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J H Kaas

Publications and source records attributed to J H Kaas.

At least 19 recordsLinked to original sources
PubMed1997

Deactivation and reactivation of somatosensory cortex after dorsal spinal cord injury.

Sensory stimuli to the body are conveyed by the spinal cord to the primary somatosensory cortex. It has long been thought that dorsal column afferents of the spinal cord represent the main pathway for these signals, but the physiological and behavioural consequences of cutting the dorsal column have been reported to range from mild and transitory to marked. We have re-examined this issue by sectioning the dorsal columns in the cervical region and recording the responses to hand stimulation in the contralateral primary somatosensory cortex (area 3b). Following a complete section of the dorsal columns, neurons in area 3b become immediately and perhaps permanently unresponsive to hand stimulation. Following a partial section, the remaining dorsal column afferents continue to activate neurons within their normal cortical target territories, but after five or more weeks the area of activation is greatly expanded. After prolonged recovery periods of six months or more, the deprived hand territory becomes responsive to inputs from the face (which are unaffected by spinal cord section). Thus, area 3b of somatosensory cortex is highly dependent on dorsal spinal column inputs, and other spinal pathways do not substitute for the dorsal columns even after injury.

Animals↗
PubMed1997

Organization of somatosensory cortex and distribution of corticospinal neurons in the eastern mole (Scalopus aquaticus).

The somatotopic organization of somatosensory cortex of the eastern mole (Scalopus aquaticus) was explored with multiunit microelectrode recordings from middle layers of cortex. The recordings revealed the presence of at least parts of two systematic representations of the body surface in the lateral cortex. One of the representations appears to be primary somatosensory cortex (S1), and it contained cytochrome oxidase dark regions, separated by light septa that formed isomorphs with some body parts. The rostral portion of this presumptive S1 cortex contained a face representation with a series of barrel-like cytochrome oxidase dark ovals that corresponded to the vibrissae on the snout. In caudolateral S1, light septa outline the palm and digits of the forepaw. Cortex caudal to S1, in the expected region of auditory cortex, responded to vibration, suggesting a modification of auditory cortex. Injections of wheat germ agglutinin-horseradish peroxidase into the cervical enlargement of the spinal cord revealed two dense foci of cortical cells that project to the spinal cord. The focus medial to the face region in S1 may correspond to primary motor cortex (M1). The second focus was coextensive with the somatosensory representation of the forelimb and the trunk in S1. The dense corticospinal projections from the forelimb representation of S1 and motor cortex may reflect sensorimotor specializations related to digging behaviors in moles.

Animals↗
PubMed1996

Movement representation in the dorsal and ventral premotor areas of owl monkeys: a microstimulation study.

We used intracortical microstimulation to investigate the lateral premotor cortex and neighboring areas in 14 hemispheres of owl monkeys, focusing on the somatotopic distribution of evoked movements, thresholds for forelimb movements, and the relative representation of proximal and distal forelimb movements. We elicited movements from the dorsal and ventral premotor areas (PMD, PMV), the caudal and rostral divisions of primary motor cortex (M1c, M1r), the frontal eye field (FEF), the dorsal oculomotor area (OMD; area 8b), the supplementary motor area (SMA), and somatosensory cortex (areas 3a and 3b). Area PMD was composed of architectonically distinguishable caudal and rostral subdivisions (PMDc, PMDr). Stimulation of PMD elicited movements of the hindlimb, forelimb, neck and upper trunk, face, and eyes. Hindlimb and forelimb movements were represented in the caudalmost part of PMDc. Face, neck, and eye movements were represented in the lateral and rostral parts of PMDc and in PMDr. Stimulation of PMV elicited forelimb and orofacial movements, but not hindlimb movements. Both proximal and distal forelimb movements were elicited from PMDc and PMV, although PMD stimulation elicited mainly shoulder and elbow movements, while PMV stimulation evoked primarily wrist and digit movements. Distal movements were evoked more frequently from PMV than from M1r or M1c. Across cases, the median forelimb thresholds for PMDc and PMV were 60 and 36 microA, respectively, values that differ significantly from each other and from the value of 11 microA obtained for M1r. Our observations indicate that premotor cortex is much more responsive to electrical stimulation than commonly thought, and contains a large territory from which eye movements can be elicited. These results suggest that in humans, much of the electrically excitable cortex located on the precentral gyrus, including cortex sometimes considered part of the frontal eye field, is probably homologous to the premotor cortex of nonhuman primates.

