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Spatiotemporal contrast sensitivity and colour vision in multiple sclerosis.

Measures of contrast sensitivity and colour vision were taken from a group of 18 multiple sclerosis patients. Contrast sensitivity losses, measured at 5 spatial frequencies and 4 temporal frequencies, were found to be significant in 11 patients. Red/green (Rayleigh equation) and green/blue (Engelking-Trendelenburg equation) Pickford-Nicolson anomaloscope settings were abnormal in 15 patients. Correlating each of the 20 spatiotemporal losses with the colour losses revealed that in 19 conditions the red/green loss was greater than the green/blue loss. None of the green/blue losses correlated significantly with spatiotemporal losses while between 2 and 8 cycles/deg 11/12 spatiotemporal conditions showed significant correlations with red/green colour loss. These results support a locus of damage before the cortex at a stage in the visual pathway where red/green chromatic information may be encoded in pathways which also code luminance information.

Adult↗

Invariant visual responses from attentional gain fields.

Inferotemporal (IT) neurons exhibit a substantial degree of invariance with respect to translation of images used as visual stimuli. Through theoretical and computer-modeling methods, we show how translation-invariant receptive fields, like those of IT neurons, can be generated from the responses of V4 neurons if the effects of attention are taken into account. The model incorporates a recently reported form of attention-dependent gain modulation in V4 and produces IT receptive fields that shift so they are centered at the point where attention is directed. Receptive fields of variable, attention-controlled spatial scale are obtained when the mechanism is extended to scale-dependent attentional gain fields. The results indicate that gain modulation may play analogous roles in the dorsal and ventral visual pathways, generating transformations from retinal coordinates to body- and object-centered systems, respectively.

Animals↗

Effects of parietal lesions in humans on color and location priming.

To determine whether the parietal lobes contribute tot he selection of nonspatial features known to be processed in the ventral stream, the current study examined the effect of chronic unilateral parietal lobe lesions in humans on color and location priming. Patients and normal controls performed a go/no-go color discrimination task in which either the same color and different color pairs of stimuli (prime and probe) were projected sequentially either in the same hemifield or in opposite hemifields. Control subjects and patients both showed independent effects of color and location priming. In the patients, primes in either field produced color priming for target probes in the ipsilesional field but not for probes in the contralesional field. This observation implicates the parietal cortex in processing activated codes of stimulus attributes not only for spatial information but also for visual features processed in the ventral visual pathways.

Aged↗

Postnatal development of glutamatergic, GABAergic, and cholinergic neurotransmitter phenotypes in the visual cortex, lateral geniculate nucleus, pulvinar, and superior colliculus in cats.

We have analyzed the postnatal development of glutamatergic/aspartergic, GABAergic, and cholinergic neurotransmitter systems in the visual cortical Areas 17 and 18, lateral geniculate nucleus (LGN), pulvinar, and the visual and non-visual parts of superior colliculus (SC) in kittens. High-affinity uptake of D-aspartate (HA D-Asp), glutamate decarboxylase (GAD), and choline acetyltransferase (ChAT) activities were measured as a means of probing the development of the respective transmitter systems. HA D-Asp exceeded the adult level several-fold in all areas during the postnatal period which corresponded with the period of maximal dendritic/axonal branching patterns and synapse densities in the respective regions. GAD exhibited a gradual increase towards adult levels during the first month. The adult level was reached during postnatal week (PNW) 5-6 in Areas 17 and 18, during PNW3 within LGN, pulvinar, and the visual part of SC. In the nonvisual part of SC, the adult GAD level was reached as early as PNW2. ChAT exhibited biphasic developmental profiles in Areas 17 and 18. An initial peak of near adultlike activity in PNW2 was followed by a decline and subsequently by a slow increase towards adult levels during PNW5-17. ChAT developed very slowly in LGN and pulvinar, and in the latter structure only approximately 70% of the adult activity had been attained by PNW17. In both subdivisions of SC, ChAT had reached adult levels during PNW3-5. Dark-rearing from birth until PNW6 moderately attenuated GAD development in all areas and increased ChAT activity in Areas 17 and 18 but did not affect development of HA D-Asp in any part of the kitten visual system. Our neurochemical findings in the developing cat visual system are consistent with available evidence regarding localization of neurotransmitter systems, as well as postnatal changes in terms of cytoarchitectonics, synaptogenesis, functional development, and susceptibility to neonatal dark-rearing in visual pathways.

