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G Sclar

Publications and source records attributed to G Sclar.

At least 19 recordsLinked to original sources
PubMed2001

Tumefactive fibroinflammatory lesion of the neck with progressive invasion of the meninges, skull base, orbit, and brain.

SUMMARY: Tumefactive fibroinflammatory lesions of the head and neck are rare. CNS involvement has not been reported. We present a histologically proven case of a tumefactive fibroinflammatory lesion that originated in the left side of the neck and progressed over 2 years to involve the meninges, the cavernous sinuses, the right temporal lobe, and the right orbit. The lesion caused destruction of the skull base and a subdural hematoma. The relationship of the present lesion to idiopathic hypertrophic pachymeningitis and Tolosa-Hunt syndrome is discussed.

Adult↗
PubMed1999

Encephalomyeloradiculoneuropathy following exposure to an industrial solvent.

A 19-year-old male developed complaints including weakness of the lower extremities and right hand, numbness, dysphagia and urinary difficulties following a 2 month exposure to an industrial solvent constituted mainly of 1-bromopropane, but also containing butylene oxide, 1,3 dioxolane, nitromethane, and other components. Nerve conduction studies revealed evidence of a primary, symmetric demyelinating polyneuropathy. Evidence of CNS involvement came from gadolinium enhanced MRI scans of the brain, showing patchy areas of increased T2 signal in the periventricular white matter, similar scans of the spinal cord revealing root enhancement at several lumbar levels, and SSEP studies. The patient's symptoms had started to resolve following the discontinuation of the exposure, before he was lost to follow-up. Similar findings have been reported following 1-bromopropane exposure in rats. I hypothesize that this patient's symptoms may have been due to 1-bromopropane-induced neurotoxicity.

Adult↗
PubMed1991

Extraretinal representations in area V4 in the macaque monkey.

Several neurophysiological studies have shown that the visual cerebral cortex of macaque monkeys performing delayed match-to-sample tasks contains individual neurons whose levels of activity depend on the sample the animal is required to remember. Haenny et al. (1988) reported that the activity of neurons in area V4 of monkeys performing an orientation matching task depends on the orientation for which the animal is searching. It was proposed that these neurons contribute to a representation of the orientation being sought. We have further characterized these neurons by recording visual responses from individual neurons during multiple behavioral tasks. Animals were trained to perform an orientation match-to-sample task using either a visual or a tactile orientation sample. In a set of 89 neurons examined using both types of sample, 25% showed statistically significant effects of sample orientation regardless of whether the sample was visual or tactile. Most of these preferred the same sample orientation in both conditions. These results allow us to specify the nature of the information signaled by these neurons more precisely than has previously been possible. For 193 units tested using one of the matching tasks, responses were also recorded while the animal performed a simple fixation task. In this task the animal was not required to attend to the visual stimuli that were presented. A few neurons that were responsive during the matching task were silent during fixation, but a comparable number was much more responsive during fixation. Across the whole population there was no systematic change in either responsivity or selectivity for orientation under the two conditions.

Animals↗
PubMed1990

Coding of image contrast in central visual pathways of the macaque monkey.

Measurements of contrast sensitivity were obtained from isolated neurons in the lateral geniculate nucleus, striate cortex, and middle temporal visual area of macaque monkeys. Between the lateral geniculate nucleus and the middle temporal area contrast sensitivity functions become progressively steeper. Furthermore, many neurons in the middle temporal area are more sensitive than any cell encountered in early stages. Measurements made with stimuli of different sizes show that this high sensitivity depends on areal summation across the receptive field.

Action Potentials↗
PubMed1990

Chromatic mechanisms in striate cortex of macaque.

