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At least 199 records · Page 11Linked to original sources

Short-term depression in thalamocortical synapses of cat primary visual cortex.

Neurons in primary visual cortex exhibit several nonlinearities in their responses to visual stimuli, including response decrements to repeated stimuli, contrast-dependent phase advance, contrast saturation, and cross-orientation suppression. Thalamocortical synaptic depression has been implicated in these phenomena but has not been examined directly in visual cortex in vivo. We assessed depression of visual thalamocortical synapses in vivo using 20-100 Hz trains of electrical stimuli delivered to the LGN. Cortical cells receiving direct input from the LGN, identified by short latency and low jitter of LGN-evoked PSPs, showed moderate reductions in PSP amplitude during the fastest trains. Cells receiving indirect input from the thalamus via other cortical excitatory neurons show a marked reduction in PSP amplitude during a train, which could be explained either by synaptic depression in corticocortical synapses or by an inhibition-mediated suppression of the firing of their afferents. Reducing spontaneous activity in the LGN (by retinal blockade) unmasked additional depression at the thalamocortical synapse but only for the first stimulus in the train. That is, the first PSP was increased in amplitude relative to the unblocked condition, but subsequent responses were essentially unchanged. Thus, the synapses are maintained at significant levels of depression by spontaneous activity. These findings constrain the role that thalamocortical depression can play in shaping cortical responses to visual stimuli.

Animals↗

Intrinsic and environmental factors in the development of functional maps in cat visual cortex.

In the mammalian visual cortex, key neuronal response properties such as orientation preference and ocular dominance (OD) are mapped in an orderly fashion across the cortical surface. It has been known for some time that manipulating early postnatal visual experience can change the appearance of the OD map. Similar evidence for developmental plasticity of the orientation map has been scarce. We employed optical imaging of intrinsic signals to examine the contribution of intrinsic and environmental factors to the development of cortical maps, using the paradigms of strabismus, reverse occlusion and rearing in a single-orientation environment ('stripe-rearing'). For several weeks after induction of strabismus, the pattern of OD domains remained stable in young kittens. The isotropic magnification of the OD map matched the postnatal growth of the visual cortical surface during the same period. In reverse-occluded and in stripe-reared kittens, orientation preference maps obtained through the left and the right eye were very similar, although the two eyes had never shared any visual experience. We suggest that the geometry of functional maps in the visual cortex is intrinsically determined, while the relative strength of representation of different response properties can be modified through visual experience.

Animals↗

Feeling with the mind's eye: contribution of visual cortex to tactile perception.

Visual imagery is implicated in the normal tactile perception of certain object properties. This is an example of cross-modal interactions that characterize normal perception. Here we review recent studies from our laboratory on cross-modal interactions between vision and touch in normally sighted humans. Positron emission tomography was used to demonstrate activation of a region of extrastriate visual cortex, near the parieto-occipital fissure, during tactile discrimination of grating orientation. Transcranial magnetic stimulation (TMS) over this region interfered with performance of this tactile task. In both studies, visual cortical involvement was found for tactile discrimination of orientation but not spatial frequency. Thus, this cortical region is not only active during but also necessary for optimal tactile sensing of orientation. Recent findings implicating visual cortex in Braille-reading in the blind should be evaluated from this perspective.

Animals↗

Postnatal growth and column spacing in cat primary visual cortex.

The primary visual cortex (area 17) of cats continues to grow substantially during early postnatal development. To assess the implications of this growth for the organization of visual cortical maps, we analysed both postnatal growth of area 17 and the spacing of ocular dominance columns in the same animals using 2-deoxyglucose autoradiography to label cortical activation patterns. Quantitative analyses of area size and column spacing were performed on flat-mount sections of the cortical hemispheres. Our analysis of the surface area revealed an average increase of the size of area 17 between the third and tenth postnatal weeks by about 51%. About 75% of this increase occurred during the third and sixth postnatal weeks (size increase of 37%). However, the distance between adjacent columns did not exhibit a similar increase but rather remained constant during the same postnatal period. Since cortical growth is not accompanied by an increased spacing of ocular dominance columns, new functional modules must somehow be added during the first postnatal weeks to occupy the enlarging cortical sheet. Possible mechanisms underlying the formation of new modules are discussed.

Age Factors↗

Orientation-tuned FMRI adaptation in human visual cortex.

