Temporal response properties of the primary and secondary rod-signaling pathways in normal and Gnat2 mutant mice.

Multiple signaling pathways have been proposed for rod vision in the mammalian retina. The primary and secondary rod pathways have been characterized in humans with the scotopic 15-Hz flicker electroretinogram (ERG). The purpose of this study was to determine whether the response properties of these pathways in the mouse are similar to those of humans. C57BL/6J and Gnat2(cpfl3) mutant mice lacking functional cones were used in these experiments. Standard ERG recording techniques were employed. Response functions were obtained for a range of flash intensities (-4.7logcd-s/m(2) to -0.2logcd-s/m(2)) and temporal modulation frequencies (1-30Hz). The mouse intensity-response functions to 15-Hz flickering stimuli possessed the same features as that of humans - a local amplitude minimum and a rapid phase change in the intensity region where the primary and secondary pathways are mutually inhibitory. However, the secondary pathway in the mouse did not achieve the same level of sensitivity as previously shown for humans, suggesting inter-species differences in post-receptoral signal processing. In Gnat2(cpfl3) mutant mice, the secondary pathway was completely abolished. Measurements of temporal acuity indicated that the primary and secondary rod pathways could mediate temporal frequencies as high as 30 and 50Hz, respectively. The response functions for mice are similar to those of humans, although the evidence suggests that the primary rod pathway dominates all rod-mediated signal processing in the mouse. Nevertheless, these results demonstrate the feasibility of measuring non-invasively the performance characteristics of the primary and secondary rod retinal pathways in the mouse and provide a mechanism for testing hypotheses about the action of disease where post-receptoral cells are differentially affected.

Cortical visual function in the rd12 mouse model of Leber Congenital Amarousis (LCA) after gene replacement therapy to restore retinal function.

One eye of rd12 mice received a sub-retinal injection of a vector carrying normal human RPE65 cDNA at post-natal day 18, and at 6- and 13-months of age. Electroretinograms (ERGs) and visual-evoked potentials (VEPs) were recorded to luminance, and to spatially and temporally modulated stimuli to assess the consequences of delayed treatment on visual pathway function. Early treatment resulted in better overall retinal rescue and better rescue of cone-mediated function. VEPs to low temporal frequency luminance modulation were well preserved at all but the oldest treatment age and corresponded to predictions based on the amount of retinal rescue. In contrast, VEPs to high frequency spatially and temporally modulated stimuli were impaired even at the earliest age. These results provide further support that early treatment in human LCA will have the most hope for optimal visual performance.

The visual evoked potential in the mouse--origins and response characteristics.

The visual evoked potential (VEP) in the mouse is characterized and compared to responses obtained with the electroretinogram (ERG). The results indicate that: 1, the VEP originates in the visual cortex; 2, the rod and cone pathways contribute separately to the VEP; 3, temporal tuning functions for rod and cone ERGs are low pass and band pass, respectively; VEP tuning functions are both band pass; and 4, VEP acuity is 0.62+/-0.156 cycles/degree. The differences in the spatial and temporal tuning functions obtained from the retina and visual cortex provides a tool to investigate signal processing through the visual system.

All developmental dyslexic subtypes display an elevated motion coherence threshold.

PURPOSE: Psychophysical studies indicate that many dyslexics have a motion-processing deficit. The purpose of this study was to determine whether elevated motion coherence thresholds correlate with the specific dyslexic subtypes as defined by the Boder classification scheme. METHODS: Twenty-one dyslexics (seven dyseidetics, six dysphonetics, and eight dysphoneidetics) and 19 age- and gender-matched controls participated in the study. The dyslexics were identified by an exclusionary approach and then subtyped with the Adult Dyslexia Test or the Dyslexia Determination Test. Motion coherence thresholds were determined with random dot kinematograms composed of signal dots and noise dots. Signal dots moved either left or right on each trial, whereas noise dots moved in random directions. The percentage of dots that comprised the signal was varied randomly on each trial (0 to 21% in 3% increments). Subjects guessed the direction of signal dot motion on each trial (two-alternative forced-choice task). A 75% correct threshold was determined with a Weibull equation fit to the psychometric function. RESULTS: All three dyslexic subtypes had elevated motion coherence thresholds (t-test; dyseidetics p = 0.01, dysphonetics p = 0.039, dysphoneidetics p = 0.048). CONCLUSION: Motion-coherence deficits are not correlated with a specific dyslexic subtype, but, rather, are common to all subtypes. However, some individuals in each of the dyslexic subtypes were found to have normal motion coherence thresholds, suggesting that other factors must be considered to predict the motion sensitivity deficits found in dyslexia.