We measured the responses of 305 neurons in striate cortex to moving sinusoidal gratings modulated in chromaticity and luminance about a fixed white point. Stimuli were represented in a 3-dimensional color space defined by 2 chromatic axes and a third along which luminance varied. With rare exceptions the chromatic properties of cortical neurons were well described by a linear model in which the response of a cell is proportional to the sum (for complex cells, the rectified sum) of the signals from the 3 classes of cones. For each cell there is a vector passing through the white point along which modulation gives rise to a maximal response. The elevation (theta m) and azimuth (phi m) of this vector fully describe the chromatic properties of the cell. The linear model also describes neurons in l.g.n. (Derrington et al., 1984), so most neurons in striate cortex have the same chromatic selectivity as do neurons in l.g.n. However, the distributions of preferred vectors differed in cortex and l.g.n.: Most cortical neurons preferred modulation along vectors lying close to the achromatic axis and those showing overt chromatic opponency did not fall into the clearly defined chromatic groups seen in l.g.n. The neurons most responsive to chromatic modulation (found mainly in layers IVA, IVC beta, and VI) had poor orientation selectivity, and responded to chromatic modulation of a spatially uniform field at least as well as they did to any grating. We encountered neurons with band-pass spatial selectivity for chromatically modulated stimuli in layers II/III and VI. Most had complex receptive fields. Neurons in layer II/III did not fall into distinct groups according to their chromatic sensitivities, and the chromatic properties of neurons known to lie within regions rich in cytochrome oxidase appeared no different from those of neurons in the interstices. Six neurons, all of which resembled simple cells, showed unusually sharp chromatic selectivity.

Animals↗
PubMed1989

Contrast adaptation in striate cortex of macaque.

We have characterized the contrast-response relationships for simple and complex cells in striate cortex of macaque monkey, before and during adaptation to high-contrast sinusoidal gratings of the optimal spatial-frequency and orientation. Adaptation brings about systematic changes in the steepness of contrast-response curves and in the effective contrast of stimuli. Adaptation reduces the detectability of low-contrast gratings by almost a factor of three, but by extending the operating range of most cells it appears to improve the discriminability of high-contrast stimuli that previously gave rise to responses of saturating amplitude.

Adaptation, Ocular↗
PubMed1987

Expression of "retinal" contrast gain control by neurons of the cat's lateral geniculate nucleus.

This paper describes the temporal tuning of cells in the lateral geniculate nucleus of the cat (27 X cells, 51 Y cells) and how this changes with stimulus contrast. Drifting sinusoidal gratings of optimal spatial frequency were presented at 7 temporal frequencies (0.5, 1, 2, 4, 8, 16 and 32 Hz) and 4 contrasts (10, 20, 40, 80%). For some cells response growth at all temporal frequencies was proportional to changes in contrast. Thus, their temporal tuning functions, on log-log axes, were displaced vertically with increasing contrast. This shift also largely characterizes the response to low temporal frequencies of the other neurons studied. For these other cells, however, responses to high temporal frequencies grew disproportionately large with increasing contrast generally causing their tuning functions to change shape. Typically the peaks of these functions shifted to higher frequencies at higher contrasts. Most of the X cells studied displayed behavior of the first type, while Y cells usually followed the second pattern. This qualitative impression was confirmed quantitatively. Cubic spline functions were fit to the temporal tuning functions obtained at different contrast levels and the peaks of the curves were extracted. X and Y cells preferred similar temporal frequencies at low contrast levels (X mean = 8.1 Hz; Y mean = 8.4 Hz) but Y cell values were significantly higher at higher contrasts (80%) (X mean = 12.0 Hz; Y mean = 16.8 Hz).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1987

Visual orientation and spatial frequency discrimination: a comparison of single neurons and behavior.

Neurons in the visual cortex respond selectively to stimulus orientation and spatial frequency. Changes in response amplitudes of these neurons could be the neurophysiological basis of orientation and spatial frequency discrimination. We have estimated the minimum differences in stimulus orientation and spatial frequency that can produce reliable changes in the responses of individual neurons in cat visual cortex. We compare these values with orientation and spatial frequency discrimination thresholds determined behaviorally. Slopes of the tuning functions and response variability determine the minimum orientation and spatial frequency differences that can elicit a reliable response change. These minimum values were obtained from single cells using receiver operating characteristic (ROC) analysis. The average minimum orientation and spatial frequency differences that could be signaled reliably by cells from our sample were 6.4 degrees (n = 22) and 21.3% (n = 18), respectively. These values are approximately 0.20 of the average full tuning width at one-half height of the cells. Although these average values are well above the behaviorally determined thresholds, the most selective cells signaled orientation and frequency differences of 1.84 degrees and 5.25%, respectively. These values are of the same order of magnitude as the behavioral thresholds. We show that, because of slow fluctuations in a cell's responsivity, ROC analysis overestimates response variability. We estimate that these slow response fluctuations elevated our estimates of single cell "thresholds" by, on average, 30%. Our data point to an approximate correspondence between orientation and spatial frequency discrimination "thresholds" determined behaviorally and those estimated from the most selective single cortical cells. Interpretation of this quantitative correspondence is considered in the discussion.

