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Results for “Motor Cortex”

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At least 811 records · Page 45Linked to original sources

PubMed2004

Facilitatory effect on the motor cortex by electrical stimulation over the cerebellum in humans.

Electrical stimulation over the cerebellum is known to transiently suppress the contralateral motor cortex in humans. However, projections from the cerebellar nuclei to the primary motor cortex are disynaptic excitatory pathways through the ventral thalamus. In the present investigation we studied facilitatory effects on the motor cortical excitability elicited by electrical stimulation over the cerebellum by recording surface electromyographic (EMG) responses from the first dorsal interosseous (FDI) muscle in nine normal volunteers. For primary motor cortical activation magnetic stimuli were given over the contralateral hand motor area with a figure-of-eight shaped coil with a current to preferentially elicit I3-waves (test stimulus). For cerebellar stimulation high-voltage electric stimuli were given with an anode on the ipsilateral mastoid process and a cathode over the contralateral process as previously described (conditioning stimulus). The effect of conditioning-test interstimulus intervals was investigated. Anodal cerebellar stimuli increased the size of EMG responses to magnetic cortical stimulation at an interstimulus interval of 3 ms. Reversing the current of conditioning stimulus abolished the facilitation. The same (anodal) conditioning stimuli did not affect electrically evoked cortical responses. Based on the effective polarity of the conditioning stimulus and the time course of facilitation we consider that this effect is due to motor cortical facilitation elicited by activation of the excitatory dentatothalamocortical pathway at the deep cerebellar nuclei or superior cerebellar peduncle. We conclude that the motor cortical facilitation is evoked by cerebellar stimulation in humans.

Adult↗

PubMed2003

Modulation of motor cortex excitability in the left hemisphere during action observation: a single- and paired-pulse transcranial magnetic stimulation study of self- and non-self-action observation.

Motor system excitability was tested by transcranial magnetic stimulation (TMS), and F-wave and H-reflex evaluation in different action observation tasks. Our aim was to investigate the effects produced by self- versus non-self-hand movement observation (MO). No significant differences were found between the self- and non-self-conditions. Movement observation significantly modulated motor cortex excitability, producing an increase in the amplitude of motor evoked potentials (MEPs) with a single magnetic pulse and a reduction in intracortical inhibition (ICI) with paired-pulse stimulation. No significant changes were found in motor cortex excitability during the observation of geometric objects. Motor imagery produced similar effects to those of action observation; no significant differences in modulation of motor system excitability between motor imagery and action observation were found in those muscles involved in actual motor execution. No significant effect on spinal excitability was found in any of the test conditions.

Adult↗

PubMed1998

Prior information preshapes the population representation of movement direction in motor cortex.

Single neuron activity was recorded in monkey motor cortex during the execution of pointing movements in six directions. The amount of prior information was manipulated by varying the range of precued directions. A distribution of neural population activation was constructed in the space of movement directions. This population representation of movement direction was preshaped by the precue. Peak location and width reflected the precued range of movement directions. From this preshaped form, the population representation evolved continuously in time and gradually in parameter space toward a more sharply peaked distribution centered on the parameter value specified by the response signal. A theoretical model of motor programming generated a similar temporal evolution of an activation field representing movement direction.

Animals↗

PubMedDate not supplied

[The effect of the iontophoretic administration of glutamate on the organization of interneuronal interactions in the rabbit motor cortex].

The multiunit activity of neurons in the motor cortex was recorded in 6 rabbits during glutamate (or physiological saline) iontophoretic application. Interaction between the neighboring neurons was evaluated by means of statistical cross-correlation analysis of spike trains. It was found that glutamate did not produce significant changes in cross-correlations.

Action Potentials↗

PubMed1994

Two mechanisms underlying the induction of long-term potentiation in motor cortex of adult cat in vitro.

