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PubMed1993

Cerebral response to pyramidal tract stimulation in wood rats and its relation to laboratory rats.

The cerebral response evoked by stimulation of the bulbar pyramidal tract in wood rats, like that of laboratory rats, consisted of a small alpha wave, almost obscured by a very large, superimposed r wave. The alpha wave behaved like a purely antidromic response, whereas the r wave behaved like a postsynaptic response, including a marked variability in amplitude on repeated trials. The contralateral forepaw and hindpaw motor sites mapped onto the somatic sensory foci for these two paws; further examination showed that the somatic sensory and motor representations were largely superimposed. An incipient sagittal fissure 1.5 mm lateral to the midline marked the boundary between limbic and neocortex. Because of their structural similarities and their differences in somatic sensory and motor organization, wood rats and laboratory rats are prime subjects for comparative study of the role of amalgamated and separate sensory and motor cortices in regulating movement and behavior.

Animals↗
PubMed1987

Activity-related changes in electrical thresholds of pyramidal tract axons in the behaving monkey.

In monkeys generating torques about the wrist we investigated changes in the excitability of pyramidal tract (PT) axons, measured as the probability of evoked antidromic responses in motor cortex with constant juxtathreshold stimuli delivered in the brain stem. When PT stimuli were delivered 2-20 ms after an orthodromic action potential in the PT neuron, the excitability of axons was elevated, with a characteristic post-spike time course. Excitability peaked at a post-pike delay of 7.0 +/- 2.7 ms (n = 33). Axonal thresholds typically dropped to 80-90% of the unconditioned values (obtained for stimuli with no preceding spike). Controlling for such post-spike threshold changes by delivering stimuli at fixed post-spike delays, we found that excitability of many PT axons also fluctuated with the wrist responses, being slightly higher during flexion or extension. The place of movement in which excitability increased had no consistent relation to the phase of movement in which the PTN fired. Task-related threshold changes were also seen in PTNs whose discharge was not modulated with the wrist response. Delivering a subthreshold conditioning stimulus also increased the excitability of most PT axons to a subsequent test stimulus. Such post-stimulus changes may be mediated by the effects of adjacent fibers activated by the conditioning stimuli. The post-spike and post-stimulus changed added in a nonlinear way. All three types of threshold change may be mediated by a common mechanism: changes in the ionic environment of the axon produced by activity of the axon itself or its neighbors.(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗
PubMed1991

Pyramidal tract lesions in comatose patients.

In 197 comatose patients transcranial magnetic evoked potentials were registered to investigate the integrity of the pyramidal tract. Findings were compared to somatosensory, visual and auditory evoked potentials. Preservation, abnormalities and absence of evoked potentials were related to survival and non-survival. Transcranial magnetic and somatosensory evoked potentials proved to be of high prognostic value. While the accuracy of prediction of a fatal outcome based on transcranial magnetic evoked potentials was close to 90%, the prediction of survival was less dependable. Transcranial magnetic evoked potentials are concluded to be a valuable adjunct to the neurophysiological assessment of the comatose patient.

Adolescent↗
PubMed1989

Modulation of spinal reflexes by pyramidal tract stimulation in an in vitro brainstem-spinal cord preparation from the hamster.

Electrophysiological evidence is presented showing that the pyramidal tract (PT) of the hamster modulates spinal reflexes in an in vitro brainstem-spinal cord preparation. Three spinal reflexes were studied. Stimulation of a dorsal root (DR) while recording from a ventral root (VR) of the same spinal segment evoked two reflexes: the monosynaptic reflex, and a long latency polysynaptic reflex. Stimulation of a DR while recording from a DR immediately rostral to it elicited a volley of antidromic discharges characteristic of the dorsal root reflex (DRR). The effect of PT stimulation on reflex transmission was tested by stimulating the PT at varying intervals prior to evoking a reflex. The results show that the amplitude of the monosynaptic reflex is progressively inhibited when preceded at shorter delays by a train of PT stimuli. Similarly, PT stimulation also suppresses the long latency reflex. In contrast, the PT facilities the DRR and repeated stimulation of the PT may evoke antidromic discharges recorded from the DRs. These data from the in vitro brainstem-spinal cord preparation indicate that the PT of the hamster exerts both inhibitory and facilitatory effects on reflex transmission in the spinal cord. The present study shows that it is possible to examine the descending control of spinal circuitry using an in vitro brainstem-spinal cord preparation.

Action Potentials↗
PubMed1980

Antidromic latency of the monkey pyramidal tract neuron related to ipsilateral hand movements.