Animals↗
PubMed1987

The effects of contrast on visual orientation and spatial frequency discrimination: a comparison of single cells and behavior.

We have compared the effects of contrast on human psychophysical orientation and spatial frequency discrimination thresholds and on the responses of individual neurons in the cat's striate cortex. Contrast has similar effects on orientation and spatial frequency discrimination: as contrast is increased above detection threshold, orientation and spatial frequency discrimination performance improves but reaches maximum levels at quite low contrasts. Further increases in contrast produce no further improvements in discrimination. We measured the effects of contrast on response amplitude, orientation and spatial frequency selectivity, and response variance of neurons in the cat's striate cortex. Orientation and spatial frequency selectivity vary little with contrast. Also, the ratio of response variance to response mean is unaffected by contrast. Although, in many cells, response amplitude increases approximately linearly with log contrast over most of the visible range, some cells show complete or partial saturation of response amplitude at medium contrasts. Therefore, some cells show a clear increase in slope of the orientation and spatial frequency tuning functions with increasing contrast, whereas in others the slopes reach maximum values at medium contrasts. Using receiver operating characteristic analysis, we estimated the minimum orientation and spatial frequency differences that can be signaled reliably as a response change by an individual cell. This analysis shows that, on average, the discrimination of orientation or spatial frequency improves with contrast at low contrasts more than at higher contrasts. Using the optimal stimulus for each cell, we estimated the contrast threshold of 48 neurons. Most cells had contrast thresholds below 5%. Thresholds were only slightly higher for nonoptimal stimuli. Therefore, increasing the contrast of sinusoidal gratings above approximately 10% will not produce large increases in the number of responding cells. The observed effects of contrast on the response characteristics of nonsaturating cortical cells do not appear consistent with the psychophysical results. Cells that reach their maximum response at low-to-medium contrasts may account for the contrast independence of psychophysical orientation and spatial frequency discrimination thresholds at medium and high contrasts.

Animals↗
PubMed1986

Binocular summation in normal, monocularly deprived, and strabismic cats: visual evoked potentials.

We have studied visual evoked potentials (VEP) in the cat using dichoptically presented sinusoidal gratings. Our goals were to determine if binocular disparity causes differential responses in the VEP, and to examine the effects of monocular deprivation and convergent or divergent strabismus on the degree of binocular summation. Binocular disparity in stimuli causes no regular alterations of visual evoked responses, except at very low spatial frequencies. However, this apparent selectivity is probably due to luminance modulation in the central retina at low frequencies. The insensitivity to binocular disparity establishes that binocular summation in the VEP may be estimated without regard to the relative phase of gratings presented to the two eyes. Binocular summation of the VEP was examined in normal animals. We found that the ratio of the binocularly evoked response to the largest monocular response (averaged across spatial frequency) ranged from 1.27 to 2.12 (4 animals) and had a mean of 1.48. These values fall within the range which has been reported for human subjects. The degree of summation might be expected to be greatly reduced in strabismic and monocularly deprived animals, in which the majority of the cells are functionally monocular. While summation was found to be reduced in 5 esotropic (convergent) animals (range = 1.13-1.24; mean = 1.18) it was approximately normal in three exotropic (divergent) animals (range = 1.29-2.12; mean = 1.61). However, single unit recordings carried out on the same animals show similar reductions of cells that can be driven through either eye for both groups of animals. Recordings from three monocularly deprived animals, on the other hand, show evidence of binocular interaction in the form of suppression. In this case, response amplitudes obtained using binocular stimulation were consistently and substantially smaller than those obtained from the normal eye alone (range = 0.76-0.85; mean = 0.80). We conclude that convergent and divergent strabismus differ substantially in the degree to which binocular summation is exhibited in the VEP, which in the latter condition, is indistinguishable from the normal cat. Monocular deprivation causes an effect which is markedly different from either form of strabismus in that the deprived eye suppresses the response of the normal eye.

Animals↗
PubMed1985

Contrast gain control in the cat's visual system.

