SEARCH · PubMed Health

Results for “cortex”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 793 records · Page 44Linked to original sources

PubMed2000

Localization of area prostriata and its projection to the cingulate motor cortex in the rhesus monkey.

Area prostriata is a poorly understood cortical area located in the anterior portion of the calcarine sulcus. It has attracted interest as a separate visual area and progenitor for the cortex of this modality. In this report we describe a direct projection from area prostriata to the rostral cingulate motor cortex (M3) that forms the fundus and lower bank of the anterior part of the cingulate sulcus. Injections of retrograde tracers in M3 resulted in labeled neurons in layers III, V and VI of prostriate cortex. However, injections of anterograde tracers in M3 did not demonstrate axon terminals in area prostriata. This connection was organized topographically such that the rostral part of M3 received input from the dorsal region of prostriate cortex, whereas middle and caudal levels of M3 received input from more ventral locations. Injections of retrograde and anterograde tracers in the caudal cingulate motor cortex (M4) did not produce labeling in prostriate cortex. Cytoarchitectural analysis confirmed the identity of area prostriata and further clarified its extent and borders with the parasubiculum of the hippocampal formation rostrally, and V1 of the visual cortex caudally. This linkage between cortex bordering V1 and cortex giving rise to a component of the corticofacial and corticospinal pathways demonstrates a more direct visuomotor route than visual association projections coursing laterally.

Animals↗

PubMed1995

Cortico-cortical mediation of short-latency (lemniscal) sensory input to the motor cortex in deeply pentobarbitone anaesthetized cats.

In pentobarbitone-anaesthetized cats, responses were recorded as surface positive potentials in the motor cortex on forelimb and brachium conjunctivum stimulation. In such a preparation, the forelimb nerve responses are mediated via the spino-cervical tract and the dorsal column-lemniscal pathway. Lesions of the sensory cortex (sparing only the depth of the coronary sulcus) abolished or reduced short-latency peripheral responses, in the motor cortex, on both skin and muscle nerve stimulation to less than 10% of control, while brachium conjunctivum responses were unchanged. Lesions of the second somatosensory area alone reduced the motor cortex responses on peripheral nerve stimulation by 10-20%. When the sensory cortex was inactivated by spreading depression, peripheral responses in the motor cortex were abolished before the spreading depression reached the recording point, as judged from the brachium conjunctivum response. The depth distribution of positive and negative field potentials, constituting the early components of a peripheral response in the motor cortex, closely resembled that of a cortico-cortical response evoked on stimulation in area 3. It differed from that of thalamo-cortical response evoked on brachium conjunctivum stimulation. These data suggest that most, if not all, sensory input through the dorsal column and spino-cervical tract to the motor cortex is mediated via the sensory cortex.

Anesthesia↗

PubMed1992

Synaptic proliferation in the motor cortex of adult cats after long-term thalamic stimulation.

1. One of the hypotheses for information storage in the CNS postulates the induction of structural changes in synaptic circuits. This postulate predicts that behavioral experiences produce changes in neural activity that subsequently induce synaptogenesis in the mature CNS. Available data indicate that the establishment of engrams for novel motor acts may involve alterations of synaptic interactions within the primary motor cortex. The present study examines the hypothesis that patterns of synaptic circuitry and of synaptic activation are rearranged after enhanced neural activity in pathways projecting to the motor cortex. 2. Electrodes implanted in the ventroposterolateral (VPL) nucleus of the thalamus were used for long-term stimulation (20 microA, 4 days) of afferents to the motor cortex in freely behaving, adult cats. This stimulation primarily affected corticocortical inputs from the somatosensory cortex (area 2) to area 4 gamma of the motor cortex. Electron microscopy and stereological procedures were used to compare the numerical density (Nv) of various types of synapses in layers II/III of the stimulated (experimental) motor cortex with the Nv of the corresponding synapses in the contralateral (control) hemisphere. 3. Long-term stimulation produced a significant increase (25.6%) in synaptic Nv in experimental motor cortex. This increase was due primarily to an increase in the Nv of asymmetrical synapses with dendritic spines. The numbers of symmetrical synapses, and of asymmetrical synapses with dendritic shafts, were not affected by long-term stimulation. 4. Synaptic active zones [calculated by measuring the lengths of postsynaptic densities (PSDs)] were significantly longer in experimental motor cortex. Lengthening of PSDs occurred selectively in asymmetrical synapses with dendritic shafts (28% increase). 5. The Nv of synapses having perforations in their PSDs (perforated synapses) was significantly higher in experimental hemispheres. Also increased was the incidence of synapse-associated polyribosomes, which are most commonly found at the base of dendritic spines. An increase in the number of perforated synapses and of polyribosomes are both morphological hallmarks of synaptogenesis. 6. The percentages of synapses having different curvatures (i.e., presynaptically concave, convex, or flat) were similar in experimental and in control motor cortex.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1997

