Swallow-evoked action potentials in vagal preganglionic efferents

1984 ◽  
Vol 52 (6) ◽  
pp. 1169-1180 ◽  
Author(s):  
J. S. Gidda ◽  
R. K. Goyal
Keyword(s):  
Action Potentials ◽  
Discharge Rate ◽  
Stimulus Frequency ◽  
Superior Laryngeal Nerve ◽  
Bimodal Distribution ◽  
Short Latency ◽  
The Body ◽  
Inhibitory Neurons ◽  
Discharge Rates ◽  
Long Latency

Swallow<evoked potentials in the preganglionic vagal fibers were studied using the single<fiber recording technique in anesthetized opossums. Swallows were evoked by tactile pharyngeal stimulation or electrical stimulation of the cut central end of the superior laryngeal nerve (SLN). Swallowing activity was recorded by the mylohyoid electromyogram and esophageal motility. Sixty<six fibers were studied in which swallowing evoked action potentials. The latencies (from the onset of mylohyoid activity) of evoked responses in different fibers varied from 100 ms to 5 s. The discharge rate of the evoked response was 3<8 action potentials per burst. Each burst lasted 1.1 +/- 0.02 (SE)s. The latencies of evoked spike bursts showed a bimodal distribution. In 34 fibers the latencies were less than 1 s, and in 32 fibers the latencies ranged between 1 and 5 s; these are the short- and long-latency fibers, respectively. Short-latency fibers could easily be distinguished from long-latency fibers based on the influence of SLN-stimulus frequency. Short-latency discharges had low thresholds of activation and were sensitive to changes in the frequency of SLN stimulation, since their latencies decreased and their discharge rate increased with increasing SLN-stimulus frequency. On the other hand, the latencies and discharge rates of long-latency discharges were not modified with changing SLN stimulus frequencies. The conduction velocities of 6 short- and 9 long-latency fibers were 5.64 +/- 0.12 and 5.78 +/- 0.12 (SE) m/s, respectively (P greater than 0.05). The relationship between the latencies of swallow-evoked discharges in the short- and long-latency fibers and the esophageal smooth muscle responses suggested that the short-latency discharges may correlate with the latency of initial inhibition, and the long-latency fibers may correlate with latencies of peristaltic contractions. Based on these temporal relationships, we speculate that vagal efferent fibers showing swallow-evoked, short-latency discharges make contact with intramural inhibitory neurons. They may mediate deglutitive inhibition in the body of the esophagus, relaxation of the lower esophageal sphincter, and receptive relaxation of the fundus of the stomach. The fibers showing late discharges make contact with intramural excitatory neurons and participate in their sequential activation. This dual pathway of activation may be responsible for physiological esophageal peristalsis.

Neuronal Mechanisms Underlying the Laryngeal Adductor Reflex

2011 ◽  
Vol 120 (11) ◽  
pp. 755-760 ◽  
Author(s):  
Qi-Jian Sun ◽  
Jia Min Chum ◽  
Tara G. Bautista ◽  
Paul M. Pilowsky ◽  
Robert G. Berkowitz
Keyword(s):  
Action Potentials ◽  
Superior Laryngeal Nerve ◽  
Laryngeal Nerve ◽  
Short Latency ◽  
Occurrence Rate ◽  
Sprague Dawley ◽  
Single Action ◽  
Long Latency ◽  
Laryngeal Adductor Reflex ◽  
Stimulation Of

