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Michela Gamberini

Publications and source records attributed to Michela Gamberini.

8 recordsLinked to original sources
PubMed2006

Somatosensory cells in area PEc of macaque posterior parietal cortex.

PEc is an area defined on cytoarchitectural grounds, located in the posterior part of the superior parietal lobule of macaque brain (Pandya and Seltzer, 1982). The aim of this work was to assess whether passive somatosensory stimulation elicited responses in PEc neurons. Extracellular recordings were performed in three awake Macaca fascicularis. Passive somatosensory stimulation was performed in darkness, and eye movements were monitored continuously. Recording sites were assigned to different areas according to the cytoarchitectonic criteria described by Pandya and Seltzer (1982) and Luppino et al. (2005). Only recording sites within the limits of the cytoarchitecturally defined area PEc were taken into account in this work. Of 147 PEc cells, 83 (56%) were modulated by passive somatosensory stimulation. The majority of them (73%) responded to joint rotations, and 24% responded to tactile skin stimulation. The majority of PEc somatosensory responses (90%) were evoked by contralateral stimulation. Joint-modulated cells were mostly activated by the upper limbs (82%). The majority of tactile receptive fields (61%) were located on the arms, and a minority was located on the legs and trunk. One-half of PEc somatosensory cells were polysensory, because they were sensitive to visual stimulation. The majority of PEc somatosensory cells were activated by active reaching movements. Somatosensory cells, somatosensory submodalities, and body part representations were not clustered in PEc subregions; in other words, PEc does not show a somatotopic organization. Although the caudal sector of the superior parietal lobule has been traditionally considered as a somatosensory area, this is the first demonstration of the presence of somatosensory cells in this cortical region.

Animals↗
PubMed2006

Cytoarchitectonic subdivisions of the dorsolateral frontal cortex of the marmoset monkey (Callithrix jacchus), and their projections to dorsal visual areas.

We describe the organization of the dorsolateral frontal areas in marmoset monkeys using a combination of architectural methods (Nissl, cytochrome oxidase, and myelin stains) and injections of fluorescent tracers in extrastriate areas (the second visual area [V2], the dorsomedial and dorsoanterior areas [DM, DA], the middle temporal area and middle temporal crescent [MT, MTc], and the posterior parietal cortex [area 7]). Cytoarchitectural field 8 comprises three subdivisions: 8Av, 8Ad, and 8B. The ventrolateral subdivision, 8Av, forms the principal source of frontal projections to the "dorsal stream," having connections with each of the injected visual areas. The cytoarchitectural characteristics of 8Av suggest that this subdivision corresponds to the marmoset's frontal eye field. The intermediate subdivision of area 8 (8Ad) has efferent projections to area 7, while the dorsomedial subdivision (8B) has few or no connections with extrastriate cortex. Area 46, located rostrolateral to area 8Av, has substantial connections with the medial extrastriate areas (DM, DA, and area 7) and with MT, while the cortex lateral to 8Av (area 12/45) projects primarily to MT and to the MTc. The rostromedial prefrontal (area 9) and frontopolar (area 10) regions have very few extrastriate projections. Finally, cells in dorsal area 6 (6d) have sparse projections to DM, MT, and the MTc, as well as strong projections to DA and to area 7. These results illuminate aspects of the evolutionary development of the primate frontal cortex, and serve as a basis for further research into cognitive functions using a marmoset model.

Amidines↗
PubMed2005

Resolving the organization of the New World monkey third visual complex: the dorsal extrastriate cortex of the marmoset (Callithrix jacchus).

We tested current hypotheses on the functional organization of the third visual complex, a particularly controversial region of the primate extrastriate cortex. In anatomical experiments, injections of retrograde tracers were placed in the dorsal cortex immediately rostral to the second visual area (V2) of New World monkeys (Callithrix jacchus), revealing the topography of interconnections between the "third tier" cortex and the primary visual area (V1). The data indicate the presence of a dorsomedial area (DM), which represents the entire upper and lower quadrants of the visual field, and which receives strong, topographically organized projections from the superficial layers of V1. The visuotopic organization and boundaries of DM were confirmed by electrophysiological recordings in the same animals and by architectural characteristics which were distinct from those found in ventral extrastriate cortex rostral to V2. There was no electrophysiological or histological evidence for a transitional area between V2 and DM. In particular, the central representation of the upper quadrant in DM was directly adjacent to the representation of the horizontal meridian that marks the rostral border of V2. The present results argue in favor of the hypothesis that the third visual complex in New World monkeys contains different areas in its dorsal and ventral components: area DM, near the dorsal midline, and a homolog of area 19 of other mammals, located more lateral and ventrally. The characteristics of DM suggest that it may correspond to visual area 6 (V6) of Old World monkeys.

