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PubMedDate not supplied

Changes in color vision after a single dose of vigabatrin or carbamazepine in healthy volunteers.

In patients with epilepsy the older antiepileptic drugs induce distinct electroencephalographic changes and may also alter visual function. Although the effects of the newer antiepileptic drugs on the electroencephalogram remain less clear, long-term treatment with vigabatrin (VGB) has been reported to induce severe and permanent visual impairment. Our aim in this study was to investigate the effects of a single oral dose of VGB and carbamazepine (CBZ) on visual function in normal healthy volunteers randomly assigned to three groups according to a single-blind, placebo-controlled design. All subjects underwent color visual evoked potential tests and color perimetry at baseline and after receiving placebo, VGB (2,000 mg) or CBZ (400 mg). Whereas CBZ induced a mild overall impairment of the chromatic and achromatic systems, VGB induced a selective blue impairment. The differential changes the two antiepileptic drugs induced in visual tests presumably depend on their different mechanisms of action. The selective blue impairment in color visual tests in VGB-treated healthy subjects is consistent with gamma-aminobutyric acid (GABA)-ergic inhibition also at retinal level. Hence, color visual tests may be suitable to detect initial visual abnormalities in VGB-treated patients with epilepsy.

Adult↗
PubMed1977

Color vision in the peripheral retina. II. Hue and saturation.

Hue and saturation of spectral lights were measured (direct scaling) in the fovea and at 45 degrees in the periphery; all lights were of equal photopic retinal illuminance (1200 trolands). At each retinal location both large and small targets were used. As shown by previous studies, small peripheral targets appear desaturated and of uncertain hue, except long wavelengths which appear red. However, if target size is increased, saturation increases and a full range of hues is seen; the hue functions for large peripheral targets are comparable to foveal ones for very small targets. From a modified form of color matching, it was concluded that the color deficiency in the periphery is more tritanlike than deutanlike; this is strengthened by the observation, that, for small peripheral targets, hues are generally apportioned between two hue categories and the change from one to the other is at about 580 nm.

Adult↗
PubMed2000

Infant color vision: sharp chromatic edges are not required for chromatic discrimination in 4-month-olds.

In our previous demonstrations of chromatic discrimination in infants, we have used test and surround fields of different chromaticities that abutted each other at sharp chromatic edges. In order to see whether sharp chromatic edges are necessary for infants to make chromatic discriminations, 16-week-old infants were tested with three stimulus configurations in which sharp chromatic edges were eliminated. The three edge manipulations involved black borders, a dark surround, or blurred edges around the chromatic test field. In each case red, green, and violet test fields were used. Although performance decreased when sharp chromatic edges were eliminated, observers' percent correct scores remained clearly above chance for eight of the nine discriminations (three colors x three edge manipulations). We argue that all three edge manipulations reduce the likelihood of mediation of chromatic discrimination by M (magnocellular) cells. These data thus provide evidence that young infants have functional P (parvocellular) pathways, and use them for making chromatic discriminations.

Color Perception↗
PubMed1992

[Color vision in pseudophakia].

The authors compare colour differentiation of 30 phakic and 30 pseudophakic eyes, using the Farnsworth-Munsell 100-hue test. No significant difference was found between the two groups as regards differentiation of colours although theoretically it could be expected that colour differentiation will be better in eyes with a synthetic intraocular lens. The factor which has the greatest influence on colour sense is the subject's age.

Adult↗
PubMedDate not supplied

[The comparative neurobiology of human and animal color vision].

Discrimination of colours was studied using instrumental learning paradigm in monkeys (Macaque rhesus) and fishes (Carpio Cyprinus L.). The confusion matrices composed of probabilities of instrumental responses were treated by factor analysis. The spherical structure of perceptual colour space revealed in both animals was close to one in humans. Four eigenvectors constituting four-dimensional Euclidean hyperspheres correspond to red-green, blue-yellow, bright and dark neuronal channels.