Management of the Pulfrich phenomenon secondary to pigmentary glaucoma.

BACKGROUND: The Pulfrich phenomenon can cause annoying symptoms for a patient due to a difference in interocular optic nerve conduction. There are very few reports that describe the successful use of tinted lenses as a treatment modality, while the majority of cases in the literature describe the condition without any reference to treatment. Although there are two previous reported cases of the Pulfrich phenomenon secondary to glaucoma, this article relates the first case of a patient with this phenomenon with glaucoma treated by tinted lenses. CASE REPORT: A 42-year-old woman, who was previously diagnosed with asymmetric pigmentary glaucoma, reported dramatic changes in visual perception-especially with driving and motion-related tasks. The evaluation showed asymmetric optic nerve function and a spontaneous Pulfrich phenomenon. The effects of different grades of neutral-density filters over the better eye were quantified by means of the Pulfrich phenomenon, subjective brightness comparison, and the visual-evoked potential. Relief of some of the symptoms from the Pulfrich phenomenon was achieved using an ophthalmic tint. CONCLUSION: The majority of patients (89%) reported in the literature who are symptomatic of the Pulfrich phenomenon received no treatment. This report illustrates that the traditional optometric tool of tinted lenses can be dramatically effective in relief of the motion-related symptoms secondary to the Pulfrich phenomenon in a patient with pigmentary glaucoma.

Rod multifocal electroretinograms in mice.

PURPOSE: To test the feasibility of recording rod multifocal electroretinograms (ERGs) from the mouse eye. METHODS: Multifocal ERGs were recorded from normal mice (C57BL/6J) using an array of equal-sized hexagons. Local stimuli were blue (W47A), and the number of blank frames between successive flashes at the same location was fixed at 14 (minimum 200 msec between flashes). Flash and surround intensity, and the number of hexagons, were varied to optimize the stimulus conditions for the mouse, and alterations in adaptation level were used to assess cone intrusion. Local response isolation was evaluated by comparing multifocal responses to full-field ERGs and by mapping local defects in laser-treated mice. RESULTS: Rod multifocal ERGs, although small, were clearly recordable and well formed under many conditions. Decreasing flash intensity or the size of stimulus elements, and/or increasing the surround intensity or adaptation level, decreased local response amplitudes. At the dimmest flash intensity (-0.70 log scotopic trolands [scot td]/s) and the smallest stimulus element (2.9 degrees x 3.5 degrees), local responses were nondetectable. Comparisons with full-field ERGs supported the hypothesis that the local responses were not contaminated by contributions from dark-adapted retinal areas surrounding the multifocal display. With sufficiently bright (0.30 log scot td-s) and relatively large (5.6 degrees x 6.9 degrees) stimulus elements, multifocal responses clearly revealed local retinal defects created with laser treatment. CONCLUSIONS: Rod multifocal ERGs can be recorded from the mouse eye to provide topographical maps of retinal function that have sufficient spatial resolution to be of practical use. The technique will be useful in characterizing the natural history of regional loss in mouse models of human retinal disease and in evaluating some forms of interventional therapy.

Stimulus duration, neural adaptation, and sweep visual evoked potential acuity estimates.

