Magnocellular Research Articles

Determinants of Contrast Sensitivity for the Tumbling E and Landolt C

To compare the object spatial frequencies that underlie contrast sensitivity for the tumbling E and Landolt C across a range of optotype sizes and under conditions biased toward the magnocellular (MC) and parvocellular (PC) pathways. Contrast thresholds of two visually normal observers were measured using tumbling E optotypes that were either low-pass filtered or high-pass filtered with a two-dimensional Gaussian filter. Optotypes were presented using steady-pedestal and pulsed-pedestal paradigms to target the MC and PC pathways, respectively. Object frequencies essential for orientation judgments of the tumbling E were derived from plots of log contrast threshold vs. log filter cutoff frequency, and results were compared with those obtained previously for the Landolt C under identical testing conditions. The object frequency used to judge the orientation of the tumbling E increased systematically with increasing target angular subtense, and the effect of target size differed depending on whether performance was mediated by the inferred MC or PC pathway. The overall pattern of results was similar for the tumbling E and Landolt C, but there was generally less dependence of object frequency on target angular subtense for the tumbling E. The tumbling E and Landolt C are not equivalent in terms of the object frequencies that mediate orientation judgments. However, both optotypes show scale-dependent changes in object frequency, particularly under test conditions that favor the PC pathway. The scale dependence of these broadband optotypes can pose a challenge in interpreting test results using these targets. A potential solution is to use spatially filtered optotypes with limited, known object frequency content.

The chromatic input to cells of the magnocellular pathway of primates

Parasol ganglion cells of the magnocellular (MC) pathway form the physiological substrate of a luminance channel underlying photometric tasks, but they also respond weakly to red-green chromatic modulation. This may take the form of a first-harmonic (1F) response to chromatic modulation at low temporal frequencies, and/or a second-harmonic (2F) response that is more marked at higher frequencies. It is shown here that both these responses originate from a receptive field component that is intermediate in size between center and surround, i.e., a discrete, chromatic receptive field is superimposed upon an achromatic center-surround structure. Its size is similar to the receptive field (center plus surround) of midget, parvocellular cells from the same retinal eccentricity. A 2F MC cell chromatic response component is shown to be present under cone silent substitution conditions, when only the middle- (M) or long-wavelength (L) cone is modulated. This and other features suggest it is a rectified response to a chromatic signal rather than a consequence of non-linear summation of M- and L-cone signals. A scheme is presented which could give rise to such responses. It is suggested that this chromatic input to MC cells can enhance motion signals to red-green borders close to equiluminance.

Transmission of blue (S) cone signals through the primate lateral geniculate nucleus

This study concerns the transmission of short-wavelength-sensitive (S) cone signals through the primate dorsal lateral geniculate nucleus. The principal cell classes, magnocellular (MC) and parvocellular (PC), are traditionally segregated into on- and off-subtypes on the basis of the sign of their response to luminance variation. Cells dominated by input from S-cones ('blue-on and blue-off') are less frequently encountered and their properties are less well understood. Here we characterize the spatial and chromatic properties of a large sample of blue-on and blue-off neurons and contrast them with those of PC and MC neurons. The results confirm that blue-on and blue-off cells have larger receptive fields than PC and MC neurons at equivalent eccentricities. Relative to blue-on cells, blue-off cells are less sensitive to S-cone contrast, have larger receptive fields, and show more low-pass spatial frequency tuning. Thus, blue-on and blue-off neurons lack the functional symmetry characteristic of on- and off-subtypes in the MC and PC pathways. The majority of MC and PC cells received no detectible input from S-cones. Where present, input from S-cones tended to provide weak inhibition to PC cells. All cell types showed evidence of a suppressive extra-classical receptive field driven largely or exclusively by ML-cones. These data indicate that S-cone signals are isolated to supply the classical receptive field mechanisms of blue-on and blue-off cells in the LGN, and that the low spatial precision of S-cone vision has origins in both classical and extraclassical receptive field properties of subcortical pathways.