Multiple nonprimary motor areas in the human cortex.

We measured the distribution of regional cerebral blood flow with positron emission tomography while three subjects moved their hand, shoulder, or leg. The images were coregistered with each individual's anatomic magnetic resonance scans. The data were analyzed for each individual to avoid intersubject averaging and so to preserve individual gyral anatomy. Instead of inspecting all pixels, we prospectively restricted the data analysis to particular areas of interest. These were defined on basis of the anatomic and physiological literature on nonhuman primates. By examining only a subset of areas, we strengthened the power of the statistical analysis and thereby increased the confidence in reporting single subject data. On the lateral convexity, motor related activity was found for all three subjects in the primary motor cortex, lateral premotor cortex, and an opercular area within the premotor cortex. In addition, there was activation of somatosensory cortex (SI), the supplementary somatosensory area (SII) in the Sylvian fissure, and parietal association areas (Brodmann areas 5 and 40). There was also activation in the insula. We suggest that the activation in the dorsal premotor cortex may correspond with dorsal premotor area (PMd) as described in the macaque brain. We propose three hypotheses as to the probable location of vental premotor area (PMv) in the human brain. On the medial surface, motor-related activity was found for all three subjects in the leg areas of the primary motor cortex and somatosensory cortex and also activity for the hand, shoulder, and leg in the supplementary motor area (SMA) on the dorsal medial convexity and in three areas in the cingulate sulcus. We suggest that the three cingulate areas may correspond with rostral cingulate premotor area, dorsal cingulate motor area (CMAd), and ventral cingulate motor area (CMAv) as identified in the macaque brain. Somatotopic mapping was demonstrated in the primary motor and primary somatosensory cortex. In all three subjects, the arm region lay anterior to the leg region in parietal area 5. Also in all three subjects, the arm region lay anterior to the leg region in the supplementary motor cortex.

Adult↗

PubMed1984

Primary visual cortex in the brushtailed possum: receptive field properties and corticocortical connections.

The corticocortical connections and receptive field properties of primary or striate visual cortex of the brushtailed possum, Trichosurus vulpecula, have been examined. In this Australian marsupial species primary visual cortex has connections with four other visual areas in the occipital lobe. In these adjacent visual areas fibers from striate cortex terminate mainly in layers 3 and 4 and in some cases also in layers 1 and 2. In all four areas return connections to striate cortex originate predominantly in layers 2 and 3, and to a much lesser extent in layers 5 and 6. Interhemispheric connections of striate cortex are limited to the boundary of striate and peristriate cortex. In addition to its cortical connections, striate cortex makes reciprocal connections with the claustrum. Most neurons in striate cortex are highly binocular. Of our sample of 113 visually responsive neurons, only 30% were orientation selective. On the basis of these observations we have compared striate cortex of the marsupial brushtailed possum with striate cortices of the American marsupial opossum and those of placental mammals.