During three different motor tasks of finger, wrist and arm movements on either side, 80 pyramidal tract neuron (PTN) activities were recorded in the monkey motor cortex. They were divided into three groups; PTNs related to contralateral movement (contra-PTNs), those related to ipsilateral and contralateral movement (bilateral-PTNs) and those related to ipsilateral movement (ipsi-PTNs). The latency histogram of the antidromic activation was similar for contra-PTNs as well as ipsi- and bilateral-PTNs in the fast PTN group, but most of slow PTNs appeared among contra-PTNs. Intracortical microstimulation (ICMS) was delivered to correlate muscular contraction with PTN activity. Most of slow PTNs were related to proximal muscular contraction and PTNs related to proximal muscles appeared more in ipsi- and bilateral-PTNs than in contra-PTNs.

Animals↗
PubMed1991

Immuno-electronmicroscopic visualization of cell adhesion molecule L1 in adult rat pyramidal tract: localization on neuronal and oligodendrocytic processes.

The immuno-electronmicroscopic localization of cell adhesion molecule L1 is investigated in adult rat pyramidal tract (PT) at the fifth/sixth cervical spinal cord segment, both by pre-embedding on vibratome sections and by immunogold-labelling on ultra-cryosections. L1-immunoreactivity (L1-IR) can be noted not only on the surface of unmyelinated PT axons, the outer axonal membrane, but also within the axoplasm of myelinated PT axons as well as periaxonally between axolemma and compact myelin. Compact myelin is L1-negative. Interestingly, L1-IR is found in between the inner oligodendrocytic mesaxon and compact myelin. Hence, L1 is expressed by this type of glial cell in adult rat PT. In conclusion, L1 is suggested to be important in the adult rat PT, not only with respect to the adhesion between unmyelinated PT axons but also during stabilization of the mature neuron-oligodendrocyte interaction.

Animals↗
PubMed2006

Quantitative analysis along the pyramidal tract by length-normalized parameterization based on diffusion tensor tractography: application to patients with relapsing neuromyelitis optica.

In this study, we introduced a length-normalized parameterization method to establish anatomical correspondence of white matter fiber tracts across subjects and applied this method to investigate the presence of abnormal diffusion along the pyramidal tract (PYT) of relapsing neuromyelitis optica (RNMO) patients without visible brain lesions. In this approach, the part of the PYT between the lowest slice of the cerebral peduncle and the uppermost slice of the lateral ventricle was reconstructed to establish the anatomical correspondence across subjects using diffusion tensor tractography. Then it was parameterized by normalizing its length and dividing equally the normalized length into a certain number of segments, so that the comparability of each segment across subjects along the PYT was established. Tract-specific diffusion indices, including directionally averaged diffusivity (D(av)), fractional anisotropy (FA), primary diffusivity (lambda(1)) and transverse diffusivity (lambda(23)), were obtained from each segment. Thus, the distribution maps of these indices along the PYT were obtained. The distribution maps of D(av), FA, and lambda(23) of RNMO patients were significantly different from those of healthy controls, especially in the lower part of the PYT. The differences may be caused by secondary degeneration to lesions in the spinal cord. In conclusion, a length-normalized parameterization method is proposed to establish anatomical correspondence for the PYT. Compared with existed methods, a major merit of our method is to provide comparability across subjects along the PYT on the basis of diffusion tensor tractography and to make it possible for the quantitative analysis along the fiber tract. This method can also be used to quantitatively analyze other white matter fiber tracts between two definite anatomic landmarks in many neurological or psychiatric diseases.

Adult↗
PubMed1991

The intracortical position of pyramidal tract neurons in the motor cortex of the reeler changes from postnatal day 10 to adulthood.

To determine whether or not the intracortical distribution pattern of pyramidal tract (PT) neurons in the motor cortex (hindlimb area) of normal and reeler mutant mice changes during early postnatal development of the cortex, we injected HRP into the pyramidal decussation of postnatal day (P) 8 and adult animals of the normal and reeler strains, and killed the animals 2 days later. In the normal P10 and adult mice, such an injection resulted in a band of labelled neurons confined to the layer of large pyramids (LP), suggesting that the intracortical localization of PT neurons does not change from P10 to adulthood in the normal strain. In the P10 and adult reeler mice, labelled PT neurons were scattered radially from the deepest zone to the superficial zone of the motor cortex. However, while the HRP-labelled PT neurons are located bilaminarly in both the deepest zone and the superficial zone of the motor cortex of the P10 reeler mouse, the majority of PT neurons were found in the upper third of the motor cortex of the adult reeler mouse. Thus, the intracortical distribution pattern of PT neurons of the reeler mouse changes during the postnatal period.

