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PubMedDate not supplied

[Reorganization of changes in the receptive fields of cat visual cortex neurons during light anesthesia].

The activity of 127 neurones of the primary visual cortex (17th field) was recorded in unanaesthetized cats immobilized with d-tubocurarine, during calm alertness and during short sleep caused by intravenous administration of 5% water solution of sombrevine in a dose of 1.5 mg/kg. In all of the studied cells, considerable rearrangements in sizes and in form of the receptive fields (RF) were recorded. The studied neurones with excitatory RF centres formed two main groups. The first one comprised 52% of cells; the central excitatory zone of their RF became considerably wider due to administration of sombrevine. In the second group (48%), the drug produced a significant reduction of RF. Neurones with an inhibitory RF centre exhibited a different relation of RF changes: the RFs became larger in 68% and narrower in 32% of the studied cells. Cortical and reticular mechanisms are discussed of the observed rearrangements in the RFs of visual cortical neurones under the action of sombrevine--a general anaesthetic, provoking a short-term decrease in the brain functional state.

Anesthesia, General↗
PubMed2003

Visual and electrical evoked response recorded from subdural electrodes implanted above the visual cortex in normal dogs under two methods of anesthesia.

Sensitive methods are required to record electrical evoked potentials over the visual cortex to evaluate the efficacy and safety of a retinal prosthesis before it can be implanted on the retinal surface of patients afflicted by outer retinal diseases. This study was designed to examine subdural electrodes as a mean to evaluate cortical evoked potentials in response to light and electrical stimulation of the retina in three dogs under two methods of anesthesia-halothane and propofol. Results showed that subdural electrodes could be stabilized over the visual cortex for several (3-5) months, and that they were 6.95 times more sensitive than subdermal electrodes in recording cortical visual evoked potentials (VEPs) and 4.31 times more sensitive in recording cortical electrical evoked potentials under both methods of anesthesia. The waveforms' shape changed for each electrode in the subdural array during 6/6 (100%) and 20/38 (52%) multi-channel recording sessions under halothane and propofol, respectively. This change could point to a cortical retinotopic organization versus hierarchical organization of different cortical areas for a given retinal stimulus. In summary, subdural electrodes show promising results for recording visual and electrical evoked responses (EERs) and thus for evaluation of the retinal prosthesis.

Anesthesia↗
PubMed1996

Laminar distribution of MK-801, kainate, AMPA, and muscimol binding sites in cat visual cortex: a developmental study.

We used quantitative autoradiography to determine whether the development of glutamate receptors correlates with the sensitive period for monocular deprivation in the visual cortex. To study glutamate receptors, we incubated sections of cat visual cortex with tritiated (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5,10imin e-maleate (MK-801), tritiated kainate, and tritiated amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid (AMPA). [3H]MK-801 is a noncompetitive ligand for the N-methyl-D-aspartate (NMDA) receptor. [3H]kainate and [3H]AMPA are competitive ligands for non-NMDA receptors. We used [3H]muscimol, which binds to GABAA receptors, so that we would have one control ligand that binds to a nonglutamate receptor. When all layers were combined, the results confirmed our previous studies with homogenate binding. [3H]MK-801 and [3H]kainate binding were significantly greater at 42 days than at earlier or later times. [3H]AMPA and [3H]muscimol binding did not show such a peak. This suggests that MK-801 and kainate binding sites are more likely to be involved in plasticity than are AMPA and muscimol binding sites. In layers 2/3, MK-801 had the greatest age-dependent changes; in layers 5 and 6, kainate binding changed most with age. This suggests that the mechanisms of plasticity may vary with cortical layer.

Animals↗
PubMed2001

Oriented axon projections in primary visual cortex of the monkey.