Animals↗
PubMed1996

Topographic patterns of V2 cortical connections in macaque monkeys.

Patterns of connections of dorsal and ventral portions of the second visual area (V2) were used to evaluate and extend current theories of cortical organization and processing streams in macaque monkeys. Injections of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) and up to four different fluorochromes in V2 labeled neurons and terminations in V2 and in 1) caudal (DLc) and rostral (DLr) subdivisions of dorsolateral cortex between V2 and the middle temporal area (MT); 2) regions we define as dorsomedial (DM) and dorsointermediate (DI) areas; 3) MT, medial superior temporal area (MST), and fundal superior temporal area (FST); 4) the dorsal part of inferior temporal (TEO) cortex; and 5) two locations in posterior parietal cortex. The largest extrastriate connection zone was DLc, which occupied the caudal one-third to one-half of the fourth visual area (V4) region of other proposals. Based on the connection pattern, foveal vision in DLc is represented adjacent to foveal vision in V2, with the lower quadrant represented dorsally and the upper quadrant ventrally, as in V2, but within a much less extensive region of cortex. The sparser connections of DLr formed a more compressed but parallel visuotopic pattern. A third visuotopic pattern of connections was located in a moderately myelinated region of cortex just rostral to dorsomedial V2. Whereas the region would include parts of dorsal visual area 3 (V3), V3a, and possibly other areas of other proposals, we interpret the connection pattern as reflecting a dorsomedial visual area, DM, with foveal vision represented caudolaterally and other parts of the lower and upper quadrants represented more medially and rostrally. A fourth pattern of label in dorsointermediate cortex suggested the location and organization of another visual area (DI). Most of a fifth connection pattern with MT was congruent with the known visuotopic organization of MT area, but visuotopically mismatched foci of connections were observed as well. Sparser foci of label in MST suggested a rostrodorsal representation of foveal vision, with paracentral vision represented more caudally. Separate dorsal and ventral foci of label in FST were consistent with previous evidence for dorsal (FSTd) and ventral (FSTv) visual areas. Finally, connections with TEO and posterior parietal cortex were sparse. Our results suggest that much of visual cortex organization is similar in New and Old World monkeys.

Animals↗
PubMed1996

Central reorganization of sensory pathways following peripheral nerve regeneration in fetal monkeys.

Transection of a sensory nerve in adults results in profound abnormalities in sensory perception, even if the severed nerve is surgically repaired to facilitate accurate nerve regeneration. In marked contrast, fewer perceptual errors follow nerve transection and surgical repair in children. The basis for this superior recovery in children was unknown. Here we show that there is little or no topographic order in the median nerve to the hand after median nerve section and surgical repair in immature macaque monkeys. Remarkably, however, in the same animals the representation of the reinnervated hand in primary somatosensory cortex area (area 3b) is quite orderly. This indicates that there are mechanisms in the developing brain that can create cortical topography, despite disordered sensory inputs. Presumably the superior recovery of perceptual abilities after peripheral nerve transection in children depends on this restoration of somatotopy in the central sensory maps.

Afferent Pathways↗
PubMed1996

Parvalbumin-like immunoreactivity of layer V pyramidal cells in the motor and somatosensory cortex of adult primates.

