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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 3 (1967), S. 58-80 
    ISSN: 1432-1106
    Keywords: Mossy fibres ; Cerebellar cortex ; Golgi cells ; Granule cells ; Purkinje cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Potential fields and unitary spikes in the cat cerebellar cortex were generated specifically by mossy fibre volleys and recorded by means of microelectrodes. The mossy fibres were excited by trans-folial (T. F.) stimulation which was compared with juxtafastigial (J.F.) stimulation. Both were conditioned by local stimuli of parallel fibres. 2. In the granular layer, an incoming mossy fibre volley evoked a small diphasic potential (P1 N1) and about 0.4 msec later a second negative wave (N2) due to the excitatory synaptic current generated by synapses of mossy fibres with granule cells and Golgi cells. In the typical configuration the N2 wave usually had a superimposed double spike potential, which is due to impulses discharged first by Golgi cells and then, about 0.5 msec later, by granule cells. 3. The transmission of impulses along the perpendicular axons of the granule cells and thence along the parallel fibres gave the fairly sharp positive potential (P2) in the granular layer, and simultaneously the negative wave (N3) in the molecular layer. The parallel fibre impulses, in turn, synaptically excited and so evoked local responses and action potentials in the dendrites of Purkinje and other cells, which aided in the production of the latter part of the N3 wave. 4. The impulses in the Purkinje cell dendrites propagate into the granular layer via the Purkinje cell somata and axons so producing the negative wave (N4) in the Purkinje and the granular layer. 5. The late and prolonged positive wave (P3) may be attributable to the deep active sources produced by postsynaptic inhibition of Purkinje cells and of granule cells by basket and Golgi cells respectively. 6. There has been good correlation between the physiological findings and the anatomical structures of the various types of cells and the synaptic connections, even to the synapses of mossy fibres on Golgi cell dendrites that have been recently described by HÁmori and SzentÁgothai.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 37 (1979), S. 193-198 
    ISSN: 1432-1106
    Keywords: Cerebello-cerebral projection ; Dentate nucleus ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Stimulation of the cerebellar dentate nucleus in monkeys elicited responses in the frontal association cortex (area 9) on the contralateral side to the stimulation, in addition to those in the motor (area 4) and premotor (area 6) cortices which were reported previously. The responses in the frontal association cortex were characterized by surface positive-deep negative field potentials in the cortex. They contrasted with surface negative-deep positive potentials in the motor and premotor cortices on the same dentate nucleus stimulation. In the rostral part of the premotor cortex (area 6) on the border of area 9, both types of responses were induced and admixed. The relay nucleus of the thalamus was suggested for the dentate-induced responses in the frontal association cortex.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 46 (1982), S. 29-36 
    ISSN: 1432-1106
    Keywords: Premovement cortical potential ; Visually initiated movement ; Cerebellum ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Cortical field potentials preceding hand movements initiated by a visual stimulus were recorded with chronically implanted electrodes in premotor, motor and somatosensory cortices of monkeys, and the influences of cerebellar hemispherectomy on cortical potentials as well as reaction time of movements were examined. As reported previously, early surface-positive, depth-negative (2.5–3 mm depth from the cortical surface) premovement potentials emerged at about 40 ms latency after onset of the light stimulus bilaterally in premotor and forelimb motor areas. Early potentials in the forelimb motor area contralateral to the moving hand were followed at about 120 ms latency by surface-negative, depth-positive late premovement potentials which are considered to be mainly composed of superficial thalamo-cortical (T-C) responses. Unilateral hemispherectomy of the cerebellum contralateral to the motor area immediately eliminated the surface-negative, depth-positive potentials. Reaction time from onset of the light stimulus to the hand movement was prolonged by 90–250 ms after cerebellar hemispherectomy. If the dentate and interpositus nuclei were also lesioned, disappearance of the late potentials and delay of the movement continued for many months. However, if the interpositus was spared, there was earlier recovery of reaction time with simultaneous reappearance of the late premovement potentials in the motor cortex. The conclusion is drawn that the cerebellar hemisphere (neocerebellum) activates the motor cortex via superficial T-C projections and participates directly in the initiation of reaction movements in response to an external stimulus.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 55 (1984), S. 60-68 
    ISSN: 1432-1106
    Keywords: Compensatory motor function ; Somatosensory cortex ; Motor cortex cooling ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The motor cortex was temporarily impaired by local cooling during repeated execution of visually initiated hand movements in monkeys. The effects of cooling were examined by recording premovement cortical field potentials in the forelimb motor and somatosensory cortices and by measuring reaction time and force exerted by the movement. The cortex was cooled by perfusing cold water (about 1° C) through a metal chamber placed on the cortical epidural surface. Cooling of the forelimb motor area lowered temperature of the cortex under the chamber to 20–29° C within 4–5 min. Recording electrodes for cortical field potentials were implanted chronically on the surface and at 2.5–3.0 mm depth of various cortical areas including that being cooled. Spread of cooling to surrounding cortical areas was prevented by placing chambers perfused with warm water (38–39° C) on the areas. Cooling of the forelimb motor area greatly reduced its premovement cortical field potentials, followed by prolonged reaction times of weakened contralateral wrist muscles. Simultaneous recording from the primary somatosensory cortex revealed an enhancement of its premovement field potentials. All changes were completely reversible by rewarming of the motor cortex. Concomitant cooling of the motor and somatosensory cortices entirely paralysed the contralateral wrist muscles. These results suggest that the motor function of the somatosensory cortex becomes predominant and compensates for dysfunction of the motor cortex when it is temporarily impaired.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1106
