Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Motor Cortex”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,333 records · Page 74Linked to original sources

Neonatal frontal lesion in unilateral hemisphere enhances the development of the intact higher motor cortex in the rat.

The influence of the neonatal frontal lesion in unilateral cerebral hemisphere for the organization of intact forelimb motor cortex in the rat was investigated by intracortical microstimulation (ICMS). The relative size of the rostral forelimb area (RFL) compared to the caudal forelimb area (CFL) in the ipsilateral motor field of lesioned rat was significantly greater than those of contralateral in normal and lesioned rats. The optimal sites of the stimulation for ipsilateral responses in lesioned rats were located in the RFL, while the optimal sites for contralateral were located caudolaterally, as for those of normal rats. At the ipsilateral optimal sites within the RFL in the lesioned animals, the threshold for the ipsilateral responses was lower than that for the contralateral responses. That is, the intact hemisphere of the animal preferentially developed the RFL rather than the CFL, for the ipsilateral forelimb. This may suggest a critical role for the RFL in individual forelimb motor control within the normal hemisphere.

Animals↗

Effects of intracellularly applied aminopyridine on firing activities and synaptic responses of electrophysiologically identified cell types in the motor cortex of cats.

Effects of 3-aminopyridine (3-Ap) applied intracellularly into electrophysiologically identified cortical neurons in the cat motor cortex were studied. Actions on the membrane and firing activity properties, excitatory and inhibitory postsynaptic responses were investigated. Intracellular microelectrode techniques and single electrode voltage clamp methods were used in experiments on anesthetized and chronic nonanesthetized cats. In addition to changes in neuronal excitability and firing activity properties the evoked postsynaptic responses were significantly altered. Augmentation of EPSPs was accompanied by increases of the total duration and amplitude of the second slow component of IPSPs without influencing the early fast IPSP component. It is concluded that most actions of 3-Ap reported here are derived from direct effects of 3-Ap on the postsynaptic membrane.

Aminopyridines↗

Distribution of synapses on an intracellularly labeled small pyramidal neuron in the cat motor cortex.

The morphological characteristics and distribution of synapses on a small pyramidal neuron in layer III of the cat motor cortex have been studied by combining intracellular HRP staining and electron microscopic examination. The stained neuron showed spiny apical and basal dendritic profiles under the light microscope, and exhibited the morphological features of a pyramidal neuron. Ultrastructural analysis indicated that about 80% of the presynaptic terminals formed asymmetrical synapses with spines of distal apical and basal dendrites. On proximal apical dendrites, 64% of the synapses were found to make contact with spines, and 16.7% of the synapses were of symmetrical type and formed with dendritic shafts. Two types of terminal could be identified on the soma; they were alternately located and established symmetrical and asymmetrical synaptic contacts respectively. Possible functional implications are discussed.

Animals↗

Relationship between finger movement rate and functional magnetic resonance signal change in human primary motor cortex.

Functional magnetic resonance imaging (FMRI) is a noninvasive technique for mapping regional brain changes in response to sensory, motor, or cognitive activation tasks. Interpretation of these activation experiments may be confounded by more elementary task parameters, such as stimulus presentation or movement rates. We examined the effect of movement rate on the FMRI response recorded from the contralateral primary motor cortex. Four right-handed healthy subjects performed flexion-extension movements of digits 2-5 of the right hand at rates of 1, 2, 3, 4, or 5 Hz. Results of this study indicated a positive linear relationship between movement rate and FMRI signal change. Additionally, the number of voxels demonstrating functional activity increased significantly with faster movement rates. The magnitude of the signal change at each movement rate remained constant over the course of three 8-min scanning series. These findings are similar to those of previous rate studies of the visual and auditory system performed with positron emission tomography (PET) and FMRI.

Adult↗

Examinations of the motor conduction time between the motor cortex and the Erb point in patients suffering from tumors of the central nervous system.

The cortical latency and the motor conduction time between the motor cortex and the Erb point were investigated in 85 patients with intracranial and in 9 patients with space-occupying spinal tumors. Electrophysiological examinations revealed pathological changes in 19% of intracranial events, and in 100% of cases of spinal tumors. In these latter cases close correlation was registered between the motor evoked potentials and the clinical symptoms of the patients.

Adult↗

Dynamical changes and temporal precision of synchronized spiking activity in monkey motor cortex during movement preparation.