Adaptation is a general property of almost all neural systems and has been a longstanding tool of psychophysics because of its power to isolate and temporarily reduce the contribution of specific neural populations. Recently, adaptation designs have been extensively applied in functional MRI (fMRI) studies to infer neural selectivity in specific cortical areas. However, there has been considerable variability in the duration of adaptation used in these experiments. In particular, although long-term adaptation has been solidly established in psychophysical and neurophysiological studies, it has been incorporated into few fMRI studies. Furthermore, there has been little validation of fMRI adaptation using stimulus dimensions with well-known adaptive properties (e.g., orientation) and in better understood regions of cortex (e.g., primary visual cortex, V1). We used an event-related fMRI experiment to study long-term orientation adaptation in the human visual cortex. After long-term adaptation to an oriented pattern, the fMRI response in V1, V2, V3/VP, V3A, and V4 to a test stimulus was proportional to the angular difference between the adapting and test stimuli. However, only V3A and V4 showed this response pattern with short-term adaptation. In a separate experiment, we measured behavioral contrast detection thresholds after adaptation and found that the fMRI signal in V1 closely matched the psychophysically derived contrast detection thresholds. Similar to the fMRI results, adaptation induced threshold changes strongly depended on the duration of adaptation. In addition to supporting the existence of adaptable orientation-tuned neurons in human visual cortex, our results show the importance of considering timing parameters in fMRI adaptation experiments.

Adaptation, Physiological↗

Glucose utilization of visual cortex following extra-occipital interruptions of the visual pathways by tumor. A positron emission tomography study.

To assess the effect of extra-occipital lesions on the local cerebral glucose utilization of the primary and associative visual cortex, 29 patients were studied in the unstimulated state by positron emission tomography and [18F]2-deoxyglucose. Quantitative Goldmann perimetry was done in each patient at the time of the positron emission tomographic study. Nine patients showed homonymous defects, either hemianopsia or quadrantanopsia, whereas nine patients had heteronymous defects. Eleven control subjects, free of any neurological symptoms and with normal visual fields, were also studied with [18F]2-deoxyglucose positron emission tomography. In the normal control subjects and in patients with a heteronymous defect, left-to-right differences in the local cerebral metabolic rate for glucose of the visual cortex varied less than 10%. In patients with hemianopic defects, differences ranged from 8 to 38%, with the hypometabolic cortex always contralateral to the field defect. In patients with quadrantanopic defects, the visual cortex contralateral to the field defect demonstrated differences from 14 to 24% above and below the calcarine fissure, the cortex that received greater input from the affected field being hypometabolic.

Adult↗

Critical period for the marked loss of retinal X-cells following visual cortex damage in cats.

Visual cortex damage in newborn kittens produces a 78% loss of retinal X-cells whereas damage in adult cats produces only a 22% loss. Retinal Y- and W-cells are unaffected. The present experiment showed that the critical period for the severe loss of retinal X-cells ends between birth and 2 weeks of age. These results have implications for understanding the neural mechanisms of recovery from early visual cortex damage.

Age Factors↗

Spatiotemporal structure of nonlinear subunits in macaque visual cortex.

The primate visual system is arranged hierarchically, starting from the retina and continuing through a series of extrastriate visual areas. Selectivity for motion is first found in individual neurons in the primate visual cortex (V1), in which many simple cells respond selectively to the direction and speed of moving stimuli. Beyond simple cells, most studies of direction selectivity have focused on either V1 complex cells or neurons in the middle temporal area (MT/V5). To understand how visual information is transferred along this pathway, we have studied all three types of neurons, using a reverse correlation procedure to obtain high spatial and temporal resolution maps of activity for different motion stimuli. Most complex and MT cells showed strong second-order interactions, indicating that they were tuned for particular displacements of an apparent motion stimulus. The spatiotemporal structure of these interactions showed a high degree of similarity between the populations of V1 complex cells and MT cells, in terms of the spatiotemporal limits and preferences for motion and their two-dimensional spatial structure. Much of the structure in the V1 and MT second-order kernels could be accounted for on the basis of the first-order responses of V1 simple cells, under the assumption of a Reichardt or motion-energy type of computation.

Animals↗

System-wide repercussions of damage to the immature visual cortex.

Damage of the primary visual cortex in mammals, including humans, severely disrupts vision by disconnecting much of the cognitive-processing machinery of extrastriate cortex from its source of visual signals in the retina. Studies of the anatomical consequences of damage to the immature primary visual cortex in cats reveal system-wide repercussions on neural circuitry that includes the retina, thalamus, midbrain and extrastriate cortex. The repercussions modify circuits that support relatively normal signal processing and the sparing of certain visually guided behaviors such as aspects of complex-pattern recognition and orienting to novel stimuli introduced into the visual field. These studies have implications for understanding the consequences of damage to the visual cortex in infant monkeys and humans, and for devising therapeutic strategies to attenuate defects in vision induced by cortical lesions.

