Biomedical subjects

Y Laouris

Publications and source records attributed to Y Laouris.

15 recordsLinked to original sources

PubMed1992

Fatigue-related changes in motor unit action potentials of adult cats.

The purpose of this study was to quantify the changes in motor-unit action potentials (MUAP) and force during a standard motor-unit fatigue test. MUAP waveforms were characterized by the measurement of amplitude, duration, area, and shape (as reflected in a coefficient of proportionality). Fatigue-resistant motor units exhibited small, but statistically significant, changes in MUAP amplitude and area during the fatigue test, whereas fatigable motor units displayed variable changes in MUAP amplitude, duration, and area. For all motor-unit types, the coefficient of proportionality did not change, and hence the change in MUAP area was proportional to the combined changes in amplitude and duration. The between- and within-train changes in MUAP were also distinct for the fatigue-resistant and fatigable motor units. Although several mechanisms could be responsible for the changes in the MUAP as the fatigue test proceeded, the dissociation of the time courses for MUAP and force indicated that these MUAP changes were not the principal reason for the decline in force under these conditions.

Action Potentials↗

PubMed1992

The effect of the stimulation pattern on the fatigue of single motor units in adult cats.

1. The main purpose of this study was to examine the effects of two subtly different stimulus patterns on the force developed by fast-twitch, fatiguable motor units in a cat hindlimb muscle during control (pre-fatigue) and fatiguing contractions. 2. The peak force and the force-time integral responses of nineteen high fatigue (FF) and three intermediate fatigue (FI) motor units of the tibialis posterior muscle in five deeply anaesthetized adult cats were measured at selected times during the course of a 360-s fatigue test. 3. The fatigue test involved a pseudo-random alternation of two patterns of stimulation. One pattern (regular) was composed of a train of stimuli with constant interpulse intervals, set at 1.8 x the twitch contraction time of each unit (interval range, 27-51 ms), and delivered for 500 (or 400) ms. For the total (FF + FI) motor-unit sample, the mean (+/- S.D.) stimulation frequency was 26 +/- 4 Hz (range, 19-37 Hz). The other stimulus pattern (optimized) consisted of three initial stimuli with short (10 ms) interpulse intervals, followed by a constant interpulse-interval train that was adjusted (interval range, 29-62 ms; frequency, 23 +/- 5 Hz; frequency range, 16-36 Hz) such that the total train had the same number of pulses, and the same average frequency and duration as the regular train. 4. The stimulus trains were delivered at 1 s-1 for 360 s, using three-train sequences of each pattern, randomly alternating with one another. The response of the third train in each sequence was selected for the force measurements. The force profile obtained from the fatigue test was subsequently decomposed into two profiles: one attributable to regular and one to optimized stimulation. 5. During the initial responses to the fatigue test, the optimized stimulus pattern produced significantly more force than the regular stimulus pattern. For FF units, the mean increase in peak force (141%) was significantly greater than the increase in the force-time integral (59%). 6. All motor units exhibited an initial potentiation of peak force with the regular stimulation pattern, whereas peak force declined monotonically with the optimized pattern. In contrast, the force-time integral potentiated in the first 30 s for both regular and optimized stimulus patterns. 7. Each motor unit maintained an increased force response to optimized stimulation during the fatigue test, with the greatest relative increase occurring about 120 s into the test, well after the potentiation effect had subsided.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1991

Measurement systems calibration: microcomputer implementation.

Measurement systems used in the collection and processing of laboratory data must be calibrated periodically to obtain accurate results. Because calibration factors can change over time or may be reset to optimize measurements for specific tests, care must be taken to assure that calibration factors and data are aligned correctly. Users should be able to process current data or re-process older data using appropriate calibration factors. The alignment of calibration factors and data should occur in a simple, automatic and transparent way. This document describes one approach to calibration procedures and computer programs used to collect, process, document, measure and display laboratory data. The examples are from our neurophysiology laboratory, where investigators study the mammalian spinal cord and peripheral neuromuscular system. Typical calibration problems, some workable solutions, and computer programs (described in pseudocode) are presented.