Objectives: Electromyographic studies of the laryngeal adductor reflex, glottal closure occurring in response to laryngeal stimulation, have demonstrated an early ipsilateral response (R1) and a late bilateral response (R2). To better define the physiologic properties of these responses, we recorded responses from expiratory laryngeal motoneurons (ELMs) in rats during stimulation of the superior laryngeal nerve (SLN). Methods: Single unit extracellular recordings were obtained from 5 ELMs, identified by their antidromic responses to recurrent laryngeal nerve stimulation and postinspiratory firing pattern, in 4 Sprague-Dawley rats. Results: Unilateral stimulation of the SLN (at 20 Hz) stopped both phrenic nerve inspiratory activity and ELM postinspiratory activity. However, the ELMs displayed robust tonic firing, consisting of non-respiratory burst activity and single action potentials. The single action potentials were identified as short-latency ones (5 to 10 ms) activated by ipsilateral SLN stimulation, with an occurrence rate of 90%, and long-latency ones (20 to 50 ms) activated by bilateral SLN stimulation, with occurrence rates of 47% on the ipsilateral side and 58% on the contralateral side. Conclusions: The R1 response appears to be the result of the short-latency action potentials, orthodromically activated by ipsilateral stimulation of the SLN. The R2 response is likely to be a result of the long-latency action potentials that can be recorded from ELMs on both sides.

Activity of respiratory neurons during NREM sleep

1985 ◽  
Vol 54 (5) ◽  
pp. 1144-1156 ◽  
Author(s):  
J. Orem ◽  
I. Osorio ◽  
E. Brooks ◽  
T. Dick
Keyword(s):  
Respiratory Activity ◽  
Discharge Rate ◽  
Active Phase ◽  
Nrem Sleep ◽  
Bimodal Distribution ◽  
Respiratory Neurons ◽  
Discharge Rates ◽  
Cell Groups ◽  
Respiratory Cells ◽  
Number Of Discharges

The purpose of this study was to analyze differences in the activity of medullary respiratory neurons in the unanesthetized, intact cat during wakefulness and non-rapid-eye-movement (NREM) sleep. We studied single respiratory neurons located within a 1-2 mm deep, 8-10 mm long zone that followed, and included in its dorsal aspect, the retrofacial and ambiguus nuclei. The analysis of variance was used to detect respiratory activity, and cycle-triggered histograms were plotted. The respiratory signal strength and consistency of the respiratory activity were quantified with the eta 2 statistic. We determined for each breath in wakefulness and NREM sleep the average discharge rate during the active phase of the cell, the number of action potentials during the active phase of the cell, and durations of both the cycle and inspiration. Differences in discharge rates and in the number of discharges between wakefulness and NREM sleep were tested with the t test. A bimodal distribution of eta 2 values for the population of neurons indicated there were two groups of respiratory cells: those with eta 2 values less than 0.3 and those with values greater than 0.3. The former we call weak respiratory cells; the latter, strong respiratory cells. Strong and weak cells were classified further as inspiratory or noninspiratory on the basis of the shape of their cycle-triggered histograms. Within the class of strong inspiratory cells, those with the highest eta 2 values 1) reached their peak discharge rate early, 2) discharged at high rates throughout inspiration, and 3) were inactive during expiration. The values of these variables diminished progressively in inspiratory cell groups with lower eta 2 values. Most cells were less active in NREM sleep than in wakefulness. Similar proportions of weak and strong cells and inspiratory and noninspiratory cells were affected by sleep. The reduction in sleep of the activity of strong inspiratory cells was consistent with a general relationship between this activity and the duration of inspiration. Lower discharge rates were associated with longer breaths; higher rates with shorter breaths. This relationship existed within both NREM sleep and wakefulness, and the plot of the relationship across these states formed a continuous function. The reduction in discharge rate in sleep was greater for weak than for strong inspiratory cells: the correlation coefficient between percent change in rate and eta 2 values was -0.636 for inspiratory cells, but it was not significant (-0.265) for noninspiratory cells.(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals Differences in Human Motoneuron Excitability Between Functionally Diverse Muscles

CommonHealth ◽  
2020 ◽  
Vol 1 (1) ◽  
pp. 12-23
Author(s):  
Christopher Taylor ◽  
Tyler Kmiec ◽  
Christopher Thompson
Keyword(s):  
Motor Unit ◽  
Discharge Rate ◽  
Statistical Significance ◽  
Spike Trains ◽  
The Body ◽  
Intrinsic Excitability ◽  
Functional Movement ◽  
Discharge Rates ◽  
Density Surface ◽  
Functionally Diverse