Animals↗

PubMed2005

Comparing the effects of auditory deprivation and sign language within the auditory and visual cortex.

To investigate neural plasticity resulting from early auditory deprivation and use of American Sign Language, we measured responses to visual stimuli in deaf signers, hearing signers, and hearing nonsigners using functional magnetic resonance imaging. We examined "compensatory hypertrophy" (changes in the responsivity/size of visual cortical areas) and "cross-modal plasticity" (changes in auditory cortex responses to visual stimuli). We measured the volume of early visual areas (V1, V2, V3, V4, and MT+). We also measured the amplitude of responses within these areas, and within the auditory cortex, to a peripheral visual motion stimulus that was attended or ignored. We found no major differences between deaf and hearing subjects in the size or responsivity of early visual areas. In contrast, within the auditory cortex, motion stimuli evoked significant responses in deaf subjects, but not in hearing subjects, in a region of the right auditory cortex corresponding to Brodmann's areas 41, 42, and 22. This hemispheric selectivity may be due to a predisposition for the right auditory cortex to process motion; earlier studies report a right hemisphere bias for auditory motion in hearing subjects. Visual responses within the auditory cortex of deaf subjects were stronger for attended than ignored stimuli, suggesting top-down processes. Hearing signers did not show visual responses in the auditory cortex, indicating that cross-modal plasticity can be attributed to auditory deprivation rather than sign language experience. The largest effects of auditory deprivation occurred within the auditory cortex rather than the visual cortex, suggesting that the absence of normal input is necessary for large-scale cortical reorganization to occur.

Adolescent↗

PubMed1991

The distribution of corticocortical, thalamocortical, and callosal inputs on identified motor cortex output neurons: mechanisms for their selective recruitment.

Motor cortex neurons were identified antidromically in anesthetized cats by their axonal projections to one of six targets: (1) somatosensory cortex, (2) opposite motor cortex, (3) red nucleus, (4) lateral reticular nucleus, (5) spinal cord, and (6) ventrolateral thalamus. Three inputs to motor cortex were tested for their influences on the identified cortical efferent neurons. The tested inputs originated from ipsilateral somatosensory cortex, opposite motor cortex, and ventral thalamus. Subthreshold effects of input pathways were detected by monitoring latency variations of antidromic responses. The three afferent sources, when activated by electrical stimulation, were not equally effective on motor cortex neurons. Ipsilateral corticocortical and thalamocortical excitation were found for the majority of neurons; the influenced proportions ranged from 55% to 100%, according to the target of the output neurons. Effects from the opposite hemisphere were found for only 5% to 30% of the neurons in the same projection classes. Many neurons (36 of 81, or 44%) were excited from more than one source, but few (5 of 37, or 14%) were influenced by all three possible sources of input, even in small regions of cortex innervated by all three of the inputs. Among 19 electrode tracks where all three inputs were present, there were only 2 tracks where all the neurons shared the same combination of inputs. Even for neurons in closest anatomical proximity ("clusters"), it was unusual (only 7 of 25 clusters) for all the neurons to have the same input pattern. Among the seven clusters where all the neurons shared the same input pattern, five of the clusters projected to the same target. These variable combinations of inputs to motor cortex neurons support the conclusion that efferent neurons could be recruited selectively from separate cortical layers or from within clusters of nearby neurons, according to the target of their axonal projection.

Afferent Pathways↗

PubMed1984

Direct connections of rat visual cortex with sensory, motor, and association cortices.

