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 1,675 records · Page 93Linked to original sources
PubMed2006

Integrity of lateral and feedbackward connections in visual processing in children with pervasive developmental disorder.

Enhanced visual detail processing in subjects with pervasive developmental disorder (PDD) has been related to impairments in feature integration. The functional integrity of two types of neuronal connections involved in visual feature integration, namely horizontal and feedbackward connections, were tested. Sixteen children with PDD and 17 age- and IQ-matched control children (mean age 13.3 years) were included. In a texture segregation task the difference in ERP response to homogeneous and checkered visual stimuli was determined. Additionally, in a contour integration task subjects had to point out a contour consisting of colinearly aligned Gabor signals in backgrounds increasing in noise. Children with PDD showed a normal performance on the contour integration task, suggesting that neurons in the primary visual cortex of children with PDD can effectively integrate the activity of local detectors that process different aspects of the same object information by making use of long-range lateral connections. The amplitude of ERP activity related to texture segregation was also not different between the PDD and control groups, indicating functional visual feedback mechanisms between V1 and higher order areas in subjects with PDD. However, a difference in latency of texture-segmentation related activity between the groups was noted. This effect did not reach significance, which could be due to the small N of the study. Therefore, the data need replication in a study with larger samples before more definitive conclusions can be drawn.

Adolescent↗
PubMed2006

More accurate sound localization induced by short-term light deprivation.

Crossmodal reorganization processes in the brain are mainly associated with early blindness, on the assumption that recruitment of genuine visual areas, such as primary visual cortex, for non-visual functions results in superior auditory and tactile performance of blind, compared to sighted, humans. This study shows that in sighted subjects the accuracy of sound localization, measured by a task of head pointing to acoustic targets, is reversibly increased after short-term light deprivation of 90 min. However, only the systematic deviations from target positions (constant error) were reduced after light deprivation, while the general precision of head pointing remained unchanged. Return to pre-deprivation values was observed after 180 min of re-exposure to light. The post-deprivation change was similar, though less in magnitude, to the effect of blindness that was demonstrated previously. Generally, these findings indicate that auditory-visual crossmodal plasticity can be quite rapidly initiated by deprivation of the visual cortex from visual input. It seems possible that visual deprivation has an influence on neuronal circuits, that are involved in processing of auditory information in visual brain areas of normal sighted humans. Since exclusively the constant error in sound localization, not general performance, was changed, the present effect of visual deprivation may, however, not be attributable to reorganization processes in the sense of a compensation for the absence of vision. It is more likely that the observed change in accuracy was specifically induced by the absence of visual calibration of the neural representation of auditory space during light deprivation.

Acoustic Stimulation↗
PubMed2005

Early computational processing in binocular vision and depth perception.

Stereoscopic depth perception is a fascinating ability in its own right and also a useful model of perception. In recent years, considerable progress has been made in understanding the early cortical circuitry underlying this ability. Inputs from left and right eyes are first combined in primary visual cortex (V1), where many cells are tuned for binocular disparity. Although the observation of disparity tuning in V1, combined with psychophysical evidence that stereopsis must occur early in visual processing, led to initial suggestions that V1 was the neural correlate of stereoscopic depth perception, more recent work indicates that this must occur in higher visual areas. The firing of cells in V1 appears to depend relatively simply on the visual stimuli within local receptive fields in each retina, whereas the perception of depth reflects global properties of the stimulus. However, V1 neurons appear to be specialized in a number of respects to encode ecologically relevant binocular disparities. This suggests that they carry out essential pre-processing underlying stereoscopic depth perception in higher areas. This article reviews recent progress in developing accurate models of the computations carried out by these neurons. We seem close to achieving a mathematical description of the initial stages of the brain's stereo algorithm. This is important in itself--for instance, it may enable improved stereopsis in computer vision--and paves the way for a full understanding of how depth perception arises.

Animals↗
PubMed2006

Zap! Magnetic tricks on conscious and unconscious vision.

Blindsight, the remarkable capability to react to unseen visual stimuli, has thus far only been demonstrated in patients and monkeys with a lesion to primary visual cortex. A recent study by Boyer, Harrison and Ro demonstrates blindsight in normal human observers, using TMS to block visual processing. Combined with other work, this opens new vistas towards understanding mechanisms of conscious and unconscious vision.

