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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 17 (1973), S. 144-151 
    ISSN: 1432-1106
    Keywords: Lateral reticular nucleus ; Pyramidal tract ; Internal feedback loops
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The properties of the corticospinal fibres which also influence the contralateral lateral reticular nucleus (LRN) were investigated in 16 cats anaesthetised with α-chloralose or N2O/O2. Measurements of conduction velocity by stimulation of pericruciate cortex and cerebral peduncle showed that the corticofugal fibres to the LRN can be divided into fast and slow conducting groups corresponding to the known two classes of corticospinal fibres. Results obtained by stimulation of the spinal cord after degeneration of ascending fibre tracts suggest that the LRN neurones are activated via collaterals from descending fibres, possibly corticospinal or rubrospinal. This circuitry may fulfill the requirements for an internal feedback loop. In particular, the fast pyramidal tract fibres to the LRN appear to constitute a component of a fast positive feedback loop from the motor cortex to the cerebellar nuclei and back to the motor cortex, as discussed by Blomfield and Marr.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Pyramidotomy ; Reaction time ; Precision grip ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Two monkeys (Macaca fascicularis) were trained to perform fast conditioned fingergrip on a small transducer. When performance was stabilized to the shortest possible reaction time, the pyramidal tract was transected on one side in one monkey, bilaterally in another. Retraining was resumed 1–3 weeks after surgery. Response latency as well as electromyographic latency and summation time were measured before and up to several months after pyramidotomy. The data show that pyramidotomy induced a long-lasting slowing in the performance of the fingergrip. This slowing was due mainly to a delay in the execution of the movement. However, a short-lasting significant delay of the onset of the EMG activity preceding the movement shows that not only the execution but also the initiation contributes to the increase of the mean response latency. The deficits were more severe and of longer duration in the monkey with bilateral pyramidotomy, especially the delay in the onset of the EMG activity. The mechanisms underlying these deficits and the role of the pyramidal tract in rapid movements are discussed, specifically in consideration of the possible function of the ipsilateral pyramidal tract.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 45 (1982), S. 410-416 
    ISSN: 1432-1106
    Keywords: Supplementary motor area ; Microstimulation ; Pyramidal tract ; Primate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The supplementary motor area of threeMacaca fascicularis was mapped using intracortical microstimulation (ICMS). Both forelimb and hindlimb movements were evoked using currents of 30 μA or less. However, thresholds for evoking movements were higher than those in the primary motor cortex. Proximal motor effects predominated, but distal joint movements were also elicited. Forelimb points were clustered in mesial cortex of area 6, anterior to the precentral hindlimb and tail region. Distal joint effects were located deep in the cortex, intermingled with proximal effects. Hindlimb responses which were less spatially localized, were found both ventral to the forelimb area, in the dorsal bank of the cingulate sulcus, and in mesial cortex, well anterior to area 4. No movements of facial muscles were elicited. Injections of HRP were made into the spinal cord at the cervical level in two animals and the lumbar level in the third one. An area of labelled cells was seen in mesial area 6 which corresponded closely to the region from which ICMS effects were elicited. No movements were evoked from the anterior portions of the fundal region of the cingulate sulcus which were also labelled.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 59 (1985), S. 91-104 
    ISSN: 1432-1106
    Keywords: Supplementary motor cortex ; Motor cortex ; Monkey ; Tracing studies ; Thalamocortical relationship
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The interrelationship of medial area 6 (supplementary motor area) with the thalamus was investigated by means of anterograde and retrograde tracing methods. Nine monkeys were prepared for autoradiography or histochemistry with the marker HRP conjugated to the lectin wheat germ agglutinin. Three of the monkeys received injections into the precentral cortex for comparison. 2. Previous observations were confirmed that the thalamic relays to the motor areas are organized as crescent-shaped lamellae which transgress cytoarchitectonic boundaries. The thalamic VA-VL complex receiving fibres from areas 4 and medial area 6 also sends fibres to these same areas. 3. The thalamic relay to medial area 6 comprised the following subdivisions: VLo, VLc, area X of Olszewski, VLm and, to a smaller extent VA. 4. Labeling (mostly anterograde only) was also prominent in some thalamic compartments outside the ‘motor’ thalamus: R, CL, CM-Pf, MD, LP, PULo. 5. It was noted that rostral and caudal injections into the medial area 6 resulted in different thalamic labeling: The rostral portion was found to be related mainly with VApc, area X and VLc, the central portion with VLo, and the caudal portion with VLc/VLo. This structural inhomogeneity may reflect also a functional rostro-caudal differentiation of the medial area 6. 6. The thalamic territory projecting to the precentral cortex is separate from the above relay and includes principally VPLo. 7. The present anatomical labeling study is in agreement with the conclusion of Schell and Strick (1984) that the SMA, especially its central portion, is an important target of basal ganglia outflow via the thalamic relay VLo. In addition consistent labeling was also found in thalamic subdivisions (area X, VLc) which had been found to receive cerebellar fibres.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1106
