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Biomedical subjects

R Camarda

Publications and source records attributed to R Camarda.

At least 37 records · Page 2Linked to original sources
PubMed1986

Afferent and efferent projections of the inferior area 6 in the macaque monkey.

The rostral part of the agranular frontal cortex (area 6) can be subdivided on the basis of its cytoarchitecture, enzymatic properties, and connections into two large sectors: a superior region, lying medial to the spur of the arcuate sulcus, and an inferior region, lying lateral to it. In this study we traced the afferent and efferent connections of the inferior region of area 6 by injecting small amounts of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) and fluorescent tracers (fast blue and diamidino yellow) into restricted parts of inferior area 6 and in physiologically determined fields of area 4. There is an ordered topographic pattern of connections between inferior area 6 and area 4. The region near the spur of the arcuate sulcus (hand field) projects to the area 4 hand field while the lateral part of inferior area 6 (mouth field) is connected with the corresponding field in area 4. The organization of the connections between the two fields is, however, different. The hand fields in area 6 and 4 have direct reciprocal projections, whereas the mouth field in the postarcuate cortex relays information to area 4 via a zone intermediate between the arcuate and the central sulcus. This zone corresponds to the cytochrome oxidase area F4 (Matelli, Luppino, and Rizzolatti: Behav. Brain Res. 18: 125-137, '85). The inferior area 6 also has topographically organized connections with the supplementary motor area. The inferior area 6 receives and sends fibers to a series of discrete cortical areas located in the lower cortical moiety (Sanides: The Structure and Function of the Nervous Tissue, Vol. 5. New York: Academic Press, pp 329-453, '72). These areas that form a broad ring around the central sulcus are the ventral bank of the principal sulcus and the adjacent area 46, the precentral operculum (PrOC), area SII (Jones and Burton: J. Comp. Neurol. 168:197-248, '76), the parietal operculum, and the rostral part of the inferior parietal lobule including the lower bank of the intraparietal sulcus. Finally, the inferior area 6 has sparse but consistent connections with insular and cingulate cortices. The functional significance of this complex pattern of connections is discussed.

Afferent Pathways↗
PubMed1984

Interconnections within the postarcuate cortex (area 6) of the macaque monkey.

Small amounts of horseradish peroxidase conjugated with wheat germ were injected in restricted parts of the postarcuate premotor area of the macaque monkey. It was found that regions of this area having different somatotopic representations are richly interconnected among them. This pattern of intra-areal connectivity was not observed in the precentral motor area. It appears therefore that the postarcuate area is organized according to anatomical principles which are different from those of the primary motor cortex.

Animals↗
PubMed1984

[Intrinsic and extrinsic connections of the postarcuate premotor area of the monkey].

Horseradish peroxidase conjugated with wheat germ agglutinine was injected in restricted parts of the postarcuate cortex in the macaque monkey. Anterograde and retrograde transport was found in the parietal and frontal lobes. In the parietal lobe two areas were marked: the antero-lateral part of area 7 and the superior bank of the sylvian fissure. In the frontal lobe the marked areas were the precentral motor cortex, the supplementary motor area and the gyrus cinguli. The intrinsic connections within the postarcuate cortex were rich and widespread. The hand representation was connected anterogradely and retrogradely with the mouth representation and anterogradely with the leg representation; the mouth representation was connected both ways with the hand representation but not with the leg area. The richness of intrinsic connections in the postarcuate cortex supports the suggestion that this area is involved in the organization of sequential motor acts.

Animals↗
PubMed1984

[Functional organization of the intermediate and deep layers of the superior colliculus of the monkey].