Introduction: Spinal motoneurons (MN) transmit neural commands from the brain to the muscles they innervate and, as a result, produce functional movement. However, MNs are not simply passive conduits of these command and, instead, actively shape motor output through alterations in intrinsic excitability. We hypothesize that the excitability of MNs is not fixed across the body; instead, MNs are functionally tuned to the tasks they control. Here, we investigate this mapping of MN excitability across motor pools. Methods: High-density surface electromyography of the tibialis anterior (TA) and first dorsal interosseous (FDI) was recorded from four neurologically intact participants while they performed low-level, isometric contractions. The data were decomposed into underlying motor unit action potentials and paired motor unit analyses were subsequently performed on these spike trains to quantify MN excitability (ΔF). Results: 1,638 motor unit spike trains were extracted across all contractions. Mann-Whitney U test revealed that all subjects (4/4) had significantly higher maximal discharge rates in FDI, 19.13 [17.62 – 20.59] pps, when compared to the TA, 13.08 [11.51 – 15.46] pps. All subjects (4/4) had a higher ΔF in the TA (4.22 [2.89 – 5.61] pps) than the FDI (3.62 [1.23 – 5.94] pps), with 3/4 reaching statistical significance. Conclusions: Our findings suggest that the discharge rate and intrinsic excitability of human MNs differs across TA and FDI motor pools during similar isometric tasks. These results support the notion that motor pools are functionally tuned to their environmental demands.

The ENT emergency clinic: does senior input matter?

2012 ◽  
Vol 127 (1) ◽  
pp. 15-19 ◽  
Author(s):  
A Mirza ◽  
L McClelland ◽  
M Daniel ◽  
N Jones
Keyword(s):  
Quality Of Care ◽  
Discharge Rate ◽  
Surrogate Marker ◽  
Operating Theatre ◽  
Number Of Children ◽  
Discharge Rates ◽  
Time Period ◽  
Number Of Patients

AbstractBackground:Many ENT conditions can be treated in the emergency clinic on an ambulatory basis. Our clinic traditionally had been run by foundation year two and specialty trainee doctors (period one). However, with perceived increasing inexperience, a dedicated registrar was assigned to support the clinic (period two). This study compared admission and discharge rates for periods one and two to assess if greater registrar input affected discharge rate; an increase in discharge rate was used as a surrogate marker of efficiency.Method:Data was collected prospectively for patients seen in the ENT emergency clinic between 1 August 2009 and 31 July 2011. Time period one included data from patients seen between 1 August 2009 and 31 July 2010, and time period two included data collected between 1 August 2010 and 31 July 2011.Results:The introduction of greater registrar support increased the number of patients that were discharged, and led to a reduction in the number of children requiring the operating theatre.Conclusion:The findings, which were determined using clinic outcomes as markers of the quality of care, highlighted the benefits of increasing senior input within the ENT emergency clinic.

scholarly journals Extracellular detection of neuronal coupling

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Elmer Guzman ◽  
Zhuowei Cheng ◽  
Paul K. Hansma ◽  
Kenneth R. Tovar ◽  
Linda R. Petzold ◽  
...  
Keyword(s):  
Action Potentials ◽  
Microelectrode Arrays ◽  
Short Latency ◽  
Spike Sorting ◽  
Neuronal Connectivity ◽  
Direct Stimulation ◽  
Multiple Electrodes

AbstractWe developed a method to non-invasively detect synaptic relationships among neurons from in vitro networks. Our method uses microelectrode arrays on which neurons are cultured and from which propagation of extracellular action potentials (eAPs) in single axons are recorded at multiple electrodes. Detecting eAP propagation bypasses ambiguity introduced by spike sorting. Our methods identify short latency spiking relationships between neurons with properties expected of synaptically coupled neurons, namely they were recapitulated by direct stimulation and were sensitive to changing the number of active synaptic sites. Our methods enabled us to assemble a functional subset of neuronal connectivity in our cultures.