    Keywords: Supplementary motor cortex ; Cerebrocerebellar linkage ; Transcellular transport of WGA-HRP ; Corticothalamic relationship ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The possibility of a cerebellar linkage, via the thalamus with medial area 6 of the cerebral cortex was further explored in the present experiments (cf. preceding companion paper). 2. It was found that HRP conjugated to the lectin wheat germ agglutinin injected into motor cortical areas was transported beyond the thalamus to the contralateral intracerebellar nuclei when the survival time was 4–7 days. 3. It is suggested that the labeling in the deep cerebellar nuclei occurred via the thalamic relay where cerebellofugal fibre terminals had taken up the marker substance released by corticothalamic fibre terminals or by the retrogradely labeled thalamic perikarya. 4. In general, transcellular labeling of perikarya was weaker than retrograde labeling in the thalamic cells. Some of the nuclear zones in the cerebellum showed relatively dense granulations of the reaction product; in other zones only cells with few granules were seen, and large parts of the nuclei were not labeled at all. 5. The topography of secondary labeling in the cerebellar nuclei depended on the cortical injection sites. In all cases, most labeling was found in the contralateral dentate nucleus. The interposed nucleus received a fair amount of heavy labeling only in the precentral arm and face cases. Very little labeling was seen in the fastigial nucleus and in the cerebellar nuclei ipsilateral to the cortical injections. A somatotopic organization of secondary labeling was noted in the precentral cases with the face being represented caudally, the hindlimb rostrally and the arm between the face and the hindlimb representation. This is in agreement with previous anatomical and electrophysiological investigations. 6. These observations thus lend support to the conclusion that the SMA receives a transthalamic input not only from the basal ganglia but also from the cerebellum, especially from its lateral, neocerebellar portion.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1106
    Keywords: Supplementary motor area ; Premotor area ; Somatosensory responses ; Somatotopy ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Kinesthetic responses of neurones in the motor cortex, including the primary motor (MI), the supplementary motor (SMA) and the postarcuate premotor (PMC) areas, were investigated in the awake, chronically prepared monkey. In all three subareas, neurones were recorded which responded to passive elbow flexions and extensions induced by a torque motor. In the SMA, such cells were restricted to its posterior portion where intracortical microstimulation produced limb and trunk movements. The majority of SMA cells responds to both displacement directions, a quarter to either flexion or extension. Although the total proportion of SMA neurones responding to arm displacements was low (15%), it was noted that in ‘correct’ somatotopic penetrations, the responsiveness could be prominent. The latency distribution of the kinesthetic responses was similar to that of MI neurones with slightly less response latencies shorter than 20 ms in the SMA. With manually applied stimuli, SMA neurones responded mostly to joint rotations, but not to light cutaneous stimuli. Only two SMA neurones with somatosensory responses were identified as descending projection neurones, and some neurones were found to be modulated also during active grasping. In the PMC, a higher proportion of neurones (27%) reacted to the standardized arm displacements, the majority again responding to both directions. The latency distribution of the kinesthetic responses was similar to that of SMA neurones. In contrast to SMA neurones, many PMC neurones responded to light cutaneous stimuli. It was found that some of the ‘somatosensory’ PMC neurones were sometimes driven also by moving visual and, rarely, by auditory stimuli. Although there are obvious differences in the nature and possibly also in the amount of sensory inputs to the three motor cortical areas, the present results indicate that all three subareas receive somatosensory feedback and that they might therefore all be implicated in the generation of sensorydriven motor output.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-1106
    Keywords: Motor cortex ; Supplementary motor area ; Tracing ; Corpus callosum ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The goal of the present neuroanatomical study in macaque monkeys was twofold: (1) to clarify whether the hand representation of the primary motor cortex (M1) has a transcallosal projection to M1 of the opposite hemisphere; (2) to compare the topography and density of transcallosal connections for the hand representations of M1 and the supplementary motor area (SMA). The hand areas of M1 and the SMA were identified by intracortical microstimulation and then injected either with retrograde tracer substances in order to label the neurons of origin in the contralateral motor cortical areas (four monkeys) or, with an anterograde tracer, to establish the regional distribution and density of terminal fields in the opposite motor cortical areas (two monkeys). The main results