Animals↗
PubMed1996

Study of paired-pulse inhibition of transcallosal response in the pyramidal tract neuron in vivo.

The effects of a specific GABAB receptor antagonist, p-(3-aminopropyl)-p-diethoxymethyl-phosphonic acid (CGP 35348), on pyramidal tract neuron responses to transcallosal stimulation were investigated in the cat motor cortex in vivo. The paired-pulse method was used to obtain more insight into the role of GABAB receptors. At a 200-ms inter-stimulus interval the spike response was inhibited in 75% of the neurons. There was an approximately 40% depression of the mean spike value in the control. CGp 35348 reduced paired-pulse inhibition, while (-)-baclofen increased it. Stronger drug effects on the second stimulation-induced response possibly indicate their presynaptic action on GABAB receptors.

Animals↗
PubMed1988

Excitatory synaptic actions between pairs of neighboring pyramidal tract cells in the motor cortex.

1. By spike-triggered averaging, we documented recurrent individual excitatory postsynaptic potentials (EPSPs) produced in 33 pyramidal tract (PT) cells (target) by the activity of axon collaterals of neighboring single PT cells (reference) in the motor cortex of the cat. 2. The computer was triggered by the spontaneous activity of reference PT cells or by current pulses applied to reference PT cells through the extracellular recording electrode. 3. The threshold for direct activation of PT cells was less than 0.1 microA with an anodal current pulse and 0.2-0.3 microA with a cathodal current pulse. 4. Application of an anodal current pulse directly activated only a single reference PT cell, the surface membrane of which was presumably touched by and sucked with the extracellular recording electrode. 5. When a cathodal current pulse was used, simultaneous activation of neurons or axons other than the reference PT cell was checked by changing the stimulus parameters along the characteristic strength-duration curve for the reference PT cell and/or by comparing averaged EPSPs obtained by cathodal stimulation with those obtained from spontaneous spikes of the reference PT cell. 6. Recurrent individual EPSPs were produced in fast PT cells by activation of neighboring slow PT cells and also of neighboring fast PT cells. Some recurrent individual EPSPs were also observed in slow PT cells. 7. The mean latencies of recurrent individual EPSPs produced by the spontaneous activity of reference slow and fast PT cells were 1.61 (n = 12) and 1.12 ms (n = 8), respectively. Their amplitudes ranged between 30 and 390 microV (n = 33). The rise time observed in fast PT cells with activation of slow and fast PT cells ranged from 1.6 to 3.6 ms (n = 20) and from 0.8 to 1.9 ms (n = 10), respectively. 8. The average conduction velocity of axon collaterals of slow and fast PT cells was estimated to be as slow as that of unmyelinated fibers in the cat. 9. It is suggested that axon collaterals of slow PT cells synapse onto more distal dendrites of fast PT cells than axon collaterals of fast PT cells.

Action Potentials↗
PubMed2002

The effects of prolonged intracortical microstimulation on the excitability of pyramidal tract neurons in the cat.

This study was conducted to examine the excitability changes induced in cerebral cortical neurons during prolonged microstimulation with a spatially dense microelectrodes array. The arrays of 16 iridium microelectrodes were implanted chronically into the postcruciate gyrus of cats. Neuronal responses characteristic of single pyramidal tract axons (ULRs) were recorded in the medullary pyramid. 7 h of pulsing of individual electrodes at 50 Hz and at 4 nC/ph induced little or no change in the ULRs' electrical thresholds. The thresholds also were quite stable when 4 of the 16 microelectrodes were pulsed on each of 14 consecutive days. However, when all 16 microelectrodes were pulsed for 7 h at 4 nC/ph, the threshold of approximately half of the ULRs became elevated. Recovery of excitability required 2-18 days. Prolonged sequential (interleaved) pulsing of the 16 microelectrodes induced less depression of excitability than did simultaneous pulsing, but only when the stimulus amplitude was low (12 A, 1.8 nC/ph). Stimulation at a higher amplitude (15 nC/ph) induced much more depression of excitability. These findings imply that multiple processes mediate the stimulation-induced depression of neuronal excitability. The data also demonstrate that the depression can be reduced by employing a stimulus regimen in which the inherent spatial resolution of the array is maximized (sequential pulsing at an amplitude in which there is minimal overlap of the effective current fields).

Adaptation, Physiological↗
PubMedDate not supplied

[The late excitatory responses of the motor cortex neurons in the cat to stimulation of the pyramidal tract].

