Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Primary Visual Cortex”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

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

At least 1,405 records · Page 78Linked to original sources

Specializations for chromatic and temporal signals in human visual cortex.

Neurological case studies and qualitative measurements suggest that regions within human extrastriate cortex are specialized for different perceptual functions, including color. However, there are few quantitative measurements of human extrastriate color specializations. We studied the chromatic and temporal responses in several different clusters of human visual field maps using functional magnetic resonance imaging. Contrast response functions were measured for luminance [(L + M)-cone], red-green [(L - M)-cone] and blue-yellow (S-cone) modulations at various temporal frequencies. In primary visual cortex (V1), temporal responsivities to luminance and red-green modulations are approximately constant up to 10 Hz, but responsivities to blue-yellow modulations decrease significantly. In ventral occipital cortex (VO), all colors elicit strong responses, and, for each color, low temporal frequency modulations are more effective than high temporal frequency modulations. Hence, VO represents the full range of color information but does not respond well to rapid modulations. Conversely, in human motion-selective cortex (MT+) and V3A, blue-yellow modulations elicit very weak responses, whereas luminance and red-green high temporal frequency modulations are equally or more effective than low temporal frequency modulations. Hence, these dorsal occipital regions respond well to rapid modulations, but not all color information is represented. Similar to human motion perception, MT+ and V3A respond powerfully to all temporal frequencies but only to some colors. Similar to human color perception, VO responds powerfully to all colors but only to relatively low temporal frequencies.

Brain Mapping↗

How the blind "see" Braille: lessons from functional magnetic resonance imaging.

What does the visual cortex of the blind do during Braille reading? This process involves converting simple tactile information into meaningful patterns that have lexical and semantic properties. The perceptual processing of Braille might be mediated by the somatosensory system, whereas visual letter identity is accomplished within the visual system in sighted people. Recent advances in functional neuroimaging techniques, such as functional magnetic resonance imaging, have enabled exploration of the neural substrates of Braille reading. The primary visual cortex of early-onset blind subjects is functionally relevant to Braille reading, suggesting that the brain shows remarkable plasticity that potentially permits the additional processing of tactile information in the visual cortical areas.

Blindness↗

A linear model fails to predict orientation selectivity of cells in the cat visual cortex.

1. Postsynaptic potentials (PSPs) evoked by visual stimulation in simple cells in the cat visual cortex were recorded using in vivo whole-cell technique. Responses to small spots of light presented at different positions over the receptive field and responses to elongated bars of different orientations centred on the receptive field were recorded. 2. To test whether a linear model can account for orientation selectivity of cortical neurones, responses to elongated bars were compared with responses predicted by a linear model from the receptive field map obtained from flashing spots. 3. The linear model faithfully predicted the preferred orientation, but not the degree of orientation selectivity or the sharpness of orientation tuning. The ratio of optimal to non-optimal responses was always underestimated by the model. 4. Thus non-linear mechanisms, which can include suppression of non-optimal responses and/or amplification of optimal responses, are involved in the generation of orientation selectivity in the primary visual cortex.

Animals↗

Comparison of discharge variability in vitro and in vivo in cat visual cortex neurons.

1. In neocortical slices, the majority of neurons fire quite regularly in response to constant current injections. But neurons in the intact animal fire irregularly in response to constant current injection as well as to visual stimuli. 2. To quantify this observation, we developed a new measure of variability, which compares only adjacent interspike intervals and is therefore less sensitive to rate variations than existing measures such as the coefficient of variation of interspike intervals. 3. We find that the variability of firing is much higher in cells of primary visual cortex in the anesthetized cat than in slice. The response to current injected from an intracellular electrode in vivo is also variable, but slightly more regular and less bursty than in response to visual stimuli. 4. Using a new technique for analyzing the variability of integrate-and-fire neurons, we prove that this behavior is consistent with a simple integrate-and-fire model receiving a large amount of synaptic background activity, but not with a noisy spiking mechanism.

Animals↗

Dynamics of responses of V1 neurons evoked by stimulation of different zones of receptive field.