Assessment of contrast gain signature in inferred magnocellular and parvocellular pathways in patients with glaucoma

Purpose Contrast gain signatures of inferred magnocellular and parvocellular postreceptoral pathways were assessed for patients with glaucoma using a contrast discrimination paradigm developed by Pokorny and Smith. The potential causes for changes in contrast gain signature were investigated using model simulations of ganglion cell contrast responses. Methods Foveal contrast discrimination thresholds were measured with a pedestal-Δ-pedestal paradigm developed by Pokorny and Smith [Pokorny, J., & Smith, V. C. (1997). Psychophysical signatures associated with magnocellular and parvocellular pathway contrast gain. Journal of the Optical Society of America A, 14(9), 2477–2486]. Stimuli were 27 ms luminance increments superimposed on 227 ms pulsed Δ-pedestals. Contrast thresholds and contrast gain signatures mediated by the inferred magnocellular (MC) and parvocellular (PC) pathways were assessed using linear fits to contrast discrimination thresholds at either lower or higher Δ-pedestal contrasts, respectively. Twenty-seven patients with glaucoma were tested, as well as 16 age-similar control subjects free of eye disease. Results Contrast sensitivity and contrast gain signature mediated by the inferred MC pathway were lower for the glaucoma group, and reduced contrast gain signature was correlated with reduced contrast sensitivity ( r 2 = 45%, p < .0005). These two parameters mediated by the inferred PC pathway were little affected for the glaucoma group. Model simulations suggest that the reduced contrast sensitivity and contrast gain signature were consistent with the hypothesis that reduced MC ganglion cell dendritic complexity can lead to reduced effective retinal illuminance, and hence increased semi-saturation contrast of the ganglion cell contrast response functions. Conclusions The contrast sensitivity and contrast gain signature of the inferred MC pathway were reduced in patients with glaucoma. The results were consistent with a model of ganglion cell dysfunction due to reduced synaptic density.

Psychophysical analysis of contrast processing segregated into magnocellular and parvocellular systems in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy

We examined achromatic contrast discrimination in asymptomatic carriers of 11778 Leber's hereditary optic neuropathy (LHON 18 controls) and 18 age-match were also tested. To evaluate magnocellular (MC) and Parvocellular (PC) contrast discrimination, we used a version of Pokorny and Smith's (1997) pulsed/steady-pedestal paradigms (PPP/SPP) thought to be detected via PC and MC pathways, respectively. A luminance pedestal (four 1 degree x 1 degree squares) was presented on a 12 cd/m2 surround. The luminance of one of the squares (trial square, TS) was randomly incremented for either 17 or 133 ms. Observers had to detect the TS, in a forced-choice task, at each duration, for three pedestal levels: 7, 12, 19 cd/m2. In the SPP, the pedestal was fixed, and the TS was modulated. For the PPP, all four pedestal squares pulsed for 17 or 133 ms, and the TS was simultaneously incremented or decremented. We found that contrast discrimination thresholds of LHON carriers were significantly higher than controls' in the condition with the highest luminance of both paradigms, implying impaired contrast processing with no evidence of differential sensitivity losses between the two systems. Carriers' thresholds manifested significantly longer temporal integration than controls in the SPP, consistent with slowed MC responses. The SPP and PPP paradigms can identify contrast and temporal processing deficits in asymptomatic LHON carriers, and thus provide an additional tool for early detection and characterization of the disease.

Spatial frequencies used in Landolt C orientation judgments: Relation to inferred magnocellular and parvocellular pathways

