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Biomedical subjects

J Tanji

Publications and source records attributed to J Tanji.

At least 37 records · Page 2Linked to original sources
PubMed1997

Neuronal activity in the ventral part of premotor cortex during target-reach movement is modulated by direction of gaze.

We recorded 200 neurons from the ventral part of the premotor cortex (PMv) and 110 neurons from the primary motor cortex (MI) of a monkey performing a visually cued arm-reaching task with a delay. We compared neuronal activity in the premovement period while the monkey reached the target with the eyes fixating on either a left or right fixation target. Our data demonstrate that about half of the movement-related activity in the PMv was modulated by the direction of gaze. In contrast, a vast majority of the activity of MI neurons and about half of PMv neurons were not influenced by the direction of gaze. We further analyzed the movement-related activity during the reaching movement to targets at the top, bottom, left, and right of each fixation point. The magnitude of activity of neurons showing the gaze-direction selectivity was primarily determined by the position of the reaching target relative to the eye-fixation target, and not by the position of the target relative to the animal's body. These data suggest that a part of the coordinate transformation of the motor command signals concerning the direction of reaching from the retinotopic to body-centered frame of reference may occur at the level of premotor cortex but not in MI.

Animals↗
PubMed1996

Overlapping corticostriatal projections from the supplementary motor area and the primary motor cortex in the macaque monkey: an anterograde double labeling study.

The purpose of the present study was to determine if the cortical efferents from homologous body regions of the supplementary motor area (SMA) and the primary motor cortex (MI) project to separate or to overlapping regions in the striatum. In order to investigate the dual corticostriatal projections, we employed an anterograde double labeling paradigm in which two tracers could be simultaneously detected in the same histological section. Prior to the injections, the forelimb representation in the two cortical motor areas was identified by using intracortical microstimulation in four Japanese monkeys (Macaca fuscata). Multiple injections of biotinylated dextran amine (BDA) were made into the forelimb regions of MI and wheat germ agglutinin conjugated horseradish peroxidase (WGA-HRP) was injected into the arm region of the SMA. In additional animals, the tracers were reversed such that BDA was injected into the SMA and WGA-HRP was injected into the MI. The tissue was processed sequentially using different chromogens in order to visualize both tracers in a single section. We analyzed the distribution of the ipsilateral anterograde label. The striatal labeling from each cortical area basically consisted of a wide band of patchy dense labeling interrupted by lighter labeling. The SMA striatal projections were located mainly within the putamen, distributing from the level of the anterior commissure to the most posterior extent of the putamen. At an intermediate level, the label spread obliquely from the ventrolateral edge of the putamen dorsomedially as far as the lateral edge of the caudate nucleus. The label from the MI was observed in comparable portions of the putamen, although the SMA projections were shifted more anterior and dorsomedial to the MI projections and the heaviest projections from the SMA and the MI were separately located. On the basis of the double anterograde labeling technique, we found considerable overlap mainly in the central portion of the putamen from the SMA and MI forelimb representation. These results suggest that the homologous body regions of the SMA and MI send widespread, and substantially overlapping projections, to portions of the striatum.

Animals↗
PubMed1996

Role for cells in the presupplementary motor area in updating motor plans.

Two motor areas are known to exist in the medial frontal lobe of the cerebral cortex of primates, the supplementary motor area (SMA) and the presupplementary motor area (pre-SMA). We report here on an aspect of cellular activity that characterizes the pre-SMA. Monkeys were trained to perform three different movements sequentially in a temporal order. The correct order was planned on the basis of visual information before its execution. A group of pre-SMA cells (n = 64, 25%) were active during a process when monkeys were required to discard a current motor plan and develop a plan appropriate for the next orderly movements. Such activity was not common in the SMA and not found in the primary motor cortex. Our data suggest a role of pre-SMA cells in updating motor plans for subsequent temporally ordered movements.

Animals↗
PubMed1996

Comparison of cerebellothalamic and pallidothalamic projections in the monkey (Macaca fuscata): a double anterograde labeling study.