PURPOSE: Results in several studies have suggested that the visual evoked potential (VEP) amplitude can vary with stimulus duration. The purpose of this study was to determine whether acuity estimates obtained by extrapolation of the sweep VEP are altered by this adaptation effect. METHODS: Sweep VEP data were obtained from 16 healthy observers under binocular viewing conditions. Data were acquired with a commercially available VEP unit using standard electrode recording techniques. Three sweeps (high spatial frequencies, medium spatial frequencies, and low spatial frequencies) were run. The subjects' visual acuity at the monitor distance was 6/6 for the high spatial frequency sweep. For the medium and low spatial frequency sweeps, the subjects were dioptrically blurred to 6/15 (medium spatial frequencies) or 6/30 (low spatial frequencies) at the monitor distance. Each sweep consisted of six spatial frequencies (contrast 80%; temporal frequency (TF) = 7.5 Hz; screen luminance = 100 candela [cd]/m2). For each spatial frequency, the stimulus duration was 8 seconds, partitioned into 1-second bins. A minimum of eight sweeps were obtained per subject. An acuity estimate was obtained for each second's data by fitting a line to the high spatial frequencies (excluding noise) and extrapolating this line to the x-axis. With this technique, estimates could not be obtained for 29 of 384 possible acuities. RESULTS: The sweep VEP acuities for the 16 subjects did not change significantly over the 8 seconds of data collection for the high, medium, or low spatial frequency sweep (repeated measures analysis of variance [ANOVA]: high, P = 0.25; medium, P = 0.50; low, P = 0.23). In any given subject, there was a 1- to 2-octave range in acuity estimates over the 8 seconds of stimulus presentation (high, 1.23+/-0.417 octaves; medium, 1.41+/-0.593 octaves; low, 1.52+/-0.475 octaves; mean +/- SD). CONCLUSIONS: These results suggest that there is not a significant change in sweep VEP acuity estimates over an 8-second stimulus presentation. Thus, neural adaptation does not significantly affect the clinical use of the sweep VEP.

Binocular spatial phase tuning characteristics of neurons in the macaque striate cortex.

We employed microelectrode recording techniques to study the sensitivity of individual neurons in the striate cortex of anesthetized and paralyzed monkeys to relative interocular image disparities and to determine the effects of basic stimulus parameters on these cortical binocular interactions. The visual stimuli were drifting sine wave gratings. After the optimal stimulus orientation, spatial frequency, and direction of stimulus movement were found, the cells' disparity tuning characteristics were determined by measuring responses as a function of the relative interocular spatial phase of dichoptic grating pairs. No attempts were made to assess absolute position disparities or horizontal disparities relative to the horopter. The majority (approximately 70%) of simple cells were highly sensitive to interocular spatial phase disparities, particularly neurons with balanced ocular dominances. Simple cells typically demonstrated binocular facilitation at the optimal phase disparity and binocular suppression for disparities 180 degrees away. Fewer complex cells were phase selective (approximately 40%); however, the range of disparity selectivity in phase-sensitive complex cells was comparable with that for simple cells. Binocular interactions in non-phase-sensitive complex cells were evidenced by binocular response amplitudes that differed from responses to monocular stimulation. The degree of disparity tuning was independent of a cell's optimal orientation or the degree of direction tuning. However, disparity-sensitive cells tended to have narrow orientation tuning functions and the degree of disparity tuning was greatest for the optimal stimulus orientations. Rotating the stimulus for one eye 90 degrees from the optimal orientation usually eliminated binocular interactions. The effects of phase disparities on the binocular response amplitude were also greatest at the optimal spatial frequency. Thus a cell's sensitivity to absolute position disparities reflects its spatial tuning characteristics, with cells sensitive to high spatial frequencies being capable of signaling very small changes in image disparity. On the other hand, stimulus contrast had relatively little effect on a cell's disparity tuning, because response saturation occurred at the same contrast level for all relative interocular phase disparities. Thus, as with orientation tuning, a cell's optimal disparity and the degree of disparity selectivity were invariant with contrast. Overall, the results show that sensitivity to interocular spatial phase disparities is a common property of striate neurons. A cell's disparity tuning characteristics appear to largely reflect its monocular receptive field properties and the interocular balance between excitatory and inhibitory inputs. However, distinct functional classes of cortical neurons could not be discriminated on the basis of disparity sensitivity alone.