Animals↗
PubMed2005

Circuits that build visual cortical receptive fields.

Neural sensitivity to basic elements of the visual scene changes dramatically as information is handed from the thalamus to the primary visual cortex in cats. Famously, thalamic neurons are insensitive to stimulus orientation whereas their cortical targets easily resolve small changes in stimulus angle. There are two main types of cells in the visual cortex, simple and complex, defined by the structure of their receptive fields. Simple cells are thought to lay the groundwork for orientation selectivity. This review focuses on approaches that combine anatomy with physiology at the intracellular level, to explore the circuits that build simple receptive fields and that help to maintain neural sensitivity to stimulus features even when luminance contrast changes.

Animals↗
PubMed2003

Colour and luminance selectivity of spatial and temporal interactions in orientation perception.

Previous studies have commented upon the similar phenomenology of simultaneous and successive interactions in the perception of orientation. These similarities have been taken as evidence of common mechanisms underlying the simultaneous tilt illusion (TI) and the successive tilt aftereffect (TAE). We measured the TI and TAE for four subjects for combinations of test and inducing stimuli modulated along either the same or orthogonal axes of colour space within the L+M+S, L-M colour-luminance plane. The largest TI and TAE were found when test and inducer were modulated along the same axis of colour space. The TI consistently showed greater selectivity for colour/luminance than the TAE. The results are discussed in relation to the known chromatic properties of the primate visual pathways. Specifically, we suggest that both the TI and TAE involve colour- and luminance-specific neurons in primary visual cortex as well as cue-invariant mechanisms in extrastriate cortex.

Color Perception↗
PubMed2004

Temporal dependence of local motion induced shifts in perceived position.

It has been shown that a moving visual pattern can influence the perceived position of outlying, briefly flashed objects. Using a rotating bar as an inducing stimulus we observed a shift, in the direction of motion, of the perceived position of small bars flashed together on either side of the moving bar. The greatest shift occurred when the 13 ms flashes were presented 60 ms before the rotating bar came closest to their locations. By varying rotation speed we showed that the peak effect was determined by the temporal rather than the spatial interval. The motion induced shift could be attenuated by introducing background flickering dots. The perceived shift decreased with distance from motion when the eccentricity of the flashes was kept constant. We conclude that the shift reflects feedback to primary visual cortex from motion selective cells in extrastriate cortex with receptive fields that overlap the retinal location of the flash.

Feedback, Psychological↗
PubMed2004

A visual motion sensor based on the properties of V1 and MT neurons.

The motion response properties of neurons increase in complexity as one moves from primary visual cortex (V1), up to higher cortical areas such as the middle temporal (MT) and the medial superior temporal area (MST). Many of the features of V1 neurons can now be replicated using computational models based on spatiotemporal filters. However until recently, relatively little was known about how the motion analysing properties of MT neurons could originate from the V1 neurons that provide their inputs. This has constrained the development of models of the MT-MST stages which have been linked to higher level motion processing tasks such as self-motion perception and depth estimation. I describe the construction of a motion sensor built up in stages from two spatiotemporal filters with properties based on V1 neurons. The resulting composite sensor is shown to have spatiotemporal frequency response profiles, speed and direction tuning responses that are comparable to MT neurons. The sensor is designed to work with digital images and can therefore be used as a realistic front-end to models of MT and MST neuron processing; it can be probed with the same two-dimensional motion stimuli used to test the neurons and has the potential to act as a building block for more complex models of motion processing.

Humans↗
PubMed2005

Aftereffect of adaptation to Glass patterns.

Our visual systems constantly adapt their representation of the environment to match the prevailing input. Adaptation phenomena provide striking examples of perceptual plasticity and offer valuable insight into the mechanisms of sensory coding. Here, we describe an aftereffect of adaptation to a spatially structured image whereby an unstructured test stimulus takes on illusory structure locally perpendicular to that of the adaptor. Objective measurement of the strength of the aftereffect for different patterns suggests a neural locus of adaptation prior to the extraction of complex form in the visual processing hierarchy, probably at the level of primary visual cortex. This view is supported by further experiments showing that the aftereffect exhibits partial interocular transfer but complete transfer across opposite contrast polarities. However, the aftereffect does show weak position invariance, suggesting that adaptation at higher levels of the visual system may also contribute to the effect.