Calibration↗

PubMed1991

Computer-aided extraction of the features of the EMG of single motor units.

A software-based system is presented for feature extraction of compound, action-potential (EMG) recordings from single motor units. It simplifies and automates the measurement and analysis of several parameters of the action potential: peak-to-peak amplitude, total duration, peak-to-peak duration, and total area. The software is based on a simple algorithm that first finds the baseline (isoelectric line; including a noise level) of each single EMG potential (waveform) and then searches for the minimum and maximum values in the array of data points representing it. The algorithm searches in both directions starting from the minimum and maximum data points (the waveform peaks) to find the beginning and ending points of the waveform. Using the indices (i.e., array-point numbers) of the four data points provided by the algorithm, the desired features are extracted and/or calculated and saved in a standard-format spreadsheet. The algorithm has a potentially widespread usefulness in a broad array of electrophysiological studies.

Action Potentials↗

PubMed1991

Triggering module for waveform digitization.

A full circuit description is provided for a triggering module used to assist a small laboratory computer in digitizing muscle force- and EMG waveforms. During the stimulation of individual motor units using a standard fatigue test, a train of 13 pulses are delivered at a rate of 40 pps either intracellularly to a motor neuron, or extracellularly to functionally isolated single motor axons from among divided ventral-root nerve filaments. Trains are delivered at a rate of 1/s for the duration of the test, which may range from 120 to 3600 s. Both the force and EMG profiles undergo changes during such tests and the quantification of parameters associated with their waveforms are of interest to neurobiologists. The triggering module allows a typical small laboratory computer to capture user-selected waveforms and thereby reduces the programming problems, timing constraints, storage requirements and analysis time associated with obtaining these parameters. The versatile circuit may be easily adapted to solve similar data-acquisition problems. The method was implemented on an Apple Macintosh II computer but can also be applied to other systems equipped with appropriate software and a data-acquisition card.

Animals↗

PubMed1990

The influence of altered head, thorax and pelvis mass on the postnatal development of the air-righting reaction in albino rats.

The experiments were performed on 18 albino newborn rats of both sexes. The postnatal development of the air-righting-reaction (ARR) of the rats was tested for 4 different falling heights (30, 40, 50 and 60 cm) with 3 different loading conditions: artificial alteration of the head, thorax and pelvis mass, respectively. The reaction was analyzed in terms of a three-segment model of the rat (three rotatable parts: head-thorax-pelvis with only one degree of freedom between successive segments). Loading of the head resulted in a delayed development of the first phase of the ARR, whereas loading of the trunk or pelvis slowed the second phase of development. In general, it appears that loading of a body segment results in a delayed development of the rotation of that segment during free fall. Furthermore, loading of a caudal region was associated with an earlier rotation of cranial segments. The completion of the ARR maturation process showed no dependency on either the location or the size of the load, suggesting that the postnatal development of the ARR is pre-programmed.

Animals↗

PubMed1990

The postnatal development of the air-righting reaction in albino rats. Quantitative analysis of normal development and the effect of preventing neck-torso and torso-pelvis rotations.

The aim of this study was to describe the ontogenesis of the air-righting reaction (ARR) in rats. The first experiment was performed on 6 newborn albino rats of both sexes and followed the development of the ARR over postnatal days 1-21. The degree of rotation achieved after falling from different heights was quantified according to a rating scheme. It appeared that the air-righting reaction is effected by a spiral movement which spreads in a cranio-caudal direction. The reaction develops between postnatal day 8 and 18. On postnatal day 10 only a few animals are able to turn their heads, this being possible only from a falling height of 60 cm and corresponding to a falling time of 350 ms. A rapid development of the reaction was found between days 10 and 14. The second experiment on 8 rats involved the use of immobilization in order to isolate the mechanisms that trigger the ARR. The immobilization prevented neck-torso rotation, torso-pelvis rotation, and both rotations in different animals. Despite the disruption of important (afferent) feedback systems, the reaction developed within the same age period as in control rats. Thus, the Magnus "chain reflex hypothesis' as basis for the ARR is rejected in favor of a central motor program hypothesis.