The purpose of this study was to define the spatial frequencies that underlie judgments of Landolt C orientation under test conditions designed to favor either the magnocellular (MC) or parvocellular (PC) pathway. Contrast thresholds of two observers were measured for briefly presented Landolt Cs of four sizes, using steady- and pulsed-pedestal paradigms to bias performance toward the MC and PC pathways, respectively. Contrast thresholds were derived from a two-alternative forced-choice orientation judgment task using the QUEST procedure. The Landolt Cs were either low-pass or high-pass Gaussian filtered with a range of cutoff object spatial frequencies (cycles per letter) to limit their frequency content. Center object frequencies were derived from plots of log contrast threshold for orientation judgments vs. log filter cutoff object frequency. The function relating center object frequency to Landolt C angular subtense was nonlinear on log–log coordinates for both the steady- and pulsed-pedestal paradigms, indicating that different object frequencies were used to judge Landolt C orientation at different optotype sizes. However, the function was substantially steeper under the pulsed-pedestal than under the steady-pedestal paradigm, such that a large change in optotype size produced a relatively small change in retinal spatial frequency (cycles per degree). The pattern of results is consistent with previously reported differences between the spatial contrast sensitivity functions of the inferred MC and PC pathways.

Systematic misestimation in a vernier task arising from contrast mismatch

Luminance signals mediated by the magnocellular (MC) pathway play an important role in vernier tasks. MC ganglion cells show a phase advance in their responses to sinusoidal stimuli with increasing contrast due to contrast gain control mechanisms. If the phase information in MC ganglion cell responses were utilized by central mechanisms in vernier tasks, one might expect systematic errors caused by the phase advance. This systematic error may contribute to the contrast paradox phenomenon, where vernier performance deteriorates, rather than improves, when only one of the target pair increases in contrast. Vernier psychometric functions for a pair of gratings of mismatched contrast were measured to seek such misestimation. In associated electrophysiological experiments, MC and parvocellular (PC) ganglion cells' responses to similar stimuli were measured to provide a physiological reference. The psychophysical experiments show that a high-contrast grating is perceived as phase advanced in the drift direction compared to a low-contrast grating, especially at a high drift rate (8 Hz). The size of the phase advance was comparable to that seen in MC cells under similar stimulus conditions. These results are consistent with the MC pathway supporting vernier performance with achromatic gratings. The shifts in vernier psychometric functions were negligible for pairs of chromatic gratings under the conditions tested here, consistent with the lack of phase advance both in responses of PC ganglion cells and in frequency-doubled chromatic responses of MC ganglion cells.

Magno-and Parvocellular Visual Cortex Activation in Anisometropic Amblyopia, as Studied with Functional Magnetic Resonance Imaging

Purpose: We studied the functional magnetic resonance imaging (fMRI) of the visual cortex in order to activate preferentially the parvocellular (PC) or the magnocellular (MC) visual system by manipulation of the spatiotemporal characteristics of the stimuli. Then we applied this technique to a patient with amblyopia to see how these two visual systems are affected in amblyopia. Methods: We acquired the fMRI at 1.5 T in 8 normal subjects and in one patient with anisometropic amblyopia, each receiving their best refractive correction. Each subject underwent experimentation under five conditions. The MC stimulus had a low contrast, a large check size, and a high temporal frequency. The PC stimulus had a high contrast, a small check size, and a low temporal frequency. After the activation in each condition had been determined by contrasting the visual stimulation conditions with the condition at rest, the inter-eye difference was determined. Results: In normal subjects, the activation map showed different visual areas as well as some overlap between the MC and PC stimuli, and similar visual cortex activations were obtained under the right-eye and the left-eye stimulation conditions. In the patient with amblyopia, the inter-eye difference was within a 95% confidence interval for the MC stimulation, but not for the PC stimulation. Conclusions: Our fMRI results show a good localization of the activity in the MC and PC pathways, and they are consistent with the findings in the literature, suggesting that the PC visual pathway is primarily defective in amblyopia.

