Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Visual Pathways”

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 1,639 records · Page 91Linked to original sources
PubMed1988

Retinal projections in the red belly squirrel (Callosciurus erythraeus Roberti): an autoradiographic study.

Tritiated labeled materials, [3H]proline and [3H]fucose, were used as tracers of the visual pathway by injection into the right eve of the red belly squirrel, After a designated survival period, the animals were sacrificed, and the brains were removed and processed using standard autoradiographic procedures. Sections were then examined under a microscope and some subcortical nuclei including the suprachiasmatic nucleus (SCN), dorsal and ventral lateral geniculate nuclei(dLGN and vLGN), three optic accessory nuclei (i.e., the medial, lateral and dorsal terminal nuclei - MTN, LTN and DTN), the nuclei of the pretectal area(PTN) and the superior colliculus(SC) in the subcortical regions were marked by labeled isotopes. Radioactive materials were found in the pulvinar nucleus(Pul), parabigeminal nucleus(PB) and dorsal lateral pontine gray(DLP). Some nuclei among the targets of retinal projection in the red belly squirrel received their projection bilaterally while others only did contralaterally. In addition, layered structures of the SC and LGN were clearly demonstrated in the brain of the red belly squirrel. Some differences in the optic system between the red belly squirrel and its near relative, the grey squirrel of North American, and other mammals are discussed.

Animals↗
PubMed2001

An fMRI study of the functional neuroanatomy of picture encoding in younger and older adults.

Age-related changes in the neural mechanisms of picture encoding were investigated using functional magnetic resonance imaging (fMRI). Seven younger and seven older adults were studied while they were encoding pairs of concrete-related, concrete-unrelated, and abstract pictures. Functional (T2*-weighted) and anatomical (T1-weighted) images of the brain were obtained using a 1.5 T MRI scanner. The results in the younger adults showed that the left dorsal prefrontal cortex (PFC) was activated during associative learning of the concrete-unrelated or abstract pictures. The results also suggest that both ventral and dorsal visual pathways are involved in the encoding of abstract pictures, and that the right superior parietal lobule likely mediates spatial information of the abstract pictures. The older adults showed significant activation in the left dorsal PFC under concrete-unrelated and abstract conditions. However, the older adults failed to activate either the left ventral and right dorsal PFC under the concrete-unrelated condition, or the parietal areas under abstract condition. A direct comparison between the two age groups demonstrates that the older adults had a reduced activation in the bilateral parieto-temporo-occipital areas under abstract condition, and in the right temporo-occipital area extending to the fusiform gyrus under the concrete-unrelated condition. Finally, age difference was found in correlation between memory performance and amplitude of signal change in the parahippocampal gyrus and fusiform gyrus under the concrete-unrelated and abstract conditions. These changes in neural response likely underlie the age-related memory decline in relation to pictorial information.

Adult↗
PubMed1984

Callosal connections of the posterior neocortex in normal-eyed, congenitally anophthalmic, and neonatally enucleated mice.

Following multiple injections of horseradish peroxidase into the posterior neocortex of one hemisphere, we examined the distribution of retrogradely labeled cells and anterogradely labeled terminations in tangential and coronal sections through contralateral areas 17 and 18 in three groups of adult mice: normal-eyed (ZRDCT-n and C57Bl/6J strains), congenitally anophthalmic (ZRDCT-an strain), neonatally enucleated (ZRDCT-n strain). In agreement with previous studies, we observed that the pattern of callosal connections in areas 17 and 18 of normal-eyed mice contains the following features: (1) a dense band of callosal cells and terminations separating the interiors of areas 17 and 18, which have relatively few callosal connections, (2) a ring-like configuration anterolateral to area 17, (3) a region of dense labeling lateral to area 18, (4) a narrow band of labeling bridging the posterior portion of area 18, and (5) a region of labeling anteromedial to area 17. We find that all these features of the normal callosal pattern are recognizable in congenitally anophthalmic mice. Their presence in mice that never had eyes supports the hypothesis that central visual pathways can develop many aspects of their connectivity in the absence of input from the periphery. However, we also find that the details of certain features of the callosal pattern in congenitally eyeless mice often differ from those of the same features in normal-eyed mice, and that the between-animal variability in the appearance of these features is higher in eyeless mice. These latter findings indicate that the eyes are needed during normal development to fine-tune the pattern of callosal connections. Our results also reveal that the callosal pattern in neonatally enucleated mice does not differ significantly from that in congenitally anophthalmic mice, indicating that the period in which the eyes guide callosal development extends into postnatal life. While the present data do not delineate the time course of this period, the finding of similarly abnormal callosal patterns in congenitally anophthalmic and neonatally enucleated mice suggests that the eyes exert little if any influence prenatally. Finally, examination of coronal sections indicates that the laminar distribution of callosal connections develops normally in both groups of eyeless mice.