Age Factors↗

PubMed1990

Higher-order non-linear phenomena in Renshaw cell responses to random motor axon stimulation.

Renshaw cell responses to random motor axon stimulation exhibit second-order non-linearities in that they depend on the occurrence of a preceding stimulus, although these non-linearities are not strong enough to significantly depress the coherence. However, higher-order non-linearities have not been checked for so far. This is carried out here. Lumbosacral Renshaw cells were recorded with micropipettes in anaesthetized cats. Their responses to random (pseudo-Poisson) stimulation of motor axons in peripheral nerves or ventral roots were quantified by calculating peristimulus-time histograms of various sorts, conventional and conditional. Conventional peristimulus-time histograms were computed with respect to all the stimuli in a train. Conditional peristimulus-time histograms were calculated with respect to "test" stimuli which were sorted out (by computer) from the original stimulus train when they were preceded by "conditional" stimuli at average intervals of delta 1 or delta 2 or both. These conditioned responses were compared with those to be expected from hypothetical linear superposition. Renshaw cell responses showed small third-order non-linearities to pairs of conditioning stimuli at small intervals (up to some tens of milliseconds before the test stimuli). These third-order effects were smaller than each of the second-order non-linearities elicited by any of the single-conditioning stimuli. Also, further higher-order non-linearities were apparent, but of little average significance. Hence, the non-linearities in Renshaw cell responses to random inputs are essentially of second-order and fairly small.

Animals↗

PubMed1990

Frequency characteristics and nonlinear features of responses of cat dorsal horn neurons to random stimulation of cutaneous afferents.

The system between cutaneous (suralis) afferents and dorsal horn neurons was studied for comparison with studies previously performed on the motor axon-Renshaw cell system, using the same methods. In anaesthetized or decerebrated cats, 27 dorsal horn neurons of segments L5 to S1 were recorded extracellularly in depths of 1-2.3 mm from cord dorsum. Cutaneous afferents in branches of the ipsilateral suralis nerve were stimulated with sequences of randomly occurring electrical pulses at two levels of mean rate. The responses of the dorsal horn neurons to the stimuli were evaluated in the frequency and time domain. Calculation of coherence, gain and phase functions (via spectral analysis) showed that the frequency response depended on the precise pattern on cell discharge and could vary from broad-band to low-pass or occasionally band-pass characteristics. There were minor differences in these characteristics with those of Renshaw cells. A special type of nonlinear analysis, using conditional peristimulus-time histograms, showed that the responses to test stimuli were facilitated, depressed or both by conditioning stimuli occurring some tens to a few hundred milliseconds before. Early and late response components could be conditioned individually and differently. Exponential fits to such conditioning curves yielded two time constants for depression (means of 21 and 94 ms) and one for facilitation (14 ms). Similar conditioning effects and time constants were previously found for the motor axon-Renshaw cell system although a few differences were apparent. By analogy, it is suggested that part of the long-lasting conditioning effects (with long time constants) are probably due to presynaptic mechanisms.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1989

A method to estimate the effects of parallel inputs on neuronal discharge probability.

We here present a method to study the interaction of parallel neural input channels regarding their effects on a neurone. In particular, the method allows to disclose the effects of oligosynaptic pathways that may exist in parallel to direct monosynaptic connections to the cell. Two (or more) inputs (nerves) are stimulated with random patterns of stimuli. The response of the cell to these patterns is evaluated by the computation of peristimulus-time histograms (PSTHs). One of the two stimulus trains is selected as the one to yield reference events for the PSTH computation. From this stimulus train are selected those stimuli as reference events which are preceded, at defined mean intervals, by stimuli in the same or a parallel channel. These "conditioning" stimuli are determined (1) separately from each single stimulus train and (2) concomitantly from the two trains as events occurring simultaneously in both. The effects exerted by these various conditioning events on the effects of the "test" pulses on the cell response yield insights into the interactions between the two (or more) inputs. These methods are demonstrated on spinal Renshaw cells activated by independent random stimulation of two muscle nerves and on dorsal horn neurones responding to cutaneous nerve stimulation.

