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C Galletti

Publications and source records attributed to C Galletti.

At least 37 records · Page 2Linked to original sources

'Real-motion' cells in area V3A of macaque visual cortex.

The stability of visual perception despite eye movements suggests the existence, in the visual system, of neural elements able to recognize whether a movement of an image occurring in a particular part of the retina is the consequence of an actual movement that occurred in the visual field, or self-induced by an ocular movement while the object was still in the field of view. Recordings from single neurons in area V3A of awake macaque monkeys were made to check the existence of such a type of neurons (called 'real-motion' cells; see Galletti et al. 1984, 1988) in this prestriate area of the visual cortex. A total of 119 neurons were recorded from area V3A. They were highly sensitive to the orientation of the visual stimuli, being on average more sensitive than V1 and V2 neurons. Almost all of them were sensitive to a large range of velocities of stimulus movement and about one half to the direction of it. In order to assess whether they gave different responses to the movement of a stimulus and to that of its retinal image alone (self-induced by an eye movement while the stimulus was still), a comparison was made between neuronal responses obtained when a moving stimulus swept a stationary receptive field (during steady fixation) and when a moving receptive field swept a stationary stimulus (during tracking eye movement). The receptive field stimulation at retinal level was physically the same in both cases, but only in the first was there actual movement of the visual stimulus. Control trials, where the monkeys performed tracking eye movements without any intentional receptive field stimulation, were also carried out. For a number of neurons, the test was repeated in darkness and against a textured visual background. Eighty-seven neurons were fully studied to assess whether they were real-motion cells. About 48% of them (42/87) showed significant differences between responses to stimulus versus eye movement. The great majority of these cells (36/42) were real-motion cells, in that they showed a weaker response to visual stimulation during tracking than to the actual stimulus movement during steady fixation. On average, the reduction in visual response during eye movement was 64.0 +/- 15.7% (SD).(ABSTRACT TRUNCATED AT 400 WORDS)

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Gaze-dependent visual neurons in area V3A of monkey prestriate cortex.

Extracellular recordings from single neurons of the prestriate area V3A were carried out in awake, behaving monkeys, to test the influence of the direction of gaze on cellular activity. The responsiveness to visual stimulation of about half of the studied neurons (88/187) was influenced by the animal's direction of gaze: physically identical visual stimuli delivered to identical retinotopic positions (on the receptive field) evoked different responses, depending upon the direction of gaze. Control experiments discount the possibility that the observed phenomenon was due to changes in visual background or in depth, depending on the direction in which the animal was looking. The gaze effect modulated cell excitability with different strengths for different gaze directions. The majority of these neurons were more responsive when the animal looked contralaterally with respect to the hemisphere they were recorded from. Gaze-dependent neurons seem to be segregated in restricted cortical regions, within area V3A, without mixing with non-gaze-dependent cells of the same cortical area. The most reliable differences between V3A gaze-dependent neurons and the same type of cells previously described in area 7a (Andersen and Mountcastle, 1983) concern the small receptive field size, the laterality of gaze effect, and the lack of straight-ahead facilitated or inhibited neurons in area V3A. Since the present results show that V3A gaze-dependent neurons combine information about the position of the eye in the orbit with that of a restricted retinal locus (their receptive field), we suggest that they might directly encode spatial locations of the animal's field of view in a head frame of reference. These cells might be involved in the construction of an internal map of the visual environment in which the topographical position of the objects reflects their objective position in space instead of reflecting the retinotopic position of their images. Such an objective map of the visual world might allow the stability of visual perception despite eye movement.

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'Real-motion' cells in visual area V2 of behaving macaque monkeys.