The temporal properties of the response of macaque ganglion cells and central mechanisms of flicker detection

This analysis assesses sensitivity of primate ganglion cells to sinusoidal modulation as a function of temporal frequency, based on the structure of their impulse trains; sensitivity to luminance and chromatic modulation was compared to human psychophysical sensitivity to similar stimuli. Each stimulus cycle was Fourier analyzed, and response amplitudes subjected to neurometric analysis; this assumes a detector with duration inversely proportional to frequency, that is, the stimulus epoch analyzed is a single cycle rather than a fixed duration, and provides an upper bound for a detection by an observer who bases judgments on a single cell. Signal-to-noise ratio for a given Fourier amplitude rapidly decreased with temporal frequency. This is a consequence of the statistics of impulse trains making up the response; at higher temporal frequencies, there are fewer impulses per cycle. Performance of this "single-cell" observer was then compared with that of modeled central detection mechanisms of fixed duration. For chromatic modulation, a filter/detector with a time constant of approximately 40 ms operating upon the parvocellular (PC) pathway provided a match to psychophysical results, whereas for luminance modulation, a filter/detection mechanism operating upon the magnocellular (MC) pathway with a time constant of approximately 5-10 ms provided a suitable match. The effects of summation and nonlinear interactions between cell inputs to detection are also considered in terms of enhanced sensitivity and "sharpness" of thresholds, that is, the steepness of the neurometric function. For both luminance (MC cells) and chromatic modulation (PC cells), restricted convergence (<20 cells) appears adequate to provide sharp thresholds and sensitivity comparable to psychophysical performance.

Anisometropic Amblyopia: Spatial Contrast Sensitivity Deficits in Inferred Magnocellular and Parvocellular Vision

To measure achromatic spatial contrast sensitivity in patients with anisometropic amblyopia under conditions favoring inferred parvocellular (PC) or magnocellular (MC) pathway mediation. Fourteen anisometropic amblyopes (VA amblyopic eye 6/12 or lower; better eye greater than 6/7.5) and 10 age-matched, nonamplyopic controls (VA 6/6) participated. Foveal spatial contrast sensitivity was measured using localized, spatially narrow band targets (0.25-8.0 cpd) presented in the center of a steady pedestal (favoring MC detection) or a pulsed pedestal (favoring PC detection) that was set within a uniform surround. Spatial contrast sensitivity functions were bandpass for the steady-pedestal and lowpass for the pulsed-pedestal. Under steady-pedestal adaptation, the amblyopes showed reduced spatial contrast sensitivity at intermediate frequencies (1-2 cpd), consistent with MC sensitivity loss. For the pulsed-pedestal condition, a generalized loss of sensitivity was observed across all spatial frequencies (0.5-4 cpd), consistent with PC sensitivity loss. The magnitudes of inferred MC and PC loss were similar. In the steady- and pulsed-pedestal paradigms, results for the better eye of greater than 75% of the amblyopes were normal or near normal at low and intermediate spatial frequencies. Anisometropic amblyopia produces spatial contrast sensitivity losses in inferred PC- and MC-mediated vision, suggesting there may be anomalous processing of MC and PC signals in higher visual areas, including those with orientation and spatial frequency selective cells in the visual cortex. With spatially localized stimuli and a paradigm designed to distinguish between MC and PC vision under conditions that differ only in the interstimulus adaptation, the better eye of the amblyopes was normal or near normal.

L/M Speed-Matching Ratio Predicts Reading in Children

Many behavioral studies have found impaired perception of dynamic visual stimuli in dyslexia and several neuroimaging studies have found reduced activation of the human motion area MT+ in dyslexia. These results are often interpreted as a magnocellular (MC) deficit in dyslexia. It has also been claimed that colored filters can help dyslexics to read. One defining feature of the MC-pathway is a greater weight for L-cone input than M-cone input, and at most very weak S-cone input. We measured the subjective speed matches between L-, M-, and S-cone isolating stimuli in good and poor readers. Subjects performed a speed-matching task with drifting cone-isolating stimuli to find the point of subjective equality between two drifting patterns. Such a task is known to activate cortical area MT+, presumably via the MC-pathway. L- to M-cone speed-match ratios were negatively correlated with single-word (r=-0.46) and irregular-word reading (r=-0.56) but not with non-word reading. Results suggest that relative L-cone sensitivity within the MC-pathway may limit orthographic reading performance.