Animals↗
PubMed1993

Preattentive discrimination of relative phase modelled by interacting Gabor or by difference-of-Gaussian filters.

A computer simulation of the human preattentive visual pathway used Gabor and difference-of-Gaussian (DOG) filters to model two-dimensional relative phase discrimination. There is a hierarchy of hexagonally packed levels: (i) an image layer; (ii) an intermediate level of on- and off-centre DOG filters; (iii) a partial set of broadband oriented Gabor-like filters with high-level DOG filters in parallel. Connections between layers use half-wave rectification and a compressive nonlinearity. Local feedback interactions between oriented Gabor filters, together with spatial averaging, allow the model to discriminate both two-dimensional relative phase and orientation differences. There were two separate simulations for the Gabor filters, one with even-symmetric filters and another with odd-symmetric. Textures were formed by superposing three high contrast sine-wave gratings with successive rotations of 60 degrees. Relative phase and global orientation were the varied parameters. Psychophysical rating data for peripheral viewing of texture pairs resemble the results from the even-symmetric simulation, showing discrimination of relative phase and orientation. In contrast, the DOG filters in the model simulate only the relative phase aspects of the data.

Discrimination, Psychological↗
PubMed2000

Expression of presynaptic proteins is closely correlated with the chronotopic pattern of axons in the retinotectal system of the chick.

Newly synthesized presynaptic integral membrane proteins in neurons are transported in precursor vesicles from the site of protein biosynthesis in the cell body by fast axonal flow to the presynaptic terminal. We followed the path that presynaptic proteins travel on the way to their central targets of the highly ordered primary visual pathway of the chick and analyzed the developmental changes in the expression of synaptic vesicle protein 2 (SV2), synaptotagmin, and syntaxin. Immunofluorescences revealed that: (1) the onset of protein expression in the retinal ganglion cells occurs in a central to peripheral developmental pattern from embryonic day 4 (E4) onward; (2) the proteins were found first in the inner and later in the outer plexiform layer of the retina; and (3) they were redistributed from the photoreceptor inner segments and cell bodies to the terminals in the outer plexiform layer. From E4 onward, immunopositive axons for SV2, synaptotagmin, and syntaxin were found in the optic nerve, disappearing after E9 for SV2 and synaptotagmin. The optic tract was stained for SV2 and synaptotagmin between E7 and E12, for syntaxin until the posthatching period. Finally, immunoreactivities for the investigated proteins were present at the surface of the tectum from E8 onward, when first retinal axons arrived there. The present study revealed that SV2 and synaptotagmin, but not syntaxin, are, expressed in a transient wave that follows the advancement of optic axons and the proteins towards the optic tectum.

Animals↗
PubMed1995

Polarized expression of the receptor protein tyrosine kinase Cek5 in the developing avian visual system.

Receptor protein tyrosine kinases of the Eph subfamily have been proposed to play roles in pattern formation based on their distribution during embryonic development. Cek5 (chicken embryo kinase 5) and Cek8 (chicken embryo kinase 8) are Eph-related kinases highly expressed in the chicken embryonic retina. To assess their potential roles in the development of the visual pathway, we examined their distribution by immunoperoxidase labeling. Cek8 is expressed throughout the pathway of the retinal ganglion cell axons, including the nerve fiber layer of the retina, optic nerve, optic chiasm, and stratum opticum of the tectum. Cek5 immunoreactivity is highly concentrated in only a portion of the optic nerve and optic chiasm, and in retinal cultures, Cek5 is detected in neurons. This prompted us to examine the regional distribution of Cek5 in the developing retina and led to the observation that Cek5 is most concentrated in the ventral aspect. RT-PCR established that the differential regulation of Cek5 expression in different portions of the retina occurs at the transcriptional level. Immunoblotting analysis revealed that this unusual expression pattern is distinctive for Cek5, as three other members of the Eph subfamily, Cek4, Cek8, and Cek9, are evenly expressed across the dorsal-ventral axis of the retina. Both Cek5 and Cek8 are distributed in manners which are consistent with their regulating the outgrowth of retinal ganglion cell axons to the tectum. Furthermore, Cek5 represents the first signal transduction molecule found to exhibit the polarized pattern of expression predicted for proteins that control the specificity of the retinotectal projections.