Animals↗

Response of astrocytes in the visual system to Wallerian degeneration: an immunohistochemical analysis of laminin and glial fibrillary acidic protein (GFAP).

Eye removal in adult rats resulted in an increase in immunohistochemical staining with antibodies to glial fibrillary acidic protein in the optic nerve, optic tract, and primary visual nuclei. Astrocytes along the primary visual pathway did not stain with antibodies to laminin in response to eye removal. There was an increase in laminin immunoreactivity associated with blood vessels along the injured pathway. These blood vessels were also shown to have an increased size. The lack of laminin induction in astrocytes along the path of degenerating optic axons may be responsible in part for the inability of axons to regenerate in the primary visual system.

Animals↗

Contrast gain control in the cat visual cortex.

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

Adaptation, Ocular↗

Vestibular unitary responses to visual stimulation in the rabbit.

Vestibular nucleus (VN) neurons, identified by sinusoidal rotation about the vertical axis, were tested for their response to moving visual field, and to electric stimulation on the optic chiasm (OX) and super colliculus (SC). Incremental responses during the rotation were inhibited by visual stimulus in cerebellectomized animals. Single-pulse stimulation applied to the OX was ineffective in producing a positive response in these neurons as well or in any other unit. Thus, such a visual pathway to VN must be located inside the brainstem and contains multi-synapses. Effects of repetitive stimulations (60 Hz) to OX and SC were more predominant in the cerebellectomized animal than in the intact animal. Cerebellar inhibitory control on visual-vestibular kinkage was suggested.

Animals↗

Encoding light intensity by the cone photoreceptor synapse.

How cone synapses encode light intensity determines the precision of information transmission at the first synapse on the visual pathway. Although it is known that cone photoreceptors hyperpolarize to light over 4-5 log units of intensity, the relationship between light intensity and transmitter release at the cone synapse has not been determined. Here, we use two-photon microscopy to visualize release of the synaptic vesicle dye FM1-43 from cone terminals in the intact lizard retina, in response to different stimulus light intensities. We then employ electron microscopy to translate these measurements into vesicle release rates. We find that from darkness to bright light, release decreases from 49 to approximately 2 vesicles per 200 ms; therefore, cones compress their 10,000-fold operating range for phototransduction into a 25-fold range for synaptic vesicle release. Tonic release encodes ten distinguishable intensity levels, skewed to most finely represent bright light, assuming release obeys Poisson statistics.

Animals↗

Using eye movements to assess brain function in mice.

Examining eye movements is an important part of the neurological evaluation of humans; the distribution of the neural circuits that control these movements is such that they are disrupted--often in highly characteristic fashions--by many disease processes. Technical advances have made it possible to measure accurately the eye movements of mice, so it is now possible to use the detective power of eye movement recording to characterize neurological dysfunction in genetically altered strains. Here we introduce analytical tools used in ocular motor research and demonstrate their ability to reveal disorders of the visual pathways, inner ear, and cerebellum.

Animals↗

Cortical blindness.

A 79-year-old woman with persistent cortical blindness caused by bilateral temporo-occipital infarctions was followed for 8 months. She had no light or visual motion perception. Our patient's visual imagery was intact, which was demonstrated when drawing elementary shapes; however, her drawing of objects was poor. Optokinetic nystagmus could not be elicited, but the vestibulo-ocular reflex (VOR) seemed intact. Although she was able to suppress her VOR by 'fixating' her outstretched hand which moved in phase with her head and body, she showed saccadic tracking eye movements in an attempt to visually 'follow' the self-generated movements of her outstretched hand, while her body and head were stationary. Such saccadic tracking seemed to be different from the previously described smooth tracking of self-moved targets by patients with acquired blindness caused by anterior visual pathway dysfunction.

