradely labeled cells are found in the A layers, which normally have no projection to PMLS cortex in adult cats. The purpose of the present study was to investigate the mechanisms of this enhanced projection by examining the normal development of projections from the thalamus, especially the LGN, to PMLS cortex. Injections of HRP were made into PMLS cortex on the day of birth or at 1, 2, 4, or 8 weeks of age. Retrogradely labeled neurons were present in the lateral posterior nucleus, posterior nucleus of Rioch, pulvinar, and medial interlaminar nucleus, as well as in the LGN, at all ages studied. Within the LGN of the youngest kittens, a small number of retrogradely labeled cells was present in the interlaminar zones and among the cells in the A layers that border these zones. Such labeled cells were virtually absent by 8 weeks of age, and they are not found in normal adult cats. Sparse retrograde labeling of C-layer neurons also was present in newborn kittens.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗

Retinal ganglion-cell densities and soma sizes are unaffected by long-term monocular deprivation in the cat.

Three cats were raised with monocular deprivation for 5.2-7.2 years, and ganglion-cell densities and soma sizes were measured in their flat-mounted retinae. The retinae were Nissl-stained so that ganglion cells could be measured whether or not they maintained normal central projections. Measurements were made in the area centralis, peripheral binocular segment, and monocular segment of the retinae. There were no significant differences between the deprived and non-deprived retinae in the densities or soma-sizes of alpha cells or other (non-alpha) ganglion cells at any of these retinal locations. These results support the view that the most distal effects of monocular deprivation occur at the retino-geniculate contact, and they suggest that even after long-term monocular deprivation, effects in the lateral geniculate nucleus do not produce secondary, retrograde changes in the retina.

Animals↗

Functional compensation in the lateral suprasylvian visual area following bilateral visual cortex damage in kittens.

Previous studies have shown that functional compensation is present in the cat's posteromedial lateral suprasylvian (PMLS) area of cortex after damage to areas 17, 18, and 19 (visual cortex) early in life but not after damage in adults. These studies all have investigated animals with a unilateral visual cortex lesion, whereas all behavioral studies of compensation for early visual cortex damage have investigated animals with a bilateral lesion. In the present experiment, we investigated whether functional compensation also is present in PMLS cortex after a bilateral visual cortex lesion early in life. We recorded from single neurons in the PMLS cortex of adult cats that had received a bilateral lesion of areas 17, 18, and 19 on the day of birth or at 8 weeks of age. We found that PMLS cells in both groups of cats had functional compensation (normal direction selectivity and ocular dominance) similar to that seen after a unilateral lesion at the same ages. These results are consistent with the hypothesis that PMLS cortex is involved in the behavioral compensation seen after early visual cortex damage. In addition, the results indicate that inputs from contralateral visual cortex are not necessary for the development of functional compensation seen in PMLS cortex.

Age Factors↗

Afferent bases of spatial- and temporal-frequency processing by neurons in the cat's posteromedial lateral suprasylvian cortex: effects of removing areas 17, 18, and 19.

1. We investigated whether spatial- and temporal-frequency processing by neurons in the cat's posteromedial lateral suprasylvian (PMLS) extrastriate cortex depends on inputs from ipsilateral areas 17, 18, and 19 (visual cortex; VC) or occurs in parallel with those cortical areas. 2. Single neurons were recorded in PMLS cortex of normal adult cats and adult cats that had ipsilateral VC removed within 24 h before recording. Receptive-field properties were characterized, and responses to sine-wave gratings of different spatial frequencies, contrasts, and temporal frequencies were measured and Fourier analyzed. 3. As in previous studies, removing inputs from VC led to a reduction in the proportion of direction-selective PMLS cells. In addition there were statistically significant reductions in response amplitude and variability, although signal-to-noise ratios were unchanged. Contrast sensitivity also was reduced at all spatial frequencies. Spatial resolution was reduced slightly; however, this reduction appears to be secondary to the overall reduction in response amplitude and sensitivity. 4. The shape of the spatial-frequency contrast-sensitivity functions and the distribution of optimal spatial frequencies were unaffected by removing inputs from VC. In addition, once response threshold was reached, the slope of the contrast-response function (contrast gain) at the optimal spatial frequency was similar for PMLS cells in normal cats and cats with a VC lesion. 5. When tested at the optimal spatial frequency, temporal-frequency bandwidths, high and low temporal-frequency cutoffs, and optimal temporal frequencies were similar for PMLS cells in normal cats and cats with VC removed. 6. The results thus indicate that inputs from VC are important for the elaboration of direction selectivity and affect response amplitude and contrast sensitivity among PMLS neurons. However, visual-cortical inputs have little or no influence on spatial- and temporal-frequency processing by PMLS neurons. These properties depend on inputs from other cortical areas or the thalamus and are processed in parallel with areas 17, 18, and 19.

Animals↗

W-and Y-cells in the C layers of the cat's lateral geniculate nucleus: normal properties and effects of monocular deprivation.

1. Previous studies have shown that rearing with monocular visual deprivation (MD) produces a loss of Y-cells and a reduction in spatial resolution among X-cells in layers A and A1 of the cat's dorsal lateral geniculate nucleus (dLGN). However, there have been no studies of the effects of visual deprivation on the function of the retinogeniculate W-cell pathway, which terminates in the C layers of the dLGN. It also is not known if Y-cells in the C layers are affected by MD in the same way as Y-cells in the A layers. These questions were addressed by the present experiment. 2. Single-cell recordings were made from the C layers of 5 normal adult cats (112 cells) and from the nondeprived (94 cells) and deprived (95 cells) C layers in 10 cats monocularly deprived by lid suture for 3-7 yr. The cells were classified as X, Y, or W on the basis of their receptive-field properties and responses to electrical stimulation of the optic chiasm. In addition, quantitative measures were made of responses to sine-wave gratings of different spatial frequencies. 3. Receptive-field organization, receptive-field center size, spatial and temporal linearity to counterphased sine-wave gratings, and latency to optic chiasm stimulation were similar for C-layer cells in normal cats and in the deprived and nondeprived layers of MD cats. On the basis of these properties, 23% of normal layer-C cells were classified as Y-cells and 72% were classified as W-cells. The Y-cells tended to be located in the magnocellular division of layer C and most (though not all) W-cells were in the parvocellular division. Normal layers C1 and C2 contained almost exclusively W cells. The incidence of Y and W cells was similar to normal in the nondeprived and deprived C-layers of MD cats. 4. In normal cats, W cells typically had the lowest amplitude first-harmonic (F1) response rates to drifting sine-wave gratings. However, many W cells gave quite brisk responses and, overall, there was no significant difference between F1 response amplitudes of Y and W cells. Response amplitudes of Y- and W-cells in the deprived and nondeprived C-layers of MD cats were not significantly different from normal. 5. Normal Y- and W-cells tended to have low optimal spatial frequencies (0.2 c/deg or lower) and spatial resolutions (generally 0.4-1.6 c/deg) to drifting sine-wave gratings.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