Long-term potentiation of synaptic transmission (LTP), as documented by the enhancement of evoked field potentials in layer III following stimulation of the underlying white matter, has been studied in slices of motor cortex from adult cats. With a 1 M NaCl-filled recording electrode, LTP was induced only in one out of eight slices. When the recording electrode in addition contained 5 mM bicuculline metiodide, LTP was obtained with a much higher rate of success (15/19), suggesting that reduction of GABAA receptor-mediated inhibition facilitated the induction of LTP in the motor cortex. Bath application of DL-2-amino-5-phosphonovaleric acid (APV, 100 microM) or Ni2+ (100 microM) significantly reduced the success rate for LTP occurrence (6/16 and 5/16, respectively); but when LTP was induced, it did not show significant change in magnitude and time course. In slices perfused with APV (100 microM) plus Ni2+ (100 microM), LTP induction was completely blocked (0/12). These results suggest that two different mechanisms may subserve LTP induction in the cat motor cortex: one is mediated by N-methyl-D-aspartate receptors and can be blocked by APV; the other may be mediated by low-threshold calcium channels and can be blocked by Ni2+.

2-Amino-5-phosphonovalerate↗

PubMed1997

Changes in human motor cortex excitability induced by dopaminergic and anti-dopaminergic drugs.

Transcranial magnetic stimulation was used to probe the acute effect of a single oral dose of various dopaminergic (levodopa, selegiline, bromocriptine) and antidopaminergic drugs (sulpiride, haloperidol) on motor cortex excitability in healthy volunteers. Motor threshold, intracortical inhibition and intracortical facilitation were tested in the abductor digiti minimi muscle. The latter two parameters were studied in a conditioning-test paired stimulus paradigm. The principal findings were an increase in intracortical inhibition by bromocriptine, and, conversely, a decrease in intracortical inhibition and an increase in intracortical facilitation by haloperidol. Effects peaked at delays consistent with the pharmacokinetics of the two drugs and were fully reversible. In conclusion, dopamine receptor agonists and antagonists can be considered inverse modulators of motor cortex excitability: the former enhance inhibition while the latter reduce it. The relation of the present findings to current models of motor excitability abnormalities in movement disorders will be discussed.

Administration, Oral↗

PubMedDate not supplied

Neuron activity in rat hippocampus and motor cortex during discrimination reversal.

Chronic unit activity and gross movement were recorded from rats during two discrimination reversals in a classical appetitive conditioning situation. The anticipatory movement decreased in response to the former CS+ tone and increased to the previous CS- tone after each reversal. Hippocampus and motor cortex were differently related to these two kinds of behavioral change. Response rates of hippocampal neurons were more closely related to the increased movement response to the former CS- which now signaled food. Motor cortex neuron responses were more closely correlated with the decrease in movement responses to the former CS+ which became neutral after the reversal. It appeared that hippocampal neurons could have been involved in one cognitive aspect of the situation, motor cortex neurons in another. The data were related to current functional concepts of these brain regions.

Animals↗

PubMed1993

Motor cortex stimulation as treatment of trigeminal neuropathic pain.

A report is given on first experiences with motor cortex stimulation in 10 patients with different forms of neuropathic pain. Three of them had central pain as sequelae of cerebrovascular disease. In none of them did the stimulation provide pain relief. Two patients had pain from peripheral nerve injuries. One did not respond, but the other obtained about 50% pain relief. The remaining 5 patients with trigeminal neuropathy experienced definite pain relief varying between 60 and 90%. During test stimulation most patients had one or two short-lasting generalized seizures. But no one had any motor effects after permanent implantation. Motor cortex stimulation appears to be a new and promising possibility of pain treatment, especially in cases with trigeminal neuropathy, but many problems have yet to be solved, before a clear indication could be given.

Electric Stimulation↗

PubMed2000

Reorganization of the motor cortex in a patient with congenital hemiparesis and mirror movements.

Abnormal branching of corticospinal fibers from the unaffected motor cortex is responsible for mirror movements in patients with congenital hemiparesis, but it is unknown which mechanisms enable these patients to lateralize motor activity. Using multiunit electromyographic analysis and transcranial magnetic stimulation, the authors provide evidence for nonbranched crossed and uncrossed corticospinal projections and intracortical inhibition of the mirror hand. They propose that this remarkable reorganization of the unaffected motor cortex helps these patients to reduce mirror movements.

Adult↗

PubMed1993

Spinal and supraspinal mechanisms contribute to the silent period in the contracting soleus muscle after transcranial magnetic stimulation of human motor cortex.