Each division of rat visual cortex, areas 17, 18a, and 18b, has connections with sensory, motor, and association cortices. These corticocortical connections were sampled using anterograde autoradiographic and retrograde horseradish peroxidase labeling techniques. Area 17 is connected via reciprocal pathways with each division of visual cortex, the posterior one-third of motor area 8, association area 7, and posteroventral area 36 of temporal cortex. It also receives projections from perirhinal areas 13 and 35. Area 18a has reciprocal connections with areas 17 and 18b, a patch in posterior somatosensory area 3, and dorsal auditory area 41. Like area 17, area 18a receives afferents from and projects to the posterior one-third of motor area 8. The connections of area 18a with association cortices are extensive; these regions include parietal areas 7, 39, 40, and 14, posteroventral and dorsal area 36, and perirhinal cortex. Area 18b is connected with areas 17 and 18a, a patch in medial area 3, and dorsal area 41. There are reciprocal projections between area 18b and posterior area 8. As for association cortex, area 18b projects to frontal area 11, area 7, posteroventral and dorsal area 36, and perirhinal cortex. In addition, area 18b receives input from and projects efferents to the dorsal claustrum. Most of the interconnections among areas 17, 18a, and 18b originate from neurons in layers II, III, and V and end in terminal fields in layers I-III and V. In contrast, projections of other sensory, motor, and association cortices to visual cortex originate mainly from neurons in layer V and to a lesser extent from layer II. The reciprocal pathways from visual cortex terminate predominantly in the supragranular layers. In conclusion, these corticocortical pathways provide the basis for cortical visuosensory and visuomotor integration that may aid the rat in the coordination of visually guided behaviors.

Animals↗

PubMed1991

Patterns of sensory intermodality relationships in the cerebral cortex of the rat.

Patterns of connections underlying cross-modality integration were studied by injecting distinguishable, retrograde tracers (Fluoro-Gold and diamidino yellow) in pairwise manner into different sensory representations (visual, somatosensory, and auditory) in the cerebral cortex of the rat. In agreement with previous single tracer studies, our results indicate that the central core of sensory areas receives projections mainly from a set of association areas located in a ringlike fashion along the margin of the cortical mantle. The visual cortex received projections from areas 48/49, area 29d, posterior agranular medial cortex (AGm), area 11, area 13, and area 35. All these areas were also connected to the auditory cortex with the exception of areas 29d and AGm. However, lateral to area 29d and posterior AGm, a band of neurons projecting to the auditory cortex was present. Somatosensory cortex was connected mainly with the more anterior aspect of the hemisphere, which included primary motor area, area 11, and area 13. The patterns of intermodality relationships revealed in the present study were of two main categories. In the anterior and lateral areas, an intermingling of cells projecting to different sensory modalities was observed. In contrast, in areas located along the medial aspect of the hemisphere, cells connected to different sensory modality representations tended to be segregated from each other. Postsubicular cortex (areas 48/49) contained both intermingled and segregated groups of cells. The incidence of clearly identified double-labeled cells concurrently projecting to two different sensory representations was extremely rare. These patterns may form a substrate for different levels of cross-modal sensory integration in the rat cortex.

Animals↗

PubMed2004

Cyto- and chemoarchitecture of the cerebral cortex of the Australian echidna (Tachyglossus aculeatus). I. Areal organization.

We have examined the topography of the cerebral cortex of the Australian echidna (Tachyglossus aculeatus), using Nissl and myelin staining, immunoreactivity for parvalbumin, calbindin, and nonphosphorylated neurofilament protein (SMI-32 antibody), and histochemistry for acetylcholinesterase (AChE) and NADPH diaphorase. Myelinated fibers terminating in layer IV of the cortex were abundant in the primary sensory cortical areas (areas S1, R, and PV of somatosensory cortex; primary visual cortex) as well as the frontal cortex. Parvalbumin immunoreactivity was particularly intense in the neuropil and somata of somatosensory regions (S1, R, and PV areas) but was poor in motor cortex. Immunoreactivity with the SMI-32 antibody was largely confined to a single sublayer of layer V pyramidal neurons in discrete subregions of the somatosensory, visual, and auditory cortices, as well as a large field in the frontal cortex (Fr1). Surprisingly, SMI-32 neurons were absent from the motor cortex. In AChE preparations, S1, R, V1, and A regions displayed intense reactivity in supragranular layers. Our findings indicate that there is substantial regional differentiation in the expanded frontal cortex of this monotreme. Although we agree with many of the boundaries identified by previous authors in this unusual mammal (Abbie [1940] J. Comp. Neurol. 72:429-467), we present an updated nomenclature for cortical areas that more accurately reflects findings from functional and chemoarchitectural studies.