Animals↗
PubMed1986

Spectral sensitivity functions derived from brightness matching: implication of intensity invariance for color-vision models.

It is demonstrated that brightness sensitivity functions are self-similar; i.e., unique up to multiplication by a positive constant. This invariance leads to a structural restriction for sensitivity models that are formulated in terms of action spectra of cone systems. The heuristic value of this restriction is demonstrated through simulations on various kinds of data on direct brightness matching and brightness magnitude estimation on the basis of a new model for brightness sensitivity that accounts for both superadditivity and subadditivity.

Color Perception↗
PubMed2005

Variations in normal color vision. IV. Binary hues and hue scaling.

We used hue cancellation and focal naming to compare individual differences in stimuli selected for unique hues (e.g., pure blue or green) and binary hues (e.g., blue-green). Standard models assume that binary hues depend on the component responses of red-green and blue-yellow processes. However, variance was comparable for unique and binary hues, and settings across categories showed little correlation. Thus, the choices for the binary mixtures are poorly predicted by the unique hue settings. Hue scaling was used to compare individual differences both within and between categories. Ratings for distant stimuli were again independent, while neighboring stimuli covaried and revealed clusters near the poles of the LvsM and SvsLM cardinal axes. While individual differences were large, mean focal choices for red, blue-green, yellow-green, and (to a lesser extent) purple fall near the cardinal axes, such that the cardinal axes roughly delineate the boundaries for blue vs. green and yellow vs. green categories. This suggests a weak tie between the cone-opponent axes and the structure of color appearance.

Adaptation, Ocular↗
PubMed1999

Electronic circuit model of retina in color vision.

Based on previous works, outer retinal cell network is modeled with a simplified electronic circuit. Gap junction is represented by conductance, chemical synaptic junction is by trans-admittance. Results of simulations are appropriate to physiological responses of retina. And it is deduced in standard regularization approach that retinal network should be to minimize energy function which consists of the second or higher order smoothness constraints, residuals and their spatial derivatives. From the point of views, we illustrate some function of retina, extraction of contour and reduction of input random noises. The spatial frequency responses and effects of parameters are also discussed.

Animals↗
PubMed1999

[Color vision in relation to age: a study of normal values].

BACKGROUND: It is difficult to quantify thresholds in most colour vision tests, and this is especially the case for tritan hues, where a strong age-related increase of threshold has been reported. With the development of computer-graphic methods it is possible to remove brightness clues caused by lens absorption. This study attempts to give normative values for colour contrast thresholds and assess the age related changes therein. PATIENTS AND METHODS: 115 patients aged between 6 & 71 years were tested for central and peripheral colour contrast sensitivity. No patient had any systemic or eye disease. As a preliminary, heterochromatic flicker balance between the luminosities of the R and G and B and G phosphors was established, so that all colours subsequently generated were isoluminant for the person tested. Then, using a modified binary search technique, colour contrast thresholds were established using both 2 degree optotypes, for central vision, and a ring, 12.5 degrees in radius for peripheral vision. In the latter case, the observer had to name the position of the missing quadrant in the ring. Stimuli were presented for 200 msec at 1 Hz. Colours were modulated on protan, deutan or tritan colour axis. RESULTS: No correlation between age and central colour vision thresholds was observed. By contrast a significant but only minor increase of peripheral colour vision threshold was observed for the peripheral protan and tritan axis. DISCUSSION: The present system removes luminance clues from colour vision tests and permits both central and peripheral retina to be tested. The results are simple in that the influence of age can be neglected. The variability of threshold results is small, and it is easy to detect the relatively large changes associated with disease. Since high-quality monitors are standardised and calibrated, providing the stimulus parameters described are adhered to, the results given here for upper limits of normal may be used for other similar systems.

Adolescent↗
PubMed1993

Development of color vision in goldfish: selective delayed maturation of blue vision.

