Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “connectivity mapping”

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 1,153 records · Page 64Linked to original sources
PubMed2001

Geometric visual hallucinations, Euclidean symmetry and the functional architecture of striate cortex.

This paper is concerned with a striking visual experience: that of seeing geometric visual hallucinations. Hallucinatory images were classified by Klüver into four groups called form constants comprising (i) gratings, lattices, fretworks, filigrees, honeycombs and chequer-boards, (ii) cobwebs, (iii) tunnels, funnels, alleys, cones and vessels, and (iv) spirals. This paper describes a mathematical investigation of their origin based on the assumption that the patterns of connection between retina and striate cortex (henceforth referred to as V1)-the retinocortical map-and of neuronal circuits in V1, both local and lateral, determine their geometry. In the first part of the paper we show that form constants, when viewed in V1 coordinates, essentially correspond to combinations of plane waves, the wavelengths of which are integral multiples of the width of a human Hubel-Wiesel hypercolumn, ca. 1.33-2 mm. We next introduce a mathematical description of the large-scale dynamics of V1 in terms of the continuum limit of a lattice of interconnected hypercolumns, each of which itself comprises a number of interconnected iso-orientation columns. We then show that the patterns of interconnection in V1 exhibit a very interesting symmetry, i.e. they are invariant under the action of the planar Euclidean group E(2)-the group of rigid motions in the plane-rotations, reflections and translations. What is novel is that the lateral connectivity of V1 is such that a new group action is needed to represent its properties: by virtue of its anisotropy it is invariant with respect to certain shifts and twists of the plane. It is this shift-twist invariance that generates new representations of E(2). Assuming that the strength of lateral connections is weak compared with that of local connections, we next calculate the eigenvalues and eigenfunctions of the cortical dynamics, using Rayleigh-Schrödinger perturbation theory. The result is that in the absence of lateral connections, the eigenfunctions are degenerate, comprising both even and odd combinations of sinusoids in straight phi, the cortical label for orientation preference, and plane waves in r, the cortical position coordinate. 'Switching-on' the lateral interactions breaks the degeneracy and either even or else odd eigenfunctions are selected. These results can be shown to follow directly from the Euclidean symmetry we have imposed. In the second part of the paper we study the nature of various even and odd combinations of eigenfunctions or planforms, the symmetries of which are such that they remain invariant under the particular action of E(2) we have imposed. These symmetries correspond to certain subgroups of E(2), the so-called axial subgroups. Axial subgroups are important in that the equivariant branching lemma indicates that when a symmetrical dynamical system becomes unstable, new solutions emerge which have symmetries corresponding to the axial subgroups of the underlying symmetry group. This is precisely the case studied in this paper. Thus we study the various planforms that emerge when our model V1 dynamics become unstable under the presumed action of hallucinogens or flickering lights. We show that the planforms correspond to the axial subgroups of E(2), under the shift-twist action. We then compute what such planforms would look like in the visual field, given an extension of the retinocortical map to include its action on local edges and contours. What is most interesting is that, given our interpretation of the correspondence between V1 planforms and perceived patterns, the set of planforms generates representatives of all the form constants. It is also noteworthy that the planforms derived from our continuum model naturally divide V1 into what are called linear regions, in which the pattern has a near constant orientation, reminiscent of the iso-orientation patches constructed via optical imaging. The boundaries of such regions form fractures whose points of intersection correspond to the well-known 'pinwheels'. To complete the study we then investigate the stability of the planforms, using methods of nonlinear stability analysis, including Liapunov-Schmidt reduction and Poincaré-Lindstedt perturbation theory. We find a close correspondence between stable planforms and form constants. The results are sensitive to the detailed specification of the lateral connectivity and suggest an interesting possibility, that the cortical mechanisms by which geometric visual hallucinations are generated, if sited mainly in V1, are closely related to those involved in the processing of edges and contours.

Animals↗
PubMedDate not supplied

Three-dimensional segmentation of MR images of the head using probability and connectivity.

