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Convergent inputs from the dentate and the interpositus nuclei to pyramidal tract neurons in the motor cortex.

Effects of stimulation of the cerebellar nuclei were investigated by intracellular recordings from fast and slow pyramidal tract neurons and thalamocortical neurons in the cat. The present study demonstrated that: (1) the interpositus and the dentate nuclei excite PTNs in the motor cortex; (2) single pyramidal tract neurons receive convergent inputs from both nuclei, and (3) the convergence of the inputs from both nuclei occurs at the level of the ventrolateral nucleus of the thalamus.

Animals↗

Electrophysiological proof of diffusion-weighted imaging-derived depiction of the deep-seated pyramidal tract in human.

In the living human brain the pyramidal tract (PT) can be displayed with magnetic resonance diffusion-weighted imaging (DWI). Although this imaging technique is already being used for planning and performing neurosurgical procedures in the PT vicinity, there is a lack of verification of DWI accuracy in other areas outside the directly subcortical PT parts. Before definitive electrode placement into the subthalamic nucleus (STN) in patients with Parkinson disease (PD) for chronic stimulation, the stimulation effect on PD symptoms and the side-effects, namely PT activation at the level of the internal capsule (IC), are electrophysiologically tested. To analyze DWI accuracy by matching the stereotactic coordinates of the electrophysiologically proven IC position with these of the DWI-derived IC display, DWI was added to the routine MRI work-up in the stereotactic frame prior to functional surgery in 6 patients. In all of the 10 displayed fiber tracts, concordant findings for imaging and macrostimulation were made. The authors proved for the first time that DWI correctly depicts the deep seated, principle motor pathways in the living human brain. Due to methodical limitations of this study the accuracy of the proven IC display is limited to 3 mm which has proven to be sufficient for the planning and performance of neurosurgical procedures in the vicinity of large fiber tracts.

Adult↗

The intraspinal branching patterns of fast and slow pyramidal tract neurons in the cat.

Antidromic activation of single pyramidal tract neurons (PTNS) was obtained in cats by stimulating either the dorso-lateral funiculus with ball-electrodes, or the spinal gray matter with microelectrodes. The results indicate that the distribution area of single PTNS is much wider than the area of a single motor nucleus, suggesting that single PTNS may influence different motor nuclei.

Animals↗

Effect of acute spinal cord injury on axonal counts in the pyramidal tract of rats.

The concentration of axons in the pyramidal tract of normal and spinal cord-injured rats was determined by counting axons in sections of spinal cord stained by the Holmes technique. In the normal rat the axon concentration was uniform in the cervical, thoracic, and lumbar regions, although the size of the tract diminished progressively with its descent in the cord. After acute cord transection or compression injury, the axon concentration distal to the injury site diminished markedly. However, an appreciable number of distal axons persisted after injury, due to either delayed degeneration or to the presence of an admixture of afferent fibers. The axonal counting technique developed in this study should be helpful in experiments on spinal cord injury and regeneration.

Animals↗

Detection of pyramidal tract lesions in amyotrophic lateral sclerosis with magnetization-transfer measurements.

PURPOSE: To determine the presence of small lesions in the pyramidal tract in patients with amyotrophic lateral sclerosis (ALS) by using magnetization-transfer (MT) measurements and MR imaging. METHODS: MT ratios (MTRs) were measured in the posterior limb of the internal capsule in nine patients with ALS and in nine healthy volunteers. RESULTS: The mean value of MTRs (%) in patients with ALS was 15.76 +/- 1.48, while that of the control subjects was 19.83 +/- 1.54. The difference was statistically significant. CONCLUSIONS: MT measurements are useful for detecting abnormalities associated with degeneration of the pyramidal tract in patients with ALS.

Aged↗

Expression of two developmentally regulated brain-specific proteins is correlated with late outgrowth of the pyramidal tract.