We have examined the idea that the adaptation of cortical neurons to local contrast levels in a visual stimulus is functionally advantageous. Specifically, cortical cells may have large differential contrast sensitivity as a result of adjustments that center a limited response range around a mean level of contrast. To evaluate this notion, we measured contrast-response functions of cells in striate cortex while systematically adapting them to different contrast levels of stimulus gratings. For the majority of cortical neurons tested, the results of this basic experiment show that contrast-response functions shift laterally along a log-contrast axis so that response functions match mean contrast levels in the stimulus. This implies a contrast-dependent change in the gain of the cell's contrast-response relationship. We define this process as contrast gain control. The degree to which this contrast adjustment occurs varies considerably from cell to cell. There are no obvious differences regarding cell type (simple vs. complex) or laminar distribution. Contrast gain control is almost certainly a cortical function, since lateral geniculate cells and fibers exhibit only minimal effects. Tests presented in the accompanying paper (37) provide additional evidence on the cortical origin of the process. In another series of experiments, the effect of contrast adaptation on physiological estimates of contrast sensitivity was evaluated. Sustained adaptation to contrast levels as low as 3% was capable of nearly doubling the thresholds of most of the cells tested. Adaptation may therefore be an important factor in determinations of the contrast sensitivity of cortical neurons. We tested the spatial extent of the mechanisms responsible for these gain-control effects by attempting to adapt cells using both a large grating and a grating patch limited to that portion of a cell's receptive field from which excitatory discharges could be elicited directly (the central discharge region). Adaptation was found to be an exclusive property of the central region. This held even in the case of hypercomplex cells, which received strong influences from surrounding regions of the visual field. Finally, we measured the time course of contrast adaptation. We found the process to be rather slow, with a mean time constant of approximately 6 s. Once again, there was considerable variability in this value from cell to cell.

Acclimatization↗
PubMed1985

Contrast gain control in the kitten's visual system.

We have studied the effects of contrast adaptation on cortical cells from 4- and 6-wk-old kittens (49 and 47 cells, respectively) using sine-wave grating stimuli. We wished to know if the effects of adaptation to different contrast levels are more extensive than those in adult animals. Our experiments involved adapting cells to different contrasts (3.1, 12.5, and 50%) while concurrently measuring their contrast-response functions at each of these different levels. We found qualitatively that the effects of adaptation in the kitten are similar to those we have previously documented in adult animals (19). Contrast-response functions are laterally shifted along the log-contrast axis, effectively matching the response range of the cells to prevailing contrast levels. The degree to which this occurred varied from cell to cell. The average degree to which cells showed these effects, as assessed both qualitatively and quantitatively, was greater for kittens than for adult cats, and greater for 4-wk-old kittens than for those aged 6 wk. This suggests that susceptibility to adaptation varies as a function of age. Additional studies were undertaken with the intent of localizing these adaptive effects. First, lateral geniculate cells and fibers (n = 23) were studied with our standard protocol, and second, we investigated the degree to which the effects of adaptation of cortical cells transferred interocularly.(ABSTRACT TRUNCATED AT 250 WORDS)

Acclimatization↗
PubMed1985

Neurophysiological evaluation of the differential response model for orientation and spatial-frequency discrimination.

Recent models have attempted to reconcile low psychophysical orientation and spatial-frequency discrimination thresholds with relatively broad orientation and spatial-frequency tuning of cortical neurons. These models have relied on the ability of the neurons to convert small stimulus changes into reliable response changes. We have examined this ability in a sample of neurons from the cat's striate cortex. We present here data from two cells that reliably signaled the smallest orientation and spatial-frequency differences. Using receiver operating characteristic analysis, we find that these cells could reliably signal orientation differences of 1.84 deg and spatial-frequency differences of 0.073 octave. We compare these single-cell results to cat and human behavioral discrimination thresholds.

Animals↗
PubMed1982

Contrast gain control in the cat visual cortex.

The eye functions effectively over an enormous range of ambient illumination, because retinal sensitivity can be adapted to prevailing light levels. Higher order neurones in the visual pathway are presumably more concerned with relative changes in illumination, that is, contrast, because a great deal of information concerning absolute light level is processed at the retinal level. It would therefore be of considerable functional value if cells in the visual cortex could adapt their response levels to a steady-state ambient contrast, in a manner analogous to the sensitivity control mechanism of the retina. We have examined here the idea that adaptation of neurones in the visual cortex to ambient contrast is similar to adaptation in the retina to ambient illumination. The experiments were performed by measuring contrast response functions (response amplitude as a function of contrast) of striate neurones, while systematically adapting them to different contrast levels. Our results show that, for the majority of cortical neurones, response-contrast curves are laterally shifted along a log-contrast axis so that the effective domains of neurones are adjusted to match prevailing contrast levels. This contrast gain control mechanism, which was not observed for lateral geniculate (LGN) fibres, must be of prime importance to visual function.

Adaptation, Ocular↗