We describe a three-dimensional (3D) segmentation method that comprises (a) user interactive identification of tissue classes; (b) calculation of a probability distribution for each tissue; (c) creation of a feature map of the most probable tissues; (d) 3D segmentation of the magnetic resonance (MR) data; (e) smoothing of the segmented data; (f) extraction of surfaces of interest with connectivity; (g) generation of surfaces; and (h) rendering of multiple surfaces to plan surgery. Patients with normal head anatomy and with abnormalities such as multiple sclerosis lesions and brain tumors were scanned with a 1.5 T MR system using a two echo contiguous (interleaved), multislice pulse sequence that provides both proton density and T2-weighted contrast. After the user identified the tissues, the 3D data were automatically segmented into background, facial tissue, brain matter, CSF, and lesions. Surfaces of the face, brain, lateral ventricles, tumors, and multiple sclerosis lesions are displayed using color coding and gradient shading. Color improves the visualization of segmented tissues, while gradient shading enhances the perception of depth. Manipulation of the 3D model on a workstation aids surgical planning. Sulci and gyri stand out, thus aiding functional mapping of the brain surface.

Algorithms↗
PubMed2005

The plastic human brain cortex.

Plasticity is an intrinsic property of the human brain and represents evolution's invention to enable the nervous system to escape the restrictions of its own genome and thus adapt to environmental pressures, physiologic changes, and experiences. Dynamic shifts in the strength of preexisting connections across distributed neural networks, changes in task-related cortico-cortical and cortico-subcortical coherence and modifications of the mapping between behavior and neural activity take place in response to changes in afferent input or efferent demand. Such rapid, ongoing changes may be followed by the establishment of new connections through dendritic growth and arborization. However, they harbor the danger that the evolving pattern of neural activation may in itself lead to abnormal behavior. Plasticity is the mechanism for development and learning, as much as a cause of pathology. The challenge we face is to learn enough about the mechanisms of plasticity to modulate them to achieve the best behavioral outcome for a given subject.

Blindness↗
PubMed2003

Laminar development of receptive fields, maps and columns in visual cortex: the coordinating role of the subplate.

How is development of cortical maps in V1 coordinated across cortical layers to form cortical columns? Previous neural models propose how maps of orientation (OR), ocular dominance (OD), and related properties develop in V1. These models show how spontaneous activity, before eye opening, combined with correlation learning and competition, can generate maps similar to those found in vivo. These models have not discussed laminar architecture or how cells develop and coordinate their connections across cortical layers. This is an important problem since anatomical evidence shows that clusters of horizontal connections form, between iso-oriented regions, in layer 2/3 before being innervated by layer 4 afferents. How are orientations in different layers aligned before these connections form? Anatomical evidence demonstrates that thalamic afferents wait in the subplate for weeks before innervating layer 4. Other evidence shows that ablation of the cortical subplate interferes with the development of OR and OD columns. The model proposes how the subplate develops OR and OD maps, which then entrain and coordinate the development of maps in other lamina. The model demonstrates how these maps may develop in layer 4 by using a known transient subplate-to-layer 4 circuit as a teacher. The model subplate also guides the early clustering of horizontal connections in layer 2/3, and the formation of the interlaminar circuitry that forms cortical columns. It is shown how layer 6 develops and helps to stabilize the network when the subplate atrophies. Finally the model clarifies how brain-derived neurotrophic factor (BDNF) manipulations may influence cortical development.

Brain Mapping↗
PubMed1989

Cortical connections of areas 17 (V-I) and 18 (V-II) of squirrels.

Connections of visual cortex in squirrels were investigated by placing WGA-HRP injections, and in some cases fluorescent dyes, into area 17 (V-I) or area 18 (V-II). Results were related to architectonic fields determined in brain sections cut parallel to the surface of manually flattened cortex and to limited microelectrode mapping data. Injections in area 17 provided evidence for 1) a patchy pattern of horizontal intrinsic connections extending 1-2 mm from the injection site; 2) uneven, widely distributed connections with area 18 (V-II) and adjoining occipital-temporal (OT) cortex; and 3) callosal connections of large portions of area 17 with the 17/18 border zone. While restricted locations in area 17 had uneven interconnections over several mm of area 18, more rostral locations in area 17 related to more rostral locations in area 18, demonstrating a topographic tendency. Injections in area 18 revealed 1) zones of discontinuous connections with area 17 that followed a topographic pattern, 2) patches of intrinsic connections that spread over distances of up to 6-8 mm from the injection site; 3) two zones of uneven connections with OT cortex suggesting the locations of at least two visual areas, OTr and OTc; 4) connections with limbic cortex rostromedial to areas 17 and 18; 5) sparse connections with regions of temporal cortex lateral to OT; and 6) uneven callosal connections with area 18 and OT cortex. The widespread and unevenly distributed intrinsic callosal interconnection patterns of areas 17 and 18 contrast with the restricted excitatory receptive fields of neurons and the retinotopic patterns of representation in these fields. Although physiological evidence is presently lacking, the patchy connections suggest that areas 17 and 18 in squirrels are modularly organized.