The regulation of axon outgrowth is not well understood. In previous studies, however, axon elongation has been well correlated with expression of a small number of growth-associated proteins (GAPs). To identify other proteins whose expression could be correlated with axon outgrowth during development of CNS pathways, monoclonal antibodies were raised against growth cone particles isolated from neonatal hamster brains. Two of these antibodies recognized a brain-specific 33 kDa protein associated with intracellular membranes of axons and growth cones. Immunoblotting demonstrated a sharp developmental decline in levels of the protein in hamster brain during the first postnatal week and a more gradual decline thereafter. Immunocytochemical studies with the antibodies revealed ubiquitous staining of the neuropil during the first several days, which by the end of the first week became restricted to a few later-maturing pathways. Staining was most intense in the pyramidal tract and was well correlated with axon outgrowth, which continues until 14 d in this pathway. These results suggest that the 33 kDa protein may, like previously identified GAPs, play a role in axon elongation. Late outgrowth of the hamster pyramidal tract is also correlated with expression of another developmentally regulated protein, the high-molecular-weight neurofilament subunit (NF-H). Immunostaining with a monoclonal antibody that recognized phosphorylated NF-H demonstrated that this subunit does not begin to appear in the late-maturing pyramidal tract fibers until several weeks after birth, in striking contrast to intense immunoreactivity of other spinal cord pathways from postnatal day 1. This finding suggests that specific pathways may have a highly idiosyncratic time course for expression of neurofilament subunits.

Animals↗

On the development of the pyramidal tract in the rat. I. The morphology of the growth zone.

An electron microscopic study has been made of the tip of the growing pyramidal tract in the rat. This part of the developing bundle, designated as the growth-zone, has been examined at the levels of the medulla oblongata and the third spinal segment at embryonic day 20 and on the day of birth, respectively. The tip of the pyramidal tract contains, apart from axons, numerous larger profiles. An analysis of serial sections revealed that these represent either growth cones or preterminal periodic varicosities. In the growth cones of the corticospinal axons three zones can be distinguished: a proximal "tubular", an intermediate "vesicular-reticular" and a distal "fine-granular" zone. As distinct from the classical descriptions the corticospinal growth cones end in a single or, less frequently, in two more or less parallel filopodia. None of the growth cones analyzed in this study showed multiple filopodia radiating from the terminal expansion as observed at the end of growing axons in tissue cultures and in developing spinal fibre tracts of nonmammalian vertebrates. As regards the varicosities, most of these structures are characterized by a light cytoplasmic density. Others, however, contain a denser cytoplasm, closely resembling that of the vesiculo-reticular part of growth cones.

Animals↗

Long-lasting facilitation of pyramidal tract input to spinal interneurons.

The purpose of this study was to determine whether long-term changes in synaptic efficacy can be induced in the pyramidal tract (PT). Tetanic stimulation of the PT induced long-term facilitation of PT input to spinal cord neurons. In contrast, tetanic stimulation of the pyramidal tract did not alter the efficacy of synaptic inputs of PT cells' intracortical axon collaterals to other cortical neurons. These findings suggest that the PT participates in motor learning by modulating the excitability of spinal cord neurons. The results also indicate that induction of LTP in the PT is dependent on postsynaptic mechanisms.

Animals↗

Influence of molecular layer on pyramidal tract neurons.

Activity in layer I increases the excitability of pyramidal tract (PT) neurons, the effect being stronger on slow than on fast PT neurons. Extracellular recordings were made from lateral postcruciate cortex of domestic cats, using antidromic activation from medullary pyramid to identify and classify PT neurons. Their responses to contralateral forepaw (CFP) and direct cortical (Ctx) stimulation, 3 to 4 mm caudal to the recording site, were determined before and after placement of vertical cuts between the Ctx stimulating and recording sites. These cuts had a minor effect on the responses of PT neurons to CFP stimulation, but a strong effect on the responses to Ctx stimulation. Cuts through layers I and II markedly delayed the responses of slow PT neurons, but had no effect on fast PT neurons. After deeper cuts (II/III through V/VI), half the fast and half the slow PT neurons failed to respond to Ctx stimulation. Of those that did, fast PT responses were markedly delayed, but slow PT responses were only mildly affected. The Ctx-CFP interactions showed the familiar facilitation-depression sequence. The period of depression was unaffected by any of the vertical cuts, but disappeared after undercutting the stimulus site below layer VI. The period of facilitation depended primarily on layer I for its production, although deeper layers also contributed to the facilitation of fast PT neurons.