Most previous immunocytochemical studies have indicated that the calcium-binding protein parvalbumin is present only in non-pyramidal neurons of the adult cerebral cortex. Using nickel and cobalt to enhance the diaminobenzidine reaction product, we observed large layer V pyramidal cells with parvalbumin-like immunoreactivity in the primary motor cortex (area 4) and somatosensory cortex of adult macaque monkeys and galagos, including giant Betz cells in area 4.

Animals↗
PubMed1996

Topography, architecture, and connections of somatosensory cortex in opossums: evidence for five somatosensory areas.

Microelectrode maps of somatosensory inputs were related to cortical architecture and patterns of cortical connections to provide evidence for five subdivisions of the somatosensory or sensorimotor cortex in North American opossums (Didelphis marsupialis). Microelectrode recordings revealed three systematic representations of the body surface. A large mediolaterally oriented representation was identified as the primary somatosensory area (S1) by its relative position, somatotopy, architecture, and connections. S1 represented the hindlimb, trunk, forelimb, and face in a mediolateral sequence. Two additional representations of cutaneous receptors were found caudolateral to S1, each with face representations adjacent to the border of lateral S1 and other body-part representations progressing more caudally toward the auditory cortex. We identified the more dorsal field as the second somatosensory area (S2) and the more ventral field as the parietal ventral area (PV). Tracers injected into S1 labeled neurons and terminals in architectonically distinct fields rostral and caudal to S1, the somatosensory caudal area (SC) and the somatosensory rostral area (SR). Movements could be evoked by microstimulation from sites scattered over S1, SR, and the frontal cortex, but thresholds were high and uncharacteristic of motor cortex. S2 and PV merged caudally with the cortex responsive to auditory stimuli, possibly A1, and neurons in some caudal recording sites in PV were activated by both auditory and cutaneous stimuli. Primary (V1) and secondary (V2) visual areas were also identified by microelectrode mapping, architecture, and connections. In addition, at least part of the cortex between V2 and the somatosensory cortex had visual connections. Thus, most of the dorsolateral cortex of opossums appears to be somatosensory, auditory, or visual.

Animals↗
PubMed1996

Theories of visual cortex organization in primates: areas of the third level.

This brief review has a few main points. (1) Early proposals on how extrastriate cortex is subdivided were inconsistent with each other, and differences in interpretation were not resolved. (2) Brodmann's proposal of two ring-like areas, 18 and 19, surrounding primary visual cortex gained great acceptance despite the lack of agreement among different investigators considering the same evidence. (3) The concepts of areas 18 and 19, transposed to signify V2 and V3, have had great impact on recent and even current theories of extrastriate visual cortex organization in primates. (4) Nevertheless, Brodmann's areas 18 and 19, as defined in humans and Old World monkeys, correspond to none of the fields currently proposed for these primates. (5) All or most mammals appear to have a V2, and there is now widespread complete agreement over the extent and organization of this area in all studied primates. V2 is commonly referred to as area 18 because of its correspondence to area 18 as defined by Brodmann is some mammals. Yet, we should recognize that V2 is about half the size of Brodmann's area 18 in Old World monkeys and humans. (6) Current concepts of V3 differ greatly from the ring-like area 19 of Brodmann. We question the validity and usefulness of retaining the concept of V3 in primates. Our proposal for DM and other visual areas along the outer border of V2 seems more consistent, not only with the evidence from New World monkeys, but with evidence from Old World and prosimian primates, and even mammals most closely related to primates (see Kaas and Preuss, 1993). In all of these primates and close relatives of primates, the evidence indicates that more than one field forms the outer border of V2.

Animals↗
PubMed1996

Cytochrome oxidase 'blobs' and other characteristics of primary visual cortex in a lemuroid primate, Cheirogaleus medius.