Animals↗

Properties of the flash visual evoked potential recorded in the cat primary visual cortex.

The flash visual evoked potential (F-VEP), elicited by a 100 ms diffuse light flash presented at 2 Hz, was examined in the cat primary visual cortex (Area 17). Intracortical F-VEP depth profiles were recorded to characterize waveform changes with electrode depth. A positive surface component, with a latency of 200 ms, was the dominant waveform feature within the cortex, reversing in polarity and increasing in magnitude as the cortex was penetrated. Other prominent components with latencies of 30, 50, 100, and 125 ms were also observed. Changes in the waveform with stimulus duration and illumination were examined and revealed the sensitivity of prominent components to stimulus parameters.

Animals↗

Preserving properties of object shape by computations in primary visual cortex.

Although our visual system is extremely good at extracting objects from the visual scene, this process involves complicated computations that are thought to require image processing by many successive cortical areas. Thus, intermediate stages in object extraction should not eliminate essential properties of the objects that are still required by later stages. A particularly important characteristic of an object is its shape, and shape has the property that it is unchanged by translations, rotations, and magnifications of the image. I show that the requirement for this property of shape to be preserved in the image, as represented by the firing of neurons in the primary visual cortex (V1), is equivalent to a particular type of computation, known as a wavelet transform, determining the firing rate of V1 neurons in response to an image on the retina. Experimental data support the conclusion that the neural representation of images in V1 is described by a wavelet transform and, therefore, that the properties of shape are preserved.

Fourier Analysis↗

Protective sensitivity changes of the motor cortex due to epileptiform experience of the visual cortex.

In awake rats, experiments were performed to study early epileptiform events (interictal spike, myoclonic jerk) in relation to a) the strength of the convulsive stimulus, b) the site of the focus, and c) epileptiform experience. For this reason, Na-penicillin G (PCN) was injected either into the motor or visual cortex and, in a second test 2 weeks thereafter, into the motor cortex in all these rats. The median latencies of both the first interictal potential and jerk were independent of the applied PCN concentration in the range between 16-1,000 IU/0.5 microliter (90.5-113 s, and from 106-196 s, respectively), as well as from the injection site in the visual or motor cortex (potential: 80 vs. 69 s; jerk: 124 vs. 129 s, respectively). After epileptiform experience in the visual cortex, the latencies of the first potential and jerk were significantly (p < 0.05) increased compared to animals with an experience in the motor cortex (first potential: 100 vs. 66 s; first jerk: 159 vs. 116 s, respectively). The results show that a PCN focus in the visual cortex decreases the susceptibility of the motor cortex for the convulsant action of PCN. This means that an autoprotective mechanism is activated whose efficiency depends upon a close linkage between the visual and motor cortex.

Animals↗

Horizontal organization of orientation-sensitive cells in primate visual cortex.

In the visual cortex of the monkey the horizontal organization of the preferred orientations of orientation-selective cells follows two opposing rules: (1) neighbors tend to have similar orientation preferences, and (2) many different orientations are observed in a local region. We have described a classification for orientation maps based on the types of topological singularities and the spacing of these singularities relative to the cytochrome oxidase blobs. Using the orientation drift rate as a measure we have compared simulated orientation maps to published records of horizontal electrode recordings.

Animals↗

Orientation discrimination sensitivity of single units in cat primary visual cortex.

Responses of visual cortex (area 17) neurons to moving oriented stimuli were recorded from anesthetized cats. The variance of response (SD2) to repeated identical stimuli was directly proportional to response magnitude (R), (SD2 = C2R). The values of C were not found to differ significantly between different types of cortical cells. The relationship predicts that the coefficient of variation (SD/R) will be smallest near the peak of the tuning curve, indicating that the peak response is most reliable for detecting an orientation but not necessarily the most sensitive to a change in orientation. Tuning curves and response variability were then examined to determine the orientation at which the neuron was most sensitive to changes in stimulus orientation using signal detection theory. The discrimination index (d' = [R1-R2]/SD) for a 1 degree change in stimulus orientation was greatest along the flanks of the tuning curve. In order to generalize the experimental data, response distributions derived from a model of cells with parameters based on experimental data were examined to determine the minimal discriminable change in stimulus orientation. Changes of stimulus orientation between 0.6 and 5 deg of arc could be detected from single responses of a single cell by an optimal observer with 75% accuracy if the orientation change was centered at the most sensitive part of the tuning curve.