One important aspect of the functional architecture of primary visual cortex is the circuitry that accounts for the receptive field properties of neurons. The anatomy that underlies retinotopy and ocular dominance is well known, but no anatomical structure related to orientation selectivity has been found in primates. We examined whether the arrangement of local axon systems projecting within the cortical layers might be correlated with orientation preference in New World monkeys. We found that axons in layer 3 spread out from the site of a tracer injection in an anisotropic manner and that this elongated distribution is aligned with the preferred orientation recorded at each site. Moreover, within a few degrees of the foveal representation, the majority of the axon terminals fall within or just outside of the limits of the cortical mapping of the classical receptive field. Thus local axons produce a field of monosynaptic excitation that aligns with orientation axes and reaches neurons that have receptive fields which are adjacent in visual space.

Animals↗
PubMed2000

Rapid extragranular plasticity in the absence of thalamocortical plasticity in the developing primary visual cortex.

Monocular deprivation during early postnatal development remodels the circuitry of the primary visual cortex so that most neurons respond poorly to stimuli presented to the deprived eye. This rapid physiological change is ultimately accompanied by a matching anatomical loss of input from the deprived eye. This remodeling is thought to be initiated at the thalamocortical synapse. Ocular dominance plasticity after brief (24 hours) monocular deprivation was analyzed by intrinsic signal optical imaging and by targeted extracellular unit recordings. Deprived-eye responsiveness was lost in the extragranular layers, whereas normal binocularity in layer IV was preserved. This finding supports the hypothesis that thalamocortical organization is guided by earlier changes at higher stages.

Animals↗
PubMed2006

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↗
PubMed1981

[Dynamics of orientational tuning of visual cortex neurons in the cat].

Orientational tuning of singly units in the primary visual cortex of a nonanesthetized paralyzed cat was studied by usual criteria (number of spikes and maximal frequency of the response) and by "time slices" method. A computer plotted graphs of orientational tuning for successive time intervals with a step of 10 or 20 ms (differential slices) or for prolonged intervals with same step (integral slices). In both cases it was revealed that in all the investigated units orientational tuning markedly changed in time, most often in wideness of characteristic and in 87% of cases in preferred orientation range was detected: preferred orientation systematically moved for 15-112 degrees in successive moments during some tens of ms of the first and the second burst of spikes. A possible functional significance of the data revealed and the neurophysiological mechanisms are discussed.

Animals↗
PubMedDate not supplied

A model of contextual interactions and contour detection in primary visual cortex.

A new model of contour extraction and perceptual grouping in the primary visual cortex is presented and discussed. It differs from previous models since it incorporates four main mechanisms, according to recent physiological data: a feed-forward input from the lateral geniculate nucleus, characterized by Gabor elongated receptive fields; an inhibitory feed-forward input, maximally oriented in the orthogonal direction of the target cell, which suppresses non-optimal stimuli and warrants contrast invariance; an excitatory cortical feedback, which respects co-axial and co-modularity criteria; and a long-range isotropic feedback inhibition. Model behavior has been tested on artificial images with contours of different curvatures, in the presence of considerable noise or in the presence of broken contours, and on a few real images. A sensitivity analysis has also been performed on the role of intracortical synapses. Results show that the model can extract correct contours within acceptable time from image presentation (30-40 ms). The feed-forward input plays a major role to set an initial correct bias for the subsequent feedback and to ensure contrast-invariance. Long-range inhibition is essential to suppress noise, but it may suppress small contours due to excessive competition with greater contours. Cortical excitation sharpens the initial bias and improves saliency of the contours. Model results support the idea that contour extraction is one the primary steps in the visual processing stream, and that local processing in V1 is able to solve this task even in difficult conditions, without the participation of higher visual centers.

Feedback↗
PubMed1983

Retinotopic organization of striate and extrastriate visual cortex in the hooded rat.