Animals↗

PubMed1989

The relationship between coherence and nonlinear characteristics in Renshaw cell responses to random motor axon stimulation.

Cat spinal Renshaw cells were activated by stimulating muscle nerves or ventral roots with random (pseudo-Poisson) patterns of brief electrical stimuli. This input pattern is optimal for a comparative study in both the frequency- and time-domain. The frequency-dependent variable of particular interest in this study was the coherence as a measure of the degree to which signal transmission is linear and noise-free; it was estimated via spectral analysis. Time-domain analysis consisted of calculating peri-stimulus time histograms in order to estimate the amount of nonlinearity in the cell responses to pairs of stimuli. The main result was that the amount of nonlinearity measured in this way did not profoundly depress the coherence. Two types of peri-stimulus time histogram were calculated: the "conventional" peri-stimulus time histogram (as a reference) computed with respect to all the stimuli in a train, and the "conditional" peri-stimulus time histogram computed with respect to the second in pairs of stimuli which were separated from each other by varied intervals delta. The latter type of peri-stimulus time histogram showed that Renshaw cell responses to stimuli were conditioned by preceding stimuli, which could facilitate (at small delta s) and/or more often depress (up to several hundreds of milliseconds) the subsequent responses in a nonlinear manner. The objective of this study was to test the hypothesis that nonlinear characteristics contribute significantly to depress the coherence from its optimal value (1).(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗

PubMed1989

Early and late components in cat Renshaw cell responses to random stimulation of motor axons: their differential sensitivity to preceding activation.

Lumbosacral Renshaw cells were activated by random stimulation of motor axons in muscle nerves or ventral roots. The stimulus patterns had mean rates of 9.5-13 or 20-23 pulses per second. The Renshaw cell responses were evaluated by two kinds of peristimulus-time histograms. "Conventional" peristimulus-time histograms were calculated by averaging the cell discharge with respect to all the stimuli in a train. "Conditional" peristimulus-time histograms were determined by averaging the cell discharge with respect to the second ("test") stimulus in pairs of stimuli which were separated by varied intervals. The effects of the conditioning stimuli were evaluated after correcting for the effect of linear superposition of the conditioning and test stimuli. The conventional peristimulus-time histograms showed an excitatory response which often consisted of two distinct components: a narrow and high "early" peak and a broad and low "late" elevation of firing probability. The early and late excitatory components were conditioned in different ways. Whereas the late component was virtually always depressed, the early component showed three patterns: (1) uniform depression; (2) uniform facilitation; (3) a mixture of depression and facilitation. Frequency responses (coherence and gain estimates) were also calculated separately for the cell discharges underlying either the early or the late components. The estimates for the "late spikes" showed a stronger decline with increasing frequency than those for the "early spikes". The origin of the different conditioning effects probably lies in a combination of pre and postsynaptic factors. They may play a role in tremor mechanisms.

Action Potentials↗

PubMed1988

Relations between time-and frequency-domain measures of signal transmission from cutaneous afferents to dorsal horn neurons.

In pentobarbitone-anesthetized cats, the spike sequences of dorsal horn neurons were recorded in response to random stimulation of branches of the suralis nerve. Combined frequency- and time-domain analysis was performed on the stimulus and spike trains. Coherence function estimates computed by spectral analysis were compared with peristimulus time histograms (PSTHs). The cell responses were divided into 4 main types: PSTHs with a single high and narrow peak were associated with broad-range high coherence; PSTHs with two (or sometimes 3) distinct peaks concurred with a coherence which was high a low frequencies, low at intermediate ones and higher again at high frequencies; broad unstructured PSTH peaks of varying height concurred with coherence declining from high values at low frequencies to lower values at higher ones; and small and broad PSTH peaks were associated with generally low coherence. Thus, the variation of coherence with frequency depends on the precise pattern of cell discharge.

