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PubMed1996

Temporal-contrast discrimination and its neural correlates.

Reported differences in neuronal contrast processing between the parallel magnocellular (M) and parvocellular (P) visual pathways invite the hypothesis that contrast discrimination in the human visual system is more sensitive at low contrasts and less sensitive at high contrasts, for stimuli modulated at high compared with low temporal frequencies. In the present study, an edgeless temporally modulated uniform field was selected as the stimulus for psychophysical contrast discrimination, and contrast-increment thresholds for pedestal contrasts ranging from 5.5% to 78.2% were determined with a temporal two-alternative forced-choice staircase procedure. The increment thresholds for five normal subjects were adequately fit by power functions with exponents that shifted continuously from about 0.5 (square-root-law behavior) to about 1.0 (Weber's-law behavior) as stimulus temporal frequency increased from 1 to 30 Hz. A neural simulation, with the use of published contrast-response functions of magnocellular and parvocellular neurons, adjusted with an estimate of response variance, produced two distinct 'neural increment-threshold functions' that were similar to the psychophysical results obtained at the highest and the lowest temporal frequencies, respectively. A shift from a relatively more noise-limited neural mechanism to one whose response is predominantly determined by gain is suggested to account for the change of the contrast-increment-threshold function with increasing temporal frequency.

Adult↗
PubMed2005

Chromatic and achromatic transient VEPs in adults with Down syndrome.

Oculo-visual abnormalities such as strabismus and high refractive error are common in people with Down syndrome, and account in large part for reduced visual function in this group. In the absence of such abnormalities, however, some spatial vision deficits persist, probably reflecting abnormal function of the neural visual pathway in this population. In addition, colour vision abnormalities are reportedly common in subjects with Down syndrome. We recorded transient visual evoked potentials in response to black-white and chromatic stimuli, in seven subjects with Down syndrome and 33 controls, to investigate function of the visual pathways underpinning spatial and chromatic visual function in Down syndrome. Our findings indicate, in agreement with previous studies, that retino-striate achromatic and chromatic processing in Down syndrome are abnormal. We find, however, that abnormal retino-striate processing of chromatic signals in this group may not give rise to colour vision deficits detected by the Colour Vision Test Made Easy or the City University test.

Adult↗
PubMed2006

Retinal projections to the subcortical visual system in congenic albino and pigmented rats.

The primary visual pathway in albino mammals is characterized by an increased decussation of retinal ganglion cell axons at the optic chiasm and an enhanced contralateral projection to the dorsal lateral geniculate nucleus. In contrast to the primary visual pathway, little is known about the organization of retinal input to most nuclei of the subcortical visual system in albino mammals. The subcortical visual system is a large group of retinorecipient nuclei in the diencephalon and mesencephalon. These areas mediate a range of behaviors that include both circadian and acute responses to light. We used a congenic strain of albino and pigmented rats with a mutation at the c locus for albinism (Fischer 344-c/+; LaVail MM, Lawson NR (1986) Development of a congenic strain of pigmented and albino rats for light damage studies. Exp Eye Res 43:867-869) to quantitatively assess the effects of albinism on retinal projections to a number of subcortical visual nuclei including the ventral lateral hypothalamus (VLH), ventral lateral preoptic area (VLPO), olivary pretectal nucleus (OPN), posterior limitans (PLi), commissural pretectal area (CPA), intergeniculate leaflet (IGL), ventral lateral geniculate nucleus (vLGN) and superior colliculus (SC). Following eye injections of the neuroanatomical tracer cholera toxin-beta, the distribution of anterogradely transported label was measured. The retinal projection to the contralateral VLH, PLi, CPA and IGL was enhanced in albino rats. No significant differences were found between albino and pigmented rats in retinal input to the VLPO, OPN and vLGN. These findings raise the possibility that enhanced retinofugal projections to subcortical visual nuclei in albinos may underlie some light-mediated behaviors that differ between albino and pigmented mammals.

Albinism↗
PubMed1995

Wiring up the visual system.