Acetylcholinesterase↗

PubMed1976

Alterations in receptive field properties of superior colliculus cells produced by visual cortex ablation in infant and adult cats.

To determine if functional alterations in the superior colliculus might account for recovery of visual behaviors following visual cortex removal in infant cats, the receptive field characteristics of single units in the superior colliculus of cats whose visual cortex was removed within the first week of life were compared with those of cats which sustained visual cortex lesions in adulthood and with those of normal cats. In the normal superior colliculus, 90% of all cells responded to moving stimuli irrespective of shape or orientation. Sixty-four percent of these units were directionally selective, responding well to movement in one direction but poorly or not at all to movement in the opposite direction. Ninety percent of units were binocular, the vast majority of these responding equally to stimulation of either eye or showing only slight preference for stimulation of the contralateral eye. Responses to stationary flashes of light were observed in only 33% of all visually activated cells in the normal superior colliculus. After visual cortex ablation in adult cats, only six percent of movement sensitive cells were directionally selective. Binocular preference was shifted following adult visual cortex lesions such that sixty percent of all cells responded exclusively or predominantly to stimulation of the contralateral eye. Seventy-one percent of all visually responsive units responded to stationary lights flashed on or off within their receptive field boundaries. Lesions limited primarily to area 17 had the same effect as larger lesions of visual cortex. Infant visual cortex lesions resulted in receptive field alterations similar to those observed after adult ablation. Only fifteen percent of motion sensitive units were directionally selective. Seventy-one percent responded exclusively or predominantly to stimulation of the contralateral eye. Seventy-six percent of visually responsive cells were activated by stationary light. Lesions largely confined to area 17 produced the same alterations as more extensive lesions of visual cortex. Thus, no evidence was found that the superior colliculus is involved in the functional reorganization presumed to occur following visual cortex ablation in infant cats. Recovery of visual behaviors following neonatal injury may therefore not involve alterations in the receptive fields of single cells.

Animals↗

PubMed1976

Retrosplenial cortex in the rhesus monkey: a cytoarchitectonic and Golgi study.

The laminar and cellular structure of retrosplenial cortex in the rhesus monkey was studied with Nissl stained and rapid Golgi impregnated tissue and the results were used to evaluate morphological features of a cortical transition zone. The granular layer of retrosplenial granular cortex is composed primarily of small, density packed, star pyramidal cells. These cells branch within the granular layer itself, while the apical dendrite enters layer I where it branches infrequently or not at all. This cell type is similar to the star pyramid first described by Lorente de No except in its areal and laminar distribution. Cytoarchitectonic observations of retrosplenial agranular cortex show, that, although this area is relatively "agranular" in comparison to other cortical areas, it does possess an incipient layer II and layer IV. These layers are composed mainly of small and medium sized pyramidal cells, but many non-pyramidal cell types were found in these and other layers in this area in rapid Golgi preparations. Stellate cells with beaded or smooth, lightly spinous dendrites were found throughout layer I-IV, while fusiform cells with smooth or very lightly spinous dendrites appear in layers III-VI. Areas surrounding retrosplenial cortex in the posterior cingulate region were also evaluated in Nissl and Golgi preparations including the indusium griseum, subiculum (dorsal to the corpus callosum) and area 23. The laminar and cellular constitutents of retrosplenial cortex were then evaluated in the context of cortical architectonic transition. The transition from one cellular layer in the indusium griseum to five cellular layers in area 23 is made by the addition of layers II, III, IV and VI in retrosplenial cortex to the one ganglionic layer of the indusium griseum and subiculum. Besides the addition and subdivision of layers in retrosplenial cortex, two aspects of cell morphology were found to change in this region. First, the structure of pyramidal cells progressively changes from those in the indusium griseum which have predominently round or oval somata and a preponderance of apical and few basal dendrites to those in layer V of retrosplenial cortex and area 23 which have pyramidal shaped somata and a great number of basal dendrites which branch frequently and spread horizontally for hundreds of microns. Second, there is a change in the number and distribution of non-pyramidal cell types. Evidence was not found that the indusium griseum, dorsal subiculum or layer V of retrosplenial granular cortex contain a significant number of stellate or fusiform cells. At the retrosplenial granular/agranular border, though, these cells gradually begin to constitute a greater proportion of the cell population and in area 23 form a major component of layer IV...