Animals↗
PubMed2001

Structure and function in rhodopsin: mapping light-dependent changes in distance between residue 316 in helix 8 and residues in the sequence 60-75, covering the cytoplasmic end of helices TM1 and TM2 and their connection loop CL1.

Double-spin-labeled mutants of rhodopsin were prepared containing a nitroxide side chain at position 316 in the cytoplasmic surface helix H8, and a second nitroxide in the sequence of residues 60-75, which includes the cytoplasmic loop CL1 and cytoplasmic ends of helices TM1 and TM2. Magnetic dipole-dipole interactions between the spins were analyzed to provide interspin distance distributions in both the dark and photoactivated states of rhodopsin. In the dark state in solutions of dodecyl maltoside, the interspin distances are found to be consistent with structural models of the nitroxide side chain and rhodopsin, both derived from crystallography. Photoactivation of rhodopsin shows a pattern of increases in internitroxide distance between the reference, position 316 in H8, and residues in CL1 and TM2 that suggests an outward displacement of TM2 relative to H8 by approximately 3 A.

Amino Acid Sequence↗
PubMed2000

Imaging: window on the brain.

Given the rapid advances in neuroimaging and brain mapping, it is no surprise that a whole host of new and burgeoning techniques are on the horizon as we enter the 21st century. This brief review focuses on methods that are just entering the clinical experience or are now being explored in a research setting but have the imminent potential for clinical use. A number of brain mapping techniques now allow the clinician to monitor disease progression and therapeutic effects in either the routine clinical setting or experimental clinical trials. A battery of methods are now available for the preoperative and intraoperative evaluation of patients with lesions in or near critical cortical areas or for targeting purposes when deep nuclei of the brain are potential sites of therapeutic ablation or electrophysiologic stimulation. The development of probabilistic atlases will soon provide a means of understanding normal variants of human brain structure and function and studying brain disorders and their treatment in an objective and quantifiable fashion. Techniques that are now on the horizon for imaging gene expression, neuronal excitivity, and connectivity are presented in their current stage of development. It is clear that brain mapping and neuroimaging will continue to be ever more important parts of clinical neuroscience and may ultimately serve as the bridge between the molecular and clinical domains of this field. Arch Neurol. 2000;57:1413-1421

Brain↗
PubMed2006

Capturing patterns and symmetries in chaotic granular flow.

Segregation patterns formed by time-periodic flow of polydisperse granular material (varying in particle size) in quasi-two-dimensional (quasi-2D) tumblers capture the symmetries of Poincaré sections, stroboscopic maps of the underlying flow, derived from a continuum model which contains no information about particle properties. We study this phenomenon experimentally by varying the concentration of small particles in a bidisperse mixture in quasi-2D tumblers with square and pentagonal cross sections. By coupling experiments with an analysis of periodic points, we explain the connection between the segregation patterns and the dynamics of the underlying flow. Analysis of the eigenvectors and unstable manifolds of hyperbolic points shows that lobes of segregated small particles stretch from hyperbolic points toward corners of the tumbler, demonstrating the connection between regions of chaotic flow and the shape of the segregation patterns. Furthermore, unstable manifolds map the shape of lobes of segregated particles. The techniques developed here can also be applied to nonpolygonal tumblers such as elliptical tumblers, as well as to circular tumblers with time-periodic forcing.

Journal Article↗
PubMedDate not supplied

Specific patterns of intrinsic connections between representation zones in the rat motor cortex.

The organization of intrinsic connections in rat motor cortex was studied by combining microstimulation and tract-tracing techniques. Maps of forelimb and vibrissal movements were constructed from the distribution of cortical sites from which movements were evoked in response to intracortical microstimulation. Then, a single injection of a fluorescent dextran was placed into either a vibrissal or a wrist representation zone, or into a region bordering these zones, resulting in anterograde labeling of long intrinsic, horizontal axons. Following injection into the vibrissal area, axons were largely restricted to the whisker representation zone and to the border region with the forelimb representation. Injections into a wrist zone labeled projections largely restricted to the forelimb area and to the border with the vibrissal area. Injections into a border region labeled dense projections throughout most of the forelimb and vibrissal areas. These findings indicate that intrinsic axon collaterals in the motor cortex form specific and extensive connections among representation zones related to movements of the same body part. These connections may be involved in the coordination of activity in different representation zones for the execution of complex movement patterns. The projection of axon collaterals into border regions may be the anatomical substrate for the rapid reorganization of motor cortical maps that occurs following various experimental manipulations.