Amino Acid Sequence↗
PubMed1998

Cloning of zebrafish neurofilament cDNAs for plasticin and gefiltin: increased mRNA expression in ganglion cells after optic nerve injury.

During retinal growth and optic axon regeneration, the differential expression of the neuronal intermediate filament proteins, plasticin and gefiltin, in the goldfish visual pathway suggests that these proteins support programmed axonal growth. To investigate plasticin and gefiltin during axonogenesis, we turned to the zebrafish, a system that is more amenable to mutational analysis. As a first step, we demonstrated that the intermediate filament compositions of goldfish and zebrafish are similar. In addition, the cDNAs for zebrafish plasticin and gefiltin were cloned and characterized. Using in situ hybridization in retina, we show increased mRNA levels for these proteins following optic nerve crush. Zebrafish plasticin and gefiltin peak and return to baseline levels of expression more rapidly than in goldfish. Furthermore, in the unoperated eye of experimental fish, there was a moderate increase in the levels of plasticin and gefiltin mRNA, suggesting that soluble factors influence the expression of these proteins. The successive expression of plasticin and gefiltin suggests that these neuronal intermediate filament proteins are integral components of axonogenesis. The cloning and characterization of cDNAs for plasticin and gefiltin permit mutational analyses of these proteins during zebrafish axonogenesis.

Animals↗
PubMed1987

Factors guiding optic fibers in developing Xenopus retina.

We have characterized, by electron microscopy, the growth of pioneering axons from the retina into the visual pathway during early development of Xenopus laevis. The subsequent development of following fibers from the growing retinal margin as they accumulated in the ganglion cell fiber layer (GCFL) of the retina was also studied. Extracellular channels bordered by neuroepithelial cells appear in the developing retina in a dorsal to ventral gradient before any pioneering axons are seen. Pioneering axons are subsequently observed in these channels, usually surrounded by neuroepithelial cell processes. Ruthenium red treatment of embryonic retinas reveals extracellular matrix (ECM) within these retinal channels, while extracellular spaces in the proximal optic stalk, just beyond the optic disc, lack this material. ECM is also seen in optic tectum wherever ingrowing retinal and nonretinal axons are found. The channels and the ECM contained within them may provide guidance cues for pioneering retinal axons. The early association of pioneering retinal axons with neuroepithelial cell processes (putative glia) appears to be important in further development of the GCFL. The so-called following fibers of ganglion cells, arising later in development, fasciculate with pioneer axons in extracellular spaces and form fiber bundles of the GCFL on top of the layer of glial cell endfeet. It is not clear whether pioneering axons, glial cell surfaces, or both serve as guidance cues for following fiber migration.

Animals↗
PubMed1989

Flash evoked potentials in the ectostriatum of the zebra finch: a current source-density analysis.

Recent research has demonstrated that ipsilaterally visually evoked potentials (VEPs) can be measured within the ectostriatum, the telencephalic target area of the tectofugal visual pathway in birds. In this paper we systematically measured contra- and ipsilateral VEPs within the ectostriatal complex to obtain more detailed information on the processing of contra- and ipsilateral stimuli. The similarity of neighbouring VEPs at equal depth and a comparison of a one dimensional and a three dimensional analysis of current source-densities (CSDs) for identical coordinates suggested that a one dimensional current source-density analysis might be applicable. The one dimensional current source-density analysis demonstrated largely corresponding patterns in the sink-source sequences of the current source-density depth profiles for the contra- and ipsilateral stimulus responses. The occurrence of a large sink in the centre of the ectostriatal core, together with the results of multiunit recordings, shows that the ectostriatal core is the location of the generators for both the contra- and the ipsilaterally evoked responses. The occurrence of macroscopic sinks and sources and the fact that VEPs can be recorded from the ectostriatum shows that there is a higher degree of order in the ectostriatum than has been previously demonstrated by anatomical methods. The time coincidence between the maximum spike rate of multiunit responses, the negative peak of the evoked potential, and the large central sink demonstrates that the influence of ipsi- as well as of contralateral stimuli is predominantly excitatory.