Wavelength discriminations in juvenile and adult goldfish were measured among three sensitivity maxima (450, 525 and 625 nm) of goldfish cone photoreceptors using a "go/no-go" (electroshock avoidance) task. The ability of juveniles to discriminate was significantly poorer in 450/525 nm and 450/625 nm discriminations than that of adults. While only a few juveniles acquired clear discriminative responses, there was a greater proportion of adults. In contrast to those discriminations, the ability of juveniles to discriminate between 525 and 625 nm was similar to that of adults. These results suggest that juveniles, in contrast to adults, have selective delayed development of the blue-sensitive mechanism. Some possible explanations for the poor blue discrimination of juveniles are proposed.

Animals↗
PubMed1998

Spatial and temporal aspects of infant color vision.

The present paper constitutes a review of the literature on young infants' chromatic discrimination capabilities. A series of early studies showed that infants as young as two months postnatal can make at least some chromatic discriminations between stationary, homogeneous fields of different wavelength compositions. Current studies of spatial and temporal contrast sensitivity functions (CSFs) for red/green isoluminant stimuli suggest that spatial chromatic CSFs show developmental changes in sensitivity and spatial scale, but not curve shape; while temporal chromatic CSFs (tCSFs) show developmental changes in sensitivity and curve shape, but not temporal scale. Infants can also code the direction of motion of moving isoluminant red/green gratings, for both continuous and quadrature motion. The possible mechanisms that underlie infants' chromatic discriminations are discussed.

Adult↗
PubMed2000

Contour integration in color vision: a common process for the blue-yellow, red-green and luminance mechanisms?

We compare the performance of the red-green, blue-yellow and luminance postreceptoral mechanisms on a contour integration task requiring the linking of oriented Gabor elements across space to extract a winding 'path' or contour. We first establish that for all three mechanisms curvature and contrast are independent; losses in performance due to one cannot be compensated by changes in the other. We then compare contour integration by the three mechanisms using a method that controls for their differences in cone contrast thresholds. Our results show that despite the poor orientation discrimination thresholds and poor spatial sampling found for the blue-yellow mechanism, all three mechanisms perform similarly on contour integration over a wide range of curvatures. Furthermore, all three mechanisms have the same dependence on path curvature. We also investigate the effects of adding external orientation noise. Our results imply that the internal orientation noise for extracting 'aligned' path elements is similar in the three mechanisms and for all path curvatures, and the relative efficiencies are also similar for the three mechanisms. To account for our results, we propose that the three postreceptoral mechanisms use a common contour integration process. This linking process, however, cannot be color-blind; our last experiment shows that linking between different chromatic mechanisms or between opposite spatial phases disrupts contour integration. We thus propose that the common integration process remains sensitive to the color contrast and phase of its inputs.

Color Perception↗
PubMed1993

The normal color vision evaluated with FM 100-hue test.

One hundred and twenty normal subjects (240 eyes) aged from 10 to 69 were tested with FM 100-hue test. They were divided into 6 groups according to their age. It was shown that there were no statistically significant difference in the total error score (TES) between the males and females or between the right and left eyes, but there existed some relationships between the TES and age. The total error score (TES) was the lowest in the 20-29 age group and increased gradually with aging. The analysis of the partial error score (PES) in each age group showed that the PES was the lowest in 20-29 age group and that the larger PES appeared around the axis of titan with age increasing.

Adolescent↗
PubMed1977

Color vision in the peripheral retina. I. Spectral sensitivity.

Spectral sensitivity was measured by heterochromatic flicker photometry both in the fovea and at 45 degrees in the periphery, using a 1200 troland standard. At each location, sensitivity functions were obtained using both large and small targets. While the foveal functions were normal, the peripheral ones showed a large enhancement in sensitivity to short wavelengths relative to long wavelengths. Similar results in the past had been criticized on the ground that they might have been due to differential chromatic adaptation of cone mechanisms. In this study such an interpretation was ruled out by additional control experiments including varying luminance and wavelength of the standard light. The possibility of a rod contribution to the peripheral functions could not be eliminated although several different techniques, including the Stiles-Crawford effect, were used to try to isolate cone mechanisms.