Action Potentials↗
PubMed2005

The relationship between V6 and PO in macaque extrastriate cortex.

The cerebral cortex of three macaque monkeys, electrophysiologically studied in chronic preparations in order to recognize functionally the medial parieto-occipital area V6, was reconstructed using the software CARET. Locations of cells recorded from area V6 (n = 553) and from neighbouring cortical areas V2/V3 and V6A (n = 1341) were displayed on surface-based reconstructions of individual brains, and on a surface-based atlas of the macaque cerebral cortex. Results show that area V6 occupies the ventral part and fundus of the parieto-occipital sulcus, as well as the ventral part of the precuneate cortex. V6 borders areas V2/V3 posteriorly and laterally, and area V6A anteriorly. The visualization of individual cases on a common template (atlas), and the use of atlas datasets, allowed us to compare data coming from different individuals and different laboratories. In particular, a comparison of the location and extent of the medial parieto-occipital areas V6 and PO indicates that area PO occupies different locations according to different authors but in general includes parts of both areas V6 and V6A. We therefore suggest that the term V6 is a more appropriate designation of the visuotopically-organized area located on the anterior wall of the parieto-occipital sulcus.

Action Potentials↗
PubMed2005

Occipital (V6) and parietal (V6A) areas in the anterior wall of the parieto-occipital sulcus of the macaque: a cytoarchitectonic study.

The anterior wall of the parieto-occipital sulcus (POs) of the macaque monkey, classically considered as part of Brodmann's area 19, contains two functionally distinct areas: a ventral, purely visual area, V6, and a dorsal area, V6A, containing visual neurons and neurons related to the control of arm movements. The aim of this study was to establish whether areas V6 and V6A, so far identified only on a functional basis, have a cytoarchitectonic counterpart. The cytoarchitectonic analysis of 13 hemispheres from ten macaque brains, cut along different planes of section, showed that the anterior wall of the POs contains three distinct areas. One is located in the ventralmost part of the wall, another in the dorsalmost part of the wall, and the third occupies an intermediate position. The ventralmost region displays architectonic features typical of the occipital cytoarchitectonic domain, whereas the two dorsal areas display architectonic features typical of the posterior parietal cortex. Analysis of myeloarchitecture and of the distribution of SMI-32 immunoreactivity confirmed the cytoarchitectonic parcellation. Correlation of cytoarchitectonic maps with functional and hodological data strongly suggests that the ventral region corresponds to area V6, whereas the other two regions correspond to different subsectors of V6A, here named V6Av and V6Ad, respectively. The present data are in line with electrophysiological and hodological data, which suggest that area V6 is a classic extrastriate area, whereas V6A is an area of the posterior parietal cortex. They also suggest that V6A includes two separate cortical subdivisions, a view supported by preliminary functional and hodological data that needs further confirmation.

Animals↗
PubMed2003

Role of the medial parieto-occipital cortex in the control of reaching and grasping movements.

The medial parieto-occipital cortex is a central node in the dorsomedial visual stream. Recent physiological studies in the macaque monkey have demonstrated that the medial parieto-occipital cortex contains two areas, the visual area V6 and the visuomotor area V6A. Area V6 is a retinotopically organized visual area that receives form and motion information directly from V1 and is heavily connected with the other areas of the dorsal visual stream, including V6A. Area V6A is a bimodal visual/somatosensory area that elaborates visual information such as form, motion and space suitable for the control of both reaching and grasping movements. Somatosensory and skeletomotor activities in V6A affect the upper limbs and involve both the transport phase of reaching and grasping movements. Finally, V6A is strongly and reciprocally connected with the dorsal premotor cortex controlling arm movements. The picture emerging from these data is that the medial parieto-occipital cortex is well equipped to control both proximal and distal movements in the online visuomotor guidance of prehension. In agreement with this view, selective V6A lesions in monkey produce misreaching and misgrasping with the arm contralateral to the lesion in visually guided movements. These deficits are similar to those observed in optic ataxia patients and suggest that human and monkey superior parietal lobules are homologous structures, and that optic ataxia syndrome is the result of the lesion of a 'human' area V6A.

Animals↗
PubMed2002

Somatosensory cells in the parieto-occipital area V6A of the macaque.

The aim of this study was to assess whether neurones of area V6A, a part of Brodmann's area 19, are modulated by passive somatosensory stimulations. Extracellular activity was recorded in four awake while passive tactile stimulations of the skin and passive rotations of the joints were performed in complete darkness and under eye movement control. Out of 240 V6A units, 78 (32%) were modulated by somatosensory stimulations. The majority of somatic receptive fields were located on both proximal and distal parts of the contralateral arm. V6A somatosensory cells may play a role in the feedback control of the actual state of the arm while reaching its target in peripersonal space.

Animals↗