Not all dyslexics are created equal.

BACKGROUND: Dyslexia is a common disorder that has traditionally been treated as a homogeneous condition. However, recent evidence indicates that it is a heterogenous condition with several subtypes. For example, studies of the visual system indicate that not all dyslexics have a normal visual pathway. Approximately 75% have a processing deficit in the magnocellular pathway. Our previous study indicated that dysphoneidetic but not dyseidetic dyslexics exhibit a magnocellular pathway defect. PURPOSE: The purpose of this study was to expand our previous work by also examining dysphonetic dyslexics. Additionally, the stimulus was altered to enhance detection of a magnocellular pathway defect in any dyslexic subtype. METHODS: Temporal contrast sensitivity functions were determined with a flickering stimulus (5, 10, 15, 20, and 25 Hz) by using a temporal, two-alternative, forced-choice technique. RESULTS: The results indicate that the dyseidetic dyslexics do not have a magnocellular pathway defect, whereas the dysphoneidetics do. Furthermore, examination of the individual dysphonetics indicated that the more severely affected subjects also exhibited a magnocellular pathway defect. CONCLUSION: These results suggest that treatment strategies for dyslexics may need to be modified to take into account their specific subtype.

A comparison of saccadic and blink suppression in normal observers.

Recent research suggests that blink and saccadic suppression are produced by the same mechanism (Volkmann, 1986; Uchikawa & Sato, 1995; Ridder & Tomlinson, 1993, 1995). These studies demonstrated that blink and saccadic suppression have the same effect on various visual functions. However, none of these studies made a comparison of blink and saccadic suppression in the same individual. The purpose of this study was to compare the effects of blink and saccadic suppression on contrast sensitivity functions in the same subject. The effect of saccadic suppression on the contrast sensitivity function in three normal observers was determined. Employing a two-alternative, forced-choice technique, thresholds were measured for seven spatial frequencies. At each spatial frequency, the threshold was determined immediately following detection of a voluntary saccade. The magnitude of suppression was taken as the log ratio of the contrast sensitivities obtained while foveating the stimulus and those obtained during saccades. The magnitude of saccadic suppression was found to increase as the saccade amplitude increased and to be spatial-frequency dependent. Low spatial frequencies were suppressed more than high spatial frequencies. The blink suppression data have been measured previously (Ridder & Tomlinson, 1993). Saccadic and blink suppression were qualitatively similar. A vertical shift of the data brought the saccadic and blink suppression data into register. These results suggest that blink and saccadic suppression are produced by the same or similar mechanisms.

The presence of a magnocellular defect depends on the type of dyslexia.

Previous studies have identified a magnocellular pathway defect in approximately 75% of dyslexics. Since these experiments have not classified dyslexia into subtypes, the purpose of this experiment was to determine if adult dyseidetic dyslexics or dysphoneidetic dyslexics suffer from a defect in the magnocellular pathway. Nine dyseidetic dyslexics, eight dysphoneidetic dyslexics, and nine normal readers participated in the experiment. Contrast sensitivity functions (CSF) were determined with vertically oriented sine wave gratings (0.5, 1.0, 2.0, 4.0, 8.0, 12.0 c/deg drifting at 1 and 10 Hz) by employing a two-alternative, forced-choice technique. The results of the experiment indicated that dysphoneidetic dyslexics had reduced sensitivity to low spatial frequencies at 10 Hz, whereas dyseidetic dyslexics did not have reduced sensitivity at either 1 or 10 Hz. These results suggest that the type of dyslexia influences whether losses in perception are found which are consistent with a magnocellular deficit.

Spectral characteristics of blink suppression in normal observers.