Adult↗
PubMed2000

Molecular evolution of color vision of zebra finch.

We have isolated and sequenced the RH1(Tg), RH2(Tg), SWS2(Tg), and LWS(Tg) opsin cDNAs from zebra finch retinas. Upon binding to 11-cis-retinal, these opsins regenerate the corresponding photosensitive molecules, visual pigments. The absorption spectra of visual pigments have a broad bell shape, with the peak being called lambda(max). Previously, SWS1(Tg) opsin cDNA was isolated from zebra finch retinal RNA, expressed in cultured COS1 cells, reconstituted with 11-cis-retinal, and the lambda(max) of the resulting visual pigment was shown to be 359nm. Here, the lambda(max) values of the RH1(Tg), RH2(Tg), SWS2(Tg), and LWS(Tg) pigments are determined to be 501, 505, 440, and 560nm, respectively. Molecular evolutionary analyses suggest that specific amino acid replacements in the SWS1 and SWS2 pigments, resulting from accelerated evolution, must have been responsible for their functional divergences among the avian pigments.

Amino Acid Sequence↗
PubMed1990

[Visual pigment genes for color vision defects].

Applying recombinant DNA techniques, the structures of red pigment gene (RPG) and green pigment gene (GPG) were analyzed for 43 patients with protan or deutan (including 3 females), 4 normal relatives and 3 carriers out of 3 families, as well as 11 normal controls. Abnormality of RPG was detected in all 19 protan and that of GPG was found in 14 out of 24 deutan. In about 80% (32/40) of protan and deutan the changing of exon 5 for RPG or GPG was discovered. In protan the normal RPG was replaced by a 5' red -3' green hybrid gene. Some of the deutan had no GPG, some had 5' green -3' red hybrid gene with or without GPG. Furthermore, the exon 5 of RPG and GPG was amplified by polymerase chain reaction (PCR) and further analyzed by Rsa I digestion. The results for PCR are identical to that of Southern blot hybridization.

Color Perception↗
PubMedDate not supplied

Infant color vision: influence of surround chromaticity on spontaneous looking preferences.

When infants are tested with stimuli of various chromaticities embedded in a dark or achromatic (white) surround, they show maximal preference for stimuli of maximal colorimetric purity, and minimal preference for achromatic stimuli. We investigated how this pattern of preferences changes with changes of surround chromaticity. Sixteen-week-old infants were tested in two experimental conditions. The surrounds in the first condition were red and white; and in the second condition green and white. The three test stimuli varied in colorimetric purity from white to red in the first condition, and from white to green in the second condition. A test stimulus that appeared achromatic to adults when viewed in the chromatic surround was included. Infant spontaneous looking preferences changed with changes of surround chromaticity. The changes were consistent with the conclusion that infant looking behavior is governed by a preference for the stimuli that differ maximally in purity from the surround. The implications of this pattern of results are discussed.

Adult↗
PubMed1994

Intronic gene conversion in the evolution of human X-linked color vision genes.

Human red and green visual pigment genes are X-linked duplicate genes. To study their evolutionary history, introns 2 and 4 (1,987 and 1,552 bp, respectively) of human red and green pigment genes were sequenced. Surprisingly, we found that intron 4 sequences of these two genes are identical and that the intron 2 sequences differ by only 0.3%. The low divergences are unexpected because the duplication event producing the two genes is believed to have occurred before the separation of the human and Old World monkey (OWM) lineages. Indeed, the divergences in the two introns are significantly lower than both the synonymous divergence (3.2% +/- 1.1%) and the nonsynonymous divergence (2.0% +/- 0.5%) in the coding sequences (exons 1-6). A comparison of partial sequences of exons 4 and 5 of human and OWM red and green pigment genes supports the hypothesis that the gene duplication occurred before the human-OWM split. In conclusion, the high similarities in the two intron sequences might be due to very recent gene conversion, probably during evolution of the human lineage.

Animals↗