In the voluntarily activated muscle, transcranial magnetic stimulation (TMS) of motor cortex produces subsequently to the motor evoked potential (MEP) a silent period (SP) in the electromyogram. We studied the time course of soleus motoneuron (MN) pool excitability after conditioning TMS by Hoffmann reflex (HR) testing, to determine whether inaccessibility of MNs after corticospinal input contributes to the SP. Coincidently with the early part of the SP, and only in the contracting soleus, MN depression was obtained that covaried with the degree of preinnervation, and with the size of the preceding MN discharge. However, MN excitability recovered significantly prior to the end of the SP. It is concluded that in the contracting soleus spinal mechanisms (most likely Renshaw inhibition and MN afterhyperpolarization) contribute to the early part of the SP, while the late part of the SP is supraspinal (probably cortical) in origin.

Adult↗

PubMed1998

Neuronal activity in the primate supplementary motor area and the primary motor cortex in relation to spatio-temporal bimanual coordination.

Single neuronal activity was recorded from the supplementary motor area (SMA-proper and pre-SMA) and primary motor cortex (M1) in two Macaca fascicularis trained to perform a delayed conditional sequence of coordinated bimanual pull and grasp movements. The behavioural paradigm was designed to distinguish neuronal activity associated with bimanual coordination from that related to a comparable motor sequence but executed unimanually (left or right arm only). The bimanual and unimanual trials were instructed in a random order by a visual cue. Following the cue, there was a waiting period until presentation of a "go-signal", signalling the monkey to perform the instructed movement. A total of 143 task-related neurons were recorded from the SMA (SMA-proper, 62; pre-SMA, 81). Most SMA units (87%) were active in both unimanual contralateral and unimanual ipsilateral trials (bilateral neurons), whereas 9% of units were active only in unimanual contralateral trials and 3% were active only in unimanual ipsilateral trials. Forty-eight per cent of SMA task-related units were classified as bimanual, defined as neurons in which the activity observed in bimanual trials could not be predicted from that associated with unimanual trials when comparing the same events related to the same arm. For direct comparison, 527 neurons were recorded from M1 in the same monkeys performing the same tasks. The comparison showed that M1 contains significantly less bilateral neurons (75%) than the SMA, whereas the reverse was observed for contralateral neurons (22% in M1). The proportion of M1 bimanual cells (53%) was not statistically different from that observed in the SMA. The results suggest that both the SMA and M1 may contribute to the control of sequential bimanual coordinated movements. Interlimb coordination may then take place in a distributed network including at least the SMA and M1, but the contribution of other cortical and subcortical areas such as cingulate motor cortex and basal ganglia remains to be investigated.

Animals↗

PubMed1998

Conversion of sensory signals into motor commands in primary motor cortex.

Movement triggered by sensory stimuli requires that the networks generating the motor commands receive an adequate driving input, which, in general, is a transformed version of the initial sensory signal. We investigated the nature of this transformation in a task in which monkeys categorize the speed of tactile stimuli as either low or high, reaching for one of two pushbuttons to indicate their choice. Extracellular recordings from primary motor cortex revealed two types of neurons selective for the speed categories: ones that fire at higher rates for low versus high speeds, and others that do the opposite. These differential responses are task-specific; no firing rate modulation was seen when identical arm movements were triggered by visual cues or when stimuli were delivered passively. Analyses using decoding and modeling techniques produced two main results. First, the neurons accurately encode the chosen category; an observer measuring their responses can exhibit a psychophysical performance during categorization identical to the monkey's. Second, by analyzing separately the trials in which hits and errors were scored, it is possible to distinguish purely sensory activity from activity exclusively related to arm motion. The recorded responses did not match either of these alternatives but were consistent with a model in which the category-tuned neurons are the link between the output of the sensory categorization process and the motor command used to indicate the animal's decision. Thus, the observed activity seems to encode a preprocessed version of the sensory stimulus and to participate in driving the arm motion.

Animals↗

PubMed1980

Sequential output-input maturation of kitten motor cortex.

Average response histograms of the responses of single cortical neurons to imposed forelimb displacements in the kitten were utilized to quantify: (1) Background activity, (2) excitatory response latency, (3) percentage responding neurons, and (4) synaptic effectiveness. Motor cortical neuronal responses to the input did not attain adult values until 55--65 days of age, while adult-like responses were found in somatosensory cortical neurons as early as 9 days postnatally. Motor cortical output to alpha-motoneurons innervating triceps brachii, as tested by intracortical and subcortical microstimulation, first appeared over an interval ranging from 37--45 days postnatally. Thus, motor cortical responses to forelimb mechanoreceptors develop after completion of the output linkages from motor cortex to forelimb motoneurons and, though the motor cortex can output at 45 days, motor cortical functions requiring somatosensory feedback cannot be operative until about 60 days. This system provides a discrete and "late" maturing model in which to study the postnatal development of neuronal networks underlying normal and abnormal motor behavior.