Action Potentials↗

Differential laminar expression of AMPA receptor genes in the developing rat visual cortex using in situ hybridization histochemistry. Effect of visual deprivation.

The postnatal development of laminar pattern of AMPA receptor mRNA subtypes GluR-A through to GluR-D (flip variants) in the visual cortex of both normally raised and monocularly deprived rats (one eyelid sutured at the age of 11 days) was studied using in situ hybridization histochemistry and computer-assisted image analysis. The AMPA receptors GluR-A through to GluR-D transcripts exhibit a differential laminar expression pattern in the developing rat visual cortex. At birth the levels of GluR-A transcripts are lower by about 50% in each visual cortical layer as compared to the adult values. In contrast, GluR-B to GluR-D mRNAs are expressed in all cases at higher levels at birth than in the adult brain. Unilateral eyelid closure at postnatal day 11 for several periods of time resulted in both transient and permanent changes in the laminar development of GluR-A through to GluR-C transcripts but hardly affected the GluR-D mRNA subtype. The distinct laminar developmental pattern of AMPA receptor mRNAs in rat visual cortex as well as the differential effects of visual deprivation suggest specific roles of AMPA receptor subtypes during the early postnatal maturation of visual function.

Animals↗

Processing efficiency of divided spatial attention mechanisms in human visual cortex.

Many visual tasks require deployment of attention to multiple objects or locations. We used functional magnetic resonance imaging and behavioral experiments to investigate the relative processing efficiency of two putative attentional mechanisms for performing such tasks: the "zoom lens" and "multiple spotlights." Two key questions were investigated: (1) does splitting the spotlight into multiple foci incur an overhead cost that diminishes the efficacy of attention compared with the zoom lens, and (2) does splitting the spotlight provide a benefit relative to the zoom lens by conserving attention resources that otherwise would be directed to task irrelevant stimuli? For both mechanisms, attending to multiple object locations decreased processing efficiency at a single location, resulting in both decreased behavioral performance and decreased blood oxygenation level-dependent (BOLD) signal attentional modulation. When the two mechanisms attended to multiple objects across the same spatial extent, the multiple spotlight mechanism, which ignores intervening stimuli, yielded better performance and higher BOLD signal. When the two mechanisms processed the same number of stimuli, splitting the spotlight neither impaired performance nor diminished BOLD signal in occipital cortex. The surprising efficiency of the multiple spotlight mechanism supports the emerging view that spatial attention is easily deployed in a diverse range of spatial configurations.

Attention↗

[Acetylcholinesterase activity in visual cortex structures during early visual deprivation].

By means of quantitative histochemical methods it has been shown that an early photic deprivation (animals kept in a dark chamber for two months after their birth) leads to a decrease in the activity level of acetylcholinesterase (AChE) in the visual area of the cerebral cortex. With the recovery of the visual function (animals kept in normal photic conditions for two weeks) the AChE activity becomes markedly normalized. The obtained data allow to suggest that the decrease in AChE activity due to deprivation is functionally determined.

Acetylcholine↗

NMDA receptor-dependent oscillatory signal outputs from the retrosplenial cortex triggered by a non-NMDA receptor-dependent signal input from the visual cortex.

The retrosplenial cortex is located at a critical juncture between the visual cortex and hippocampal formation. Functions of the retrosplenial cortex at the local circuit level, however, remain unclear. Herein, we show how signals traveling from the visual cortex behave in local circuits of the retrosplenial cortex, using optical recording methods and application of caffeine to rat brain slices. Electrical signals evoked in the primary visual cortex penetrated into the deep layer of the retrosplenial granular a cortex (RSGa) and propagated further toward postsubiculum and upper layer. Non-N-methyl-D-aspartate (NMDA) receptor-dependent initial traveling signal from the visual cortex triggered NMDA receptor-dependent neural oscillation in the RSGa. Oscillatory signals originated from the local area in the deep layer of the RSGa, and the signal spread back and forth toward the visual cortex and postsubiculum, in addition to spreading toward the upper layer. From the perspective of the RSGa, extrinsic signal inputs from the visual cortex switched on neural oscillators in the RSGa that deliver NMDA receptor-dependent intrinsic signal outputs. Opening and strengthening of non-NMDA receptor-dependent input pathways from the visual cortex required NMDA receptor-dependent oscillatory neural activities. These input and output relationships indicate that the retrosplenial cortex may represent an important relay station between the visual cortex and hippocampal formation.

Animals↗