Movement preparation is considered to be based on central processes which are responsible for improving motor performance. For instance, it has been shown that motor cortical neurones change their activity selectively in relation to prior information about movement parameters. However, it is not clear how groups of neurones dynamically organize their activity to cope with computational demands. The aim of the study was to compare the firing rate of multiple simultaneously recorded neurones with the interaction between them by describing not only the frequency of occurrence of epochs of significant synchronization, but also its modulation in time and its changes in temporal precision during an instructed delay. Multiple single-neurone activity was thus recorded in monkey motor cortex during the performance of two different delayed multi-directional pointing tasks. In order to detect conspicuous spike coincidences in simultaneously recorded spike trains by tolerating temporal jitter ranging from 0 to 20 ms and to calculate their statistical significance, a modified method of the 'Unitary Events' analysis was used. Two main results were obtained. First, simultaneously recorded neurones synchronize their spiking activity in a highly dynamic way. Synchronization becomes significant only during short periods (about 100 to 200 ms). Several such periods occurred during a behavioural trial more or less regularly. Second, in many pairs of neurones, the temporal precision of synchronous activity was highest at the end of the preparatory period. As a matter of fact, at the beginning of this period, after the presentation of the preparatory signal, neurones significantly synchronize their spiking activity, but with low temporal precision. As time advances, significant synchronization becomes more precise. Data indicate that not only the discharge rate is involved in preparatory processes, but also temporal aspects of neuronal activity as expressed in the precise synchronization of individual action potentials.

Animals↗

Effects of reversible bilateral inactivation of face primary motor cortex on mastication and swallowing.

The effects of reversible cold block-induced bilateral inactivation of the face primary motor cortex (face MI) on mastication and swallowing were studied in awake monkeys. A warm or cold alcohol-water solution was pumped through thermodes placed bilaterally on the dura overlying the intracortical microstimulation-defined face MI while the monkey chewed and swallowed food during pre-cool (thermode temperature 37 degrees C), cold block (4 degrees C), and post-cool (37 degrees C) sessions. Vertical and horizontal jaw movements and electromyographic (EMG) activity of several muscles were monitored. Each masticatory sequence was divided into three masticatory phases (i.e. food preparatory, rhythmic chewing, preswallow). The cold block markedly affected the ability of the monkey to carry out mastication although it did not prevent mastication from occurring. The masticatory deficit was characterized by a significant elongation of the total masticatory time, including in particular elongation of the food preparatory phase. The coordination of the jaw- and tongue-muscle activities was severely disrupted during the food preparatory phase. Face MI cold block also significantly affected the duration of some masticatory-related EMG activities and had some limited effects on the temporal relationships of the EMG activities during mastication. Although cold block significantly affected the duration and some EMG parameters of the preswallow phase, it had no significant effect on swallow duration or the EMG parameters during swallowing. These findings provide further evidence that the primate face MI plays a critical role in the regulation of mastication and that it plays a role in the preparation for swallowing.

Animals↗

Thalamic connections of the primary motor cortex (M1) of owl monkeys.

To determine the relative contributions of transthalamic cerebellar and pallidal projections to the primary motor cortex (M1) of owl monkeys, we examined the thalamic labeling resulting from injections of fluorescent tracers and wheatgerm agglutinin/horseradish peroxidase conjugate (WGA-HRP) into regions of M1 identified by intracortical microstimulation. Injections were placed in the major somatotopic divisions of M1 (the hindlimb, trunk, forelimb, and face representations) and in the caudal and rostral M1 subareas. In most cases, we injected several differentiable tracers into different parts of M1. Our results indicate that the strongest connections of M1 are with subdivisions of the ventral lateral thalamus (VL); other connections are mainly with intralaminar nuclei (the central lateral, paracentral, and center median nuclei) and the reticular nucleus. Most projections are reciprocal and topographically organized. M1 is strongly connected with the principal (VLp), medial (VLx), and anterior (VLa) subdivisions of the VL complex but has at most weak connections with the dorsal division (VLd). Each of the major somatotopic divisions of M1 is connected with an anteroposteriorly elongated territory within the VL complex. The connections are somatotopically organized such that the M1 hindlimb representation is connected with a band of cells in the lateral and anterior portions of the VL complex (spanning VLa and VLp), whereas the trunk, forelimb, and face representations are connected with successively more medially and posteriorly situated cell bands (spanning VLa, VLp, and VLx). There is some degree of overlap between the somatotopic territories within VL, although the absence of double-labeled cells in cases with injections of adjacent somatotopic divisions of M1 suggests that individual thalamic neurons project to single somatotopic regions. In addition to somatotopic differences, the connections of the caudal and rostral subdivisions of M1 differ to some extent. Caudal M1 is connected most strongly with VLp, a target of cerebellar projections, but it is also connected with VLa, which receives pallidal inputs. In complementary fashion, rostral M1 is most strongly connected with VLa, but it is also connected with VLp. VLx, a target of cerebellar projections, has significant connections with both caudal and rostral M1. These results indicate that all parts of M1 are influenced by both the cerebellum and globus pallidus in owl monkeys, as has been suggested in some recent studies of macaque monkeys.