Afferent Pathways↗

PubMed1982

On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex.

The activity of single cells in the motor cortex was recorded while monkeys made arm movements in eight directions (at 45 degrees intervals) in a two-dimensional apparatus. These movements started from the same point and were of the same amplitude. The activity of 606 cells related to proximal arm movements was examined in the task; 323 of the 606 cells were active in that task and were studied in detail. The frequency of discharge of 241 of the 323 cells (74.6%) varied in an orderly fashion with the direction of movement. Discharge was most intense with movements in a preferred direction and was reduced gradually when movements were made in directions farther and farther away from the preferred one. This resulted in a bell-shaped directional tuning curve. These relations were observed for cell discharge during the reaction time, the movement time, and the period that preceded the earliest changes in the electromyographic activity (approximately 80 msec before movement onset). In about 75% of the 241 directionally tuned cells, the frequency of discharge, D, was a sinusoidal function of the direction of movement, theta: D = b0 + b1 sin theta + b2cos theta, or, in terms of the preferred direction, theta 0: D = b0 + c1cos (theta - theta0), where b0, b1, b2, and c1 are regression coefficients. Preferred directions differed for different cells so that the tuning curves partially overlapped. The orderly variation of cell discharge with the direction of movement and the fact that cells related to only one of the eight directions of movement tested were rarely observed indicate that movements in a particular direction are not subserved by motor cortical cells uniquely related to that movement. It is suggested, instead, that a movement trajectory in a desired direction might be generated by the cooperation of cells with overlapping tuning curves. The nature of this hypothetical population code for movement direction remains to be elucidated.

Animals↗

PubMed1989

[Spinal and muscular evoked response following single stimulation of the motor cortex of the rat].

The general characteristics of motor evoked potentials recorded from muscle and spinal cord in response to single electrical stimulation of motor cortex were examined in 30 rats. 5 other rats were additionally examined before and after full muscle relaxation, to differentiate the volume-conducted muscle response from spinal cord responses. The first positivity (P1) recorded from the lower thoracic cord following anodal stimulation was 1.1 +/- 0.1 ms and the second positivity (P2) was 2.1 +/- 0.2 ms. P1 was present in 11 animals and P2 in 20. The later components after 2.3 ms latency recorded from the epidural spinal electrode were lost with full muscular relaxation and seem to originate from volume conducted muscular activity. A relatively stable early MEP muscle response (6.1 +/- 0.9 ms) was observed in contralateral lower extremity muscles of all animals. Following this early response, a late MEP muscle response (16.0 +/- 1.9 ms) has been recorded in 43% of all animals. This relatively inconstant and multiphasic late muscle response disappeared during vibration of same extremity tendons and has similar characteristics as Hoffmann's reflex response. Additionally, with increasing stimulus intensities, the amplitude ratio of early to late response was similar to M response/H reflex amplitude ratio. The results suggest that the late MEP muscle response is probably the result of a reflex response caused by the first/early descending volley and traveled back to the spinal cord possibly through the Ia afferents similar to that in the H-reflex.

Animals↗

PubMed2002

Changes of cortical excitability of human motor cortex in spinocerebellar ataxia type 2. A study with paired transcranial magnetic stimulation.

The aim of this study was to evaluate motor cortex excitability in spinocerebellar ataxia type 2 (SCA2). Cortical silent period (CSP), motor thresholds, and intracortical inhibition and facilitation by paired transcranial magnetic stimulation (TMS) were investigated in 18 SCA2 patients and in 20 controls. The mean CSP duration and motor threshold after TMS were significantly increased in the patient group. Intracortical inhibition by paired TMS at short interstimulus intervals (ISIs) showed no significant differences between patients and controls; at longer ISIs, the expected facilitation of test responses, observed in control subjects, resulted significantly less marked in SCA2 patients at all the tested intervals. Our findings extend previous findings on cerebellar dysfunctions of varying aetiologies by investigating intracortical excitability in SCA2. In addition, this study demonstrates that the cortical excitability involvement found in SCA2 is independent on the cytosine-adenine-guanine repeat expansion. The neurophysiological alterations seen in our patients relate to the worsening of general clinical condition. Thus, we might speculate that changes of motor cortex excitability in SCA2 represent a slow neurodegenerative process characterized by gradual loss of cerebellar neurons leading to an increasing disturbance of the balance between inhibitory and excitatory circuits in the motor system.

