PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “visualization”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,297 records · Page 72Linked to original sources

Optimal response of eye and hand motor systems in pointing at a visual target. II. Static and dynamic visual cues in the control of hand movement.

The closed loop situation of hand pointing at a target has been experimentally divided into its static and dynamic components. When the subjects see their hand at first (closed loop) until the start of the hand movement cuts off the vision of the hand (open loop), the pointing is significantly more accurate than when it is performed without any vision of the hand before and throughout the movement (fully open loop). This suggests that initial cues as regards hand and target position, improve the motor program by a better identification of initial and final states. As poor as it is, the extra retinal signal (encoding of eye position) improves performance when the foveation is done under closed loop; it allows a better redefinition of target position, and thus modulates the hand motor program through a direct central pathway, which is quicker than the processing of the visual feedback of the hand movement error.

Eye Movements↗

Neuroplasticity in the cat's visual system. Origin, termination, expansion, and increased coupling of the retino-geniculo-middle suprasylvian visual pathway following early ablations of areas 17 and 18.

We used anterograde and retrograde transsynaptic pathway tracing techniques to reveal the retinal origin and the cortical termination of the expanded retino-geniculo-middle suprasylvian (MS) cortex pathway in adult cats which sustained lesions of areas 17 and 18 on the day of birth (P1) or at 1 month of age (P28). Following anterograde transsynaptic transport of tritiated amino acids from the eye, four major results were obtained: (1) a strong and specific pathway from retina through dorsal lateral geniculate nucleus (dLGN) to the posterior half of MS cortex was identified; this pathway is a substantial expansion of an insignificant pathway present in intact cats; (2) the terminus of the pathway was lower layer III and layer IV; (3) contralateral projections were stronger than ipsilateral projections; (4) projections in P28 cats were stronger than those in P1 cats. Following retrograde transsynaptic transport of WGA-HRP from posterior MS cortex, four additional results were obtained: (1) the pathway was enlarged and visuotopically organized; (2) the pathway arose primarily from alpha- and gamma-retinal ganglion cells; (3) a small number of beta-cells in P1 cats and a modest number in P28 cats also contribute to the pathway; (4) the combined numbers of gamma- and beta-cells relative to alpha-cells was greater in temporal retina than in nasal retina. The combined demonstration of both origin and terminus of the pathway with transsynaptic tracers argued strongly for high levels of coupling between primary and secondary pathway limbs in both P1 and P28 cats. This level of coupling, as well as other features of the pathway, have much in common with the retino-geniculo-17/18 pathway of intact cats. However, the retino-geniculo-MS system in P1 cats transmits primarily Y and W signals, in P28 cats X, Y, and W signals; whereas the retino-geniculo-17/18 pathway transmits primarily X and Y signals. These results have implications for understanding the repercussions of early visual cortex lesions in monkeys and humans.

Amino Acids↗

Task dependency of visual processing in the human visual system.

In this review we contrast passive, attribute driven processing in the visual system with an active, task-dependent view and summarize the evidence from our Positron Emission Tomography (PET) work supporting the task-dependent view. The PET studies involved comparison of regional Cerebral Blood Flow (rCBF) in closely related detection and discrimination tasks. The major finding reported is that the same retinal input or input containing only a single cue activates different extrastriate areas depending on the task.

Adult↗

Visual performance and synapses in the visual cortex of rabbits.

The density of synaptic connections, the length of the contact zones and the number of synaptic vesicles are quantitatively studied in the left and right hemisphere of a group of rabbits a number of which showed marked ocular dominance. No systematic differences in the parameters studied could be observed in the visual cortex between symmetric animals, indicating that the ocular dominance cannot be explained by hemispheric differences in density of synapses.

Animals↗

Instructive effect of visual experience in mouse visual cortex.

We describe a form of experience-dependent response enhancement in the visual cortex of awake mice. Repeated presentations of grating stimuli of a single orientation result in a persistent enhancement of responses evoked by the test stimulus. Response potentiation is specific to the orientation of the test stimulus, develops gradually over the course of several training sessions, and occurs in both juvenile and adult mice. The stimulus-selective response potentiation (SRP) can mask deprivation-induced response depression in adult mice. SRP requires NMDA receptor activation and is prevented by viral delivery of a peptide that interferes with AMPA receptor trafficking. SRP may reveal the mechanisms involved in certain forms of perceptual learning.

Animals↗

Visual receptive fields of neurons in primary visual cortex (V1) move in space with the eye movements of fixation.