The visuotopic organization of the primary visual cortex (area 17) and the extrastriate visual regions surrounding it (areas 18a and 18) has been studied in gray rats using standard microelectrode mapping techniques. The results confirm and extend previous observations in the rat. Apart from the representation of the contralateral visual field (VF) in area 17, in which the upper VF is represented caudally and the nasal VF laterally, there are additional representations of the VF in the extrastriate cortex. In lateral extrastriate cortex (area 18a) there are at least 4 such representations, namely lateromedial (LM), anterolateral (AL), laterointermediate (LI) and laterolateral (LL). In LM (second visual area) the upper VF is represented caudally and the nasal VF medially, being thus a mirror image of V1. In AL (third visual area) the upper VF is represented rostrally and the nasal VF, medially, being thus a mirror image of LM. In LI, the upper VF is medial and the nasal VF, lateral, being thus a mirror image of LM, or a reduced copy of V1. In medial extrastriate cortex (area 18) there are two representations of the temporal VF, labeled anteromedial (AM) and posteromedial (PM). In AM, the upper temporal VF is medial and the lower temporal VF, lateral, the extreme temporal field being rostral. The 30 degrees azimuth provides the boundary between AM and PM. Thus, AM is organized as a counter-clockwise rotation by 90 degrees of the V1 representation. In PM, the upper lower VF topography is like in AM, but the extreme temporal VF is caudal, being thus a mirror image of AM.

Animals↗
PubMed1980

Annual review of section on ocular disease: diseases of the optic nerve, tracts, and visual cortex.

The ophthalmic literature dealing with diseases of the optic nerve, tracts, and visual cortex was reviewed for the period November 1977 to December 1978. Fifty-nine papers of interest to optometrists have been abstracted. Main areas of interest include: role of axoplasmic transport in production of disc edema and cotton-wool spots; ocular effects of local and systemic vascular disturbances; congenital abnormalities of the eye alone and in association with other bodily malformation; field testing, including an ingenious ophthalmoscopic method which can lead to detection of very small scotomas; a new quantitative method for assessing integrity of the optic nerve in multiple sclerosis and related conditions; stimulating questions on the development of optic atrophy and on its relation to retinal vascularity; considerations of acquired and congenital abnormalities of the cavernous sinus and their ocular manifestations; swinging-flashlight test in hemianoptic patients; a case of subacute sclerosing panecephalitis; methods to enhance magnification during opthalmoscopy; methods enabling a closer investigation of the retinal nerve fiber layer.

Adolescent↗
PubMed1990

An analysis of neural spike-train distributions: determinants of the response of visual cortex neurons to changes in orientation and spatial frequency.

A previously unexploited method of examining neural spike-trains was applied to data obtained from cells in the visual cortex. Distributions of interspike intervals recorded extracellularly from cat visual cortex under four conditions were analyzed. Stimuli were gratings differing in orientation and spatial frequency. The probability density function of first passage time for a random walk with drift process, which is defined by its barrier height and drift coefficient, was used to characterize the generating process of axonal discharge under resting and stimulus conditions. Drift coefficient and barrier height were derived from the sample mean and standard deviation of the measured inter-spike intervals. For cells with simple receptive fields, variations in the drift coefficient were produced by changes in orientation and spatial frequency. Variations in barrier height were produced only by changes in orientation of the stimulus.

Animals↗
PubMed1995

[The effect of stimulation of the suprachiasmatic and supraoptic nuclei of the anterior hypothalamus on the evoked activity of the visual cortex in rabbits].

Stimulation of the hypothalamus' suprachiasmatic (SCH) and supraoptic (SO) nuclei induced short-latency hypothalamo-cortical responses in the visual cortex affecting the light-induced responses. Possible mechanisms of the differential effects of the stimulation upon different phases of the visual EPs, and participation of the RF in these mechanisms, are discussed. There seems to exist an interconnection between the hypothalamic and light stimuli in the visual cortex.

Animals↗
PubMed1983

Structural development of the lateral geniculate nucleus and visual cortex in monkey and man.

This study concerns the development of the primary visual pathway of the primate. The lateral geniculate nucleus (LGN) is the principal thalamic relay to the visual cortex (area 17), and its neurons have similar morphological characteristics in both monkey and man, as identified by Golgi impregnation. The commonest neuron is the multipolar with a radiate or tufted dendritic tree; next is the bipolar neuron with two or three diametrically opposed dendritic trunks. Less frequent are neurons with beaded dendrites and others with fine, axon-like dendritic processes, possibly interneurons. The dendritic tree of all neurons remains generally within a lamina, but some dendrites cross interlaminar zones. LGN neurons are identifiable before birth and differ from their adult form by the presence of immature features, especially numerous dendritic and somatic spines, most frequent at birth in monkeys and at about 4 months postnatally in man. They disappear almost completely by 3 months in monkeys and 9 months in man. The human LGN has reached its 'adult' volume by this age. Two stages in the development of the human area 17 can be defined. The first is marked by a rapid growth to its 'adult' volume by about 4 months, and by intense synaptogenesis beginning in the foetus and reaching a maximum around 8 months. The second stage is one of stabilization in the volume of area 17 and loss of synapses to reach 'adult' synaptic density around 11 years, at about 60% of the maximum values.