Animals↗

PubMed1981

An ultrastructural and biochemical analysis of norepinephrine-containing varicosities in the cerebral cortex of the turtle Pseudemys.

The fine structure and norepinephrine content of small granular vesicle-containing profiles were studied in normal and norepinephrine-depleted cerebral cortex of the turtle, Pseudemys. The cortex was fixed for electron microscopy with the KMnO4 procedure of Koda and Bloom ('77), while the norepinephrine content was assayed wit the radioenzymatic method of Coyle and Henry ('73). Green fluorescent fibers have been described by Parent and Poitras ('74) as located almost exclusively in the outer half of the molecular layer in turtle cortex. Small granular vesicle-containing profiles are found down to 100 microns below the pial surface, but over 50% lie within 20 microns of the surface. Within the outer 100 microns of cortex, the frequency of labeled varicosities is 1.39/1,000 microns2. The average area of the norepinephrine-containing varicosities is 0.61 microns2, and there is a mean of 18.4 vesicles per single section. The average number of large plus small vesicles in an entire varicosity was estimated to be 72. Synaptic membranes are not well-preserved with KMnO4 fixation, but good examples were found of small granular vesicle-containing profiles forming both symmetrical and asymmetrical membrane differentiations. Only a small percentage of the small granular vesicle profiles were associated with a synaptic membrane differentiation in single sections. When norepinephrine-fiber synapses are seen, they usually share a postsynaptic element with another unlabeled vesicle-containing profile. Normal turtle cortex contains an average norepinephrine concentration of 1.95 micrograms/gr, which is about eight times higher than in rat cortex. The ratio of norepinephrine to dopamine is about 18 to one, suggesting that dopamine is present predominantly in a precursor pool for norepinephrine. Small granular vesicle-containing profiles were eliminated after treatment with reserpine and 6-hydroxydopamine in concentrations that were shown to reduce norepinephrine concentration by 94% and 86%, respectively. The labeled varicosities were partially depleted by midbrain hemisection and by an inhibitor of dopamine-beta-hydroxylase (FLA-63). The norepinephrine-containing varicosities are remarkably coextensive with the distribution of thalamic fibers, both in the total extent of cortex where they are found and in the depth of cortex where they terminate. The results support the idea that there is a close structural and functional association between locus coeruleus and thalamic fibers in cerebral cortex, and the apparent difference in frequency of synapses suggests that each fiber system exerts its influence on cortical cells in a different way.

Animals↗

PubMed1983

The laminar distribution of intracortical fibers originating in the olfactory cortex of the rat.