To address the question of segregated projections from the internal segment of the globus pallidus (GPi) and the cerebellar nuclei (Cb) to the thalamus in the monkey, we employed a double anterograde labeling strategy combining the anterograde transport of horseradish peroxidase conjugated to wheat germ agglutinin (WGA-HRP) with biotinylated dextran amine (BDA) transport. The tissue was processed sequentially for WGA-HRP, and then BDA immunohistochemistry using two different chromogens. Since the two labels were easily distinguishable on the same histological section, the interrelationship between the cerebellar and pallidal projection systems could be directly evaluated. We found that both the cerebellothalamic and pallidothalamic label consisted of dense plexuses of labeled fibers and swellings in a patch-like configuration. The patches or foci of labeling were distributed either as dense single label or as interdigitating patches of double label. We found dense single label in the central portion of the ventral anterior nucleus pars principalis (VApc) and the ventral lateral nucleus pars oralis (VLo) following the GPi injections or in the central portion of the ventral posterior lateral nucleus pars oralis (VPLo) and nucleus X (X) following the cerebellar nuclei injections. Complementary interdigitating patches of WGA-HRP and BDA labeling were found primarily in transitional border regions between thalamic nuclei. On occasion, we found overlap of both labels. We observed a gradient pattern in the density of the pallidothalamic and cerebellothalamic projections. The pallidothalamic territory included VApc, VLo, and the ventral lateral nucleus pars caudalis (VLc), with the density of these projections decreasing along an anterior to posterior gradient in the thalamus. Occasional patches of pallidal label were found in VPLo and nucleus X. Conversely, the density of cerebellothalamic projections increased along the same gradient, with the cerebellothalamic territory extending anteriorly beyond the cell-sparse zones of VPLo, X, and VLc to include VLo and VApc also. These data suggest that although the cerebellar and pallidal projections primarily occupy separate thalamic territories, individual thalamic nuclei receive differentially weighted inputs from these sources.

Animals↗
PubMed1996

Comparison of neuronal activity in the supplementary motor area and primary motor cortex.

Neuronal activity in the supplementary motor area (SMA) and primary motor cortex (MI) have been compared in many experiments during performance of many different motor tasks. On one hand, the activity in both areas may appear similar, especially when the motor task is simple. On the other hand, if the motor tasks are more demanding, neuronal activity in the SMA exhibits a variety of complex relationship to many different aspects of motor behavior, while the activity in MI is mostly related to execution of motor task itself. Of particular interest is the neuronal activity in the SMA during preparation and execution of motor tasks when no external cues for the retrieval of appropriate motor act is available. Temporal sequencing of multiple movements is a typical example of the kind of motor task that requires profound activity in the SMA.

Animals↗
PubMed1996

New concepts of the supplementary motor area.

The supplementary motor area, although traditionally defined as a single motor area, is now viewed as including at least three different areas that can be distinguished anatomically and physiologically. The differential use of these three areas for various motor behaviors has been the subject of recent studies that are beginning to provide novel concepts of the functional differentiation of each area.

Animals↗
PubMed1996

Visually guided saccade versus eye-hand reach: contrasting neuronal activity in the cortical supplementary and frontal eye fields.

1. We studied neuronal activity in the supplementary eye field (SEF) and frontal eye field (FEF) of a monkey during performance of a conditional motor task that required capturing of a target either with a saccadic eye movement (the saccade-only condition) or with an eye-hand reach (the saccade-and-reach condition), according to visual instructions. 2. Among 106 SEF neurons that showed presaccadic activity, more than one-half of them (54%) were active preferentially under the saccade-only condition (n = 12) or under the saccade-and-reach condition (n = 45), while the remaining 49 neurons were equally active in both conditions. 3. By contrast, most (97%) of the 109 neurons in the FEF exhibited approximately equal activity in relation to saccades under the two conditions. 4. The present results suggest the possibility that SEF neurons, at least in part, are involved in signaling whether the motor task is oculomotor or combined eye-arm movements, whereas FEF neurons are mostly related to oculomotor control.

Animals↗
PubMed1996

Neuronal activity in the claustrum of the monkey during performance of multiple movements.