We tested the hypothesis that receptive field (RF) locations of visual cortex cells maintain a fixed location on the retina and move in space with movements of the eye. Responses to a bar swept across the RF were recorded from 29 neurons in V1 (26) and V2 (3) of alert monkeys while precisely monitoring the eye movements of fixation. There was a tight correlation and a near unity ratio between eye position and RF position. This implies that RFs of V1 neurons and at least some V2 neurons are fixed to specific retinal locations, rather than being shifted on the retina by attention-controlled mechanisms. V1 neurons thus differ from those polysensory neurons whose RF locations on the retina are dynamically altered to maintain a desired position in space.

Animals↗

Determining progressive visual field loss in serial Humphrey visual fields.

PURPOSE: To evaluate the three commercially available computerized statistical algorithms for determining progression of glaucomatous field loss in serial Humphrey fields. METHODS: Serial Humphrey fields of 102 ocular hypertensive and glaucomatous eyes were analyzed by linear regression analysis of Statpac, glaucoma change probability and Progressor Programme, and the results compared with a retrospectively determined clinical outcome. RESULTS: Linear regression analysis of Statpac identified progression in 11 field series, glaucoma change probability identified progression in 23 field series, and Progressor Programme identified progression in 27 field series. Clinical outcome identified much less-progression than any of the three algorithms, determining that only seven eyes showed deterioration. There was a wide variation of results from analysis of the same group of field series by the three different algorithms. In contrast to the other two algorithms, which detected progression in similar percentages of both ocular hypertension and glaucoma field series. Progressor Programme detected progression predominantly in glaucoma field series. CONCLUSIONS: There was a high degree of variability among the three different algorithms for determining visual field progression, and none of them correlated well with clinical impression.

Algorithms↗

Propagating waves in visual cortex: a large-scale model of turtle visual cortex.

This article describes a large-scale model of turtle visual cortex that simulates the propagating waves of activity seen in real turtle cortex. The cortex model contains 744 multicompartment models of pyramidal cells, stellate cells, and horizontal cells. Input is provided by an array of 201 geniculate neurons modeled as single compartments with spike-generating mechanisms and axons modeled as delay lines. Diffuse retinal flashes or presentation of spots of light to the retina are simulated by activating groups of geniculate neurons. The model is limited in that it does not have a retina to provide realistic input to the geniculate, and the cortex and does not incorporate all of the biophysical details of real cortical neurons. However, the model does reproduce the fundamental features of planar propagating waves. Activation of geniculate neurons produces a wave of activity that originates at the rostrolateral pole of the cortex at the point where a high density of geniculate afferents enter the cortex. Waves propagate across the cortex with velocities of 4 microm/ms to 70 microm/ms and occasionally reflect from the caudolateral border of the cortex.

Algorithms↗

The pattern electroretinogram in anterior visual pathway dysfunction and its relationship to the pattern visual evoked potential: a personal clinical review of 743 eyes.

The pattern electroretinogram (PERG) has now been in routine clinical use for sufficiently long to allow a personal clinical review of its relationship to the cortically generated pattern visual evoked potential (PVEP). The PERG and PVEP findings are presented from 520 eyes with optic nerve demyelination (382 eyes), optic nerve compression (90 eyes) or heredofamilial optic atrophy (48 eyes), and these are compared with the findings obtained in 223 eyes with dysfunction anterior to the retinal ganglion cells. Dysfunction anterior to the retinal ganglion cells gives a reduction in the P50 component of the PERG, but this component is usually spared in optic nerve disease where selective loss of the N95 component is by far the most frequently occurring abnormality. A diagnostic strategy is presented.

Diagnosis, Differential↗

Flicker in the visual background impairs the ability to process a moving visual stimulus.

For the detection of a moving object, segregating the object from the background is a necessary first step. This segregation can be achieved by detection of differences in the spatial, temporal and spatio-temporal properties of the object and background. Here we investigate how flicker influences the perception of a moving object in man and monkey, and we examine the neuronal responses in extrastriate medial temporal and medial superior temporal areas (MT and MST) of two rhesus monkeys. The performance of humans and monkeys in a direction discrimination task was impaired in the presence of flicker in the background compared to the static background condition. A similar effect was found in recordings from 155 single units in areas MT and MST during the discrimination task. The discriminability (d') of the neuronal responses in preferred and nonpreferred directions was reduced by 33% on average in the presence of a flicker background compared to the static background. This reduction in discriminability was not caused by differences in variance of the neuronal activity for the two background conditions, but was due to a reduction of the difference between the activities in preferred and nonpreferred direction. This reduction in directional selectivity could be traced back to two different mechanisms: in 32 out of 155 neurons (21%), the decrease resulted from an increase in the response to the stimulus moving in the nonpreferred direction; in 62 out of 155 neurons (40%), the reduction in directional selectivity was due to a decrease in the response to the preferred direction. These results give deeper insights into how moving stimuli are processed in the presence of background flicker as present in natural visual scenes.