Prokineticin 2 depolarizes paraventricular nucleus magnocellular and parvocellular neurons

Blind whole-cell patch-clamp techniques were used to examine the effects of prokineticin 2 (PK2) on the excitability of magnocellular (MNC), parvocellular preautonomic (PA), and parvocellular neuroendocrine (NE) neurons within the hypothalamic paraventricular nucleus (PVN) of the rat. The majority of MNC neurons (76%) depolarized in response to 10 nm PK2, effects that were eliminated in the presence of tetrodotoxin (TTX). PK2 also caused an increase in excitatory postsynaptic potential (EPSP) frequency, a finding that was confirmed by voltage clamp recordings demonstrating increases in excitatory postsynaptic current (EPSC) frequency. The depolarizing effects of PK2 on MNC neurons were also abolished by kynurenic acid (KA), supporting the conclusion that the effects of PK2 are mediated by the activation of glutamate interneurons within the hypothalamic slice. PA (68%) and NE (67%) parvocellular neurons also depolarized in response to 10 nm PK2. However, in contrast to MNC neurons, these effects were maintained in TTX, indicating that PK2 directly affects PA and NE neurons. PK2-induced depolarizations observed in PA and NE neurons were found to be concentration-related and receptor mediated, as experiments performed in the presence of A1MPK1 (a PK2 receptor antagonist) abolished the effects of PK2 on these subpopulations of neurons. The depolarizing effects of PK2 on PA and NE neurons were also shown to be abolished by PD 98059 (a mitogen activated protein kinase (MAPK) inhibitor) suggesting that PK2 depolarizes PVN parvocellular neurons through a MAPK signalling mechanism. In combination, these studies have identified separate cellular mechanisms through which PK2 influences the excitability of different subpopulations of PVN neurons.

Do magnocellular and parvocellular ganglion cells avoid short-wavelength cone input?

We recently developed a new technique to measure cone inputs to visual neurons and used this technique to seek short-wavelength-sensitive (S) cone inputs to parasol, magnocellular (MC) and midget, parvocellular (PC) ganglion cells. Here, we compare our physiological measurements of S-cone weights to those predicted by a random wiring model that assumes cells' receptive fields receive input from mixed cone types. The random wiring model predicts the average weights of S-cone input to be similar to the total percentage of S-cones but with considerable scatter, and the S-cone input polarity to be consistent with that of PC cells' surround and of MC cells' center. This is not consistent with our physiological measurements. We suggest that the ganglion cells' receptive fields may have a mechanism to avoid S-cone inputs, as is the case in the H1 horizontal cells. Previous reports of S-cone inputs, in particular substantial input to MC cells, are likely to reflect variation in prereceptoral filtering and/or the failure to correct for variation in macular pigment.

Contrast sensitivity for letter optotypes vs. gratings under conditions biased toward parvocellular and magnocellular pathways

This study examined the extent to which letter optotypes and grating stimuli provide equivalent measures of contrast sensitivity under conditions designed to favor the magnocellular (MC) and parvocellular (PC) pathways. The contrast sensitivity functions (CSFs) of three visually normal observers were measured for Sloan letters and Gabor patches, using steady- and pulsed-pedestal paradigms to bias processing toward MC and PC pathways, respectively. CSFs for Gabor patches were low-pass for the steady-pedestal paradigm and band-pass for the pulsed-pedestal paradigm, in agreement with previous reports. However, CSFs for letters were low-pass for both testing paradigms. CSFs for letters restricted in frequency content by spatial filtering were equivalent to those for Gabor patches for both testing paradigms. Results indicate that conventional letter optotypes can provide a misleading measure of contrast sensitivity, especially under conditions emphasizing the PC pathway. The use of spatially band-pass filtered letters can provide a more appropriate evaluation of spatial contrast sensitivity while maintaining some of the potential advantages of letters.