1. In this review we describe some of our recent studies on the developing marsupial visual pathway. The description focuses on retinal ganglion cells, considering the formation of their dendritic trees, the outgrowth of axons and the formation of connections within the brain. 2. Both dendritic trees and outgrowing axons undergo a period of exuberance, followed by one of refinement. The dendritic tree transiently develops a more complex branching pattern than is found in adults. Short side branches, referred to as spines, are a feature of immature dendrites and, to a lesser extent, of axons. These structures are mostly lost as development proceeds. However, they are retained on the dendritic trees of small-field ganglion cells and, for a proportion of axons, on that part within the nerve fibre layer of the retina. Although most axons navigate fairly direct routes towards their targets, a minority follow inappropriate courses, such as doubling back towards the eye or entering the opposite optic nerve at the chiasm. As such errant axons are not seen in the adult, we assume that their parent cell bodies die during development. 3. Throughout development, optic axons are arranged in an approximate retinotopic order along the length of the visual pathway; as a result, axons approach the visual centres aligned to form, at least, a crude retinotopic map. Axons from dorsal and ventral retina exchange locations along the optic nerve and in this way correct for the inversion of the image brought about by the lens.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1995

The optic tract and tectal ablation influence the composition of neurofilaments in regenerating optic axons of Xenopus laevis.

Neurofilaments have been proposed to regulate axonal stability and diameter through changes in number and subunit composition. We have found that pathway and target innervation directly influence the molecular composition of neurofilaments within regenerating optic axons of Xenopus laevis. Immunocytochemistry was used to examine neurofilaments within two abnormal visual pathways. The first was an aberrant, transient retinoretinal projection, which formed when some axons entered the contralateral optic nerve at the chiasm. The second was formed by regenerating axons deprived of their normal targets by surgical ablation of both optic tecta. Distal to an orbital nerve crush, the neurofilament proteins NF-L, NF-M, NF-H, and XNIF disappear from degenerating fibers. In normally regenerating axons, these neurofilament proteins emerge in a progression reminiscent of development. In the aberrant retinoretinal projection, levels of XNIF, NF-L, and -M remained lower than in normally regenerating axons, whereas NF-H and a phosphorylated form of NF-M were undetectable for at least 35 d after nerve crush. Normally, these two latter forms reappear between 15 and 21 d after surgery. Thus, this transient, incorrect axonal projection expressed neurofilaments in a very different pattern from correctly regenerating axons. In tecta-ablated frogs, staining of phosphorylation independent epitopes of XNIF, NF-L, and -M increased normally after axons entered the tract, but that of NF-H and phosphorylated NF-M remained low for at least 42 d after axotomy. Thus, separate parts of the visual pathway influence the complexity of neurofilaments.

Animals↗
PubMed1994

A unique achiasmatic anomaly detected in non-albinos with misrouted retinal-fugal projections.

In mammals with binocular vision, projections of retinal axons to primary retino-recipient nuclei establish a strict visuotopic and eye-segregated arrangement. Normal primate visual pathway organization is characterized by orderly hemiretina separation in which nasal-retinal axons cross at the optic chiasm and project to primary contralateral subcortical and cortical structures while temporal-retinal fibres project ipsilaterally to corresponding visual structures. We report here, in two unrelated children, an unusual visual pathway malformation in which nasal-retinal cortical projections, unable to decussate due to the inborn absence of an optic chiasm, erroneously route ipsilaterally to visual projection targets. We have termed this newly documented achiasmatic condition the non-decussating retinal-fugal fibre syndrome (Apkarian et al., Invest. Ophthalmol. Vis. Sci., 34, Suppl., 711, 1993).

Adolescent↗
PubMed1983

Organization and function of a central nervous system circadian oscillator: the suprachiasmatic hypothalamic nucleus.