Aged↗

Disruption of retinogeniculate afferent segregation by antagonists to NMDA receptors.

Afferent activity has an important role in the formation of connections in the developing mammalian visual system. But the extent to which the activity of target neurons shapes patterns of afferent termination and synaptic contact is not known. In the ferret's visual pathway, retinal ganglion cell axons from each eye segregate early in development into eye-specific laminae in the lateral geniculate nucleus (LGN). The dorsal laminae (termed laminae A and A1) then segregate further into inner and outer sublaminae that retain input from on-centre and off-centre retinal axons, respectively. Thus, individual retinogeniculate axons form terminal arbors within laminae A and A1 that are restricted to one inner or outer sublamina. We report here that blockade of N-methyl-D-aspartate (NMDA) receptors on LGN cells with specific antagonists during the period of sublamina formation prevents retinal afferents from segregating into 'On' and 'Off' sublaminae. Retinogeniculate axons have arbors that are not restricted appropriately, or are restricted in size but inappropriately positioned within the eye-specific laminae. NMDA receptor antagonists may specifically disrupt a mechanism by which LGN neurons detect correlated afferent and target activity, and have been shown to reduce retinogeniculate transmission more generally, causing LGN cells to have markedly reduced levels of activity. These results therefore indicate that the activity of postsynaptic cells can significantly influence the patterning of inputs and the structure of presynaptic afferents during development.

2-Amino-5-phosphonovalerate↗

Diagnostic validity for different components of pattern shift visual evoked potentials in multiple sclerosis.

Visual evoked potentials, elicited by checkerboard-pattern reversal were recorded from multiple sclerosis patients with different probabilities of diagnosis. Latencies and amplitudes of the different components were analyzed for diagnostic validity. It was demonstrated that the latency of the main positive peak (P2) was the most sensitive parameter. But in a few cases determination of P2 latency and interocular difference of this peak alone failed to detect involvement of the visual system. Additional evaluation of absolute latencies, asymmetries in latency and amplitudes of other components would give evidence in predicting abnormalities of the visual pathways.

Adolescent↗

Morphological changes in the optic nerve after chronic exposure of neonatal rats to cocaine and amphetamine.

We determined the effects of cocaine hydrochloride (15 mg/kg body weight/day) or amphetamine sulfate (25 mg/kg body weight/day) on the optic nerve in groups of rats exposed from postnatal day 1 to 30. Qualitative and quantitative studies of cross-sections of the optic nerves showed different patterns of organization, namely the presence of degenerative features in drug-treated animals and significant differences in the proportion of the nerve occupied by glial cells and their processes and nerve fiber bundles. No significant differences of the total number of fibers were found. Taken together, these data indicate that the optic nerve is vulnerable to early exposure to cocaine and amphetamine which cause developmental changes in this link of the visual pathways.

Amphetamine↗

Reconstruction of natural scenes from ensemble responses in the lateral geniculate nucleus.

A major challenge in studying sensory processing is to understand the meaning of the neural messages encoded in the spiking activity of neurons. From the recorded responses in a sensory circuit, what information can we extract about the outside world? Here we used a linear decoding technique to reconstruct spatiotemporal visual inputs from ensemble responses in the lateral geniculate nucleus (LGN) of the cat. From the activity of 177 cells, we have reconstructed natural scenes with recognizable moving objects. The quality of reconstruction depends on the number of cells. For each point in space, the quality of reconstruction begins to saturate at six to eight pairs of on and off cells, approaching the estimated coverage factor in the LGN of the cat. Thus, complex visual inputs can be reconstructed with a simple decoding algorithm, and these analyses provide a basis for understanding ensemble coding in the early visual pathway.

Algorithms↗

Temporal and spatial resolution in foveal vision of multiple sclerosis patients.