Action Potentials↗

PubMed1988

Time constants of facilitation and depression in Renshaw cell responses to random stimulation of motor axons.

In 9 adult anaesthetized cats, 22 lumbosacral Renshaw cells recorded with NaCl-filled micropipettes were activated by random stimulation of ventral roots or peripheral nerves. The stimulus patterns had mean rates of 9.5-13 or 20-23 or 45 pulses per second and were pseudo-Poisson; short intervals below ca. 5 ms (except in two cases) were excluded. The Renshaw cell responses were evaluated by two kinds of peristimulus-time histograms (PSTHs). "Conventional" PSTHs were calculated by averaging the Renshaw cell discharge with respect to all the stimuli in a train. These PSTHs showed an early excitatory response which was often followed by a longer-lasting slight reduction of the discharge probability. These two response components were positively correlated. "Conditional" PSTHs were determined by averaging the Renshaw cell discharge with respect to the second ("test") stimulus in pairs of stimuli which were separated by varied intervals, delta. The direct effect of the first "conditional" response was subtracted from the excitation following the second ("test") stimulus so as to isolate the effect caused by the second stimulus per se. After such a correction, the effect of the first "conditioning" stimulus showed pure depression, pure facilitation or mixed facilitation/depression. Analysis of such conditioning curves yielded two time constants of facilitation (ranges: ca. 4-35 ms and 93-102 ms) and two of depression (ranges: ca. 7-25 ms and 50-161 ms). It is concluded that these time constants are compatible with processes of short-term synaptic plasticity known from other synapses. Other processes such as afterhyperpolarization and mutual inhibition probably are of less importance.

Animals↗

PubMed1988

Facilitation and depression in the responses of spinal Renshaw cells to random stimulation of motor axons.

1. We investigated the responses of cat lumbosacral Renshaw cells to pseudo-Poison stimulus sequences (of three different mean rates) delivered to motor axons in ventral roots or various muscle nerves. The Renshaw cell responses were evaluated by computation of peristimulus time histograms (PSTHs). 2. PSTHs computed with respect to all the stimuli showed, before the reference time, near-constant bin contents corresponding to the mean firing probability (rate), and an initial excitatory component (increase in discharge probability) after the reference time, followed by a small but longer-lasting reduction of firing rate. These two response components were strongly correlated linearly. It is suggested that the postexcitatory rate reduction is predominantly due to afterhyperpolarization. 3. In general, Renshaw cell responses to any stimulus in a stimulus train depended upon the stimulation history. In the averaged record, the response to the second of a pair of stimuli was affected by the first stimulus independently of intervening (random) stimuli. Very often, the second response showed a long-lasting depression (from 25 to greater than 250 ms). In a number of cases a briefer facilitating effect preceded the depression. 4. These conditioning effects were largely homosynaptic, i.e., confined to the particular input channel that was stimulated. This was shown by stimulating two different nerves (or nerve branches) with independent random patterns of similar mean rates and determining the cross-conditioning exerted by one input channel on the excitatory effects of the other. At small intervals between conditioning and test stimuli of some tens of milliseconds, a facilitatory effect could often be seen, which almost certainly reflected spatial summation. However, the subsequent depressant effect was largely accounted for by the postexcitatory rate reduction consequent to the conditioning stimulus in the parallel channel. Autoconditioning was still present. 5. The amount of facilitation and depression as well as their balance depended on the average Renshaw cell response. This in turn depended, at each mean stimulus rate, on the strength of synaptic coupling between an input channel and the cell, and on the mean stimulus rate, declining with an increase in mean rate. That is, the facilitation increased and the depression decreased with decreasing synaptic coupling and increasing mean stimulus rate. 6. Several factors may contribute to facilitation and depression; these are discussed with respect to their relative quantitative significance.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