Adolescent↗
PubMed1999

Relationships between cytochrome oxidase (CO) blobs in primate primary visual cortex (V1) and the distribution of neurons projecting to the middle temporal area (MT).

The cytochrome oxidase (CO) blobs and interblobs in layer 3B of primate visual cortex have different sets of corticocortical connections. Cortical layers below layer 3B also project corticocortically, but the relationship of efferent projections from the deeper layers to the overlying blob/interblob architecture is less clear. We studied the tangential organization of neurons projecting from primary visual cortex (V1) to the middle temporal visual area (MT) and their relationship to the CO blobs. MT-projecting neurons in two primate species, bush babies and owl monkeys, were retrogradely labeled, then charted in tangential sections, and compared to the positions of the overlying CO blobs. In both primate species, MT-projecting neurons in layer 3C were unevenly distributed in the tangential plane, with dense patches of labeled cells that were aligned with the CO blobs. A novel two-dimensional spatial correlation method was used to show the colocalization of MT-projecting cells with the overlying blobs. Chi-square analyses performed with the cortical surface equally divided into compartments of blob, interblob, and blob/interblob borders showed that blob columns tended to have about 1.5 times more MT-projecting cells (P < 0.0001) than interblob columns. Similar analyses were applied to published data on V1 cells projecting to area MT in macaque monkey (Shipp and Zeki [1989] Euro J Neurosci 1:310-332). Again, the results showed a significant correlation between the cell distribution and CO blobs. Taken together, these results suggest that layer 3C is not uniform but is made up of a mosaic of cells that project to area MT and cells that project to some other location. These findings also indicate that the mosaic organization of layer 3C is related in some unique way to the overlying CO architecture.

Animals↗
PubMed1994

Polyneuronal innervation of spiny stellate neurons in cat visual cortex.

Our hypothesis was that spiny stellate neurons in layer 4 of cat visual cortex receive polyneuronal innervation. We characterised the synapses of four likely sources of innervation by three simple criteria: the type of synapse, the target (spine, dendritic shaft), and the area of the presynaptic bouton. The layer 6 pyramids had the smallest boutons and formed asymmetric synapses mainly with the dendritic shaft. The thalamic afferents had the largest boutons and formed asymmetric synapses mainly with spines. The spiny stellates had medium-sized boutons and formed asymmetric synapses mainly with spines. We used these to make a "template" to match against the boutons forming synapses with the spiny stellate dendrite. Of the asymmetric synapses, 45% could have come from layer 6 pyramidal neurons, 28% from spiny stellate neurons, and 6% from thalamic afferents. The remaining 21% of asymmetric synapses could not be accounted for without assuming some additional selectivity of the presynaptic axons. Additional asymmetric synapses may come from a variety of sources, including other cortical neurons and subcortical nuclei such as the claustrum. Of the symmetric synapses, 84% could have been provided by clutch cells, which form large boutons. The remainder, formed by small boutons, probably come from other smooth neurons in layer 4, e.g., neurogliaform and bitufted neurons. Our analysis supports the hypothesis that the spiny stellate receives polyneuronal innervation, perhaps from all the sources of boutons in layer 4. Although layer 4 is the major recipient of thalamic afferents, our results show that they form only a few percent of the synapses of layer 4 spiny stellate neurons.

Animals↗
PubMed2003

An egalitarian network model for the emergence of simple and complex cells in visual cortex.