Previous studies of the characteristics of suppression occurring under various visual conditions show similarities and differences which may indicative of the mechanism of suppression. The primary purpose of this study was to determine if the suppression that occurs in response to an eyelid blink (blink suppression) is similar to that which occurs during a saccade (saccadic suppression). In addition, the characteristics of blink suppression and other forms of suppression (i.e. permanent and binocular rivalry suppression) are compared. A test probe paradigm was utilized to determine the effect of blink suppression on the spectral sensitivity function in three normal observers. Employing a two alternative forced choice technique, thresholds were determined for wavelengths from 420 to 680 nm in 20 nm steps. At each wavelength, the threshold was determined at 0 and 400 msec after the onset of a voluntary blink. The magnitude of suppression was taken as the difference between the 0 and 400 msec thresholds. Similar to saccadic suppression, the magnitude of blink suppression increased as the stimuli biased detection towards the luminance channel. These results suggest that blink suppression and saccadic suppression are the result of a single mechanism. Similarities between blink suppression and other forms of visual suppression are also considered.

Blink-induced variations in visual performance with toric soft contact lenses.

BACKGROUND: Blink-induced lens movement causes a reduction in visual performance that is potentially greater with toric than with spherical soft contact lenses because of the combination of vertical lens movement and rotation. This study examined the effect of the two most common methods of toric lens stabilization (prism ballast and dynamic stabilization) on vision. METHOD: Four toric soft contact lens wearers were the subjects (astigmatic range 1.25 to 2.25 D). Stimulus presentation (10.5 cpd sine wave grafting flashed for 16 ms) occurred at specified times up to 400 ms after the blink. Contrast thresholds were determined monocularly with spectacles and the two types of contact lenses. RESULTS: For the grouped data, the prism balasted lens gave better overall visual performance than the dynamic stabilization at all times after the blink. Separate analysis of subject data suggested that this general pattern was not true for all individuals. CONCLUSIONS: Clinical evaluation of different lens designs on individual patients is required for achieving the optimum visual performance with toric soft lenses.

Suppression of contrast sensitivity during eyelid blinks.

Each blink of the eyelids is associated with a concurrent suppression of vision that lasts as long as 200 msec. Saccadic eye movements are also associated with a concurrent suppression of vision. Previous studies suggested that blink and saccadic suppression may be the result of a single mechanism. Volkmann, Riggs, White and Moore [(1978) Vision Research, 18, 1193-1199] demonstrated that saccadic suppression is most evident for low spatial frequency stimuli. However, the effect of stimulus spatial frequency on blink suppression has not been evaluated. If blink suppression and saccadic suppression result from a single mechanism, then blink suppression should also exhibit its greatest effect at low spatial frequencies. The purpose of this study was to determine the effect of stimulus spatial frequency on blink suppression. The stimulus was a sine-wave grating presented at different times after the blink. Psychometric functions were produced from the data for each post-blink, stimulus onset time and a Weibull function was fit to the data to determine threshold. The magnitude and duration of blink induced contrast sensitivity suppression was found to depend on the spatial frequency of the stimulus employed (similar to saccadic suppression). This is further evidence that a single mechanism may produce both blink induced visual suppression and saccadic suppression.

Effect of ibuprofen on contrast sensitivity.

Therapeutic doses of ibuprofen (2-4'-isobutylphenyl-propionic acid) have been shown to have many deleterious effects on the nervous system. However, visual disturbances have been reported in fewer than 1% of the patients taking recommended doses of ibuprofen. The most commonly reported visual disturbances include: amblyopia, scotomata, and changes in color vision. To our knowledge, no studies have examined the effects of ibuprofen therapy on the contrast sensitivity function of an affected individual. Contrast sensitivity, Snellen visual acuity, color vision (D-15 test), and Goldmann visual fields were measured on 1 affected subject during and after ibuprofen therapy (800 mg/day for 2 days). Snellen visual acuity, color vision, and Goldmann visual fields were unaffected by the treatment. However, the contrast sensitivity was significantly depressed at low spatial frequencies while the subject was taking ibuprofen. The results, in concert with previous reports concerning the visual effects of ibuprofen, suggest that this drug can result in transient multifocal lesions of the visual pathway.