We recently obtained the brain of a rare lemuroid primate, Cheirogaleus medius. The brain was not perfused before death, but rather fixed by immersion shortly thereafter. In both flat-mounted and transversely sectioned tissue, we were able to clearly demonstrate periodic zones of high cytochrome oxidase (CO) activity in the primary visual cortex, resembling the so-called 'blobs' described in many other primate species. Our results contrast with a previous report indicating that blobs are absent in Cheirogaleus medius and provide support for the view that blobs are an evolutionary specialization of primate visual cortex that evolved only once, early in primate history. In other aspects of architectonic organization, area V1 of this Cheirogaleus individual closely resembles that of other strepsirhine primates, such as Galago. We were able to identify additional divisions of cortex in this individual, including the middle temporal visual area (MT), auditory cortex, and the primary somatosensory area (S1 or area 3b). These observations indicate that valuable neuroanatomical information can, in favorable cases, be obtained from rare mammalian species that die of natural causes in captivity or which must be euthanized, even though the animals have not been perfused.

Animals↗
PubMed1996

Surface-view connectivity patterns of area 18 in cats.

To determine surface-view connectivity patterns of area 18, separate injections of up to six anatomical tracers were delivered to various rostrocaudal locations of area 18 in six normal cats. Subsequently, cortex was separated from subcortical structures, manually flattened, and cut parallel to the surface. Results reveal that ipsilateral cortical connections of area 18 with three regions of cortex are topological. In areas 17 and 19, separate patches of cells labeled with different tracers progressed in a rostrocaudal sequence corresponding to the order of the injections. A similar but less precise pattern of rostrocaudal labeling occurred in more lateral visual cortex, even though several presumptive visual areas were involved. Thus, anteromedial suprasylvian cortex projected to anterior area 18 while more posterolateral suprasylvian cortex projected to posterior area 18. There was no evidence of double-labeled cells projecting to separate regions in area 18. These results are more consistent with the concept of a single suprasylvian area projecting to area 18 cortex than several.

Animals↗
PubMed1995

GAP-43 expression in the medulla of macaque monkeys: changes during postnatal development and the effects of early median nerve repair.

Expression of GAP-43, a neuronal specific growth associated phosphoprotein, has been highly correlated with the growth and remodeling of the nervous system during development and regeneration. As part of an effort to understand mechanisms of developmental plasticity in the somatosensory system, we determined how the expression of GAP-43 is affected by prenatal and early postnatal nerve cut and repair in macaque monkeys. We also observed normal developmental changes in the expression of GAP-43 during early postnatal life in macaque monkeys. The normal cuneate nucleus, as well as other nuclei of the ascending somatosensory pathways, had low levels of GAP-43 at birth that increased by 3 months and declined thereafter to reach adult levels between 8 and 15 months of age. Fiber tracts expressed low levels of GAP-43 at all postnatal ages, except the pyramidal tract which demonstrated high levels a birth that decreased over the first year. These observations suggest a gradual but differential synaptic maturation in lower brain stem nuclei as macaque monkeys mature. Greatly increased levels of GAP-43 were observed at the time of birth in the cuneate nucleus of two macaque monkeys with prenatal (E94 and El 14) nerve repair. Such an increase was not found after prenatal nerve repair with a postnatal survival time of 15 months, or after early postnatal nerve repair with short (80 days) or long (20 months) survivals. The results suggest that reorganization mechanisms at central terminals of peripheral nerves are very different following prenatal than postnatal nerve damage.

Animals↗
PubMed1995

Human visual cortex. Progress and puzzles.

A wealth of data is now available on the functional organization of the human visual cortex. Caution is necessary in basing interpretations of such data on information gained from studies of the monkey visual cortex.

Animals↗
PubMed1995

Organization of the somatosensory cortex of the star-nosed mole.