Animals↗
PubMed1995

Modelling the increase of contrast sensitivity with grating area and exposure time.

We extended the contrast detection model of human vision to temporal integration by taking into account the effect of exposure duration on contrast sensitivity for stationary gratings. The extended model thus comprised: (i) low-pass filtering due to the optical modulation transfer function of the eye; (ii) high-pass filtering (lateral inhibition) due to the neural modulation transfer function of the visual pathways; (iii) addition of internal neural noise; and (iv) detection by a local matched filter whose efficiency for gratings decreased with increasing area and exposure duration. To test the model we measured binocular contrast sensitivity in foveal photopic vision as a function of exposure duration and area for sinusoidal gratings with equiluminous surround at spatial frequencies of 0.25-16 c/deg. In agreement with the model, contrast sensitivity at all grating areas first increased in proportion to square root of t when exposure duration (t) was shorter than critical duration. Thereafter the increase saturated and contrast sensitivity became independent of exposure time. Critical exposure duration was found to be independent of grating area but increased with spatial frequency. Similarly, at all exposure durations contrast sensitivity first increased in proportion to square root of A when grating area (A) was smaller than critical area. Thereafter the increase saturated and contrast sensitivity became independent of area. Critical area was found to be independent of exposure duration but decreased with increasing spatial frequency. The extended model explained 95-97% of the total variance of our contrast sensitivity data at the spatial frequencies studied. Our results also mean that spatial and temporal integration processes are mutually independent and thus area and time are separable variables in the detection of stationary gratings.

Adult↗
PubMed1992

Induction of c-fos immunostaining in the rat brain after the systemic administration of nicotine.

To search for evidence of altered neuronal gene expression in response to exposure to the highly addictive drug nicotine, rat brains were examined by immunocytochemistry for the fos protein after the systemic administration of nicotine. The drug was administered as an IV infusion over 1 h At a dose of 2 mg/kg, the most dramatic nicotine-induced fos nuclear immunostaining was seen in central visual pathways, including the superficial superior colliculus and the medial terminal nu. of the accessory optic tract, in the interpeduncular nu. Notably, many regions with high levels of nicotine binding sites, including the medial habenula, thalamus, substantia nigra, and ventral tegmental area, failed to express the c-fos gene with this schedule of nicotine administration. A minimal increase in fos immunostaining was seen after a nicotine dose of 0.5 mg/kg, with a much greater response after 1 or 2 mg/kg. The response was seen as soon as 60 min after the beginning of the infusion, was maximal at 2-3 h, and declined thereafter. c-fos expression was substantially attenuated in the superficial gray layer of superior colliculus, medial terminal nucleus of the accessory optic tract, and the interpeduncular nucleus by pretreatment with the centrally acting nicotine antagonist mecamylamine, 5 mg/kg IP, but not with the peripherally acting antagonist hexamethonium, 4 mg/kg IP. These observations identify a subset of central nervous system neurons that respond to nicotine with altered expression of the immediate early gene c-fos. These neurons presumably undergo long-term changes in gene expression as a result of acute exposure to high doses of nicotine.

Animals↗
PubMed2004

The derivation of direction selectivity in the striate cortex.

In the central visual pathway of binocular animals, the property of directional selectivity (DS) is first exhibited in striate cortex. In this study, we sought to determine the neural circuitry underlying the transformation from non-DS neurons to DS cortical cells. In a well established model, DS receptive fields (RFs) are derived from the sum of two non-DS inputs with 90 degrees (quadrature) spatiotemporal phase differences. We explored possible input sources for this model, which include non-DS simple cells and lateral geniculate nucleus (LGN) neurons, by examination of spatiotemporal RFs of single cells and of pairs of cells. We find that distributions of non-DS simple RFs do not match the temporal predictions of the quadrature model because of a lack of long-latency responses. The long-latency inputs could potentially arise from lagged LGN afferents. However, analysis of cell pairs indicates that DS cells receive cortical input from non-DS simple cells for both short- and long-latency components, with temporal phase differences typically <90 degrees. Furthermore, the distribution of minimum phase differences needed to generate DS cells overlaps that exhibited by non-DS simple cells. Considered together, these results are consistent with a linear model whereby DS simple cells are formed from simple-cell inputs, with temporal phase differences often less than quadrature.

Animals↗
PubMed2004

Error rate of axons at the owl's optic chiasm.