Effects of interocular suppression on spectral sensitivity.

A stable form of interocular suppression, referred to as "permanent suppression," can be produced by presenting a contoured field to one eye and a spatially homogenous field to the fellow eye, a viewing condition analogous to the classic "hole-in-the-hand" illusion. We examined the relation between permanent suppression and binocular rivalry suppression by comparing the changes in the increment-threshold spectral sensitivity function produced by these two forms of suppression. Permanent suppression produced a reduction in spectral sensitivity; however, in contrast to binocular rivalry suppression, the sensitivity alterations associated with permanent suppression were independent of the test-probe wavelength. The different patterns of sensitivity loss observed during binocular rivalry and permanent suppression indicate that different neural mechanisms mediate these two forms of interocular suppression.

Binocular beat VEPs: losses of cortical binocularity in monkeys reared with abnormal visual experience.

Binocular beat VEPs were recorded from anesthetized macaque monkeys with diverse visual rearing histories, including surgically induced esotropia, optical prism dissociation, optical anisometropia, monocular form deprivation (MD), and normal rearing. Dichoptic visual stimulation was produced by temporally modulating the luminances of uniform fields presented to each eye. Five pairs of temporal frequencies were used, all of which had interocular differences of 2 Hz. While normally reared animals exhibited robust binocular beat responses strongly tuned to temporal frequency, the responses from monkeys with abnormal rearing experiences showed losses in beat signal-to-noise ratios that correlated with the age of onset or duration of the abnormal visual experience. Surgical esotropia induced early in life (2 months of age) produced a virtually complete loss of the binocular beat response; the cortical losses were less severe as the age of surgery rose to 10 months. Monkeys reared with either anisometropia or optical dissociation also manifested substantial reductions in evoked beat nonlinearity. MD monkeys sutured relatively late in development (8 and 25 months) showed mild reductions. The correspondence of these results to earlier psychophysical data obtained from these animals, and the similarity of these results to previous findings with binocularly normal and abnormal humans, supports the use of the binocular beat as an objective, noninvasive index of binocular neural integrity.

Disruption of binocularly correlated signals alters the postnatal development of spatial properties in cat striate cortical neurons.

1. Extracellular single-cell recording techniques were employed to investigate the effects of ocular misalignment on the postnatal development of the spatial response properties of striate cortical neurons. The primary objective of the study was to gain insight into the neural basis of strabismic amblyopia. 2. Two basic rearing strategies were used to study specific aspects of experimental strabismus in developing kittens. In one group, strabismus was optically induced by fitting kittens with goggles that held a 15-diopter base-in prism in front of one eye (MP) or both eyes (BP) between the ages of 4 wk and 4 mo. In the second group, a unilateral esotropia was surgically induced at 3 wks of age either by the simple resection of the lateral rectus muscle tendon (tenotomy) or by a more drastic procedure that involved removing sections of the lateral rectus and superior oblique muscles (myectomy). In addition, the eyelids of the nondeviating eyes of these kittens were sutured closed (ESO/MD). The first rearing paradigm isolated the effects of conflicting visual inputs on neural development, whereas the second procedure isolated the effects of anomalous ocular motility by producing a misalignment without putting the deviated eye at a competitive disadvantage. 3. The recording experiments were conducted when the animals were greater than or equal to 9 mo of age. A total of 445 striate cortical neurons were isolated and quantitatively studied in 17 cats (3 MPs, 3 BPs, 5 ESO/MDs, 3 goggle-reared controls, and 3 normals). In addition, we analyzed the distribution of preferred stimulus orientations of 1,205 single units that had been studied qualitatively in our previous investigation of 42 kittens reared with optically induced strabismus. 4. As expected, the proportion of binocularly driven units was reduced in both MP and BP cats. The great majority of units in ESO/MD animals were exclusively driven or highly dominated by the open deviating eye. 5. Prism-reared animals showed physiological deficits in spatial resolution, contrast sensitivity, contrast gain, and peak firing rate. These effects were manifest in both eyes, although there was always an interocular asymmetry in the deficits observed in the two eyes. In MP animals, the units dominated by the treated eye, which was contralateral to the recording hemisphere, were on the average more severely affected. The interocular asymmetry was smaller in BP cats; however, two of the three BP animals also showed a greater deficit in those units dominated by the contralateral eye.(ABSTRACT TRUNCATED AT 400 WORDS)

Orientation bias of neurons in the lateral geniculate nucleus of macaque monkeys.