New analytical solution for the study of hydraulic interaction between Alpine tunnels and groundwater

2003 ◽  
Vol 174 (5) ◽  
pp. 441-448 ◽  
Author(s):  
Jean-Christophe Maréchal ◽  
Pierre Perrochet
Keyword(s):  
Analytical Solution ◽  
Surface Waters ◽  
Discharge Rate ◽  
Water Discharge ◽  
Rate Condition ◽  
Type Curves ◽  
Discharge Rates ◽  
The Alps ◽  
Surface Monitoring ◽  
Tunnel Discharge

Abstract The present paper addresses two major problems encountered during tunnel drilling and related to the hydraulic interaction with surrounding groundwater bodies. The first one is the prediction of water discharge into the tunnel, as a function of the geometric and hydrogeological data. The second problem is related to the assessment of the draining effects on surface waters (springs, lakes, wetlands). Surface monitoring campaigns are costly and evaluating their duration is a sensitive question. Both problems are tightly related and depend on aquifer dynamics. It is shown that in a geological context with steeply dipping structures, nearly vertical, inducing series of aquifers and aquicludes such as in the Alps, the drainage of the aquifer by the tunnel can be modelled by the analytical solution of Jacob and Lohman [1952] for artesian wells. First developed for horizontal, confined unsteady flow towards a vertical well with constant drawdown, it is adapted here to a horizontal tunnel by a rotation of π/2. The main difference between this solution and more classical Theis’ solutions is that a constant drawdown condition replaces the constant discharge rate condition. Hence, a relation is obtained for the time-dependent discharge rate Q(t) detected at the tunnel after drilling, as a function of aquifer transmissivity (T), storage coefficient (S), initial drawdown (so) and tunnel radius (ro). This analytical solution is compared to a finite-elements model simulating a draining tunnel in a simplified 2D vertical cross-section. The comparisons show that the decay of the tunnel discharge can be divided into two periods. During the first period, radial drawdown develops around the tunnel and there is excellent match between analytical and numerical results. Tunnel discharge results from the decompression of rock and water (storage effects) as a response to the sudden initial drawdown at the tunnel location. During the second period, the drawdown cone reaches the aquifer limits (lateral and upper) and numerical discharge rates decrease faster than analytical rates because of hydraulic heads decline at the aquifer limits. In the Alps, such trends were observed for the discharge rates into the Simplon and Mont-Blanc tunnels, and the analytical solution of Jacob and Lohman [1952] was applied to the first discharge period to evaluate aquifer transmissivity and storage coefficients. As indicated by the simulations, and corroborated by field observations, the analytical solution is only valid during a first period after tunnel opening, the duration of which scaling with the inverse of the aquifer diffusivity (T/S). In the second part of the paper, dimensionless type-curves are presented to enable rapid evaluation of the time where a given drawdown is observed at a given distance from the tunnel. Accounting for tunnel geometry (radius and depth) and aquifer parametres (T and S), these curves could for instance help in practice to determine when surface waters would start to be affected by a draining tunnel underneath. Although neglecting the boundary effects discussed in the first part of the paper, these type-curves demonstrate the great inertia of mountain aquifers, and could be used to adjust the duration of surface monitoring campaigns according to the specific tunnel/aquifer settings.

Electrical interactions between the giant axons of a polychaete worm (Sabella penicillus L.)

1980 ◽  
Vol 84 (1) ◽  
pp. 119-136
Author(s):  
D. Mellon ◽  
J. E. Treherne ◽  
N. J. Lane ◽  
J. B. Harrison ◽  
C. K. Langley
Keyword(s):  
Safety Factor ◽  
Nerve Cord ◽  
Action Potentials ◽  
Divalent Cations ◽  
Muscular Contraction ◽  
The Body ◽  
The Other ◽  
Intracellular Recordings ◽  
Giant Axons ◽  
Other Hand