1. We studied neuronal activity in the claustrum of monkeys during performance of three different arm movements. We verified recording sites of claustral neurons by histological confirmation of microlesions. For the sake of comparison, we also recorded from the arm area of the precentral motor cortex (MI). Selection of the movements was either visually guided or determined by memorized information. 2. A striking property of claustral neurons is their nonselective relation to the three movements (push, pull, and turn a manipulandum). A vast majority (70%) of movement-related neurons exhibited increase of discharge in relation to all three movements, whereas only 16% were active in relation to one of the three movements. By contrast, about one-half of neurons in the MI were active in relation to a single movement. In both areas, the movement-related activity was similar regardless of whether the movements were selected by visual signals or by memory. 3. The study is the first to reveal involvement of claustral neurons in motor execution, and their activity property suggests that the way they are involved is different from that of MI neurons.

Animals↗
PubMed1996

Changing directions of forthcoming arm movements: neuronal activity in the presupplementary and supplementary motor area of monkey cerebral cortex.

1. To understand roles played by two cortical motor areas, the presupplementary motor area (pre-SMA) and supplementary motor area (SMA), in changing planned movements voluntarily, cellular activity was examined in two monkeys (Macaca fuscata) trained to perform an arm-reaching task in which they were asked to press one of two target buttons (right or left) in three different task modes. 2. In the first mode (visual), monkeys were visually instructed to result and press either a right or left key in response to a forth coming trigger signal. In the second mode (stay), monkeys were required to wait for the trigger signal and press the same target key as pressed in preceding trials. In the third mode (shift), a 50 Hz auditory cue instructed the monkey to shift the target of the future reach from the previous target to the previous nontarget. 3. While the monkeys were performing this task, we recorded 399 task-related cellular activities from the SMA and the pre-SMA. Among them, we found a group of neurons that exhibited activity changes related specifically to shift trials (shift-related cells). The following properties characterized these 112 neurons. First, they exhibited activity changes after the onset of the 50-Hz auditory cue and before the movement execution when the monkeys were required to change the direction of forthcoming movement. Second, they were not active when the monkeys pressed the same key without changing the direction of the movements. Third, they were not active when the monkeys received the 50-Hz auditory cue but failed to change the direction of the movements by mistake. These observations indicate that the activity of shift-related cells is related to the redirection of the forthcoming movements, but not to the auditory instruction itself or to the location of the target key or the direction of the forthcoming movements. 4. Although infrequently, monkeys made errors in the stay trials and changed directions of the reach voluntarily. In that case, a considerably high proportion of shift-related neurons (12 of 19) exhibited significant activity changes long before initiation of the reach movement. These long-lasting activities were not observed during the preparatory period in correct stay trials, but resembled the shift-related activity observed when the target shift was made toward the same direction. Thus these activity changes were considered to be also related to the process of changing the intended movements voluntarily. 5. We found another population of neurons that showed activity modulation when the target shift was induced by the visual instruction in visual trials (visually guided shift-related neurons). These neurons were active when the light-emitting diode (LED) guided the forthcoming reach to the previous nontarget but not to the previous target. Therefore their activity was not a simple visual response to the LED per se. A majority of them also showed shift-related activity in shift trials (19 of 22 in monkey 2). 6. Neurons exhibiting the shift-related activity were distributed differentially among the two areas. In the pre-SMA, 31% of the neurons recorded showed the shift-related activity, whereas in the SMA, only 7% showed such an activity. These results suggest that pre-SMA and SMA play differential roles in updating the motor plans in accordance with current requirements.

Acoustic Stimulation↗
PubMed1996

Supplementary motor cortex in organization of movement.

Traditionally, the SMA has been defined as a single motor area in the medial part of the frontal agranular cortex. Recent anatomical and physiological studies, however, defined two areas in the medial part of Brodmann's area 6. The anterior part is now called the presupplementary motor area (pre-SMA) and the posterior part, the SMA proper or the SMA. Both areas have unique combinations of cortical and thalamocortical connectivity. Although neurons in both areas take some part in simple motor tasks such as pushing buttons in response to sensory signals, characteristic activity is found in the kind of motor tasks that require temporal organization. Temporal sequencing of multiple movements, for instance, requires a role of neuronal activity in both the SMA and pre-SMA.