Extracellular recordings were made in area V2 of behaving macaque monkeys. Neurons were classified into three groups: non-oriented cells, oriented cells with antagonistic areas and oriented cells without antagonistic areas in their receptive field. All neurons were tested with standard visual stimulations in order to assess whether they gave different responses to the movement of a stimulus and to the movement of its retinal image alone, when the stimulus was motionless and the animal voluntarily moved its eyes. To do this, neuronal responses obtained when a moving stimulus swept a stationary receptive field (during steady fixation) and when a moving receptive field swept a stationary stimulus (during tracking eye movements), were compared. The receptive field stimulation at retinal level was physically the same in both cases, but only in the first was there actual movement of the visual stimulus. Control trials, where the monkeys performed tracking eye movements without any intentional receptive field stimulation, were also carried out. Out of a total of 263 neurons isolated in the central 10 deg representation of area V2, 101 were fully studied with the visual stimulation described above. Most of these (83/101; 82%) gave about the same response to the two situations. About 14% (14/101) gave a good response to stimulus movements during steady fixation and a very weak one to retinal image displacements of stationary stimuli during visual tracking. We have called neurons of this type "real-motion cells" (cf. Galletti et al. 1984). None of the non-oriented cells was a real-motion one, while about an equal percentage of real-motion cells was found among the oriented cells with and without antagonistic areas. Finally, we found only 4 neurons which showed behaviour opposite to that of real-motion cells, i.e. they showed a better response to displacement of the retinal image of stationary stimuli than to actual movement of stimuli. We suggest that real-motion cells might contribute to correctly evaluating movement in the visual field in spite of eye movements and that they might allow recognition of the movement of an object even if it moves across a non-patterned visual background. Present data on area V2, together with similar results observed in area V1 (Galletti et al. 1984; Battaglini et al. 1986), support the view that these two cortical areas analyse the movement in a parallel fashion along with many other characteristics of the visual stimulus.

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[Cavernous hemangioma confined to the tongue].

The authors relate on a case of an isolated cavernous haemangioma of the body of the tongue characterized by considerable size. Such neoplasms, usually described within the more extensive chapter of the more common angiomatous lesion of the oral cavity, are relatively rare. The authors describe a personal case discussing the diagnostic spects of such lesion and emphasizing the importance of the arteriography of the carotid artery and the of the selective arteriography of the lingual arteries, especially in considering surgery. Biopsies are not recommended. After discussing the histopathological and clinical aspects of such lesions the Authors emphasize the therapeutic ones. Even though radiotherapy, cryotherapy, laser therapy, medical treatment, injection of sclerosing substances and the selective embolization, of the lingual artery seem to have some efficacy, the authors conclude that surgery in the therapy of choice in the isolated vascular lesions of the body of the tongue.

Hemangioma↗

Effect of fast moving stimuli and saccadic eye movements on cell activity in visual areas V1 and V2 of behaving monkeys.

Extracellular recordings were carried out in the visual cortex of behaving monkeys trained on a fixation/detection task, during which a target light was displayed stationary or suddenly moving on a tangent translucent screen. The responses of visual cortical cells to fast moving stimuli during steady fixation and those obtained during rapid eye movements (saccades) which moved their receptive field across a stationary stimulus, were studied. Areas V1 and V2 were explored. When tested with rapidly moving stimuli (500 deg/sec) during steady fixation, neurons in each area behaved in almost the same way. About one fourth of them were activated, the remainder showing either no response (little more than a half of them) or a reduction of the spontaneous firing rate. In both areas, some of the neurons activated during steady fixation did not respond or responded very weakly during eye motion at saccadic velocity (500 +/- 50 deg/sec). Neurons of this type, which we refer to as 'real motion' cells, could somehow contribute to the maintenance of visual stability during the execution of large eye movements.

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Single unit activity and visual perception of motion.

Extracellular recordings were carried out in the primary visual cortex of behaving macaque monkeys. Neurons were activated by moving a visual stimulus across their receptive fields during steady fixation and by moving their receptive fields (by visual tracking) at the same velocity across a stationary visual stimulus. Out of a total number of 123 cells studied, 111 were activated by the visual stimulation both during fixation and tracking. The remaining 12 cells showed good response during fixation and very weakened response during tracking. Our results show that a small percentage of striate neurons in macaque monkey could discriminate between the real motion of an object in the visual world and the self-induced displacement of its retinal image.

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'Real-motion' cells in the primary visual cortex of macaque monkeys.

Extracellular recordings were carried out in the primary visual cortex of behaving macaque monkeys. Neurons were activated by moving a visual stimulus across their receptive fields during periods of steady fixation and by moving their receptive fields (by visual tracking) across a motionless visual stimulus, taking care that the velocities of stimulus and eye movements were the same. The total cell population (108 neurons) ws divided into 3 groups according to the cell sensitivity to visual stimulus orientation (non-oriented cell and oriented cells) and to the presence or absence of antagonistic areas in in the receptive fields (oriented cells with antagonistic areas). All the non-oriented cells (n = 14) showed almost the same response to visual stimulation both during steady fixation and during visual tracking. Out of a total number of 86 oriented cells, 77 turned out to be activated by the visual stimulation both during fixation and tracking. Eight oriented cells gave a very weak response or no response at all to visual stimulation during smooth pursuit eye movements and one neuron of the same group showed a greater response during visual tracking than during fixation. Six out of 8 oriented cells with antagonistic areas showed almost the same response to the two types of visual stimulation, while the remaining two neurons showed very weak responses during smooth pursuit eye movements. Our results show that a small percentage (about 10%) of striate neurons in macaque monkeys gave very different responses to the same physical stimulation at retinal level, according to the presence or absence of slow eye movements (smooth pursuit eye movements). The activity of these neurons seems to be related to the real movement of something in the visual world, in spite of the retinal image movement per se.