Adaptation, Ocular↗
PubMed2005

Human cortical responses to contrast modulations of visual noise.

We studied visual evoked potentials (VEPs) elicited by second-order contrast modulations of binary dynamic noise and first-order luminance modulations. Using a 3-point Laplacian operator centred on Oz, we found that contrast modulations of both low and higher spatial frequencies elicited a negative component whose latency was about 200 ms. The latency of this component was significantly longer than that of the early Laplacian components to first-order luminance modulations. These findings could be due to slower first-stage linear filters and additional processing stages of the second-order pathway. The topographical analysis of scalp recorded VEPs to central and half-field stimulation has suggested that the responses to second-order patterns are likely to be generated by neuronal structures within the primary visual cortex which may have inputs from extrastriate neurons via feedback connections.

Brain Mapping↗
PubMed2005

Two sources of error in pop-out localization.

An odd-one-out stimulus, such as a vertical bar among horizontals, pops out from the background and is easily detected, but its location may be slightly ambiguous. Four observers were asked to pinpoint these stimuli on thousands of trials, in 5 x 5 and 9 x 9 arrays of Gabor patches. We found they made frequent errors toward neighbors of the target. Over a range of performance from 41% to 96% correct, the frequency of neighbor errors was well described by a linear function of the total error frequency, a function that might result from mixing together two spatial distributions--one broad, the other narrow. We suggest that these represent two sources of error in pop-out localization; one might correspond to a higher visual area with imprecise retinotopic mapping, and the other to a more fine-grained localization process in primary visual cortex.

Depth Perception↗
PubMed2006

Short- and long-range spatial interactions: a redefinition.

First level short- and long-range spatial interactions are considered to be processed in the primary visual cortex. In psychophysics, they are measured with two kinds of stimuli, Gabor patches and lines/points. Each has its own short- and long-range definitions. We show that first, in terms of visual angle separation, the two definitions do not correspond to identical scales of interactions and second, that Gabor data can be matched to the lines/points definition by properly considering the observed effects. As a consequence, three regimes of spatial interaction are present: a case where overlapping of stimuli is present, and two others for spatially separated stimuli which we define as the short- and long-range regimes. Both types of stimuli show compatible lateral interactions and, we think, permit the measurement of the same underlying mechanisms.

Contrast Sensitivity↗
PubMed2006

Distorting visual space with sound.

Attentional repulsion is described as the perceived displacement of a vernier stimulus in a direction that is opposite to a brief peripheral visual cue (Suzuki & Cavanagh, 1997). Here, we demonstrate that visual repulsion can also be elicited using lateralized sounds. Given that repulsion is believed to be occurring in early retinotopic visual areas, these results raise the possibility that the location of a sound could directly influence the pattern of activity as early as primary visual cortex.

Acoustic Stimulation↗
PubMed2006

Luminance-contrast mechanisms in humans: visual evoked potentials and a nonlinear model.

Isolated-checks were luminance-modulated temporally to elicit VEPs. Bright or dark checks were used to drive ON or OFF pathways, and low or high-contrast conditions were used to emphasize activity from magnocellular or parvocellular pathways. Manipulation of stimulus parameters and frequency analysis of the VEP were performed to obtain spatial and contrast-response functions. A biophysical explanation is offered for why the opposite polarity stimuli drive selectively ON and OFF pathways in primary visual cortex, and a lumped biophysical model is proposed to quantify the data and characterize changes in the dynamics of the system with contrast given a limited number of parameters. Response functions were found to match the characteristics of the targeted pathways.

Adult↗
PubMed2004

Axonal transport of recombinant baculovirus vectors.