Action Potentials↗

Effect of peripheral visual field size upon visual search in children and adults.

Twenty observers in each of the age groups, three, four, five, and twenty-one years, were asked to identify pictures displayed through five different sizes of peephole. Recognition latency changes as a cube-root power function of aperture area. It was found that latency decreased as age and area increased. However, the exponent of the power function showed little age-related change. Effectiveness of the peripheral visual field size was discussed in terms of magnitude of the exponent.

Adult↗

Blindsight and shape perception: deficit of visual consciousness or of visual function?

Two people with homonymous right hemianopias were tested on a number of measures of non-conscious and conscious perception of shape in the blind field. Experiment 1 examined preparatory manual adjustments in grasping objects. Both subjects performed well above chance not only in three-dimensional location but also in preforming the hand to the shape, size and orientation of objects. In Experiment 2 single upper-case letters were briefly exposed in the blind field, and subjects made forced choices among 6 alternatives in the sighted field. Performance improved over blocks of trials and was above chance, but not dramatically. In Experiment 3 single upper-case words were briefly presented in the blind field, and subjects chose which of two words exposed after in the intact field was semantically closer. In Experiment 4 subjects had to give the meaning of single ambiguous words (e.g. BANK) presented both visually in the intact field and auditorily. Each ambiguous word was preceded by a single upper-case word briefly presented in the blind field, biasing each meaning on different blocks of trials (e.g. MONEY and RIVER). In Experiment 3, although results were in the appropriate direction, they were not consistently well above chance. By contrast, in Experiment 4 both subjects were consistently semantically biased to a high degree by words in the blind field. Experiments 2, 3 and 4 taken together suggest that indirect techniques (priming) are more sensitive to showing effects of non-conscious perception than direct ones (forced-choice). More importantly the experiments indicate that not only orientation but curvature, structural descriptions of component strokes and spatial ordering of letters are registered non-consciously in the blind field. Experiment 5 examined after-images in the blind and sighted fields, showing veridical conscious perception of shape in the blind field provided it was accompanied by a shape in the sighted field which together formed a good Gestalt. Experiment 6 showed conscious perception of illusory contours spanning the hemifields induced by Kanizsa figures. The experiments suggest that aspects of shape are much better perceived in blindsight than previously thought, that this is independent of their use in motor control, that the main deficit in blindsight is one of consciousness, and that the loss of conscious vision in the blind field is far from total. The effects and their relationship to those in other neuropsychological deficits suggest an intimate link between perceptual consciousness, attention and object perception.

Afterimage↗

Early visual processing during binocular rivalry studied with visual evoked potentials.

Visual evoked potentials (VEPs) were recorded to probes presented to the dominant and suppressed eyes in a binocular rivalry paradigm. Probes presented to the suppressed eye interrupted the current dominance phase and produced a P300-like deflection (400-700 ms). Probes delivered to the dominant eye increased the duration of the current dominance phase. VEPs to these probes included an endogenous component that overlapped the early exogenous components. The early endogenous component (rivalry-related potential, RRP) started as early as 70 ms and had a broad centroparietooccipital distribution.

Adult↗

Comparison of measures of visual acuity in infants: Teller acuity cards and sweep visual evoked potentials.

PURPOSE: This study compares the development of acuity in the same infants during one testing session using Teller acuity cards (TAC) and sweep visual evoked potentials (sVEP). We asked whether different testing methods in two centers would produce different developmental time courses. METHODS: Forty-eight infants were tested in two centers. The standard procedure for TAC was used. For sVEP acuity, the amplitude response curve derived from time-locked cortical activity was used to extrapolate to zero response, giving an acuity estimate for each infant. RESULTS: sVEP acuity was generally higher than TAC acuity. The rate of development was steeper for TAC than sVEP acuity with TAC starting at a much lower level. The ratio of sVEP to TAC acuity decreased exponentially with age reaching an asymptote of about 1.44 at 6 months. CONCLUSIONS: Results were indistinguishable between centers suggesting that comparison of acuity measures obtained using variations of these methods across centers is possible.