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Microprocessor-based system for spike and eye-movement data acquisition and storage.

A simple system for simultaneous recording of eye position and spike activity during on-line experimentation is described. The system is based on a relatively inexpensive and widely distributed personal computer. While the hardware is configured from commercially available products, the software has been developed in our laboratory. Data acquisition is controlled by a few routines whose logic is outline, together with the main limitations and the possible improvements of the system itself.

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Projections from the cortex of the superior temporal sulcus to the dorsal lateral geniculate and pregeniculate nuclei in the macaque monkey.

Cortical projections from the visual region and adjacent polysensory region of the superior temporal sulcus (STs) to the lateral geniculate body (LGb) were investigated in the macaque monkey using an autoradiographic tracing method. Solutions of tritiated aminoacids were injected into different parts of the caudal half of the STs of five animals. A survival time of 7 days was allowed. Labels were found in both subdivisions of the LGb: the dorsal lateral geniculate nucleus (DLGn) and the pregeniculate nucleus (PGn). In particular, part of the visual cortical region adjacent to the middle temporal area (MT) projects into the DLGn as well as the PGn, whereas the MT itself and the superior temporal polysensory region project into the PGn only. Afferents to the DLGn terminate in the magnocellular layers and in their adjoining interlaminar zones, completely sparing the parvocellular layers. Afferents to the PGn terminate in separate regions of this nucleus; the MT and adjacent visual cortices project into the internal layer of the PGn, whereas the polysensosy region of the STs projects into the external retinorecipient layer of the PGn. Possible functional implications of these projections are discussed.

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Non-oriented cells of the striate cortex activated during smooth pursuit eye movements and steady fixations in behaving monkeys.

Extracellular recordings were carried out in the primary visual cortex of behaving monkeys. Neurons were activated by moving a visual stimulus on their receptive fields during periods of steady fixation and by moving their receptive fields (smooth pursuit eye movements) on a motionless visual stimulus. Regarding non-oriented cells, they turned out to be activated by the visual stimulation both during steady fixations and smooth pursuit eye movements. Therefore, the non-oriented cells we studied seem not to receive an extraretinal signal related to the slow eye movements.

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Projections from the visual cortical region of the superior temporal sulcus to the striatum and claustrum in the macaque monkey.

Solutions of tritiated aminoacids were injected into the visual cortical region hidden in the depth of the superior temporal sulcus (STs) of the macaque monkey. Injection sites involved the middle temporal visual area, extending into the surrounding visual cortices. Projections were found homolaterally in both the striatum and claustrum. In the caudate nucleus labeled material affected mainly the body and spread both to the tail and the head of the nucleus. Label was also seen in the caudal third of the putamen and in the postero-ventral claustrum. Compared with the scarcity of afferents arising from occipital visual areas, the present data point to a heavy projection system from additional visual areas of the STs to the basal ganglia in the macaque monkey.

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Bilateral projections from the visual cortex to the striatum in the cat.

Direct projections from visual areas 17, 18, 19, and lateral suprasylvian visual area (LS) to the striatum were searched for in 12 adult cats using the autoradiographic technique to detect neuronal pathways. Striatal labels were found only after injections in areas 19 and LS. Projections homolateral to the injection sites were observed from both areas to the head and body of the caudate nucleus and to the putamen. Contralateral projections were found from both areas 19 and LS: however, area 19 did not project to the contralateral putamen. The extent of contralateral projections was smaller and they were confined within the same regions as the homolateral ones. Silver grains were often arranged in cluster-like patches, which were more evident ipsilaterally, in the head of the caudate nucleus and after injections in area LS. The present data support the view of a not strictly topographical segregation of striatal projections from the cat visual cortex.

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Corticopontine projections from the visual area of the superior temporal sulcus in the macaque monkey.