The nose of the star-nosed mole consists of a star-like array of 22 fleshy appendages that radiate from the nostrils and are moved about to explore the environment. The surface of each appendage, or ray, is densely packed with bulbous receptor organs (Eimer's organs) that are highly responsive to tactile stimulation. Here, we report that these rays have corresponding morphological specializations in somatosensory cortex. Using a stain for the metabolic enzyme, cytochrome oxidase (CO), to reveal subdivisions of cortex, we disclosed a complex pattern of CO-dense stripes or bands separated by sharp lines or septa of low CO staining. Multiunit microelectrode recordings of neural activity evoked by light tactile stimuli in somatosensory cortex of anesthetized moles allowed us to mark some of the bands and other CO-dark regions with small electrolytic lesions and later relate recording results to the CO pattern. The results suggest that the primary somatosensory cortex, S1, has an unusual ventrolateral location and orientation with representations of mouth, nose rays, facial vibrissae, forepaw, and trunk in a rostrocaudal sequence. Within this presumptive S1, the 11 rays of the contralateral nose are represented as a rostral-to-caudal cortical pinwheel of 11 stripes. Cortex ventral to the primary set of stripes contains a second rostrocaudal representation of the rays as a mirror image of the first. This second set of stripes may be part of the second somatosensory area, S2. A third pattern of CO stripes appears to merge partially with caudal stripes of the first two patterns, so that a full pattern of 11 stripes is not obvious. This representation may correspond to the ventral somatosensory area, VS, of other mammals. An extensive area of cortex separated from the nose by a large septum was responsive to stimulation of the forelimb. Auditory cortex is unusually caudal in this mole, and the presumptive primary visual area is relatively small. These specializations of somatosensory cortex in star-nosed moles may be more patent examples of the consequences of more general factors in brain development. The observations are consistent with the general rule that the terminations of sensory projections with discorrelated activity segregate.

Animals↗
PubMed1995

The emergence and evolution of mammalian neocortex.

Cortical variation in mammals and other terrestrial vertebrates, re-examined by current comparative methodology (out-group analysis), indicates that separate lateral (olfactory), dorsal and medial (hippocampal) pallial or cortical formations arose with the origin of vertebrates. Although the exact origin of mammalian isocortex (so-called neocortex) is still disputed, it appears that the earliest mammals already had a six-layered isocortex with ten to 20 functional subdivisions. Among placental mammals, at least, isocortex has expanded numerous times, producing additional cortical subdivisions. Because these expansions were independent transformations of a simpler cortex, they produced subdivisions that are not homologous.

Animals↗
PubMed1995

Limits on plasticity in somatosensory cortex of adult rats: hindlimb cortex is not reactivated after dorsal column section.

1. To better understand the limits and extents of plasticity in sensory systems of adult mammals, we unilaterally sectioned the dorsal funiculus at thoracic levels in nine adult rats to deactivate ascending afferents from the hindpaw and lower body. After postsurgical recovery periods of 3 h to 3 mo, the region of primary somatosensory cortex (S1) representing the limbs and trunk was extensively mapped with microelectrodes. 2. Recording sites were later identified as being within the hindlimb representation and other parts of S1 by relating locations of microlesions to the cytochrome oxidase pattern in sections of cortex cut tangential to the pial surface. The extent and effectiveness of spinal cord lesions were evaluated by injecting cholera toxin B subunit conjugated with horseradish peroxidase (B-HRP) at various sites in the deafferented hindpaw. 3. In five animals with complete section of the dorsal funiculus, we failed to detect any response to cutaneous stimulation of any part of the body in the deafferented hindlimb cortex. In four other animals with incomplete lesions, neurons in some penetrations could be activated by hindlimb stimulation, but not by stimulating other body parts. In those cases without activation of hindlimb cortex, B-HRP was detected in the spinal cord only caudal to the lesion, and it was not transported to the nucleus gracilis. Limited transport past the lesion to nucleus gracilis was detected in cases with incomplete lesions. 4. The results indicate that forelimb inputs do not substitute for missing hindlimb inputs in primary somatosensory cortex in rats and that the potential for somatotopic reorganization is more limited than previously thought.

Afferent Pathways↗