Animals↗

Post-natal development of pyramidal tract neurones in kittens.

The post-natal development of pyramidal tract neurones (p.t.n.s) was investigated in twenty-one barbiturate-anaesthetized kittens from birth to 28 days of age using a combination of electrophysiological and anatomical techniques. P.t.n. responses were recorded intracellularly as well as extracellularly with glass micropipettes filled with horseradish peroxidase (HRP) on stimulation of the medullary pyramid and cerebellar nuclei. Latency histograms of antidromic responses of p.t.n.s were compared at various ages. In the neonate, p.t.n.s were divided into two groups which were presumed to be analogous with fast and slow p.t.n.s in adult animals. During the first post-natal week, latency shortening was not conspicuous, but by the end of the second post-natal week, the faster group showed a marked decrease of latencies (up to around 10 ms at 14 days of age), while those of the slower group did not change so much. The slower group increased their conduction velocity during the third post-natal week (latencies up to around 18 ms). At the end of the fourth post-natal week, the distribution of antidromic latencies was in a narrower range, but the values were still longer than those reported in adult animals. Intracellular HRP staining revealed that apical dendrites of p.t.n.s spread fully to the pial surface even at birth. The somata of these neurones were characteristically covered with somatic appendages and development of the basal dendritic tree was immature in 0-1-day-old kittens. Basal dendrites developed nearly completely by 7 days, but somata were still covered with appendages. During the fourth post-natal week, these appendages disappeared almost completely. The sizes of the dendritic field, especially of apical dendrites, became larger in parallel with the development of cortical layers. From the morphological point of view, differentiation of fast and slow p.t.n.s was not clear until 28 days of age except in somatic volumes, which were already different in the first post-natal week. At the end of the fourth post-natal week, p.t.n.s with short antidromic latencies had a tendency to bear spines more sparsely over the secondary and tertiary dendritic surface in comparison with p.t.n.s with longer latencies. Intracortical axonal trajectories developed fairly well in the immature cerebral cortex, and the general pattern of ramification changed little during the first month after birth.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗

Spinal branching of pyramidal tract neurons in the monkey.

The branching pattern of individual pyramidal tract (PT) neurons of the monkey motor cortex was studied by activating these neurons antidromically from within the cervical motor nuclei and also from other regions of the spinal cord. 1. Fifty-four neurons were activated from motor nuclei in the cervical cord. Twenty-eight of these were activated from one segment and six (11%) were activated from motor nuclei of different segments. The remaining 20 neurons were activated from motor nuclei and also from unspecified region(s) of the gray matter. 2. Another 156 neurons were activated from unspecified regions(s) of cervical gray matter which could have been motor nuclei or outside the nuclei, and 64 of these were activated from more than one segment. 3. The branching patterns of PT neurons sending axons directly to motor nuclei innervating distal forelimb muscles suggested that they branch less than the rest of PT neurons.

Animals↗

Intracortical distribution of axonal collaterals of pyramidal tract cells in the cat motor cortex.