1. The projections from the superior temporal sulcus (STS) visual area to pontine nuclei were studied in the macaque monkey by the autoradiographic tracing method. Microinjections of a mixture of L-[5-3H] proline and L-[4,5-3H] leucine were carried out in the posterior band and the floor of the caudal half of the STS. Survival time was always 7 days. 2. The STS visual area projects to the dorsolateral part of ipsilateral pontine nuclei. Terminal projections are distributed in patches in the whole rostro-caudal extent of the pons. 3. These findings support the view that the STS visual area in the macaque monkey is homologous to the postero-medial lateral suprasylvian area in the cat.

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Cortical visual input to the orbito-insular cortex in the cat.

The anatomical pathways supplying the visual signal to the cat orbito-insular cortex (OIC) from primary visual areas were studied by an anterograde axonal transport technique. L-[5-3H]proline was injected, in different animals, in each of areas 17, 18, 19 and the lateral suprasylvian visual area (LS). Serial histological sections were processed by autoradiographic technique after long (8-16 days) or short (30 h) survival times. The axonal flow labelled direct pathways from LS to the ipsilateral orbital gyrus and the ventral bank of the anterior ectosylvian sulcus; this region seems to correspond to that from which many authors recorded photically evoked potentials. Long survival animals injected in LS showed labels also in the contralateral OIC. No axonal flow could be demonstrated from areas 17, 18 and 19 to OIC, either at short of long survival times. The results suggest that, apart from possible sub cortical afferences, a critical visual input may reach OIC from the extrageniculostriate visual system through LS. The functional relevance of extrastriate input to OIC is discussed.

Afferent Pathways↗

Bilateral cortical projections from cat visual areas 17 and 18. An autoradiographic study.

Associated and commisural connections of visual areas 17 and 18 were studied in the light of the latest knowledge about the anatomo-functional organization of the cat's visual cortices. Injections of L-[5-3H] proline were placed, in different animals, in area 17 or 18 of the right hemisphere. Serial histological sections of the whole brain were processed by autoradiographic technique, after long (8-16 days) or short (30 hours) survival times. Cortical areas labelled by axonally transported radioactive material were then correlated with electrophysiological and cytoarchitectonical maps. Areas 17 and 18 were found to send associational projections to area 19, to the anterior and posterior subdivisions of the lateral suprasylvian visual area and to two regions lying on the crown of the suprasylvian gyrus (areas 21A and 20). In addition, area 18 sends projections to ipsilateral areas 17, 7 and 5. Contralaterally, projections from areas 17 and 18 reach the homonymous areas near the margin of the other. Homotopical callosal connections of area 17 affect the band of the contralateral 17 in which part of the ipsilateral visual hemi-field is represented. Heterotopical commisural projections from the areas studied affect areas 19 and LS in regions adjoining the central vertical meridian representations. These results suggest that, on an anatomical basis, the interactions between the cortical targets of the classical geniculo-striate and the estrageniculo-striate systems are more complicated than previously believed. Furthermore, the geniculo-striate system supplies some visual input to non-visual areas through area 18.

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An autoradiographic study of bilateral cortical projections from cat area 19 and lateral suprasylvian visual area.

Associational and commissural connections of area 19 and of the lateral suprasylvian visual area (LS) of the cat were studied by means of an axonal anterograde transport technique. Multiple injections of L-[5-3H] proline were placed, in different animals, in area 19 and in two different subdivisions of LS (PMLS, PLLS). Serial histological sections of the whole brains were processed by autoradiographic technique after long (8-12 days) and short (30 hrs) survival times. Cortical areas labelled by accumulation of radioactive material were correlated with electrophysiological and cytoarchitectonic maps of cortical areas. Results showed a number of projections of areas 19 and LS not previously described. Area 19 sends ipsilateral projections to area 5 and to the medial bank of the anterior suprasylvian sulcus. The postero-medial (PMLS) and postero-lateral (PLLS) subdivisions of LS project to ipsilateral areas 5, 6, 7, 20, 21, 35, to the suprasylvian fringe (SF), to the cingulate gyrus and to the insular cortex. Contralaterally, new projections are found from area 19 to areas 20 and 5, and from LS to areas 19, 20, 21, 5, 7, SF to the cingulate gyrus and to the insular cortex. Results lead to conclude that the intra-modal and cross-modal interactions between cortical areas processing visual input are more complicated than previously assumed. The crucial role of the cat's LS in the cortico-cortical distribution of the visual message in emphasized.

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