Brain Mapping↗
PubMed1995

Microstimulation of the supplementary eye field during saccade preparation.

Electrical stimulation of the supplementary eye field (SEF) of monkeys has been reported to evoke saccades with low threshold currents. In previous reports, the evoked saccades have appeared either as 'converging', 'goal directed', or at times 'constant vector'. In the present study, a new aspect of intracortical microstimulation (ICMS) was found when the stimulus was applied at the time when an animal was prepared to initiate its own voluntary saccades. A cue signal was given to the animal that indicated targets of impending saccades. After a variable delay period, a 'go' signal told the monkey to initiate the saccade toward the target. ICMS was applied shortly (50-100 ms) before the go signal. The stimulus-evoked saccades were directed toward and captured the cued target, provided that the target direction was contralateral to the cortical stimulus site. Saccades with that property were evoked only from a limited portion of the cortical field that corresponded to the SEF, characterizing this particular oculomotor area.

Animals↗
PubMed1995

Spatial distribution of thalamic projections to the supplementary motor area and the primary motor cortex: a retrograde multiple labeling study in the macaque monkey.

The exact knowledge on spatial organization of information sources from the thalamus to the supplementary motor area (SMA) and to the primary motor cortex (MI) has not been established. We investigated the distribution of thalamocortical neurons projecting to forelimb representations of the SMA and the MI using a multiple retrograde labeling technique in the monkey. The forelimb area of the SMA, and the distal and proximal forelimb areas of the MI were identified by electrophysiological techniques of intracortical microstimulation and single neuron recording. Injections were made into these three representations with three different dyes in the same animal (horseradish peroxidase conjugated to wheat germ agglutinin, diamidino yellow, and fast blue), and the thalamic neurons were retrogradely labeled. Injections into the SMA densely labeled thalamic neurons in nuclei ventralis lateralis pars oralis (VLo), ventralis lateralis pars medialis (VLm) and ventralis lateralis pars caudalis (VLc), but not in nucleus ventralis posterior lateralis pars oralis (VPLo). Injections into the MI labeled thalamic neurons primarily in VLo, VLc, and VPLo. We found that the distribution of projection neurons to the three areas was largely separate in the thalamus. However, in the middle part of VLo, and in a limited portion of VLc, thalamic neurons projecting to the SMA partially overlapped with those to the distal forelimb area of the MI. They overlapped little with those to the proximal forelimb area of the MI. We noted no overlap between the distributions of thalamic projection neurons to the distal and proximal forelimb areas of the MI. These findings suggest that the SMA and MI receive separate information from the thalamus, while sharing minor sources of common inputs.

Animals↗
PubMed1995

Thalamic distribution of projection neurons to the primary motor cortex relative to afferent terminal fields from the globus pallidus in the macaque monkey.

To examine quantitatively the pathway from the internal segment of the globus pallidus to the primary motor cortex through the thalamus, we compared the distribution of thalamocortical neurons projecting to the motor cortex with the distribution of afferent terminal fields from the pallidum in the ventrolateral nuclear group of the thalamus in four Japanese monkeys by using the anterograde and retrograde double-labeling method. In each monkey, different fluorescent retrograde tracers (Fast Blue and Diamidino Yellow) were injected separately into the distal and proximal forelimb areas of the primary motor cortex after physiological mapping with intracortical microstimulation. In the same individual monkeys, an anterograde tracer, wheatgerm agglutinin conjugated to horseradish peroxidase, was injected into the internal segment of the globus pallidus after the forelimb part was identified physiologically. A small group of projection neurons to the distal and proximal representations of the motor cortex were found in the terminal fields from the pallidum, but a majority of the projection neurons were distributed outside the terminal area in the thalamus. These results confirm the existence of the pathway from the pallidum through the thalamus to the primary motor cortex, but also indicate that the primary motor cortex receives its major thalamic inputs from outside of the pallidal projection area, and that the pallidum sends its major outputs to nonprimary motor areas through the thalamus.

Afferent Pathways↗