Adult↗

PubMed1983

Synaptic organization of immunocytochemically identified GABA neurons in the monkey sensory-motor cortex.

Neurons in the monkey somatic sensory and motor cortex were labelled immunocytochemically for the GABA synthesizing enzyme, glutamic acid decarboxylase (GAD), and examined with the electron microscope. The somata and dendrites of many large GAD-positive neurons of layers III-VI receive numerous asymmetric synapses from unlabelled terminals and symmetric synapses from GAD-positive terminals. Comparisons with light and electron microscopic studies of Golgi-impregnated neurons suggest that the large labelled neurons are basket cells. Small GAD-positive neurons generally receive few synapses on their somata and dendrites, and probably conform to several morphological types. GAD-positive axons from symmetric synapses on many neuronal elements including the somata, dendrites and initial segments of pyramidal cells, and the somata and dendrites of non-pyramidal cells. Synapses between GAD-positive terminals and GAD-positive cell bodies and dendrites are common in all layers. Many GAD-positive terminals in layers III-VI arise from myelinated axons. Some of the axons form pericellular terminal nests on pyramidal cell somata and are interpreted as originating from basket cells while other GAD-positive myelinated axons synapse with the somata and dendrites of non-pyramidal cells. These findings suggest either that the sites of basket cell terminations are more heterogeneous than previously believed or that there are other classes of GAD-positive neurons with myelinated axons. Unmyelinated GAD-positive axons synapse with the initial segments of pyramidal cell axons or form en passant synapses with dendritic spines and small dendritic shafts and are interpreted as arising from the population of small GAD-positive neurons which appears to include several morphological types.

Afferent Pathways↗

PubMed1996

A propriospinal-like contribution to electromyographic responses evoked in wrist extensor muscles by transcranial stimulation of the motor cortex in man.

We tested the hypothesis that some of the electromyographic (EMG) responses elicited in preactivated forearm muscles by transcranial stimulation of the human motor cortex are produced by activity in a disynaptic corticospinal linkage involving propriospinal-like interneurones with cell bodies in the spinal C3-4 segments. The experimental design incorporated a previous observation that stimulation of afferents in the superficial radial nerve inhibits propriospinal-like neurones projecting to the extensor carpi radialis (ECR) muscle. Surface EMG responses were recorded from the active ECR muscle after transcranial electrical or magnetic stimulation over the motor cortex. In random trials, single conditioning stimuli at twice perceptual threshold were given to the superficial radial nerve at the wrist at different times before a cortical shock. When the cortex was stimulated electrically, the conditioning stimulus suppressed the EMG responses when the interval between the shocks was 11 ms or more. This was about 3.5 ms longer than the minimum time calculated for a possible direct cutaneous effect on spinal motoneurones. The time course of suppression began earlier and was more complex during magnetic stimulation of the cortex. It is argued that this difference is due to the repetitive I waves generated by the magnetic shock. Whether electrical or magnetic stimulation was used, the first 1-3 ms of the EMG response was relatively unaffected by superficial radial nerve stimulation at any interstimulus interval, whereas clear suppression was seen in the later portion of the response. In contrast, if the EMG response in ECR was suppressed by a conditioning stimulus to the median nerve at the elbow, then all portions of the EMG response were inhibited including the first 1-3 ms. The median nerve effect is thought to be due to direct reciprocal inhibition of the extensor motoneurones. Thus sparing of the initial part of the cortically evoked response with superficial radial stimulation suggests that the latter type of inhibition occurs at a premotoneuronal level. The timing of the effect is compatible with the explanation that corticospinal excitation is produced in ECR motoneurones through both monosynaptic and disynaptic (including propriospinal premotoneuronal) pathways, with superficial radial nerve inhibition being exerted at the propriospinal level.

Adult↗