In this study, the autoradiographic method for tracing axonal connections was used to identify the laminar distribution of intracortical fibers originating in the olfactory cortical areas of the rat. Most of the projections can be divided into two major fiber systems with different laminar patterns of termination. The first of these, termed the layer Ib fiber system, arises in the anterior olfactory nucleus, the anterior and posterior piriform cortex, and the lateral entorhinal cortex, and terminates predominantly in layer Ib and, in many cases, layer III of the entire olfactory cortex. The second system, termed the layer II-deep Ib fiber system, originates in three relatively small olfactory cortical areas--the dorsal peduncular cortex, the ventral tenia tecta, and the periamygdaloid cortex--and terminates in and around the cells of layer II in most parts of the olfactory cortex. There is significant overlap in the laminar distribution of the two systems, although the distinction between them is readily apparent. Within the layer Ib fiber system there are relatively slight but consistent differences in the lamination of fibers from different areas. The fibers from the anterior olfactory nucleus are concentrated in the deep part of layer Ib while those from the anterior piriform cortex are concentrated in the superficial part of this layer. The fibers from the posterior piriform cortex tend to be densest in the middle of layer Ib. These differences are maintained in all areas of termination of each set of fibers, both ipsilaterally and contralaterally. In addition, intracortical fibers from the anterior cortical nucleus of the amygdala are distributed throughout layer I, including layer Ia and Ib. Fibers from the nucleus of the lateral olfactory tract terminate bilaterally around the cells of the islands of Calleja and the medial edge of the anterior piriform cortex.

Amygdala↗

PubMed1984

Cortical connections of the middle temporal visual area (MT) and the superior temporal cortex in owl monkeys.

The connections of the middle temporal visual area (MT) and an adjoining superior temporal visual region (ST) were investigated with injections of 3H-proline and horseradish peroxidase (HRP) in adult owl monkeys. Injections in MT revealed an extensive pattern of intrinsic connections that appeared to be organized in a series of bands across MT. MT was found to project ipsilaterally to an array of visual areas including the first (V I) and second (V II) visual areas, the dorsolateral visual area (DL), and the dorso-medial visual area (DM). When injection sites and projection zones were related to previously described retinotopic maps, it was apparent that the projections of MT to these fields were largely homotopic. Other projections were to posterior parietal cortex, the dorsointermediate visual area (DI), the ventral visual area (V), and possibly the medial visual area (M). In addition, dense projections to cortex on the rostral border of MT were used to define a new subdivision of visual cortex, the superior temporal visual region (ST), as the major projection zone of MT. Callosal connections of MT were mainly to MT, with some terminations in DL and ST. Injections of 3H-proline into ST revealed a diffuse projection to largely layer I of MT, and dense projections to posterior parietal cortex, cortex in more rostral parts of the superior temporal sulcus, ventromedial inferior temporal cortex, and the region of the frontal eye fields. Callosal projections were largely to ST cortex of the other cerebral hemisphere. The results place MT and V II in distinctly different processing chains. While both MT and V II receive the major cortical outputs of V I, V II relays to DL and DL relays to subdivisions of inferior temporal cortex. In contrast, the most significant cortical target of MT appears to be to ST, which relays to posterior parietal cortex and other targets.

Animals↗

PubMed1985

Topographical projections of the cerebral cortex to the subthalamic nucleus.

Corticosubthalamic projections in the rat were investigated using the autoradiographic anterograde axonal tracing technique. After unilateral injections of tritiated amino acids in the cerebral cortex, projections to the ipsilateral subthalamic nucleus (STH) could be found arising only from the frontal agranular cortex and the zone of MI-SI overlap. Injections into granular areas of the cortex (e.g., somatosensory and visual areas) did not result in labeling in STH. Following injections in the frontal agranular cortex, labeling was present in the ipsilateral but not the contralateral STH. In general, injections that involved the lateral agranular field of frontal cortex, as defined by Donoghue and Wise ('82), resulted in a greater amount of labeling in STH than injections within the medial agranular area or the zone of MI-SI overlap. The projection from the frontal agranular areas to STH is topographically organized. The rostral part of the lateral agranular cortex projects to the lateral portion of the rostral two-thirds of STH, and the caudal part of this field projects to the ventral aspect of the middle third of STH. Injections in the rostral part of the medial agranular cortex resulted in labeling throughout the ventral two-thirds of the medial half of STH. The caudal part of the medial agranular cortex projects to the dorsolateral part of the caudal two-thirds of STH. The present results reveal projections from only the frontal agranular cortex and the zone of MI-SI overlap to STH in the rat. The cortico-STH projection is ipsilateral and terminates in a topographical manner in all parts of STH.