The dynamics of receptive fields of 73 neurons in area 17 of cat visual cortex were studied using the temporal slice method. Three-dimensional maps of the receptive fields were plotted using the criterion of spike number in successive fragments (step 10 or 20 ms) of responses to 100 local flashes presented at different parts of the receptive field in random order. The size and configuration of such dynamically recorded receptive fields were then estimated. This allowed us to reveal the dynamic reorganization of all receptive fields 20-400 ms after stimulation. A small zone of responses appeared in the receptive field after initial latency, then it widened, received definitive configuration, and after that decreased and disappeared. The effect was reproducible under repeated estimations. The relationships between receptive field and the previously described orientation tuning dynamics, as well as between dynamics of receptive fields and their summation zones, mechanisms and possible functional meaning of the revealed effects for signal processing in the primary visual cortex are discussed.

Animals↗

The origin and topography of long-range intrinsic projections in cat visual cortex: a developmental study.

We investigated the morphological features of long range intrinsically projecting neurons and their pattern of axonal arborization in cat area 17 at different stages of postnatal development. In one set of experiments intracortically projecting cells were retrogradely labeled in vivo with rhodamine latex beads and then visualized by in vitro filling with Lucifer yellow. In another approach, intracortical fibers including the cells of origin were labeled postmortem in fixed brains with the lipophilic carbocyanine dye Dil. The results of this study indicate that the long-range intrinsic circuitry of the primary visual cortex develops in three major steps. The first step consists of the development of unclustered long-range axons in the two outer compartments of the cerebral cortex, layer I and the subplate. These early connections could serve as a scaffold for the organization of the tangential architecture of the neocortex as they originate from cells that are the first to receive synaptic input from extrinsic afferents. The second step consists of the outgrowth of horizontal axon collaterals originating from cells located in layers II-VI. During the first 2-3 weeks these connections still differ from those in the adult because they span shorter distances, originate more often from neurons with morphological features of nonpyramidal cells, and lack the precise clustering of the mature connections. The third step consists of a selection process that leads to the elimination of axon terminals from locations between the clusters of tangentially projecting neurons. This selection starts at the end of the second postnatal week and, hence, overlaps in time with the still proceeding elongation of axons and continues beyond the end of the fourth postnatal week when axon length has reached its maximal extent. This refinement process enhances the specificity of long-range connections and is probably influenced by visual experience.

Animals↗

The locus of attentional effects in texture segmentation.

Cuing covert spatial attention can increase spatial resolution. Here we pinpointed the specific locus of this effect using texture segmentation. At the level of visual cortex, texture segmentation theoretically involves passage of visual input through two layers of spatial linear filters separated by a pointwise nonlinearity. By manipulating the textures to differentially stimulate first- or second-order filters of various scales, we showed that the attentional effect consistently varied with the latter. These psychophysical results further support the hypothesis that attention increases resolution at the attended location and are consistent with an effect of attention at stages as early as the primary visual cortex.

Attention↗

Stimulus rate dependence of regional cerebral blood flow in human striate cortex, demonstrated by positron emission tomography.

The purpose of this investigation was to determine the relationship between the repetition rate of a simple sensory stimulus and regional cerebral blood flow (rCBF) in the human brain. Positron emission tomography (PET), using intravenously administered H2(15)O as the diffusible blood-flow tracer, was employed for all CBF measurements. The use of H2(15)O with PET allowed eight CBF measurements to be made in rapid sequence under multiple stimulation conditions without removing the subject from the tomograph, thus minimizing changes in base-line CBF and in head position due to longer intervals between scans. Nine normal volunteers each underwent a series of eight H2(15)O PET measurements of CBF. Initial and final scans were made during visual deprivation. The six intervening scans were made during visual activation with patterned-flash stimuli given in random order at 1.0-, 3.9-, 7.8-, 15.5-, 33.1-, and 61-Hz repetition rates. In each subject the region of greatest rCBF increase was determined. Within this region the rCBF was determined for every test condition and then expressed as the percentage change from the value of the initial unstimulated scan (rCBF% delta). Anatomical localization of the region of greatest rCBF response was performed employing bony landmarks from a lateral skull radiograph, a template of the cranium created from a transmission attenuation scan and a stereotaxic atlas. In every subject, striate cortex rCBF% delta varied systematically with stimulus rate. Between 0 and 7.8 Hz, rCBF% delta was a linear function of stimulus repetition rate. The rCBF response peaked at 7.8 Hz and then declined. The rCBF% delta during visual stimulation was significantly greater than that during visual deprivation for every stimulus rate except 1.0 Hz. The anatomical localization of the region of peak rCBF response was determined for every subject to be the mesial occipital lobes along the calcarine fissure, primary visual cortex. We conclude that stimulus rate is a significant determinant of rCBF response in the visual cortex. Investigators of brain responses to selective activation procedures should be aware of the potential effects of stimulus rate on rCBF and other measurements of cerebral metabolism. For cerebral responses to selective activation to be meaningfully interpreted, the stimulus repetition rate must be taken into consideration. Response amplitude may be maximized by proper rate selection or be undetectable due to selection of too high or too low a repetition rate. Stimulus rate must be controlled for when responses to unlike stimuli or performance tasks are compared or ambiguities will be present as to whether response differences are