The purpose of this investigation was to analyze the influence of stimulus orientation on the responses of individual neurons in the monkey's lateral geniculate nucleus (LGN). Our specific goals were to assess the prevalence and the degree of orientation tuning in the monkey LGN and to determine if the preferred stimulus orientations of LGN neurons varied as a function of receptive-field position. The primary motivation for this research was to gain insight into the receptive-field configuration of LGN neurons and consequently into the neural mechanisms which determine the spatial organization of LGN receptive fields in primates. In both the parvocellular and magnocellular layers, the responses of the majority of individual neurons to sine-wave gratings varied as a function of stimulus orientation. The influence of stimulus orientation was, however, highly dependent on the spatial characteristics of the stimulus; the greatest degree of orientation bias was observed for spatial frequencies higher than the cell's optimal spatial frequency. On a population basis, the degree of orientation bias was similar for all major classes of LGN neurons (e.g. ON vs. OFF center; parvocellular vs. magnocellular) and did not vary systematically with receptive-field eccentricity. At a given receptive-field location, LGN neurons, particularly cells in the parvocellular laminae, tended to prefer either radially oriented stimuli or stimuli oriented more horizontally than their polar axis. Our analyses of the orientation-dependent changes in spatial-frequency response functions, which was based on the Soodak et al., (1987; Soodak, 1986) two-dimensional, difference-of-Gaussian receptive-field model, suggested that the orientation bias in LGN neurons was due to an elongation of the receptive-field center mechanism which in some cases appeared to consist of multiple subunits. Direct comparisons of the orientation-tuning characteristics of LGN cells and their retinal inputs (S potentials) indicated that the orientation bias in the monkey LGN reflects primarily the functional properties of individual retinal ganglion cells. We conclude that orientation sensitivity is a significant property of subcortical neurons in the primate's geniculo-cortical pathway.

Effects of convergent strabismus on spatio-temporal response properties of neurons in cat area 18.

Single-cell recording experiments were carried out to determine whether rearing kittens with surgically induced convergent strabismus (esotropia) alters the development of receptive field (RF) properties of neurons in area 18. In agreement with previous work on kittens with divergent strabismus (exotropia), there was a marked loss of binocularly driven cells in area 18 of esotropic cats. In contrast to the striate cortex of strabismic cats, the spatial properties of area 18 neurons, including receptive-field size and spatial frequency tuning, did not differ from those in normal controls. On the other hand, we found that contrast thresholds, measured at an optimal spatial frequency, were significantly elevated, and that the contrast gain in many cells was reduced in strabismic cats. These deficits were observed in both eyes, though the cells dominated by the deviating eye had a lower response amplitude at all contrasts. Furthermore, temporal frequency tuning curves were abnormal in strabismic cats in that the optimal frequencies and temporal resolutions were shifted to lower values. These effects were also bilateral. Velocity tuning, measured with a high-contrast bar stimulus, revealed that area 18 neurons in strabismic cats were unable to respond to very high velocities compared to normals. This reduced response was more severe when measured with the deviating eye in spite of the bilateral nature of the deficit. Finally, latencies to electrical stimulation of the optic chiasm or the optic radiation were significantly longer in strabismic cats. The magnitude of these effects was virtually the same for both eyes. From these observations, we conclude that the temporal properties of area 18 neurons, particularly the cells abilities to follow fast temporal modulations, are affected by raising kittens with surgically induced convergent strabismus.