Contrast Response Properties of Magnocellular and Parvocellular Pathways in Retinitis Pigmentosa Assessed by the Visual Evoked Potential

To evaluate the contrast response of the visual system in retinitis pigmentosa (RP) under conditions designed to emphasize the parvocellular (PC) and magnocellular (MC) pathways. Visual evoked potentials (VEPs) were measured in 10 patients with RP and in 10 age-equivalent control subjects with normal visual acuity and color vision, by using an array of isolated checks that were presented against a steady yellow background. The checks were modulated sinusoidally, either in isoluminant chromatic contrast (5.6 Hz), to favor the chromatic PC pathway, or in luminance contrast (5.6 and 11.2 Hz), to favor the MC pathway. Response amplitude and phase at the stimulus (fundamental) frequency were derived from Fourier analysis, and contrast response functions were fit with a Michaelis-Menten equation to derive R(max), the maximum response amplitude, and sigma, the contrast necessary to produce R(max)/2. In the control subjects, the mean amplitude function for chromatic modulation increased approximately linearly with increasing contrast, whereas the function for luminance modulation increased sharply at low contrasts and saturated at contrasts above approximately 30% for both temporal frequencies, as expected. The patients with RP showed primarily a reduction in R(max) with little change in sigma in all testing conditions. The reduction in R(max) was equivalent for chromatic modulation and luminance modulation at 5.6 Hz, but was substantially lower for luminance modulation at 11.2 Hz. Contrast processing was impaired within both the MC and PC pathways in these patients with RP, but the degree of impairment within the MC pathway depended on temporal frequency. These VEP results are in general agreement with recent psychophysical studies of contrast sensitivity losses in patients with RP, and further they characterize contrast processing deficits in these patients at suprathreshold levels.

Chromatic Organization of Ganglion Cell Receptive Fields in the Peripheral Retina

This study addresses the chromatic properties of receptive fields in the subcortical visual pathway of primates. There is agreement that, in the central visual field, many cells belonging to the parvocellular (PC) division of the subcortical pathway show red-green opponent responses, that a subgroup of cells belonging to the koniocellular (KC) pathway shows blue-yellow opponent responses, and that magnocellular (MC) pathway cells show only weak signs of chromatic input. However, the chromatic properties of ganglion cells in the peripheral retina are poorly understood. Here, we measured the temporal-chromatic properties of ganglion cells in extracellular in vivo recordings from peripheral macaque retina. We show that the chromatic responsivity of peripheral KC ("blue-on") and MC cells is very similar to that of their counterparts in the foveal retina. Cone-opponent responses are expressed only at low temporal frequencies (<10 Hz) in the majority of peripheral PC cells, and some peripheral PC cells show non-opponent response properties. With these exceptions, the chromatic properties of ganglion cells are essentially preserved throughout the first 50 degrees of visual eccentricity. The main change seen in passing from foveal to peripheral retina is that all ganglion cell classes become more responsive to high temporal-frequency modulation.

Characteristics of contrast processing deficits in X-linked retinoschisis

Contrast sensitivity and contrast discrimination were evaluated in six males with X-linked retinoschisis (XLRS), a form of early-onset macular degeneration, using testing paradigms designed to favor either the magnocellular (MC) or parvocellular (PC) pathway. Compared to a group of age-similar control observers, the patients with XLRS showed a pronounced loss of contrast sensitivity at high spatial frequencies, consistent with their reduced visual acuities. At low spatial frequencies, the patients’ deficits were greater under conditions favoring the MC pathway, for both contrast sensitivity and contrast discrimination. The pattern of contrast sensitivity loss shown by the patients with XLRS could be simulated in control observers by testing at a parafoveal locus, although by optical coherence tomography, none of the patients with XLRS had eccentric fixation. The pattern of findings indicates that the foveas of patients with XLRS functionally resemble the normal parafoveal retina.