Slow and fast pyramidal tract cells (Pt cells) from the cat motor cortex were identified antidromically and injected with horseradish peroxidase (HRP). The axonal collaterals of these cells were mapped following HRP histochemistry with benzidine di-hydrochloride. All cells, slow or fast, show a similar arrangement of their collaterals. A proximal axonal network of 0.5-0.8 mm in diameter delimits a local field of action for collaterals in layers V and VI. The tangential expansion of this local field corresponds to that of the basal dendritic domain of Pt neurons. Much longer collaterals running for millimeters in the lower gray or white matter were observed in all cells. They form at a cortical level a distal field of action for Pt neurons. Many of these long branches were traced to other regions of area 4 or toward other cytoarchitectonic areas. In one case a collateral was seen entering and dividing in area 3a. Due to limitations of the HRP technique most of these long branches could not be followed to their terminals. On the basis of the laminar distribution of Pt cell collaterals (mostly in layers V and VI) synaptic sites where recurrent excitation and inhibition are produced on Pt neurons are discussed.

Animals↗

Temporal changes of pyramidal tract activities after decision of movement: a study using transcranial magnetic stimulation of the motor cortex in humans.

To elucidate the effects of the decision to move on the pyramidal tract in humans, we examined the changes in the motor evoked potentials (MEP) of the forearm muscles following transcranial magnetic cortical stimulation (TMS) of the hand area during a go/no-go hand-movement task in 10 normal subjects. The subjects performed an extension of the right wrist according to the go, no-go and control signals, one of which was randomly presented on a TV. A single TMS was applied to the primary hand motor area in the left hemisphere 0-300 ms after each signal. The MEPs recorded from the wrist extensor and flexor muscles changed in amplitude after both go and no-go signals. In comparison with the control, the MEPs were significantly facilitated in the agonistic muscles (wrist extensor muscles) and attenuated in the antagonistic muscles (wrist flexor muscles), at the latencies of 100-200 ms after the go signal (P < 0.02). In contrast, the MEPs of both the extensor and flexor muscles were significantly attenuated during the period of 100-200 ms after the no-go signal (P < 0.001). We speculate that there is strong inhibition on the pyramidal tract after the no-go signal and that the inhibitory effect is non-specific to the target muscles. This inhibition differs from the reciprocal inhibition of the MEP observed in antagonistic muscles after the go signal, and it is probably related to the movement decision originating in the prefrontal cortex.

Adult↗

[A case with pyramidal tract lesion suggesting Wallerian degeneration--analysis with diffusion coefficient].

We reported a 55-year-old man, whose T2-weighted MR images disclosed abnormal high signal band along the left pyramidal tract 6 months after cerebral infarction of the left centrum semiovale. Brain CT revealed low intensity areas in the centrum semiovale, the posterior limb of the internal capsule on left side. On T2-weighted MR images, there were an irregular high signal area on the left centrum semiovale, a high signal band from the left centrum semiovale to the medullary pyramid, and a high signal band from the left centrum semiovale to the cerebral cortex. These lesions were observed as high signal areas on proton weighted images and low signal areas on T1-weighted MR images. Diffusion coefficient perpendicular to the pyramidal tract in the patient, which was calculated from diffusion weighted images at the posterior limb of the internal capsule, was higher than that in normal individuals. Diffusion anisotropy at the lesion, which is the rate between the diffusion coefficient parallel and perpendicular to nerve fiber, was higher than that of normal individuals. These data suggested that the lesion had demyelinating process, which was consistent with the pathology at stage 2 of the Wallerian degeneration.

Cerebral Infarction↗

Motor responses after transcranial electrical stimulation of cerebral hemispheres with a degenerated pyramidal tract.

Motor responses were evoked in the thenar muscles by transcranial electrical cortex stimulation in 5 stroke patients with an isolated lacuna in the internal capsule, in whom wallerian degeneration of the pyramidal tract was demonstrated in vivo. Suprathreshold stimulation of the affected hemisphere elicited bilateral motor responses; whereas, stimulation at identical intensities of the undamaged hemisphere yielded strictly unilateral responses in the contralateral hand, like the responses of all normal control subjects. Focused magnetic brain stimulation was performed in 1 patient and gave identical results. Because muscular excitability to cortical stimulation is preserved in spite of pyramidal tract disruption, other pathways must bypass the lesion. Because of the bilaterality of responses, we suggest polysynaptic corticoreticulospinal connections.

Cerebrovascular Disorders↗