We explain how simple and complex cells arise in a large-scale neuronal network model of the primary visual cortex of the macaque. Our model consists of approximately 4000 integrate-and-fire, conductance-based point neurons, representing the cells in a small, 1-mm(2) patch of an input layer of the primary visual cortex. In the model the local connections are isotropic and nonspecific, and convergent input from the lateral geniculate nucleus confers cortical cells with orientation and spatial phase preference. The balance between lateral connections and lateral geniculate nucleus drive determines whether individual neurons in this recurrent circuit are simple or complex. The model reproduces qualitatively the experimentally observed distributions of both extracellular and intracellular measures of simple and complex response.

Animals↗
PubMed2001

Consistency of encoding in monkey visual cortex.

Are different kinds of stimuli (for example, different classes of geometric images or naturalistic images) encoded differently by visual cortex, or are the principles of encoding the same for all stimuli? We examine two response properties: (1) the range of spike counts that can be elicited from a neuron in epochs representative of short periods of fixation (up to 400 msec), and (2) the relation between mean and variance of spike counts elicited by different stimuli, that together characterize the information processing capabilities of a neuron using the spike count code. In monkey primary visual cortex (V1) complex cells, we examine responses elicited by static stimuli of four kinds (photographic images, bars, gratings, and Walsh patterns); in area TE of inferior temporal cortex, we examine responses elicited by static stimuli in the sample, nonmatch, and match phases of a delayed match-to-sample task. In each area, the ranges of mean spike counts and the relation between mean and variance of spike counts elicited are sufficiently similar across experimental conditions that information transmission is unaffected by the differences across stimulus set or behavioral conditions [although in 10 of 27 (37%) of the V1 neurons there are statistically significant but small differences, the median difference in transmitted information for these neurons was 0.9%]. Encoding therefore appears to be consistent across experimental conditions for neurons in both V1 and TE, and downstream neurons could decode all incoming signals using a single set of rules.

Action Potentials↗
PubMed1985

The neuronal composition of area 17 of rat visual cortex. I. The pyramidal cells.

The pyramidal cells in area 17 of rat visual cortex have been examined by light microscopy using Golgi preparations and semithin plastic sections, and by electron microscopy. Pyramidal cells have cell bodies in layers II-VIa. The pyramidal cells in the lower portion of layer II/III are typical examples of this neuronal type in that they have pyramidal-shaped cell bodies, apical dendrites which ascend to layer I, and a skirt of basal dendrites. The pyramidal cells in upper layer II/III are similar in form but have shorter apical dendrites, while the most superficial pyramidal cells lack apical dendrites and instead have two or more primary dendrites that emanate from the upper surface of their somata. In layer V the pyramidal cells are of two sizes, medium and large, and both have a typical morphology, although the larger neurons have thicker apical dendrites and better-developed axon hillocks than the medium-sized pyramids. The medium-sized pyramidal cells of layer V outnumber the large ones to a ratio of 2.5:1. In layer IV a few typical medium-sized pyramidal cells are present, but the majority are small and can be regarded as star pyramids for they have dendrites radiating in all directions. No clearly identified spiny stellate cells have been encountered in layer IV. The pyramidal cells of layer VIa are also small, and most of them have apical dendrites which only ascend as far as layer IV. In addition to these varieties, both inverted and horizontally inclined pyramidal cells have been encountered. In electron micrographs it is apparent that although all of the pyramidal cells have symmetric axosomatic synapses, the frequency with which these synapses occur varies. The cell bodies of the various forms of pyramidal cells do not show a standard cytology. The medium-sized pyramidal cells of layer II/III usually have rounded nuclei, while the nuclei of the small pyramidal cells of layers IV and VIa are somewhat more irregular, and the large pyramidal cells of layer V have deeply indented nuclear envelopes. The appearance of the perikaryal cytoplasm also varies. The larger pyramidal cells have numerous mitochondria and well-developed Nissl bodies in their perikaryal cytoplasm, but the smaller cells have much-less-pronounced mitochondria and their rough endoplasmic reticulum is only organized into stacks at the bases of dendrites. Pyramidal cells account for about 87% of profiles of neuronal cell bodies with nuclei in layer II/III, 90% in layer IV, 89% in layer V, and 97% in layer VIa.

Animals↗