Interleukin-1β depolarizes magnocellular neurons in the paraventricular nucleus of the hypothalamus through prostaglandin-mediated activation of a non selective cationic conductance

Interleukin-1β (IL-1β) is involved in hypothalamic regulation of the neuroimmune response by influencing the synthesis and secretion of corticotropin releasing hormone (CRH), vasopressin (VP) and other stress-related mediators. VP secretion from magnocellular (MNC) neurons of the paraventricular nucleus (PVN) of the hypothalamus at the posterior pituitary and/or median eminence contributes to increasing adrenocorticotropin hormone (ACTH) output and ultimately glucocorticoid release, which then contributes to the stress response. In this study, using whole-cell patch clamp recordings from neurons in a slice preparation of the rat PVN, we show that MNC neurons are also influenced by IL-1β. In response to 1 nM IL-1β, 62% of MNC neurons tested depolarized (mean depolarization=10.9±1.4 mV); effects which were maintained in the presence of a sodium channel blocker, tetrodotoxin (TTX). The effects of IL-1β on MNC neurons were blocked in the presence of a specific cyclooxygenase (COX)-2 inhibitor, NS-398, indicating a dependence on prostaglandins (PG) in mediating these effects. In response to direct application of 1 μM PGE 2, 57% of MNC neurons depolarized, exhibiting a membrane potential change similar to that induced by IL-1β (mean depolarization=7.8±1.1 mV). Voltage clamp experiments examining the effects of PGE 2 on the currents evoked by slow voltage ramps revealed activation of a conductance characteristic of a non-selective cationic conductance (NSCC) (voltage-independent, with a reversal potential of −41.8±7.6 mV), suggesting that this prostanoid directly modifies cationic currents in MNC neurons. These data provide evidence that IL-1β depolarizes MNC neurons in the PVN as a result of prostaglandin-mediated activation of a NSCC.

Contrast Sensitivity Deficits in Inferred Magnocellular and Parvocellular Pathways in Retinitis Pigmentosa

To define the contrast sensitivity deficits of patients with retinitis pigmentosa (RP) under testing conditions designed to emphasize threshold mediation by either the magnocellular (MC) or parvocellular (PC) pathway. Contrast sensitivity was measured with spatially localized, narrow-band test patterns at peak spatial frequencies ranging from 0.25 to 8 cycles per degree (cpd), using a steady-pedestal paradigm (brief presentation of the test stimulus against a continuously presented luminance pedestal) and a pulsed-pedestal paradigm (simultaneous brief presentation of the test stimulus and luminance pedestal) to favor the MC and PC pathways, respectively. The contrast sensitivity functions of 12 patients with RP who had visual acuities ranging between 20/12.5 and 20/40 were compared to those of 10 visually normal, age-equivalent control observers. Five of the patients with RP who had Snellen visual acuities better than 20/25 had contrast sensitivity functions that were within the normal limits at all spatial frequencies for both testing paradigms. The other seven patients with RP had reduced contrast sensitivities for both paradigms, with the greatest reduction in sensitivity occurring at the highest spatial frequency. Their contrast sensitivity deficits were equivalent for the steady- and pulsed-pedestal paradigms. As observed in previous studies, the degree of contrast sensitivity loss shown by the patients with RP was greatest at the highest stimulus spatial frequency. However, in comparison to prior studies of contrast discrimination in patients with RP, there was no evidence of a preferential contrast sensitivity loss within the MC pathway. This apparent discrepancy is attributed to differences in the test targets and psychophysical judgments that were used in the studies, which emphasizes the importance of task characteristics in evaluating relative deficits within the MC and PC processing streams in visual disorders.

Macaque ganglion cells, light adaptation, and the Westheimer paradigm

Retinal adaptation mechanisms are considered relative to the Westheimer paradigm. Responses to a probe presented upon pedestals were obtained from macaque ganglion cells. On-center magnocellular (MC) cell responses decreased to a plateau as pedestal diameter increased, consistent with operation of a local adaptation pool. Off-center cells also demonstrated a vigorous response with small pedestals, but as pedestal size increased, responsivity decreased and then partially recovered as pedestals encroached upon the surround. The response trough was due to a profound suppression of maintained activity. Comparison with psychophysical data suggests a multiple physiological substrate for the Westheimer paradigm, involving an interaction between adaptation pools, changes in maintained firing due to center-surround mechanisms and a cortical component.