Single neurons and polispike activity were recorded from the superior colliculus of anesthetized, behaving monkeys. In agreement with previous findings neurons of the superficial layers responded exclusively to visual stimuli. In the intermediate layers most neurons were oculomotor, although some of them showed also a visual receptive field. No neurons responding to tactile or auditory stimuli were found. Occasionally the discharge of an oculomotor neuron increased if the ocular movement was triggered by a visual or an acoustical stimulus. Rare tacticle and auditory neurons were recorded in deep layers. However their receptive fields were difficult to map and their responses lacked the precision of the responses of the specific acoustic and tactile areas. Electrical stimulation of the SC produced contralateral eye and head movements, the threshold being high in the superficial layers and low in the intermediate and deep ones. In the deep layers complex limb and trunk movements could be also elicited. In conclusion, in contrast with carnivores and other mammals, the primate superior colliculus appears to be dominated by the visual modality.

Animals↗
PubMed1982

Inferior cortical altitudinal hemianopia: report of a case.

A case of bilateral inferior altitudinal hemianopia of cortical origin is reported. Although bilateral altitudinal hemianopias can be caused by more or less symmetrical involvement of visual pathways, it is shown how only three sites of these pathways are likely to be responsible for altitudinal hemianopias in human pathology.

Cerebrovascular Disorders↗
PubMed1981

Response properties and behavioral modulation of "mouth" neurons of the postarcuate cortex (area 6) in macaque monkeys.

Single neurons were recorded from the "mouth area" of the postarcuate cortex in macaque monkeys. According to their responses to somatosensory stimuli and their activity during the animal's movements, the neurons were subdivided into three classes: (1) neurons activated only by external stimuli; (2) neurons showing an enhancement of their response when a specific motor act followed the external stimulation; (3) neurons responding reliably to external stimuli only if the stimulation triggered a specific, related motor act. Of the recorded neurons, 50% also responded to visual stimuli.

Animals↗
PubMed1980

Neurons with complex visual properties in the superior colliculus of the macaque monkey.

Single neurons were recorded from the superficial layers of the superior colliculus of immobilized monkeys (Macaca mulatta and Macaca irus). Two main functional types of neurons were found. The neurons of the first type (Type I neurons) responded well to simple stationary and moving stimuli such as spots, bars or slits of light. The latency of their response was 41 +/- 6 ms. They were not directionally selective and responded to a large range of velocities. The neurons of the second type (Type II neurons) responded very poorly to simple visual stimuli and their activation required real objects or certain two-dimensional patterns. The mean latency of response of these units was 66 +/- 26 ms. Habituation was always present. Type II neurons were located in the lower part of the superficial layers. The characteristics of Type II neurons suggest that in the primate superior colliculus there is a mechanism that allows the recognition of the complexity and the novelty of a stimulus and guides orienting responses to those stimuli that are worth analyzing in detail.

Animals↗
PubMed1979

The effect of hemidecortication on the inhibitory interactions in the superior colliculus of the cat.

Single neurons were recorded extracellularly from the superficial layers of the superior colliculus (SC) in 21 curarized cats. Four animals were normal unoperated cats, 17 were animals in which all cortical visual areas were ablated on one side from 7 to 69 days before the electrophysiological experiments. After cortical ablation all animals were blind in the visual field contralateral to the ablated side. In both normal and hemianopsic cats the effect of a visual stimulus located very far from the excitatory part of the unit receptive field, on the neuron responses to visual stimuli was studied. The remote stimulus (extra-field stimulus) was a hand moved black spot 10 degrees in diameter. In normal animals the introduction of the extra-field stimulus in the hemifield contralateral or ipsilateral to the recorded SC produced a marked reduction of unit responses to visual stimuli presented in their receptive field. This effect was particularly strong when the extra-field stimuli were introduced in the hemifield contralateral to the recorded side. In the hemianopsic animals the neurons of the SC ipsilateral to the lesion (receptive fields in the behaviorally blind hemifield) responded well to visual stimuli, but were only weakly inhibited by the extra-field stimuli presented in the blind hemifield. The neurons of this colliculus with the exception of those in the upper part of stratum griseum superficiale were normally inhibited by stimuli presented in the normal hemifield. The neurons of the SC contralateral to the lesion responded well to visual stimuli and were normally inhibited by stimuli presented in the normal hemifield; they were virtually not affected by stimuli presented in the blind hemifield. Mechanisms responsible for the abnormal inhibitory interactions between and within colliculi after cortical lesions and the possible behavioral implications of the findings are discussed.