Deficits of spatial and temporal resolution were compared in a group of 49 definite multiple sclerosis(MS) patients showing no major evidence of previous optic neuritis attack but representative of the population of the Belgian National MS Centre as to age and the most important disease variables. Resolution in the two domains was measured foveally with forced-choice staircase psychophysical procedures using Landoldt C and double flash stimuli, respectively. The two measurements were equally sensitive to MS-induced deficits and did not exhibit cross-sensitivity. Since discrete deficits of either kind were equally prevalent and outnumbered combined deficits, this suggests a nonselective but nonuniform destruction of M and P visual pathway function in these patients.

Adult↗

Computer-assisted interpretation of resolution visual fields from patients with chiasmal and retrochiasmal lesions.

Computer-assisted interpretation of resolution visual fields was performed in 147 normal subjects and 174 consecutive patients with known chiasmal or retrochiasmal lesion. The program identified 99% of normal subjects, and provided support for the correct diagnosis in 64% of patients with chiasmal and 83% of patients with retrochiasmal lesions. In conclusion, computer-assisted interpretation of resolution visual fields can provide considerable support to the final diagnostic decision in patients with lesions of the visual pathways.

Adolescent↗

Dynamic causal modeling of evoked responses in EEG and MEG.

Neuronally plausible, generative or forward models are essential for understanding how event-related fields (ERFs) and potentials (ERPs) are generated. In this paper, we present a new approach to modeling event-related responses measured with EEG or MEG. This approach uses a biologically informed model to make inferences about the underlying neuronal networks generating responses. The approach can be regarded as a neurobiologically constrained source reconstruction scheme, in which the parameters of the reconstruction have an explicit neuronal interpretation. Specifically, these parameters encode, among other things, the coupling among sources and how that coupling depends upon stimulus attributes or experimental context. The basic idea is to supplement conventional electromagnetic forward models, of how sources are expressed in measurement space, with a model of how source activity is generated by neuronal dynamics. A single inversion of this extended forward model enables inference about both the spatial deployment of sources and the underlying neuronal architecture generating them. Critically, this inference covers long-range connections among well-defined neuronal subpopulations. In a previous paper, we simulated ERPs using a hierarchical neural-mass model that embodied bottom-up, top-down and lateral connections among remote regions. In this paper, we describe a Bayesian procedure to estimate the parameters of this model using empirical data. We demonstrate this procedure by characterizing the role of changes in cortico-cortical coupling, in the genesis of ERPs. In the first experiment, ERPs recorded during the perception of faces and houses were modeled as distinct cortical sources in the ventral visual pathway. Category-selectivity, as indexed by the face-selective N170, could be explained by category-specific differences in forward connections from sensory to higher areas in the ventral stream. We were able to quantify and make inferences about these effects using conditional estimates of connectivity. This allowed us to identify where, in the processing stream, category-selectivity emerged. In the second experiment, we used an auditory oddball paradigm to show that the mismatch negativity can be explained by changes in connectivity. Specifically, using Bayesian model selection, we assessed changes in backward connections, above and beyond changes in forward connections. In accord with theoretical predictions, there was strong evidence for learning-related changes in both forward and backward coupling. These examples show that category- or context-specific coupling among cortical regions can be assessed explicitly, within a mechanistic, biologically motivated inference framework.

Auditory Pathways↗

Ischemic lesions of the occipital cortex and optic radiations: positron emission tomography.

We used 18-F-fluoro-2-deoxyglucose positron emission tomography (PET) and computed tomography (CT) to study eight patients with homonymous hemianopias or quadrantanopias due to ischemic lesions of the visual pathways. Four patients with ischemic damage to all or part of the occipital lobe had decreased glucose metabolism in the affected region. Three patients with ischemic damage limited to the optic radiations had decreased glucose metabolism in the portion of striate cortex appropriate for the visual field defect. Changes in glucose metabolism frequently occurred in the undamaged ipsilateral thalamus and visual association areas.

Adult↗