Targeted gene delivery to neurons is crucial to effective gene therapy of neurodegenerative diseases. Several types of viral gene vectors may target neurons through retrograde axonal transport to somas of projection neurons after viral internalization at axon terminal fields. In this report we demonstrate for the first time that recombinant baculovirus vectors could migrate by axonal transport to cell bodies, resulting in transgene expression in projection neurons. After stereotaxic injection of Cy3-labeled baculovirus vectors into the rat striatum, retrograde axonal transport of the baculovirus vectors was observed along the corticostriatal pathway and nigrostriatal pathway. Furthermore, after intra-vitreous body injection, anterograde axonal transport and transsynaptic transport of the virus particles were observed in defined connections of the visual system, from the retina to the optic nerve, the lateral geniculate body, the superior colliculus, and the primary visual cortex. PCR analysis confirmed the existence of transported viral DNA in the tissue samples collected from projection fields. Driven by a neuron-specific promoter, transgene expression from the recombinant baculovirus vectors was detectable in target regions remote from injection sites. The attributes of baculovirus vectors in the bidirectional axonal transport and transneuronal transport in neural circuits of the central nervous system could be utilized for targeted gene delivery.

Animals↗
PubMed1993

Functional brain mapping by blood oxygenation level-dependent contrast magnetic resonance imaging. A comparison of signal characteristics with a biophysical model.

It recently has been demonstrated that magnetic resonance imaging can be used to map changes in brain hemodynamics produced by human mental operations. One method under development relies on blood oxygenation level-dependent (BOLD) contrast: a change in the signal strength of brain water protons produced by the paramagnetic effects of venous blood deoxyhemoglobin. Here we discuss the basic quantitative features of the observed BOLD-based signal changes, including the signal amplitude and its magnetic field dependence and dynamic effects such as a pronounced oscillatory pattern that is induced in the signal from primary visual cortex during photic stimulation experiments. The observed features are compared with the results of Monte Carlo simulations of water proton intravoxel phase dispersion produced by local field gradients generated by paramagnetic deoxyhemoglobin in nearby venous blood vessels. The simulations suggest that the effect of water molecule diffusion is strong for the case of blood capillaries, but, for larger venous blood vessels, water diffusion is not an important determinant of deoxyhemoglobin-induced signal dephasing. We provide an expression for the apparent in-plane relaxation rate constant (R2*) in terms of the main magnetic field strength, the degree of the oxygenation of the venous blood, the venous blood volume fraction in the tissue, and the size of the blood vessel.

Biophysical Phenomena↗
PubMed2000

How the brain uses time to represent and process visual information(1).

Information theory provides a theoretical framework for addressing fundamental questions concerning the nature of neural codes. Harnessing its power is not straightforward, because of the differences between mathematical abstractions and laboratory reality. We describe an approach to the analysis of neural codes that seeks to identify the informative features of neural responses, rather than to estimate the information content of neural responses per se. Our analysis, applied to neurons in primary visual cortex (V1), demonstrates that the informative precision of spike times varies with the stimulus modality being represented. Contrast is represented by spike times on the shortest time scale, and different kinds of pattern information are represented on longer time scales. The interspike interval distribution has a structure that is unanticipated from the firing rate. The significance of this structure is not that it contains additional information, but rather, that it may provide a means for simple synaptic mechanisms to decode the information that is multiplexed within a spike train. Extensions of this analysis to the simultaneous responses of pairs of neurons indicate that neighboring neurons convey largely independent information, if the decoding process is sensitive to the neuron of origin and not just the average firing rate. In summary, stimulus-related information is encoded into the precise times of spikes fired by V1 neurons. Much of this information would be obscured if individual spikes were merely taken to be estimators of the firing rate. Additional information would be lost by averaging across the responses of neurons in a local population. We propose that synaptic mechanisms sensitive to interspike intervals and dendritic processing beyond simple summation exist at least in part to enable the brain to take advantage of this extra information.

Action Potentials↗
PubMed1986

Regional distribution of [3H]naloxone binding in the brain of a newborn rhesus monkey.

The distribution of opiate receptors in the brain of a newborn monkey (Macaca mulatta) was mapped by in vitro autoradiographic localization of [3H]naloxone binding to tissue sections. The autoradiographs of the newborn brain were compared to those from two adult brains. The distribution of opiate receptors appeared to be adult-like in subcortical structures (both limbic and nonlimbic) and allocortical areas. By contrast, all neocortical areas, except the primary visual cortex, lacked at birth the laminar specific patterns that characterize the adult. The results therefore suggest that, like many other aspects of neocortical maturation, such as dendritic growth, synaptogenesis, myelination and neurotransmitter concentrations, the distribution of opiate receptors continues to develop postnatally.

Animals↗