BACKGROUND: In owls, the visual pathways from the retina are totally crossed. Attempts to find ganglion cells with uncrossed axons have failed consistently, when retrograde labeling with HRP is used for their identification. In the present investigation we have used retrograde fluorescent tracers of complementary colour in each optic tectum to demonstrate a tiny population of ipsilaterally-projecting retinal ganglion cells in the owl. METHODS: We studied two species, one from each of the two important owl families: the Southern boobook owl, Ninox boobook: (Family Strigidae); and the Barn Owl, Tyto alba: (Family Tytonidae). RESULTS: The small numbers, random distribution and heterogeneity of the mis-projecting ganglion cells, taken together, argue against a functional role for them. Instead, they appear to be the result of developmental errors in the specification of laterality. At a number of different eccentricities and ganglion cell densities, the error rate was roughly a constant fraction of the neurons involved, at around 10-4 for the tytonid owl (lacking a fovea) and around 10-5 for the strigid owl (which has a fovea and a higher overall density of ganglion cells). CONCLUSIONS: These values are close to the error rates of replicating enzymes, such as nucleic acid polymerases. The evolution of a higher retinal ganglion cell density and a fovea in the Strigidae appears to be accompanied by an improvement in the error rate.

Animals↗
PubMedDate not supplied

Use of a stenopeic semiocclusor enhances vep diagnosis.

PURPOSE: We conducted a study to assess the capability of a 2-mm stenopeic semiocclusor in improving the sensitivity of the standard full-field pattern-visual evoked potential technique to disclose abnormalities of the pre-chiasmatic visual pathway. METHODS: Nineteen control subjects and fifty-five patients with a diagnosis of definite or probable Multiple Sclerosis (MS) were evaluated. All subjects were seated in front of a 19" TV monitor depicting a black and white square pattern, standard condition (R). Two trials of 100 stimulus repetitions at 1.8 Hz, recording at Oz- Fz were performed for each eye. After two minutes the procedure was replicated using an stenopeic semiocclusor, central field condition (S). The main parameters quantified were the P100 latency in each eye (a) and P100 inter-ocular difference (b). RESULTS: Under condition R abnormalities were detected in 42 patients for parameter "a", and in 39 patients for parameter "b". If both parameters, a + b, were considered 48 patients (87%) showed abnormalities. Under condition S, abnormalities were detected in 49 patients for parameter "a" and 41 patients for parameter "b". When both parameters, a + b, were considered 53 patients (96%) showed abnormalities. DISCUSSION: The main point of interest of this study is the fact that when a pattern reversal stimulus is restricted to the central area the evoked response shows a P100 peak with prolonged latency in comparison to the full-field stimulus. Additionally, used in combination with the standard full-field technique it improves the abnormality detection rate whilst adding little extra time to the procedure.

Adolescent↗
PubMed1994

Optic nerve injury alters basic fibroblast growth factor localization in the retina and optic tract.

Basic fibroblast growth factor (bFGF) is thought to be a trophic factor for several classes of neurons. Its distribution changes in response to cortical neural injury. We have determined the effect of injury to the optic nerve on localization of bFGF in the rodent retina and visual pathways. Our observations were confirmed by using different antisera and monoclonal antibodies. While photoreceptors normally contain virtually no bFGF, crushing the optic nerve causes a striking increase, over a period of several weeks, in the amount of bFGF in retinal photoreceptors. Since photoreceptors do not synapse directly upon the injured ganglion cells, intermediary cells must participate in the cascade of events that results in the elevated bFGF. In light of the observation that exogenous bFGF protects photoreceptors from photodamage (Faktorovich et al., 1992), this increase in bFGF in photoreceptors may explain, in part, why crushing the optic nerve protects photorecptors against photodamage (Bush and Williams, 1991). Whereas bFGF is constitutively found in glia in the optic nerve, little bFGF is found in glia in the optic tract. However, damage to the optic nerve increases bFGF in astrocytes in the optic tract. This change occurs within days, suggesting that a relatively direct signal may intervene between the injured axon and the adjacent glial cells. Thus, despite the fact that the optic nerve and optic tract are contiguous structures through which axons of retinal ganglion cells project, the glial elements in these structures express distinct properties, because of differences in either glial subclasses or microenvironment.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1996

Selective broad-band spatial frequency loss in contrast sensitivity functions. Comparison with a model based on optical transfer functions.