    Keywords: Compensatory motor function ; Somatosensory cortex ; Cerebellar hemispherectomy ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Electrical activities of the motor and somatosensory cortices preceding visually-initiated hand movements were recorded with electrodes chronically implanted on the surface and at 2.5–3.0 mm depth in the cortex of monkeys, and changes in field potentials in these cortices after cerebellar hemispherectomy were observed for many weeks. As previously reported, a unilateral cerebellar hemispherectomy including the lateral and interpositus nuclei eliminates the cerebellar-mediated superficial thalamo-cortical (T-C) responses recorded in the forelimb motor cortex contralateral to the hemispherectomy. These T-C responses normally precede the hand movement, and the operation results in the delay of movement initiation. The electrodes in the forelimb area of the contralateral primary somatosensory cortex showed an enhancement of superficial T-C responses of the somatosensory cortex for 30–40 days after the operation. The enhanced potentials preceded the delayed movement as do the cerebellar-mediated superficial T-C responses of the motor cortex in normal situations. Local cooling of the somatosensory cortex following the cerebellar hemispherectomy disturbed the reaction time movement for a few weeks after the operation. This effect was rarely encountered in normal monkeys. The present study suggests the compensatory motor function of the somatosensory cortex for the dysfunction of the motor cortex in early weeks after cerebellar hemispherectomy.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 65 (1987), S. 649-657 
    ISSN: 1432-1106
    Keywords: Audio-initiated hand movement ; Cortical field potential ; Cerebellar hemispherectomy ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Monkeys were trained to respond to auditory stimulus by lifting a lever (audio-initiated hand movement), and field potentials were recorded. from various cortical areas with electrodes implanted on the surface and at a depth of 2.0–3.0mm, depending on the area. Tones of 500, 1000 and 2000 Hz were given to the monkey for about 500 or 10 ms, as auditory stimuli. In association with the movement, potentials of different configurations were recorded respectively in the primary auditory, auditory association, prefrontal, premotor, motor and somatosensory cortices. Initial surface-positive (s-P), depthnegative (d-N) potentials appeared in the primary auditory and auditory association cortices about 20 ms after the onset of the auditory stimulus, and they were often followed by s-N, d-P potentials. In the forelimb area of the motor cortex contralateral to the moving hand, s-N, d-P potentials appeared at a latency of about 100 ms. Following cerebellar hemispherectomy ipsilateral to the moving hand, the s-N, d-P potentials in the forelimb motor cortex were eliminated and reaction times prolonged. The same monkeys were also trained to perform a visuoinitiated movement, and results were compared with each other. Primary sensory and sensory association areas activated during such movements were certainly different, and the prefrontal association cortex appeared to participate much less predominantly in the audio- than in the visuo-initiated movement. Reaction times were generally longer and more variable for the audio- than for the visuo-initiated movement. Nevertheless the cerebello-thalamomotor cortical projection was found to be recruited in the same manner prior to both movements.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 55 (1984), S. 26-32 
    ISSN: 1432-1106
    Keywords: Cortical field potential ; Visually initiated movement ; Motor learning ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A monkey was trained to lift a lever by wrist extension in response to a light stimulus. During the learning process of the task over several months, field potentials related not only to the task performance but also to substitution and stimulation experiments were recorded with chronically implanted electrodes on the surface and at a depth of 2.5–3.0 mm in the prefrontal, premotor, motor and prestriate cortices. In the substitution experiment, an examiner lifted a lever for the monkey so that it was watching the light and rewarded without the hand movement. In the stimulation experiment, the same light stimulus was simply delivered to the monkey. In a naive monkey which lifted the lever independently of the stimulus, stimulus-locked potentials were evoked by the task experiment in those cortices except the motor cortex, but none was elicited by the substitution or stimulation experiment. In a welltrained monkey, the substitution and stimulation experiments induced almost the same potentials as those prior to the task movement in respective cortices except the motor cortex, in which the component of cerebellar-induced premovement potential was not observed during the substitution and stimulation experiments. At an intermediate stage of learning, the situation was intermediate between the naive and well-trained stages and most premovement potentials except those in the motor cortex were elicited by the substitution experiment in reduced sizes, but nothing by the stimulation experiment. The present study suggests that the neuronal circuits for the operantly conditioned movement are functionally organized and gradually consolidated in the learning process, and that the consolidation is made earlier for the circuit involving association and premotor cortices than the circuit including the motor cortex in the process. The circuit to the motor cortex via the cerebro-cerebellar interconnection is recruited only on the execution of movement.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 70 (1988), S. 43-49 