Circadian rhythms in mammals are generated by endogenous neural oscillating systems entrained to the light-dark cycle by specific visual pathways. We conclude from available data that the suprachiasmatic hypothalamic nuclei (SCN) are the principal circadian oscillators in the rodent brain and that a retinohypothalamic projection terminating in the SCN is the primary visual pathway subserving entrainment of circadian rhythms. Recent anatomical studies demonstrate that the SCN have distinct subdivisions in the rat. A dorsomedial component is comprised of a distinct neuronal population and contains a large population of interneurons, many of which produce peptides. It receives no direct or indirect visual input and has only very limited projections outside the SCN. A ventrolateral component is also made up of a distinctive neuronal population, receives both direct and indirect visual projections, and provides the major external projections of the SCN, which are to the hypothalamus, particularly the hypophysiotrophic area. The SCN are viewed in this review as containing multiple, mutually coupled oscillating systems that arise from a developmental process of interconnecting individual neuronal circadian oscillators into circuits that form the oscillating systems. A model for the organization of the systems is presented.

Animals↗
PubMed2006

Prevalence of abnormal pattern reversal visual evoked potentials in craniosynostosis.

BACKGROUND: The purpose of this study was to examine the prevalence and type of changes observed in the pattern reversal visual evoked potentials recorded at the first assessment of children with craniosynostosis. METHODS: Visual evoked potentials were recorded from 114 patients with craniosynostosis. Eighty-one patients were syndromic and 33 were nonsyndromic. No patient had received any craniofacial surgical intervention. At the time of the test, 22 of 40 patients were aged 6 months and younger, and 18 patients were between 6 months and 1 year of age. Pattern reversal visual evoked potentials were recorded from a midoccipital electrode positioned 3 cm above the inion. The pattern reversal visual evoked potentials elicited to 50' checks with three reversals per second viewed with both eyes were analyzed for n80-p100 amplitude, p100 latency, and breadth of waveform. RESULTS: Sixty percent of patients had abnormal pattern reversal visual evoked potentials to 50' checks. This did not show a significant association with age, or classification of craniosynostosis. CONCLUSIONS: The high prevalence of abnormal pattern reversal visual evoked potentials to a robust stimulus suggests that visual pathway dysfunction, as measured electrophysiologically, can affect a majority of patients with craniosynostosis. This study indicates that a baseline evaluation of all children with craniosynostosis at their first presentation is essential if subsequent electrophysiologic visual pathway monitoring is to take place.

Craniosynostoses↗
PubMed2002

Disparity-selective neurons in area V4 of macaque monkeys.

Area V4 is an intermediate stage of the ventral visual pathway providing major input to the final stages in the inferior temporal cortex (IT). This pathway is involved in the processing of shape, color, and texture. IT neurons are also sensitive to horizontal binocular disparity, suggesting that binocular disparity is processed along the ventral visual pathway. In the present study, we examined the processing of binocular disparity information by V4 neurons. We recorded responses of V4 neurons to binocularly disparate stimuli. A population of V4 neurons modified their responses according to changes of stimulus disparity; neither monocular responses nor eye movements could account for this modulation. Disparity-tuning curves were similar for different locations within a neuron's receptive field. Neighboring neurons recorded using a single electrode displayed similar disparity-tuning properties. These findings indicate that a population of V4 neurons is selective for binocular disparity, invariant for the position of the stimulus within the receptive field. The finding that V4 neurons with similar disparity selectivity are clustered suggests the existence of functional modules for disparity processing in V4.

Animals↗
PubMed1994

Geniculocalcarine hyperintensities on brain magnetic resonance imaging associated with visual hallucinations in the elderly.

Magnetic resonance scans of five geriatric patients presenting with formed visual hallucinations in the absence of other psychopathology were compared with those of 12 healthy elderly subjects for the presence and extent of subcortical and periventricular signal hyperintensity. While the number of discrete brain lesions did not differ between groups, scans from the patient group contained a higher incidence (100% vs. 50%) and greater mean size (11.1 vs. 2.9 mm) of periventricular signal hyperintensity in the posterior region. Peripheral visual acuity was impaired in all of the patients, but cerebrovascular risk factors were not elevated in this group. The authors suggest that structural abnormalities in the area of the primary visual pathway may predispose some older individuals, particularly those with poor peripheral visual acuity, to develop the symptom of visual hallucination.

Aged↗
PubMed1991

Perceptual filling in of artificially induced scotomas in human vision.