Adult↗

Very slow brain potential fluctuations (< 0.5 Hz) in visual thalamus and striate cortex after their successive electrical stimulation in lightly anesthetized rats.

Recently accumulating evidence demonstrates the presence of very slow activity (< 0.5 Hz) in structures of the visual system of the brain. It was found in our laboratory earlier that specific and significant alterations of this activity (mainly in the domain of seconds) occurred in the visual system in response to illumination changes. The present study was performed in order to test the hypothesis that potentials in the domain of seconds reflect specific and direct interactions of the lateral geniculate nucleus (LGN) and the primary visual cortex (V1) during neural processing of sensory information. The experimental subjects were seven adult rats with chronic stereotaxic electrodes implanted in the LGN and V1. Animals were lightly anesthetized and the recordings were made in the LGN before and after electrical stimulation of V1 and also in the V1 before and after stimulation of LGN. The main findings were significant spectral changes in the domain of seconds in the V1 after LGN electrical stimulation and similar changes in the LGN after V1 electrical stimulation. These changes were manifested as significant increases in power in the domain of seconds (0.1-0.5 Hz). Significant responses were detected in the both LGN and V1 multisecond activities (pre- vs. post-stimulus recordings). The changes were opposite in direction in the LGN and V1. The obtained results support the conclusion that very slow activity in the domain of seconds reflects specific mechanisms of forward and backward interactions within the LGN-V1 thalamic-cortical-thalamic system, while multisecond activity relates to global neuronal activity fluctuations.

Anesthesia↗

Visual imagery and visual representation.

Among many controversies in visual neuroscience is whether visual imagery of objects, scenes and living beings is based upon contributions of the early visual areas or depends on hierarchical higher visual areas only, and whether the cortical areas subserving visual imagery are identical to those underlying visual perception. These questions are important for furthering our understanding of vision, since areas active in visual imagery might tell us how the visual cortex represents objects, scenes and living beings. Here, P.E. Roland and B. Gulyás present their hypothesis, based on experimental evidence in man and primates, that the visual areas subserving visual imagery are parieto-occipital and temporo-occipital visual association areas, and that these areas form only a subset of the visual areas engaged in perception. This hypothesis is consistent with the view that objects, scenes and living beings are represented, stored and re-evoked outside the domain of the primary visual cortex and its immediate neighbours.

Animals↗

Rapid adaptation to internal states as a coding strategy in visual cortex?

Adaptation is a prominent feature of biological neuronal systems. A common interpretation of adaptation in terms of function is that it provides flexibility for a neuronal system to perform well under varying external conditions, for example by adjusting the input/output relation of a sensory system with reference to the ensemble of stimuli the organism currently perceives. This interpretation, however, only applies if the time-scale of adaptation is slower than the time-scale at which the environment changes. Experimentally it is observed, however, that adaptation can be very rapid. Spike-frequency adaptation of cortical neurons, for example, occurs on a time-scale of approximately 100 ms. Here we show that those rapid adaptation processes can also be understood within the framework of information theory. We start with the hypothesis that neuronal codes are designed to optimize the information a neuronal representation conveys about an input stimulus for any increasing time window beginning with stimulus onset, and we show that this implies a rapid adaptation of the neuronal code on the time-scale of stimulus presentation. Adaptation, however, does not occur because the state of the environment changes. Rather it is a reaction to changes of the organisms own internal state, e.g. the level of noise in the neuronal representation. We apply this approach to a model of an orientation hypercolumn in the primary visual cortex, and predict that inter-columnar interactions should adapt on the time-scale of a typical fixation period ( approximately 300 ms).

Adaptation, Psychological↗

Submillimeter functional localization in human striate cortex using BOLD contrast at 4 Tesla: implications for the vascular point-spread function.