Under conditions of partial suppression of GAMKA-dependent cortical inhibition in the motor cortex of anesthetized cats, a weak electrical stimulation of the pyramidal tract evoked the late slow (50-200 ms) excitatory reactions in the motor cortex neurons similar to those previously recorded under the same conditions in response to stimulation of the parietal cortex. This finding favors the proposal that the late excitatory component of the cortico-cortical response reflects the repetitive activation of cortical neurons due to excitation spread via the system of cortical recurrent excitatory collaterals.

Animals↗
PubMed1987

Electrophysiological relationship between claustrum and contralateral area 4 and 6 pyramidal tract neurons.

The connections between the claustrum and the contralateral motor areas were electrophysiologically investigated in cats under chloralose anesthesia. The extracellular unitary activity of 81 pyramidal tract neurons (PTNs) was recorded; 22 PTNs were inhibited by activation of the contralateral claustrum; inhibition was preceded by an early activation of 4 out of the 22 inhibited PTNs. Section of the corpus callosum abolished the contralateral claustrum effect, while the action of the ipsilateral homologous structure persisted.

Animals↗
PubMed1988

Unmyelinated corticospinal axons in adult rat pyramidal tract. An electron microscopic tracer study.

The aim of the present study was to provide experimental ultrastructural evidence for a corticospinal component in the adult rat pyramidal tract (PT). For this purpose, the entire sensorimotor and frontal cortex of the left hemisphere was labelled using the anterograde tracer horseradish-peroxidase (HRP). Six months old rats were sacrificed 24 or 48 h after implantation of 6-8 HRP-gels. The detection of anterogradely transported HRP at the cervical as well as the lumbar intumescence was carried out as described earlier (J. Histochem. Cytochem., 35 [1987] 623-626). Our results demonstrate the occurrence of labelled myelinated as well as labelled unmyelinated axons within the adult rat PT at both spinal cord levels analyzed. This implicates that at least part of the unmyelinated profiles in the adult rat PT belong to fibres originating in the cortex and therefore must be interpreted as corticospinal axons. The findings are discussed in the light of their physiological significance.

Animals↗
PubMed1998

Inhibitory influence of the ipsilateral motor cortex on responses to stimulation of the human cortex and pyramidal tract.

1. The ability of the primary motor cortex (M1) to modulate motor responses in ipsilateral hand muscles seems to be important for normal motor control and potentially also for recovery after brain lesions. It is not clear which pathways mediate this ipsilateral modulation. Transcallosal connections have been proposed, but are known to be sparse between cortical hand motor representations in primates. The present study was performed to determine whether descending ipsilateral modulation of motor responses might also be mediated below the cortical level in humans. 2. A paired-pulse protocol was used, in which motor-evoked potentials (MEPs) were produced by cortical transcranial magnetic stimulation (cTMS) or by electrical stimulation of the pyramidal tract at the level of the pyramidal decussation (pdTES), in both preactivated and relaxed hand muscles. Paired stimuli were applied at various interstimulus intervals (ISIs) between 2 and 100 ms. The conditioning stimulus (CS) was always magnetic, and delivered to the M1 ipsilateral to the target hand, prior to the test stimulus (TS). The magnetic TS was delivered to the M1 contralateral to the target hand; the electrical TS was applied through electrodes placed over the mastoid process bilaterally. Further experiments included cortical electrical stimulation and H-reflexes. The MEP amplitudes were averaged separately for each ISI and the control condition (no CS), and expressed as a percentage of the unconditioned response. 3. Conditioning stimulation of the ipsilateral M1 resulted in significant inhibition of magnetically evoked MEPs, and also of MEPs produced by pdTES. Inhibition occurred at ISIs between 6 and 50 ms, and was observed in preactivated and relaxed muscles. Higher CS intensities caused greater inhibition of both cTMS- and pdTES-evoked MEPs. 4. While the conditioning effects on magnetically evoked muscle responses could be explained by a transcallosal mechanism, the effects on pdTES-evoked MEPs cannot, because they are elicited subcortically and are therefore not susceptible to inhibitory mechanisms transmitted at the cortico-cortical level. 5. In conclusion, the present results provide novel evidence that the inhibitory influence of the human M1 on ipsilateral hand muscles is to a significant extent mediated below the cortical level, and not only through cortico-cortical transcallosal connections. They point to a concept of inhibitory interaction between the two primary motor cortices that is relayed at multiple levels along the neuroaxis, thus perhaps providing a structurally redundant system which may become important in case of lesions.

Adult↗