Afferent Pathways↗

Electrophysiological and morphological characteristics of layer VI pyramidal cells in the cat motor cortex.

1. Intracellular recordings were made from layer VI pyramidal cells in in vitro slice preparations of the cat motor cortex (area 4 gamma). Layer VI pyramidal cells were identified morphologically by intracellular injection of biocytin. 2. Of 22 layer VI pyramidal cells examined, single action potentials were followed by depolarizing afterpotentials (DAP) in 9 cells, but were not followed by DAP in the remaining 13 cells. The amplitude of DAP was 3.4 +/- 1.4 mV (mean +/- SD, n = 9) when measured from the negative peak of fast afterhyperpolarization to the peak of DAP. 3. In response to depolarizing current pulses with a duration of 300-400 ms, pyramidal cells showing DAP displayed a train of action potentials in a phasic-tonic pattern without any appreciable adaptation in the tonic firing, whereas pyramidal cells lacking DAP exhibited a weak adaptation after phasic firing. Anomalous rectification was seen in both pyramidal cells showing DAP and those lacking DAP. 4. Repetitive doublet or triplet spiking was induced in DAP-showing pyramidal cells in response to a depolarizing current pulse after injecting strong depolarizing current pulses of 400 ms duration at 1 Hz for 30-60 s, but was never induced in DAP-lacking pyramidal cells. Doublet/triplet spiking lasted 5-10 min and returned to the original single spiking. An application of CsCl induced a burst firing in DAP-showing pyramidal cells. 5. In the nine pyramidal cells showing DAP, seven cells had shorter apical dendrites that arborized extensively at layer V and terminated in the middle part of layer III. In the 13 pyramidal cells lacking DAP, 11 cells had longer apical dendrites that arborized less frequently and extended into layer II or I. Main axons could be traced into the deep white matter in 17 of the 22 layer VI pyramidal cells examined. 6. Ascending recurrent axon collaterals were more prominent in pyramidal cells with longer apical dendrites than in pyramidal cells with shorter apical dendrites. The terminal bouton-like swelling observed along the recurrent axon collaterals arising from the pyramidal cells with longer apical dendrite were distributed most densely at the level between the bottom part of layer III and the top part of layer V. In contrast, those arising from the pyramidal cells with shorter apical dendrite were distributed mainly at the levels of layers V and VI.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Thalamic connectivity of rat somatic motor cortex.