Patients with scotomas or blind-spots in their visual field resulting from damage to the visual pathways often report that the pattern from the rest of the visual field 'fills in' to occupy the scotoma. Here we describe a novel technique for generating an artificial perceptual scotoma which enabled us to study the spatial and temporal characteristics of this filling-in process. A homogeneous grey square subtending 1.5 degrees was displayed against a background of twinkling two-dimensional noise of equal mean luminance. On steady eccentric fixation for 10 s the square vanished and was filled in by the twinkling noise from the surround. Using this display we found that 'filling in' is an active visual process that probably involves creating an actual neural representation of the surround rather than merely ignoring the absence of information from the scotoma; filling in can occur separately for colour and texture, suggesting separate mechanisms; the filling-in process does not completely suppress information from the scotoma, even after an image has faded completely from consciousness it can nevertheless contribute to motion perception; and the process can be strongly influenced by illusory contours.

Humans↗
PubMed1975

Functional asymmetries of the human visual system as revealed by binocular rivalry and binocular brightness matching.

Two techniques, a binocular rivalry task and a binocular brightness matching task, were designed to yield indices of asymmetry (relative dominance weights) for the two eyes, the crossed and uncrossed visual pathways, and the two cerebral hemispheres. Twenty subjects with normal vision were run on all conditions. Intercorrelations of the dominance weights obtained by the two methods showed no relationship between the two methods, but produced three hypotheses about visual functioning: (1) the left hemisphere appears more dominant for rivalry; (2) the right hemisphere appears more dominant for brightness matching; (3) the uncrossed visual pathways are dominant over the crossed pathways in the binocular rivalry task.

Dominance, Cerebral↗
PubMed1988

[Hemianopic visual field defects--methods of study and localization problems].

In a survey of methods for determining hemianopic visual field defects, a distinction is made between gross visual field screening and actual visual field examination with kinetic and automatic static perimetry. These methods may be arranged according to increasing the concentration required as well as to ability to cooperate, as follows: hand-movement stimulation of shifts of gaze, finger-counting with repetition by the patient, brightness and color comparison among the respective halves and quadrants of the visual field, then kinetic perimetry with the Goldmann perimeter, and, most exacting of all, automated perimetry. The advantages of kinetic perimetry in cases of incipient bitemporal visual field defects are discussed. For visual field examination with automated static perimeters, test programs are chosen which have their test-point pattern shifted with respect to the principal meridian. The diagnostic situations in which visual field testing may and must not be limited to 30 degrees are presented in tabular form. Guidelines and criteria for localizing lesions have been developed, i.e., the vertical and horizontal limits of the major axes which pass through the fixation point and the temporal crescent. Consideration of the course of the nerve fibers in the retina and of the fact that exact separation between superior and inferior may only be found temporal to the foveola with corresponding nasal defects enables horizontally limited visual field defects originating within the eye to be distinguished clearly from those originating in the visual cortex. Vertical limits due to semidecussation at the chiasma permit a differentiation between prechiasmic and postchiasmic lesions. In homonymous defects, consideration of further simple anatomic features of the visual pathway, namely the knee of Wilbrand and that portion of the optic radiation which extends anteriorly to the temporal lobes and which represents the inferior retinal halves with characteristic defects, also enables lesions in the visual pathway to be localized more accurately.

Brain Mapping↗
PubMed1984

Near-field acuity changes after visual system lesions in pigeons. II. Telencephalon.

Pigeons were trained to perform in a psychophysical task that measured their minimum-separable visual acuity. After their performance stabilized, lesions were made in telencephalic components of the visual system. In one group, lesions were made in the ectostriatum, which is the telencephalic target of the tectofugal visual pathway. These cases showed severe to moderate losses of acuity. The magnitude of the loss was correlated with the extent of ectostriatal damage. In another group, lesions were made in the visual Wulst, a portion of which receives the ascending fibers of the thalamofugal visual pathway. Within this group, only lesions that were large and included all components of the visual Wulst were effective in decreasing visual acuity to a moderate degree. A partial correlation analysis indicated that the components of the visual Wulst that were responsible for the acuity changes were the accessory hyperstriatum and the hyperstriatum ventrale. However, lesions that were generally confined to these regions alone were ineffective. Also ineffective were lesions of the granular components of the visual Wulst, which receive the ascending thalamofugal fibers. The results raise questions about the presumed roles of the tectofugal pathway as a background-vision mechanism and the thalamofugal pathway as a fine-detail vision mechanism.