Intracellular recordings demonstrated a transfer of impulses between the paired giant axons of Sabella, apparently along narrow axonal processes contained within the paired commissures which link the nerve cords in each segment of the body. This transfer appears not to be achieved by chemical transmission, as has been previously supposed. This is indicated by the spread of depolarizing and hyperpolarizing voltage changes between the giant axons, the lack of effects of changes in the concentrations of external divalent cations on impulse transmission and by the effects of hyperpolarization in reducing the amplitude of the depolarizing potential which precedes the action potentials in the follower axon. The ten-to-one attenuation of electronic potentials between the giant axons argues against the possibility of an exclusively passive spread of potential along the axonal processes which link the axons. Observation of impulse traffic within the nerve cord commissures indicates, on the other hand, that transmission is achieved by conduction of action potentials along the axonal processes which link the giant axons. At least four pairs of intact commissures are necessary for inter-axonal transmission, the overall density of current injected at multiple sites on the follower axon being, it is presumed, sufficient to overcome the reduction in safety factor imposed by the geometry of the system in the region where axonal processes join the giant axons. The segmental transmission between the giant axons ensures effective synchronization of impulse traffic initiated in any region of the body and, thus, co-ordination of muscular contraction, during rapid withdrawal responses of the worm.

Pain-induced changes in motor unit discharge depend on recruitment threshold and contraction speed

2021 ◽  
Author(s):  
Eduardo Martinez-Valdes ◽  
Francesco Negro ◽  
Michail Arvanitidis ◽  
Dario Farina ◽  
Deborah Falla
Keyword(s):  
Discharge Rate ◽  
Tibialis Anterior Muscle ◽  
Maximum Voluntary Contraction ◽  
Motor Units ◽  
Inhibitory Effect ◽  
Voluntary Contraction ◽  
Recruitment Threshold ◽  
Contraction Speed ◽  
Discharge Rates ◽  
Hypertonic Saline Injection

At high forces, the discharge rates of lower and higher threshold motor units (MU) are influenced in a different way by muscle pain. These differential effects may be particularly important for performing contractions at different speeds since the proportion of lower and higher threshold MUs recruited varies with contraction velocity. We investigated whether MU discharge and recruitment strategies are differentially affected by pain depending on their recruitment threshold (RT), across a range of contraction speeds. Participants performed ankle dorsiflexion sinusoidal-isometric contractions at two frequencies (0.25Hz and 1Hz) and two modulation amplitudes [5% and 10% of the maximum voluntary contraction (MVC)] with a mean target torque of 20%MVC. High-density surface electromyography recordings from the tibialis anterior muscle were decomposed and the same MUs were tracked across painful (hypertonic saline injection) and non-painful conditions. Torque variability, mean discharge rate (MDR), DR variability (DRvar), RT and the delay between the cumulative spike train and the resultant torque output (neuromechanical delay, NMD) were assessed. The average RT was greater at faster contraction velocities (p=0.01) but was not affected by pain. At the fastest contraction speed, torque variability and DRvar were reduced (p<0.05) and MDR was maintained. Conversely, MDR decreased and DRvar and NMD increased significantly during pain at slow contraction speeds (p<0.05). These results show that reductions in contraction amplitude and increased recruitment of higher threshold MUs at fast contraction speeds appears to compensate for the inhibitory effect of nociceptive inputs on lower threshold MUs, allowing the exertion of fast submaximal contractions during pain.

Fast Inhibition Alters First Spike Timing in Auditory Brainstem Neurons

2004 ◽  
Vol 92 (4) ◽  
pp. 2615-2621 ◽  
Author(s):  
Antonio G. Paolini ◽  
Janine C. Clarey ◽  
Karina Needham ◽  
Graeme M. Clark
Keyword(s):  
Lateral Inhibition ◽  
Cochlear Nucleus ◽  
Stellate Cell ◽  
Discharge Rate ◽  
Stellate Cells ◽  
Auditory Pathway ◽  
Auditory Brainstem ◽  
Spike Timing ◽  
Inhibitory Neurons