Animals↗

PubMed1987

The entorhinal cortex of the monkey: II. Cortical afferents.

The entorhinal cortex of the monkey is commonly viewed as the major link between the cerebral cortex and the other fields of the hippocampal formation. Until recently, however, little was known about the origins of the cortical projections to the entorhinal cortex, and most of the available information is still based on degeneration studies. We have carried out a systematic analysis of these connections by placing small injections of the retrograde tracer wheat germ agglutinin conjugated to horseradish peroxidase into each of the fields of the entorhinal cortex of the Macaca fascicularis monkey. Retrogradely labeled cells were observed in several areas of the frontal and temporal lobes, the insula, and the cingulate cortex. In the frontal lobe, the greatest number of labeled cells were observed in the orbital region and specifically in areas 13 and 13a: labeled cells were also seen in areas 14, 11, and 12. In the dorsolateral frontal cortex, labeled cells were observed mainly in the rostral half of area 46; occasionally cells were also seen in areas 9, 8, and 6. In the cingulate cortex, labeled cells were observed in area 25, area 32, and rostral levels of area 24; fewer cells were observed at caudal levels of area 24 or in area 23. The retrosplenial region (areas 30 and 29), including its caudal extension along the rostral calcarine sulcus and its ventral extension into the temporal lobe, contained numerous labeled cells. In the temporal lobe, retrogradely labeled cells were arranged in two rostrocaudally oriented bands. Rostral to the hippocampal formation, the first band encompassed the piriform and periamygdaloid cortices and areas 35 and 36; the labeling in area 36 was continuous to the temporal pole. At more caudal levels this band was located immediately lateral to the hippocampal formation and included areas 35 and 36 rostrally and areas TH and TF caudally. The second band was situated in the superior temporal gyrus where labeled cells were observed in several distinct cytoarchitectonic fields, including the parainsular cortex in the fundus of the inferior limiting sulcus. In the insula proper, retrogradely labeled cells were seen mainly in the rostral or agranular division; far fewer were observed in the dysgranular and granular insula. Whereas there is little available physiological information concerning many of the cortical regions that project to the entorhinal cortex, on anatomical grounds they may be generally characterized as polysensory associational regions.

Afferent Pathways↗

PubMed1988

Organization of cortical and subcortical projections to anterior cingulate cortex in the cat.

The aim of the experiments reported here was to identify cortical and subcortical forebrain structures from which anterior cingulate cortex (CGa) receives input in the cat. Deposits of retrograde tracers were placed at nine sites spanning the anterior cingulate area and patterns of retrograde transport were analyzed. Thalamic projections to CGa, in descending order of strength, originate in the anteromedial nucleus, lateroposterior nucleus, ventroanterior nucleus, rostral intralaminar complex, reuniens nucleus, mediodorsal nucleus, and laterodorsal nucleus. Minor and inconsistent ascending pathways arise in the paraventricular, parataenial, parafascicular, and subparafascicular thalamic nuclei. The basolateral nucleus of the amygdala, the hypothalamus, the nucleus of the diagonal band, and the claustrum are additional sources of ascending input. Cortical projections to CGa, in descending order of strength, derive from posterior cingulate cortex, prefrontal cortex, motor cortex (areas 4 and 6), parahippocampal cortex (entorhinal, perirhinal, postsubicular, parasubicular, and subicular areas), insular cortex, somesthetic cortex (areas 5 and SIV), and visual cortex (areas 7p, 20b, AMLS, PS and EPp). In general, the limbic, sensory, and motor afferents of CGa are weak. The dominant sources of input to CGa are other cortical areas with high-order functions. This finding calls into question the traditional characterization of cingulate cortex as a bridge between neocortical association areas and the limbic system.

Afferent Pathways↗