Animals↗
PubMed1996

Visual evoked potentials in children with developmental coordination disorder.

Children who demonstrate problems with skilled movement in the absence of physical handicap are formally designated as suffering from developmental coordination disorder (DCD). Diagnosis of DCD was confirmed by the 'movement assessment battery for children'. Visually evoked potentials (VEPs) were recorded to evaluate the integrity of the visual pathway and to rule out the presence of any neurological lesions affecting visual input. Binocular, pattern onset VEPs were recorded in 14 children with DCD aged between five and seven years, and an age-matched control group using pattern onset, high contrast, grating stimuli. Implicit times to the first and second peaks and troughs were measured, and results between the two groups were compared. Inattention and movement artefact meant that VEPs were more difficult to record within the DCD group, resulting in smaller amplitudes of the waveform, but no significant differences in the implicit times were observed between the DCD group and controls. Further research is required to determine the specific source of the neurological deficits in DCD but a problem with the integrity of the afferent visual pathway does not appear to be a causal factor.

Apraxias↗
PubMed1999

'Natural' and artificial monocular deprivation effects on thalamic soma sizes in pigeons.

The dominance for visual pattern analysis of the left hemisphere in normal pigeons and the concomitant morphological asymmetries in the optic tectum can be attributed to a 'natural' prehatch monocular deprivation of the left eye resulting from an asymmetrical embryonic position within the egg. Using control animals and pigeons which were monocularly deprived for 10 days after hatching, the present study could show that the cellular soma sizes of the nucleus rotundus within the tectofugal visual pathway are modified by light experience depending on the timepoint and direction of lateralized stimulation. Although rotundal cell size is thus ontogenetically modified in an activity-dependent manner, a detailed comparison makes it likely that the mechanisms which govern developmental plasticity of visual pathways differ between birds and mammals.

Animals↗
PubMed1979

Pineal N-acetyltransferase and hydroxyindole-O-methyltransferase: control by the retinohypothalamic tract and the suprachiasmatic nucleus.

The visual pathway and central neural structures involved in the photic and endogenous regulation of the activity of pineal N-acetyltransferase and hydroxyindole-O-methyltransferase were investigated. The results indicate that the visual pathway regulating both enzymes is the retinohypothalamic tract, and that the inferior accessory optic tract is clearly not involved in the regulation of hydroxyindole-O-methyltransferase activity, as has been previously thought. In addition, the suprachiasmatic nucleus was found to be necessary for the generation of a rhythm in N-acetyltransferase activity in blinded animals, and to be responsible for the tonic elevation of hydroxyindole-O-methyltransferase activity in blinded animals. Finally, it was concluded that the rapid and large daily changes in N-acetyltransferase activity seen in a normal lighting cycle and the much slower and smaller changes in hydroxyindole-O-methyltransferase activity seen only after weeks in constant lighting conditions are mediated by the same neural tract; the different time courses of the effects of environmental lighting may be explained on the basis of different intracellular regulatory mechanisms.

Acetylserotonin O-Methyltransferase↗
PubMed1975

Electrophysiologic evidence for normal optic nerve fiber projections in normally pigmented squinters.

The Siamese cat, a type of albino, has a visual pathway anomaly in which too many optic nerve fibers cross at the optic chiasm, and also frequently has strabismus. The correlation of strabismus with this defect suggests that a similar pathway defect without pigmentation anomalies, may be the cause of much human strabismus. Creel, Witkop, and King have used evoked potential methods to show that such a pathway defect likely occurs in the human albino. While unpublished control experiments verified their results on human albinos, no such defect has been found in the normally-pigmented human squinter. It is concluded that the visual pathway anomaly is limited to albinism and is not a likely cause of most human strabismus.

Adolescent↗