PURPOSE: Contrast sensitivity functions (CSFs) were measured under various optical conditions in healthy observers together with CSFs from selected patients. Threshold increases across the spatial frequency range were compared with predictions of a theoretical optical model based on modulation transfer functions. METHODS: Contrast thresholds for various spatial frequencies were determined with a computer-automated method of ascending limits in a control group and a group of patients with various visual pathway diseases ranging from retinal disorders, such as diabetic retinopathy, to neural disorders, such as multiple sclerosis. For normal control subjects, simulated contrast sensitivity losses also were effected by manipulating pupil diameter and dioptric blur. Modulation transfer functions of the eye's optics in polychromatic light were calculated. The wave aberration function included standard spherical aberration, coma, and small amounts of irregular aberrations. RESULTS: Experimentally, slight dioptric blur (e.g., 0.4 to 0.75 D) introduced increased CSF thresholds within either a narrow or broad bandwidth. For the latter, decreased CSF sensitivity occurred across a spatial frequency range as broad as 1 log unit, from low spatial frequencies (2 cyc/deg), and for pupil sizes equal to or larger than 3 mm. Predictions based on an optical model are qualitatively and quantitatively in agreement with these findings. Contrast sensitivity losses of the patients were neither specific nor selective to the pathologic condition at hand. Furthermore, various CSF losses optically induced in the control subjects were indistinguishable from nonoptically induced pathologic CSF profiles. CONCLUSIONS: Selective broad-band contrast sensitivity loss may be optically induced by slight refractive error. As a result, selective contrast sensitivity loss at lower and intermediate spatial frequencies concurrent in patients with various pathologic, neuro-ophthalmologic conditions cannot be a priori attributed to neural factors without carefully controlled and well-defined optical variables.

Adult↗
PubMed1998

Neuro-ophthalmic findings in progressive multifocal leukoencephalopathy.

BACKGROUND: Progressive multifocal leukoencephalopathy (PML) is a demyelinating disorder of the central nervous system found in immunodeficient patients, most frequently now in those infected with HIV. It may represent the initial manifestation of HIV infection. Since the central visual pathways may be affected, a variety of neuro-ophthalmic signs and symptoms can manifest. We studied the clinical, radiographic and histopathological characteristics of patients with PML. METHODS: The charts of 13 patients in whom PML was diagnosed in the Neuro-AIDS clinic at the Montreal Neurological Institute between November 1987 and March 1995 were reviewed. The diagnosis of PML was established by characteristic clinical features together with typical computed tomographic or magnetic resonance imaging findings, such as nonenhancing low-density (on computed tomography) or hyperintense (on T2-weighted magnetic resonance imaging) white-matter lesions, without mass effect. Neuro-ophthalmic findings were based on clinical examination by an ophthalmologist, neuro-ophthalmologist or neurologist. Tissue for pathological examination was obtained by biopsy in one case and at postmortem study in a second case. RESULTS: The most common finding was homonymous hemianopia, in five patients (38%). Other features included nystagmus (in two patients), diplopia with cranial nerve palsy (in one) and cortical blindness (in one). One of the patients exhibited involvement of the brain stem, a site not usually affected by this demyelinating process. INTERPRETATION: The diagnosis of PML should be considered in immunocompromised patients with neuro-ophthalmic findings, particularly those with homonymous hemianopia.

AIDS Dementia Complex↗
PubMedDate not supplied

A functional hypothesis for LGN-V1-TRN connectivities suggested by computer simulation.

We employ computer simulation to investigate the function of neural circuitries between thalamic sensory relay nuclei, primary sensory cortices, and the thalamic reticular nucleus (TRN). Computational similarities exist between these circuits and the architecture of a simple artificial neural network. We impose processing parameters on this network architecture in keeping with anatomical and physiological details of the mammalian geniculo-cortical visual pathway, and then run the simulation on a task involving multiple simultaneous inputs from the simulated visual field. After two to three loops through the simulation, activity in cortical and thalamic units whose receptive fields include the stronger stimulus remains constant, while activity in other cortical and thalamic units activated by weaker stimuli declines toward resting values. These results suggest that the modeled neural circuitry functions to "prime" selective attentional mechanisms further up the visual streams toward specific portions of the total visual stimulus. Besides extending existing models and evidence about the function of these neural circuits, our results also provide physiologists with predicted activity profiles of thalamic and cortical elements of the modeled neural system for a task not yet studied experimentally.

Animals↗