Using multislice segmented echoplanar imaging at 4 T, we have measured an upper bound to the cortical vasculature point-spread function (PSF) using functional magnetic resonance imaging (fMRI) in humans. Our experiments demonstrate that cortical subunits that are approximately 700 microm apart can be resolved using the early part of the hyperoxygenation phase of the blood oxygenation level-dependent (BOLD) effect. This was accomplished using brief (4 sec) single trials of monocular and binocular stimulation of ocular dominance columns in human primary visual cortex. The data suggest that at even higher magnetic fields, the cortical vasculature PSF may be limited by the extent and nature of horizontal connections and not signal-to-noise ratio.

Adult↗

Functional projections from striate cortex and superior temporal sulcus to the nucleus of the optic tract (NOT) and dorsal terminal nucleus of the accessory optic tract (DTN) of macaque monkeys.

The nucleus of the optic tract (NOT) and the dorsal terminal nucleus of the accessory optic tract (DTN) have been recognized to be relevant structures for optokinetic and vestibuloocular reflexes. NOT-DTN neurons relay visual information to the vestibular nuclei via the nucleus prepositus hypoglossi and to the flocculus via the dorsal cap of the inferior olive. It has been previously shown that in carnivores the NOT-DTN receives information from primary visual cortical areas in addition to the direct retinal input. In this study we demonstrate the presence and some functional characteristics such as latency and evicacy of considerable cortical projections to the NOT-DTN in macaque monkeys. In anaesthetized and paralyzed monkeys NOT-DTN neurons were identified physiologically and tested for cortical input by electrical stimulation in various cortical areas. Successful sites of stimulation to activate NOT-DTN neurons orthodromically lie in the primary visual cortex (V1) and in the motion-processing areas in the superior temporal sulcus (STS). In contrast, electrical stimulation in area V4 and in parietal areas in most cases did not yield orthodromic responses. Overall latencies of action potentials elicited by stimulation in V1 were 0.5 ms longer than those elicited from STS. These short latency differences between V1 and STS stimulation suggest a direct projection from both V1 and STS to the NOT-DTN. The physiological results were supported by the results of anatomical experiments by using horseradish peroxidase as anterograde tracer. Both injections into V1 and into the lower bank of STS resulted in anterogradely labelled fibers and terminals around the recording sites of direction-specific NOT-DTN neurons. This paper is a first step in clarifying the significance of corticofugal projections from individual areas involved in the analysis of visual motion for the optokinetic reflex.

Animals↗

Structural modeling of functional visual pathways mapped with 2-deoxyglucose: effects of patterned light and footshock.

This paper describes the first application of structural modeling to the visual system. Structural modeling, or path analysis, is a mathematical method that allows for the quantification of the functional strengths of anatomical connections between the structures that form a neural system. The objective was to demonstrate how structural modeling can be used to determine the functional interrelationships between brain structures that form the visual system and how these interrelationships change under different conditions. Data were obtained from measures of 2-deoxyglucose uptake in the visual system of rats presented with either patterned light or darkness. The effects of arousing footshock on visual system operations were also investigated. Models based on the anatomical connections and the interregional correlations between metabolic activity data were used to determine path coefficients representing the magnitude of the influence of each directional path. Statistical evaluation of the models revealed that the dominant positive influences on visual system activity in the darkness were the tectocortical subsystem and the descending connections from secondary visual cortex. In the patterned light model, the total influence of the geniculocortical subsystem was higher than in the dark, and the tectocortical pathways showed both a reduction and a shift in the direction of effects. The models also revealed that the effects of footshock-induced arousal on visual system operations depended upon the visual environment and on extra-visual influences. The footshock led to an increase in the interaction of the two main subsystems at the level of connections between primary visual cortex and the lateral posterior nucleus, and a descending negative influence from the secondary visual cortex became dominant. The models are discussed in the context of conventional analyses to show how structural modeling allows for the determination of much more information about the functional interactions within the visual system of subjects under different experimental conditions.

Animals↗

Ocular dominance shift in kitten visual cortex caused by imbalance in retinal electrical activity.