The purpose of this study was to investigate certain organizational features regarding the connectional relationships between the somatic motor cortex (SMI) and dorsal thalamus in the rat. This was accomplished by applying microiontophoretically horseradish peroxidase and tritiated amino acids into low threshold stimulation sites within hindlimb, forelimb and face representations of the SMI as defined by intracortical microstimulation. Injections into the SMI produced labeling in distinct sets of specific and non-specific thalamic nuclei. The former included the ventrolateral (VL), ventromedial (VM), posteromedial (Pom) and posterior (Po) nuclei, and the latter included the centrolateral (CL), paracentral (PC), centromedial (CeM) and parafascicular (PF) nuclei. The densest labeling, both retrograde and anterograde, was found in the VL, and to a slightly lesser extent, in the Pom nuclei. Labeling of specific nuclei was more extensive than in non-specific groups. Thalamic-SMI projections were reciprocal in nature with the exception of the reticular thalamic nucleus (R). The ventrobasal (VB) nucleus was labeled only after injections into the SMI representations of the hindlimb and forelimb. A topographic organization between the SMI and dorsal thalamic nuclei was indicated by the varied position of label following injections into different cortical representations. Injections into the hindlimb representation resulted in labeling in the rostrodorsolateral VL, ventrolateral VM, rostrodorsomedial Pom, dorsal Po, rostrodorsolateral R, dorsolateral PF, CL and PC. In contrast, injections into the face representation resulted in labeling in the caudoventromedial VL, dorsolateral VM, caudoventrolateral Pom, ventral Po, caudoventromedial R, ventrolateral PF, the PC, CeM and ventral CL. The position of thalamic labeling following injections into the forelimb representation was intermediate between that for hindlimb and face representations. In coronal section, distinct patterns of labeling were identified in all specific thalamic nuclei following injections into each topographic region of the SMI. In the VL, labeling appeared as an obliquely-oriented, longitudinal strip or band (more C-shaped following injections of the hindlimb representation); in the VM as a horizontal strip; in the Pom as an irregular V-shaped band; and in the Po as a circular-to-ovoid cluster. No distinct patterns of labeling were discerned in non-specific nuclei. Labeling in the anterior grouping of non-specific nuclei overlapped to a large extent, but this was not the case in either the specific thalamic nuclei or the PF nucleus.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Reduced excitability of the motor cortex in untreated patients with de novo idiopathic "grand mal" seizures.

OBJECTIVES: Transcranial magnetic stimulation (TMS) was used to investigate motor cortex excitability, intracortical excitatory, and inhibitory pathways in 18 patients having experienced a first "grand mal" seizure within 48 hours of the electrophysiological test. All had normal brain MRI, and were free of any treatment, drug, or alcohol misuse. Results were compared with those of 35 age matched normal volunteers. METHODS: The following parameters of responses to TMS were measured: motor thresholds at rest and with voluntary contraction, amplitudes of responses, cortical silent periods, and responses to paired pulse stimulation with interstimulus intervals of 1 to 20 ms. RESULTS: In patients, there were significantly increased motor thresholds with normal amplitudes of motor evoked potentials (MEPs), suggesting decreased cortical excitability. Cortical silent periods were not significantly different from those of normal subjects. Paired TMS with short interstimulus intervals (1-5 ms) induced normal inhibition of test MEPs, suggesting preserved function of GABAergic intracortical inhibitory interneurons. On the contrary, the subsequent period of MEP facilitation found in normal subjects (ISIs of 6-20 ms) was markedly reduced in patients. This suggests the existence of abnormally prolonged intracortical inhibition or deficient intracortical excitation. In nine patients retested 2 to 4 weeks after the initial seizure, these abnormalities persisted, although to a lesser extent. CONCLUSION: The present findings together with abnormally high motor thresholds could represent protective mechanisms against the spread or recurrence of seizures.

Adolescent↗

Spinal cord transection induced c-fos protein in the rat motor cortex.

Spinal cord transection at the middle thoracic level induced the expression of c-Fos protein in the rat motor cortex detected with the immunohistochemical study. At 1 h after transection, maximal expression of c-Fos was seen in the frontal cortex and hindlimb area of the cortex. c-Fos-like immunoreactive neurons were recognized in the second to sixth layers of these cortices, although the axotomized neurons were located only in the fifth layer of these cortices. A significant difference of c-Fos-like protein expression was observed between the spinal transected group and the sham operated group 1 h after the operation. These results indicate that each layer of the motor cortical column is activated and that there is a correlation between alteration of the neuronal network and functional plasticity.

Animals↗

Postnatal development of descending motor pathways studied in man by percutaneous stimulation of the motor cortex and the spinal cord.

Using the percutaneous electrical stimulation of the brain and spinal cord, we have determined central motor pathway conduction velocities in a group of 19 healthy fullterm newborns (average post-conceptional age 39.8 weeks) and in 19 infants between 2 months and 8 years of age. The newborns were examined during the first postnatal week. The percutaneous stimulation of the motor cortex and of the cervical and lumbar enlargements of the spinal cord was made by means of bipolar electrodes. The evoked compound muscle action potentials were recorded by bipolar surface electrodes fixed on the skin overlying the thenar eminence muscles and the tibialis anterior muscle. In fullterm newborns, the responses of lower limb muscles to cortical stimulation were more difficult to obtain than those of upper limb muscles. Conduction velocities of central motor fibres along the spinal cord (between vertebrae C7 and L4) were around 10 m/sec in fullterm newborns and 38 m/sec at the age of 4 years. These values are considerably lower than those described for adult man (48-60 m/sec). The adult values are established around the age of 8 years.