Animals↗
PubMed2006

Constraints on hippocampal processing imposed by the connectivity between CA1, subiculum and subicular targets.

A long-held fundamental function of the rat hippocampus is to provide a spatial map of the environment. The principal hippocampal output region for spatial information is area CA1 and the major target of CA1 is the subiculum. Thus, one possible role of the subiculum is to receive, process and transmit information regarding location to areas outside the hippocampus. Anatomical experiments in the rat have shown that the projections from CA1 to subiculum exist in a series of 'nested loops'. Thus, each part of CA1 does not connect with each part of the subiculum. In turn, the majority of subicular principal neurons at the end of these loops have only one axonal projection target. The identity of these target areas depends on the location of the projecting cell within the subiculum, that is, neurons in different loops (and different septo-temporal levels of the subiculum) project to different sites. Principal neurons in subiculum and CA1 are not highly interconnected, suggesting that spatial information within any one of the nested loops is not shared amongst the others. This anatomical arrangement suggests that spatial information from any one part of CA1 is sent only to the sub-population of subicular principal cells within the same loop. In turn, this sub-population of subicular cells projects information to only a subset of the total range of subicular target areas. Thus, these subicular targets receive spatial information from only a subset of those in CA1. One conclusion from this is that for subicular targets to receive spatial information from the whole environment, area CA1 must have multiple spatial maps, one for each major projection (nested loop) to the subiculum.

Animals↗
PubMed2003

Learning and inference in the brain.

This article is about how the brain data mines its sensory inputs. There are several architectural principles of functional brain anatomy that have emerged from careful anatomic and physiologic studies over the past century. These principles are considered in the light of representational learning to see if they could have been predicted a priori on the basis of purely theoretical considerations. We first review the organisation of hierarchical sensory cortices, paying special attention to the distinction between forward and backward connections. We then review various approaches to representational learning as special cases of generative models, starting with supervised learning and ending with learning based upon empirical Bayes. The latter predicts many features, such as a hierarchical cortical system, prevalent top-down backward influences and functional asymmetries between forward and backward connections that are seen in the real brain. The key points made in article are: (i). hierarchical generative models enable the learning of empirical priors and eschew prior assumptions about the causes of sensory input that are inherent in non-hierarchical models. These assumptions are necessary for learning schemes based on information theory and efficient or sparse coding, but are not necessary in a hierarchical context. Critically, the anatomical infrastructure that may implement generative models in the brain is hierarchical. Furthermore, learning based on empirical Bayes can proceed in a biologically plausible way. (ii). The second point is that backward connections are essential if the processes generating inputs cannot be inverted, or the inversion cannot be parameterised. Because these processes involve many-to-one mappings, are non-linear and dynamic in nature, they are generally non-invertible. This enforces an explicit parameterisation of generative models (i.e. backward connections) to afford recognition and suggests that forward architectures, on their own, are not sufficient for perception. (iii). Finally, non-linearities in generative models, mediated by backward connections, require these connections to be modulatory, so that representations in higher cortical levels can interact to predict responses in lower levels. This is important in relation to functional asymmetries in forward and backward connections that have been demonstrated empirically.

Bayes Theorem↗
PubMed1984

Relation of callosal and striate-extrastriate cortical connections in the rat: morphological definition of extrastriate visual areas.

The main purpose of this study was to correlate the tangential distributions of visual callosal and striate-extrastriate connections in the rat. Cells of origin and terminations of the visual callosal pathway of one hemisphere were labeled by the anterograde and retrograde transport of horseradish peroxidase (HRP) after multiple injections of this enzyme in the contralateral hemisphere, while ipsilateral striate-extrastriate projection fields were revealed by using the autoradiographic method following single injections of 3H-proline in striate cortex. A remarkable complementarity in the distribution of both cortico-cortical pathways was revealed by superimposing in a camera lucida the patterns of callosal and striate-extrastriate projections from consecutive tangential sections processed for HRP and autoradiography, respectively. Projections from striate cortex are distributed into multiple extrastriate fields which are partially or totally surrounded by cortical strips containing dense and overlapping accumulations of labeled callosal cells and terminations. In addition to projections to the following striate recipient areas described in previous reports: posterior (P), posterolateral (PL), lateromedial (LM), laterolateral (LL), anterolateral (AL) and anteromedial (AM); projections to laterointermediate (LI), laterolateral anterior (LLa), anterior (A), medial (M) and pararhinal (PR) areas were defined in the present study. Striate-extrastriate projection fields occupy only a portion of the acallosal islands that contain them, and the location of the fields within these islands correlates with the retinotopic location of the isotope injection in striate cortex. When compared to previous physiological and anatomical maps of extrastriate visual areas in the rat, the present results indicate that the distribution of callosal connections correlates with the borders of extrastriate visual areas, and that the projection from striate cortex into these areas is retinotopically organized. Surprisingly, a direct projection from striate cortex to the head representation region in somatosensory cortex was labeled, a finding that challenges the view that primary sensory areas do not connect directly.