Monocular lid suture during the sensitive period early in the life of a kitten disrupts normal development of inputs from the two eyes to the visual cortex, causing a decrease in the fraction of cortical cells responding to the deprived eye. Such an ocular dominance shift has been assumed to depend on patterned visual experience, because no change in cortical physiology is produced by inequalities between the two eyes in retinal illumination or temporally modulated diffuse light stimulation. A higher-level process, involving gating signals from areas outside striate cortex, has been proposed to ensure that sustained changes in synaptic efficacy occur only in response to behaviourally significant visual inputs. To test whether such a process is necessary for ocular dominance plasticity, we treated 4-week-old kittens with visual deprivation and monocular tetrodotoxin (TTX) injections to create an imbalance in the electrical activities of the two retinas in the absence of patterned vision. After 1 week of treatment we determined the ocular dominance distribution of single units in primary visual cortex. In all kittens studied, a significant ocular dominance shift was found. In addition to this physiological change, there was an anatomical change in the lateral geniculate nucleus, where cells were larger in laminae receiving input from the more active eye. Our results indicate that patterned vision is not necessary for visual cortical plasticity, and that an imbalance in spontaneous retinal activity alone can produce a significant ocular dominance shift.

Animals↗

Modulation of connectivity in visual pathways by attention: cortical interactions evaluated with structural equation modelling and fMRI.

Electrophysiological and neuroimaging studies have shown that attention to visual motion can increase the responsiveness of the motion-selective cortical area V5 and the posterior parietal cortex (PP). Increased or decreased activation in a cortical area is often attributed to attentional modulation of the cortical projections to that area. This leads to the notion that attention is associated with changes in connectivity. We have addressed attentional modulation of effective connectivity using functional magnetic resonance imaging (fMRI). Three subjects were scanned under identical stimulus conditions (visual motion) while varying only the attentional component of the task. Haemodynamic responses defined an occipito-parieto-frontal network, including the, primary visual cortex (V1), V5 and PR A structural equation model of the interactions among these dorsal visual pathway areas revealed increased connectivity between V5 and PP related to attention. On the basis of our analysis and the neuroanatomical pattern of projections from the prefrontal cortex to PP we attributed the source of modulatory influences, on the posterior visual pathway, to the prefrontal cortex (PFC). To test this hypothesis we included the PFC in our model as a 'modulator' of the pathway between V5 and PP, using interaction terms in the structural equation model. This analysis revealed a significant modulatory effect of prefrontal regions on V5 afferents to posterior parietal cortex.

Analysis of Variance↗

Neuronal computation of disparity in V1 limits temporal resolution for detecting disparity modulation.

The human ability to detect modulation of binocular disparity over time is poor compared with detection of luminance modulation. We examined the physiological origin of this limitation by analyzing neuronal responses to temporal modulation of binocular disparity in striate cortex of awake monkeys. When neurons were presented with random-dot stereograms in which disparity varied sinusoidally over time, their responses modulated at the stimulus temporal frequency, with little change in mean firing rate. We calculated modulation amplitude as a function of temporal frequency and compared this with the psychophysical performance of four human observers. Neuronal and psychophysical functions showed similar peak frequencies (2 Hz) and comparable high-cut frequencies (10 and 5.5 Hz, respectively). Thus, V1 (primary visual cortex) neurons appear to limit psychophysical performance. The temporal resolution of the same neurons for contrast modulation was approximately 2.5 times greater, which parallels the superior psychophysical performance for contrast. There is a simple mathematical explanation for this difference: it results from calculating cross-correlation between temporally broadband monocular images that are bandpass filtered before measuring correlation. The limit on temporal resolution is a direct consequence of the binocular energy model that adds to the list of properties of human stereoscopic performance that are explained by this simple model of disparity encoding in V1: the same neurons can account for the performance of psychophysical tasks that result in either high (contrast) or low (disparity) temporal resolution. Because this principle holds whenever a broadband input is bandpass filtered before computing correlation, it may limit the resolution of other neuronal systems.

Animals↗

Functional mapping of the human visual cortex by magnetic resonance imaging.

Knowledge of regional cerebral hemodynamics has widespread application for both physiological research and clinical assessment because of the well-established interrelation between physiological function, energy metabolism, and localized blood supply. A magnetic resonance technique was developed for quantitative imaging of cerebral hemodynamics, allowing for measurement of regional cerebral blood volume during resting and activated cognitive states. This technique was used to generate the first functional magnetic resonance maps of human task activation, by using a visual stimulus paradigm. During photic stimulation, localized increases in blood volume (32 +/- 10 percent, n = 7 subjects) were detected in the primary visual cortex. Center-of-mass coordinates and linear extents of brain activation within the plane of the calcarine fissure are reported.

Blood Volume↗