Within the first processing site of the central auditory pathway, inhibitory neurons (D stellate cells) broadly tuned to tonal frequency project on narrowly tuned, excitatory output neurons (T stellate cells). The latter is thought to provide a topographic representation of sound spectrum, whereas the former is thought to provide lateral inhibition that improves spectral contrast, particularly in noise. In response to pure tones, the overall discharge rate in T stellate cells is unlikely to be suppressed dramatically by D stellate cells because they respond primarily to stimulus onset and provide fast, short-duration inhibition. In vivo intracellular recordings from the ventral cochlear nucleus (VCN) showed that, when tones were presented above or below the characteristic frequency (CF) of a T stellate neuron, they were inhibited during depolarization. This resulted in a delay in the initial action potential produced by T stellate cells. This ability of fast inhibition to alter the first spike timing of a T stellate neuron was confirmed by electrically activating the D stellate cell pathway that arises in the contralateral cochlear nucleus. Delay was also induced when two tones were presented: one at CF and one outside the frequency response area of the T stellate neuron. These findings suggest that the traditional view of lateral inhibition within the VCN should incorporate delay as one of its principle outcomes.

Human cortical potentials evoked by stimulation of the median nerve. II. Cytoarchitectonic areas generating long-latency activity

1989 ◽  
Vol 62 (3) ◽  
pp. 711-722 ◽  
Author(s):  
T. Allison ◽  
G. McCarthy ◽  
C. C. Wood ◽  
P. D. Williamson ◽  
D. D. Spencer
Keyword(s):  
Spatial Distribution ◽  
Median Nerve ◽  
Somatosensory Cortex ◽  
Sensorimotor Cortex ◽  
Preceding Paper ◽  
Short Latency ◽  
Cortical Surface ◽  
Long Latency ◽  
Area 3B ◽  
Stimulation Of

1. The anatomic generators of human median nerve somatosensory evoked potentials (SEPs) in the 40 to 250-ms latency range were investigated in 54 patients by means of cortical-surface and transcortical recordings obtained during neurosurgery. 2. Contralateral stimulation evoked three groups of SEPs recorded from the hand representation area of sensorimotor cortex: P45-N80-P180, recorded anterior to the central sulcus (CS) and maximal on the precentral gyrus; N45-P80-N180, recorded posterior to the CS and maximal on the postcentral gyrus; and P50-N90-P190, recorded near and on either side of the CS. 3. P45-N80-P180 inverted in polarity to N45-P80-N180 across the CS but was similar in polarity from the cortical surface and white matter in transcortical recordings. These spatial distributions were similar to those of the short-latency P20-N30 and N20-P30 potentials described in the preceding paper, suggesting that these long-latency potentials are generated in area 3b of somatosensory cortex. 4. P50-N90-P190 was largest over the anterior one-half of somatosensory cortex and did not show polarity inversion across the CS. This spatial distribution was similar to that of the short-latency P25-N35 potentials described in the preceding paper and, together with our and Goldring et al. 1970; Stohr and Goldring 1969 transcortical recordings, suggest that these long-latency potentials are generated in area 1 of somatosensory cortex. 5. SEPs of apparently local origin were recorded from several regions of sensorimotor cortex to stimulation of the ipsilateral median nerve. Surface and transcortical recordings suggest that the ipsilateral potentials are generated not in area 3b, but rather in other regions of sensorimotor cortex perhaps including areas 4, 1, 2, and 7. This spatial distribution suggests that the ipsilateral potentials are generated by transcallosal input from the contralateral hemisphere. 6. Recordings from the periSylvian region were characterized by P100 and N100, recorded above and below the Sylvian sulcus (SS) respectively. This distribution suggests a tangential generator located in the upper wall of the SS in the second somatosensory area (SII). In addition, N125 and P200, recorded near and on either side of the SS, suggest a radial generator in a portion of SII located in surface cortex above the SS. 7. In comparison with the short-latency SEPs described in the preceding paper, the long-latency potentials were more variable and were more affected by intraoperative conditions.

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