Animals↗
PubMed1995

Comparison of the patterns of callosal connections in lateral parietal cortex of the rat, mouse and hamster.

In a recent study of the second somatosensory area (SmII) in the rat it was reported that the somatotopic map in the cortex lateral to the primary somatosensory area (SmI) is closely related to local features of the callosal pattern. The existence of this relationship suggests that knowledge of the overall pattern of callosal connections in the cortex lateral to SmI may facilitate the description of the somatotopic organization of lateral parietal cortex in other rodents. We tested this suggestion by comparing the callosal patterns in lateral parietal cortex in the rat, mouse and hamster. Our finding that the callosal pattern in the mouse closely resembles that in the rat supports the idea that the callosal pattern reflects the underlying somatotopy because the maps of SmII described previously in the mouse and rat are very similar to each other. In addition, on the basis of our observation that the callosal pattern in the hamster is very similar to that in the rat and mouse, we predict that these three rodent species share a common somatotopic plan in lateral parietal cortex.

Animals↗
PubMed2001

Intra- and inter-areal connections between the primary visual cortex V1 and the area immediately surrounding V1 in the rat.

We have qualitatively and quantitatively analysed the anatomical connections within and between rat primary visual cortex (V1) and the rim region surrounding area V1, using both ortho- and retrograde anatomical tracers (biotinylated dextran amine, biocytin, cholera toxin b subunit). From the analysis of the projection patterns, and with the assumption that single points in the rat visual cortex, as in other species, have projection fields made up of multiple patches of terminals, we have concluded that just two V1 recipient areas occupy the entire rim region: an anterolateral area, probably homologous with V2 in other mammals, previously named Oc2L, and a medial area, corresponding to Oc2M. A non-reciprocal projection from the anterolateral area to the medial area was identified. Small injections (300-600microm uptake zone diameter) of the anatomical tracers in area V1, or in the rim region, label orthograde intra-areal connections from each injection site to offset small patches. This is found in all regions of the rim and within at least the relatively expanded central dorsal field representation of V1. From the extent of these projections in V1 and the two rim regions, we have estimated that the neurons at the injection site send diverging laterally spreading projections to other neurons whose receptive fields share any part of the area included in the pooled receptive fields of the neurons at the injection site. Orthogradely labelled inter-areal feedforward projections from V1 to either rim region are estimated to diverge in their projections to neurons that share any part of the area of the pooled receptive fields of the V1 intra-areal connectional field of the same injection. The orthogradely labelled feedback projections to V1, from injection sites in either rim region, reach V1 neurons whose pooled receptive fields match those of the neurons in the rim injection site, i.e. with no divergence. Despite patchy anatomical connectional fields, our estimates indicate that visual space is represented continuously in the receptive fields of neurons postsynaptic to each intra- or inter-areal field of orthograde label. We suggest that, despite the absence of regularly mapped functions in rat V1 (e.g. regularly arranged orientation specificity), which in other species (e.g. primates and cats) relate to the patchy connectional patterns, the rat visual cortex intra- and inter-areal anatomical connections follow similar patterns and scaling factors to those in other species.

Animals↗
PubMed2000

A new Arabidopsis thaliana root gravitropism and chirality mutant.