were: (1) The hand representation of M1 exhibited a modest homotopic callosal projection, as judged by the small number of labeled neurons within the region corresponding to the contralateral injection. A modest heterotopic callosal projection originated from the opposite supplementary, premotor, and cingulate motor areas. (2) In contrast, the SMA hand representation showed a dense callosal projection to the opposite SMA. The SMA was found to receive also dense heterotopic callosal projections from the contralateral rostral and caudal cingulate motor areas, moderate projections from the lateral premotor cortex, and sparse projections from M1. (3) After injection of an anterograde tracer (biotinylated dextran amine) in the hand representation of M1, only a few small patches of axonal label were found in the corresponding region of M1, as well as in the lateral premotor cortex; virtually no label was found in the SMA or in cingulate motor areas. Injections of the same anterograde tracer in the hand representation of the SMA, however, resulted in dense and widely distributed axonal terminal fields in the opposite SMA, premotor cortex, and cingulate motor areas, while labeled terminals were clearly less dense in M1. It is concluded that the hand representations of the SMA and M1 strongly differ with respect to the strength and distribution of callosal connectivity with the former having more powerful and widespread callosal connections with a number of motor fields of the opposite cortex than the latter. These anatomical results support the proposition of the SMA being a bilaterally organized system, possibly contributing to bimanual coordination.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 128 (1999), S. 1-5 
    ISSN: 1432-1106
    Keywords: Key words Dexterity ; Skills ; Hand ; Hominid Evolution ; Anthropology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 48 (1982), S. 81-88 
    ISSN: 1432-1106
    Keywords: Supplementary motor area ; Antidromic stimulation ; Pyramidal tract ; Primate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The direct projection from the supplementary motor area (SMA) to the spinal cord was investigated in six monkeys by means of antidromic identification of single SMA neurones. The exploration concentrated on that portion of medial area 6 from which movements were found to be elicited by stimulation at intensities of less than 30 μA in an earlier study, but also included some of medial area 4. Of 315 identified corticofugal projection neurones, 234 were found to be localized within medial area 6; of these only one third (76 cells) were corticospinal cells and the remaining two thirds were neurones which projected to the brainstem. The conduction velocities of the descending projection neurones of the SMA were slow (modal value: 10 m/s). Corticospinal cells of the SMA were found up to 6 mm rostral to the boundary between areas 4 and 6. Corticospinal neurones activated antidromically from the cervical but not from the lumbar cord (‘cervicothoracic’ neurones) were concentrated in the mesial cortex; ‘lumbo-sacral’ neurones were found both in the dorsal cortex and the dorsal bank of the cingulate sulcus. However, there was considerable intermingling between the two types of projection neurones and there was no separation in the rostro-caudal direction. Similarly, projection neurones receiving orthodromic inputs from the somatotopical subdivisions of the precentral cortex were not segregated, but were intermingled in the entire rostro-caudal extent of the SMA. It is concluded that there is a clustering of corticospinal neurones in the SMA according to their most caudal segmental projection. However, no rostro-caudal differentiation into face, arm and leg areas was established. This observation is consistent with the results of a previous study in which corticospinal neurones in the SMA were labelled with anatomical tracers and efferent zones were investigated with intra-cortical microstimulation (Macpherson et al. 1982).
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-1106
    Keywords: Supplementary motor area ; Microstimulation ; Somatotopy ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Intracortical microstimulation of the supplementary motor area (SMA) was studied in awake monkeys. With short trains of micropulses, contralateral muscle twitches mainly in shoulder and proximal arm muscles were elicited. There was an indication of a rostro-caudal representation of distal to proximal forelimb, trunk, and proximal to distal hindlimb muscles. However, an intermingling of efferent zones was much more prominent as compared to the precentral motor cortex (MI). All efferent zones to the spinal cord were clustered in the caudal half of the SMA, and we failed to detect face and ocular movements (except at one stimulation site) when microstimulating the rostral portions of the SMA. Single micropulses were also injected in efferent zones of the microexcitable cortex in order to investigate post-pulse facilitation of sustained EMG activity. For motor cortex (MI) stimulation, post-pulse facilitation was prominent and observed in 14 of 17 tested stimulation sites. The incidence of facilitation in comparable muscles obtained with SMA stimulation was only 20 out 54 tests. The onset latencies of EMG modulation obtained from the two areas were in the same range but the amount of modulation in the SMA was less conspicuous than in MI. These results indicate that the SMA has oligo- or possibly even monosynaptic connections with motoneurones, but that these connections are less dense than those from MI.
    Type of Medium: Electronic Resource
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