Animals↗
PubMed1977

Influence of the presentation of remote visual stimuli on visual responses of cat area 17 and lateral suprasylvian area.

Single units were recorded extracellularly from area 17 and lateral suprasylvian area (LSSA) in curarized cats. Visual stimuli, usually a 10 degree black spot, were introduced abruptly in the visual field remote from the discharge area of a neuron's receptive field and moved at a speed of about 30 degrees/sec. The effect of these remote stimuli (S2) on the reponse to a restricted visual stimulus (S1) crossing the discharge area was studied. It was found that most units in area 17 were not affected by the presentation of remote stimuli, the remainder being either slightly facilitated or slightly inhibited. In contrast the LSSA neurons were usually inhibited by the presentation of S2: this effect was strong, was present in all classes of LSSA neurons and was independent of the relative directions of movement of S1 and S2. On the basis of these data and those previously obtained from the superior colliculus it is concluded that the way the extrageniculate centres respond to a stimulus abruptly introduced in the visual field is substantially different from that of the striate cortex. Only in the extrageniculate centres a new stimulus, besides exciting the neurons which correspond to the position of the stimulus in the field, concomitantly decreases the responses of neurons located in positions of the visual field remote from that stimulus. Possible behavioral implications of the findings are discussed.

Animals↗
PubMed1976

Visual receptive fields in the lateral suprasylvian area (Clare-Bishop area) of the cat.

Single units were recorded from the visual area of the lateral suprasylvian gyrus (LSSA or Clare-Bishop area) in 20 unanesthetized cats. Most LSSA units were poorly responsive to stationary visual stimuli, but they responded vigorously to moving visual stimuli. Their receptive fields appeared to be constituted of a large activating region (discharge area) often surrounded by inhibitory flanks. Relating unit behavior to changes of stimulus length, the LSSA neurons could be subdivided into 5 categories. The first category (22 out of 95 units tested, 23.16%) consisted of units showing summation inside the discharge area. Expanding the stimulus outside the discharge area did not affect the response. The second category (7.37%) was formed by units which showed summation inside the discharge area and inhibition when the stimulus was extended outside the discharge area. The third category (21.05%) consisted of units largely insensitive to the stimulus length inside the discharge area, but surrounded by inhibitory flanks. The fourth category (41.05%) consisted of units which showed inhibition of the response when the stimulus, well inside the discharge area, became longer than a certain optimal lenght. They were surrounded by inhibitory flanks. The fifth category (7.37%) was formed by units insensitive to variations of the stimulus length inside as well as outside the discharge area. Almost all units, independent of their category, were directionally specific, that is their response could be decreased 50% or more by varying the direction of movement away from that which gave the maximal response (preferred direction). Typically the response was halved when the stimulus was moved +/- 50 degrees from the preferred direction. Among the directionally specific units, 71% showed the minimal response 180 degrees away from the preferred direction (direction specificity curve type 1), 20% had the minimal response 90 degrees from the preferred direction (direction specificity curve type 2); the remaining could not be classified in this respect. Of LSSA units, 87% (all those of type 1 and many of those of type 2) were directionally selective, that is their response to movement in the preferred direction was at least double that in the opposite direction. The LSSA units usually preferred stimuli moving at rather high speeds. The optimal speed for 71% of units was 20 degrees/sec or greater. Almost all units responded over a wide range of speeds, many of them from 5-10 degrees/sec to over 100 degrees/sec. Most neurons had a low spontaneous activity and some of them remained completely silent for seconds.

Action Potentials↗