A new Arabidopsis thaliana (L.) Heynh. root mutant, named clg1, was isolated from the Feldmann-Du Pont T-DNA insertional mutagenesis collection. It is characterized by primary roots that make early right-handed coils, show increased right-handed slanting, and reduced positive gravitropism. The mutant roots however did not exhibit increased resistance to IAA, but only a modest increment of resistance to the auxins 2,4 D, and NAA, and to the auxin transport inhibitors TIBA and NPA. By contrast, the mutant roots showed a notable resistance to plant hormone ethylene (given as ACC). clg1 appears to be new, since it complements the most known auxin and gravitropism mutants, maps to chromosome 5, and shows a phenotype largely different from that of the known ethylene mutants. The increased right-handed slanting (chirality) can possibly be a consequence of the reduced gravitropic response, since gravitropism and slanting are competitive growth-direction leading forces. The increased resistance to ethylene, seems to indicate that this phythormone plays a role in the gravitropic response of roots (as already proposed for shoots), and possibly in the regulation of the connected signal transduction pathway. The gene involved in the clg1 mutation, which is recessive, was mapped, as above reported, to chromosome 5, close to the visible marker tt3.

Journal Article↗
PubMed1996

High-resolution physical mapping by combined Alu-hybridization/PCR screening: construction of a yeast artificial chromosome map covering 31 centimorgans in 3p21-p14.

We describe an integrated approach to large-scale physical mapping using an Alu-PCR hybridization screening strategy in conjunction with direct PCR-based screening to construct a continuous yeast artificial chromosome map covering >20 mb in human chromosome 3, bands p14-p21, composed of 205 loci, connected by 480 yeast artificial chromosomes, with average interlocus distance of approximately equal to 100 kb. We observe an inverse distribution of Alu-PCR and (CA)n markers. These results suggest that the two screening methods may be complementary and demonstrate the utility of Alu-PCR hybridization screening in the closure of high-resolution human physical maps.

Animals↗
PubMed1993

The human decorin gene: intron-exon organization, discovery of two alternatively spliced exons in the 5' untranslated region, and mapping of the gene to chromosome 12q23.

Decorin is a chondroitin/dermatan sulfate proteoglycan expressed by most vascular and avascular connective tissues and, because of its ability to interact with collagen and growth factors, has been implicated in the control of matrix assembly and cellular growth. To understand the molecular mechanisms involved in regulating its tissue expression, we have isolated a number of genomic clones encoding the complete decorin gene. The human decorin gene spans over 38 kb of continuous DNA sequence and contains eight exons and very large introns, two of which are 5.4 and > 13.2 kb. We have discovered two alternatively spliced leader exons, exons Ia and Ib, in the 5' untranslated region. These exons were identified by cloning and sequencing cDNAs obtained by polymerase chain reaction amplification of a fibroblast cDNA library. Using Northern blotting or reverse transcriptase PCR, we detected the two leader exons in a variety of mRNAs isolated from human cell lines and tissues. Interestingly, sequences highly (74-87%) homologous to exons Ia and Ib are found in the 5' untranslated region of avian and bovine decorin, respectively. This high degree of conservation among species suggests regulatory functions for these leader exons. In the 3' untranslated region there are several polyadenylation sites, and at least two of these sites could give rise to the transcripts of approximately 1.6 and approximately 1.9 kb, typically detected in a variety of tissues and cells. Using a genomic clone as the labeled probe and in situ hybridization of human metaphase chromosomes, we have mapped the decorin gene to the discrete region of human chromosome 12q23. This study provides the molecular basis for discerning the transcriptional control of the decorin gene and offers the opportunity to investigate genetic disorders linked to this important human gene.

Alternative Splicing↗
PubMed1995

Metabolic mapping of visual areas in the behaving cat: a [14C]2-deoxyglucose study.

Visually responsive cortical areas and subcortical nuclei were studied in the awake cat using the 2-deoxyglucose technique. Visual input was confined to one hemisphere by unilaterally sectioning the optic tract, the corpus callosum and the commissura anterior. Within the intact hemisphere, numerous cortical regions were distinguishable in the autoradiographs due to differential labelling. Comparison of the intact with the visually deafferented hemisphere confirmed the visual character of eighteen cortical areas (areas 17, 18, 19, 20a, 20b, 21a, 21b, the posteromedial lateral, posterolateral lateral, anteromedial lateral, anterolateral lateral, dorsal lateral, ventral lateral, and posterior suprasylvian areas, the splenial and anterior ectosylvian sylvian areas, insular visual area and posterior area 7) and revealed the visual nature of an area in the posterior cingulate gyrus which had not been described previously. We refer to this area as cingulate visual area (CVA). This area exhibits a gradient in interhemispheric differences along a caudorostral axis similar to that observed in posterior area 7 which is in keeping with the strong and topographic connections between CVA and posterior area 7. These results support the validity of metabolic mapping for the characterisation of cortical areas.

Animals↗