Child↗

Muscle representation in the macaque motor cortex: an anatomical perspective.

How are the neurons that directly influence the motoneurons of a muscle distributed in the primary motor cortex (M1)? To answer this classical question we used retrograde transneuronal transport of rabies virus from single muscles of macaques. This enabled us to define cortico-motoneuronal (CM) cells that make monosynaptic connections with the motoneurons of the injected muscle. We examined the distribution of CM cells that project to motoneurons of three thumb and finger muscles. We found that the CM cells for these digit muscles are restricted to the caudal portion of M1, which is buried in the central sulcus. Within this region of M1, CM cells for one muscle display a remarkably widespread distribution and fill the entire mediolateral extent of the arm area. In fact, CM cells for digit muscles are found in regions of M1 that are known to contain the shoulder representation. The cortical territories occupied by CM cells for different muscles overlap extensively. Thus, we found no evidence for a focal representation of single muscles in M1. Instead, the overlap and intermingling among the different populations of CM cells may be the neural substrate to create a wide variety of muscle synergies. We found two additional surprising results. First, 15-16% of the CM cells originate from area 3a, a region of primary somatosensory cortex. Second, the size range of CM cells includes both "fast" and "slow" pyramidal tract neurons. These observations are likely to lead to dramatic changes in views about the function of the CM system.

Animals↗

Physiological demonstration of multiple representation in the forelimb region of the cat motor cortex.

Earlier studies in primates have demonstrated a double representation of the distal forelimb in area 4. In this study intracortical stimulation was used to map the representation of the forelimb in area 4 of the cat. Maps of individual animals revealed two spatially separate representations for the distal forelimb in area 4. Two "digit zones," regions in which threshold stimulation evoked contractions limited to digit musculature, were seen in all animals. Although the absolute location of the two digit zones varied among animals, the zones were always separated by a field in which more proximal musculature was represented. In some experiments EMG activity was monitored from selected forelimb muscles in order to determine the muscles represented in the two zones. Activity of the same digit muscle could be evoked by stimulation in each digit zone. The analysis demonstrated that some digit muscles were represented in both the digit zones. Thus, this study demonstrates that multiple representation of the distal forelimb in area 4 is not an isolated, species-specific phenomenon, but is likely to be a generalized pattern of motor cortex organization.

Animals↗

Mental rotation in a patient with an implanted electrode grid in the motor cortex.

We investigated the effects of cortical stimulation on mental rotation tasks in a patient with an electrode array placed over his left primary motor cortex. The array was implanted to relieve chronic pain resulting from right brachial plexus damage. Tasks involving motor imagery were slowed down by cortical stimulation, whereas those involving visual imagery were not. When the patient performed the motor-imagery task, the interference effect on response times disappeared if the stimulator was switched off. We also probed two of the sites (anterior-lateral and posterior-medial position), and found that stimulation of the more anterior-lateral one consistently disrupted motor imagery.

Brain Injuries↗

Limits on recovery in the corticospinal tract of the rat: partial lesions impair skilled reaching and the topographic representation of the forelimb in motor cortex.

Although evidence suggests that there are impairments in skilled movements following very large lesions of the pyramidal component of the corticospinal tract, the behavioral and electrophysiological effects of partial lesion has not received equal attention. Here, rats with complete lesions or partial lesions (medial, central, or lateral third) of the pyramidal tract at the medullary pyramids were evaluated for their quantitative and qualitative postsurgical performance on a skilled reaching task, following which the topographic representation of their forelimb was mapped with intracortical microstimulation (ICMS). Complete lesions impaired reaching success, impaired the qualitative features of reaching movements, and abolished ICMS evoked movement from the forelimb region of motor cortex. Although partial lesions did not impair reaching success, they did impair qualitative aspects of limb movement including forepaw aiming, supination, and food pellet release. ICMS indicated a reduction in the size of the forelimb area, especially the distal area of the caudal forelimb area (CFA), of the motor map. The behavioral and electrophysiological impairments did not vary with lesion location within the pyramidal tract. The incomplete recovery, as measured both behaviorally and electrophysiologically, demonstrates that plasticity within the corticospinal system is limited even with lesions that permit substantial sparing of pyramidal tract fibers.

Animals↗