Aging↗

The effect of visual deprivation on beta-adrenergic receptors in the visual centres of the rat brain.

The levels of binding of [3H]dihydroalprenolol to beta-adrenergic receptors in the visual centres and frontal cortex from brains of control, dark-reared and monocularly deprived rats were compared. Receptor binding is changed in monocularly deprived rats in the lateral geniculate nuclei and superior colliculi of both sides. Scatchard analyses indicated that the changes in the [3H]dihydroalprenolol binding in the lateral geniculate nuclei were due to alterations in both receptor affinity and receptor number. No effect of dark-rearing could be detected.

Aging↗

Neuronal generators of visual evoked potentials in humans: visual processing in the human cortex.

PURPOSE: We wished to define the localization of cortical generators of visual (pattern) evoked potentials (VEP) and the temporal sequence of activation in the occipital region. METHODS: In 4 candidates for epilepsy surgery, a large array of subdural electrodes was placed over occipital areas. Checkerboard pattern reversal stimuli were generated and the epileptogenic focus was localized and functionally mapped. Magnetic resonance imaging did not show any occipital lesions in any of the 4 patients. RESULTS: The area first activated was the lingual gyrus in the mesial occipital lobe (negative potential peaks at approximately 70 ms), followed by an area superior to the calcarine fissure (negative peaks at approximately 80 ms). Later (starting at approximately 90 ms), there were positive potentials over the occipital pole and lingual gyrus, followed by potentials at the lateral occipital lobe. CONCLUSIONS: These data support the idea that VEP are generated in the mesial and lateral occipital cortex by different circumscribed neuronal generators with different latencies of activation. The scalp-recorded N1 and P1 potential peaks most likely derive from the progressive activation of neuronal masses in different regions of the occipital lobe.

Brain Mapping↗

The correlation of visual evoked potentials (VEP) and visual field indices (Octopus G1) in glaucoma and ocular hypertension.

Flash evoked responses and the visual field indices (VFI) of the Octopus G1 program were recorded from 42 eyes of 21 patients, aged 23-76 years (mean 51 years); 29 eyes had open-angle glaucoma (OAG) and 10 ocular hypertension (OH). Three eyes were normal. The early component of the VEP called P 120 had lower amplitude in glaucomatous eyes compared with normal or hypertensive eyes. Mean sensitivity (MS), mean defect (MD), and short time fluctuation (SF), indicative of diffuse non-specific nerve fiber los, correlated significantly (P less than 0.05). Reliability factor (RF), which is indicative of psychodynamic factors, also correlated significantly (P less than 0.05) in eyes with OAG.

Adult↗

The effects of early visual experience on the cat's visual cortex and their possible explanation by Hebb synapses.

1. Kittens were dark-reared until 4-6 weeks old, and then for another 4-7 weeks with various combinations of cylindrical lenses, monocular occlusion, and normal vision. 2. Single unit recordings from 816 neurones of the visual cortex (area 17) were obtained after the end of exposure. Clear-cut effects on the distributions of the neurones' ocular dominance and orientation preference were found yielding close correlations with the rearing conditions. 3. It was confirmed that most cortical neurones prefer vertical stimulus orientations when experience is restricted to vertical contours in both eyes. It was further confirmed that, if the experienced orientations are different in the two eyes, each eye dominates over those neurones whose orientation preference corresponds to the orientation this eye has experienced. 4. When one eye is covered while the other sees only contours of one orientation, the ocular dominance distribution of cortical neurones shows a bias towards the open eye. Neurones dominated by this eye prefer orientations corresponding to the experienced range. Neurones preferring other orientations are shared between both eyes. 5. When vision is unimpaired in one eye and restricted to vertical contours in the other, binocularity is common among neurones preferring vertical orientations. Neurones with orientation preferences off the vertical are mainly monocular and dominated by the eye with unrestricted vision. 6. When normal monocular vision of one eye precedes restricted monocular vision of the other eye, only a few binocular units are encountered. Reversal of the initial effects of monocular experience is found only in neurones preferring the orientation that has been experienced by the newly opened eye. The other neurones remain dominated by the originally open eye. Thus, complementary distributions of orientation preferences are found for the two eyes. 7. A good correlation was found between the amount of orientational experience as determined by the number of orientations exposed and the number of normally tuned neurones. Conversely, the number of neurones responding to all orientations decreases with increasing amount of experience.

Animals↗