    ISSN: 1432-1106
    Keywords: Audio-initiated hand movement ; Cortical field potential ; Motor learning ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Field potentials on the surface and at a depth of 2.0–3.0 mm in the cerebral cortex were recorded with chronically implanted electrodes in various areas of a monkey. The potentials associated with movements in response to auditory stimuli (audio-initiated hand movement) were observed during the learning process of the movement. The monkey had to lift a lever by wrist extension within the duration of the stimulus (tone of 1000 Hz) lasting for about 900, 700 or 500 ms depending on the stage of the learning process. On the first training day, potentials appeared in the primary auditory, auditory association, prefrontal and premotor cortices of a naive monkey. The potentials of the auditory association, prefrontal and premotor cortices became less marked on the next and following days. After a few weeks of training, the potential of the auditory association cortex started to increase again, while the monkey still lifted the lever randomly. When the potential of the auditory association cortex grew to a certain extent, the monkey began to respond to the stimulus with the movement, and potentials appeared in the motor cortex in response to the auditory stimulus. After this process, the potentials in the auditory association and motor cortices gradually increased with further training, and the movement became shorter and less variable in reaction time. The potential in the motor cortex was shown to be mediated by the neocerebellum and superficial thalamo-cortical projection. The changes of potentials associated with the learning processes of audio-initiated movements were respectively compared with those of the learning processes of the visuo-initiated movement, reported previously (Sasaki and Gemba 1982), and cortical and subcortical mechanisms related to the learning process were discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 48 (1982), S. 429-437 
    ISSN: 1432-1106
    Keywords: Cortical field potential ; Visually initiated movement ; Motor learning ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Field potentials on the surface and at 2.5–3.0 mm depth in the cerebral cortex were recorded in various areas with chronically implanted electrodes and the potentials which preceded hand movements in response to a light stimulus were observed during the process of learning the skilled conditioned movement. A naive monkey had to lift a lever by wrist extension within duration of the light stimulus lasting for 900, 700 or 510 ms depending on the stage of the learning process. In addition to some responses in the striate gyrus, significant short-latency responses to the light stimulus appeared bilaterally in certain areas of the prefrontal and prestriate cortices at an early stage of learning in which the monkey still lifted the lever randomly, and they became gradually larger as the monkey was trained further. Short-latency responses were also often noted in the bilateral premotor cortices during an early stage of learning. When the monkey started to respond to the stimulus by the appropriate movement, early surface-positive (s-P), depth-negative (d-N) premovement potentials appeared in the forelimb motor cortex, and the responses in the premotor cortex increased in size. As the movement became faster and more skillful, late s-N, d-P premovement potentials, that are known to be mediated by the neocerebellum and superficial thalamo-cortical projections, emerged after the early s-P, d-N potentials and became more marked, larger and steeper in the forelimb motor cortex contralateral to the moving hand. All the premovement potentials in the different cortical areas thus developed into steady and constant states and remained so for many months thus maintaining their established patterns. Such successive appearances of premovement field potentials in various cortical areas were related to learning processes of the movement and the implication of these findings was discussed.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-1106
    Keywords: Pallidum ; Cerebellar nuclei ; Thalamus ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Thalamic projections of the pallidum and the deep cerebellar nuclei were studied by unitary recordings as well as field potential analysis in the thalamus of squirrel monkeys (Saimiri sciureus) under sodium pentobarbital anesthesia. Stimulation of the pallidum produced a positive field potential preceded by incoming afferent fiber volleys in the thalamus. Spontaneous discharges of thalamic neurons were suppressed during this positive potential, and intracellular recordings from the thalamic neurons revealed that the time course of this field potential corresponded to that of the hyperpolarizing potential. The hyperpolarization was presumed to be a monosynaptic inhibitory postsynaptic potential by the short synaptic delay (about 0.5–0.7 ms) and responsiveness to high frequency stimulation (over 150 Hz). The positive field potential on stimulation of the external pallidal segment was distributed in L.po (VA) and the reticular thalamic nucleus around L.po, whereas that on stimulation of the internal segment was in V.o.a (the anterior basal part of VL) and in Z.o (upper part of VL). The projection of the external segment appeared to be less dense than that of the internal segment. The projection of deep cerebellar nuclei was situated in V.o.a, V.o.p (posterior part of basal part of VL), V.o.i (VLm), the intralaminar nucleus (CL), and some part of V. im (the rostral part of VPLo). Projections of the interpositus and dentate nuclei were distributed in a more anterior part than those of the fastigial nucleus. A certain topographical arrangement of the projections of these three nuclei was found in V.o.p, V.o.i and V.im. No significant overlap was detected between projections of the pallidum and the deep cerebellar nuclei within the thalamus.
    Type of Medium: Electronic Resource
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