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PubMed1987

Postnatal transient expression of long-lasting descending inhibitory effect on spinal reflexes in the rat.

In the spinal cord isolated from neonatal rats, stimulation of the ipsilateral lateral column at the thoracic level strongly inhibited monosynaptic segmental reflex in the lumbar cord for about 60 s. The descending inhibition was not associated with any changes in the membrane potential or conductance in lumbar motoneurons when the excitatory postsynaptic potentials in response to stimulation of the dorsal root were depressed. The descending inhibition was diminished with age and could not be detected at 5 months of age. It is suggested that certain inhibitory pathways in the descending spinal tract are rearranged during postnatal development of rats.

Age Factors↗
PubMed2001

The bilateral reflex control of the trapezius muscle in humans.

Abstract. Electromyographic recordings were made from the trapezius muscle in 18 healthy subjects using surface electrodes placed bilaterally. A mechanical tap applied to the insertion of the lower fibres of trapezius evoked a reflex at 11.9 +/- 1.4 ms (mean plus minus SD) in the ipsilateral trapezius muscle. In addition and surprisingly, short latency, facilitatory reflexes were also seen on the contralateral side at a latency of 14.3 +/- 1.7 ms. Electrical stimulation of the afferent nerve to trapezius, the cervical nerve of C3/4, also evoked short latency, facilitatory reflexes from both the ipsilateral and contralateral muscles. Since this nerve carries the Ia fibres from trapezius, this reflex would appear to be the equivalent of the H reflex seen in the soleus muscle. The latency of this reflex was 10.9 +/- 1.4 ms ipsilaterally and 11.9 +/- 1.5 ms contralaterally, the difference being only 1.0 +/- 0.7 ms. Voluntary activity of the ipsilateral trapezius increased the amplitude of both mechanically and electrically evoked ipsilateral and crossed reflexes, and vibration of the ipsilateral trapezius decreased the amplitude of both reflexes. These results together suggest that the earliest parts of both ipsilateral and crossed reflexes are monosynaptic in origin. If the crossed reflex is, in part, due to a common Ia presynaptic input, correlation of bilateral trapezius activity should produce a peak in the cross-correlogram. Indeed, cross-correlation of the bilateral trapezius activity during elevation of the arms produced a short duration peak. Moreover, this was significantly larger when compared to that constructed from activity of the upper and lower fibres of trapezius from one side. These results imply that muscle spindle afferents from the ipsilateral trapezius monosynaptically activate motoneurones contralaterally.

Action Potentials↗
PubMed2005

Post-activation depression in various group I spinal pathways in humans.

This investigation was designed to study the effects of post-activation depression in different spinal pathways fed by group I afferents available to investigation in human subjects. It was precipitated by a recent investigation in the cat showing that-contrary to the general assumption-post-activation depression is not a widespread phenomenon in the spinal cord. In 24 healthy subjects comparison was made between the effects of low and high-test stimulus rates on the monosynaptic Ia excitation, known to be subject to post-activation depression, and on oligosynaptic pathways fed by group I afferents. Both the amplitude of monosynaptic H reflexes and the amount of heteronymous monosynaptic Ia facilitation were significantly smaller at high than at low-test stimulus rates (1-2 s compared with 6-8 s between two consecutive stimuli). So was the amount of reciprocal Ia inhibition of tibialis anterior motoneurones. In contrast, the amount of other non-monosynaptic group I effects directed to the same motor nuclei (peroneal-induced excitation of quadriceps motoneurones, disynaptic non-reciprocal group I inhibition of flexor carpi radialis motoneurones, and D1 inhibition of flexor carpi radialis and soleus H reflexes) were enhanced at high stimulus rates. Results in humans confirm that post-activation depression depends on the type of group I afferents, and/or on the target neurones. The functional significance of the discrepancy between post-activation depression in pure Ia pathways and in other group I pathways is discussed with regard to the fusimotor-driven servo-assistance from Ia afferent discharges.

Adult↗
PubMed2004

Conversion of the modulatory actions of dopamine on spinal reflexes from depression to facilitation in D3 receptor knock-out mice.

Descending monoaminergic systems modulate spinal cord function, yet spinal dopaminergic actions are poorly understood. Using the in vitro lumbar cord, we studied the effects of dopamine and D2-like receptor ligands on spinal reflexes in wild-type (WT) and D3-receptor knock-out mice (D3KO). Low dopamine levels (1 microM) decreased the monosynaptic "stretch" reflex (MSR) amplitude in WT animals and increased it in D3KO animals. Higher dopamine concentrations (10-100 microM) decreased MSR amplitudes in both groups, but always more strongly in WT. Like low dopamine, the D3 receptor agonists pergolide and PD 128907 reduced MSR amplitude in WT but not D3KO mice. Conversely, D3 receptor antagonists (GR 103691 and nafadotride) increased the MSR in WT but not in D3KO mice. In comparison, D2-preferring agonists bromocriptine and quinpirole depressed the MSR in both groups. Low dopamine (1-5 microM) also depressed longer-latency (presumably polysynaptic) reflexes in WT but facilitated responses in D3KO mice. Additionally, in some experiments (e.g., during 10 microM dopamine or pergolide in WT), polysynaptic reflexes were facilitated in parallel to MSR depression, demonstrating differential modulatory control of these reflex circuits. Thus, low dopamine activates D3 receptors to limit reflex excitability. Moreover, in D3 ligand-insensitive mice, excitatory actions are unmasked, functionally converting the modulatory action of dopamine from depression to facilitation. Restless legs syndrome (RLS) is a CNS disorder involving abnormal limb sensations. Because RLS symptoms peak at night when dopamine levels are lowest, are relieved by D3 agonists, and likely involve increased reflex excitability, the D3KO mouse putatively explains how impaired D3 activity could contribute to this sleep disorder.

Animals↗
PubMed1994

N-methyl-D-aspartate (NMDA)-mediated muscle relaxant action of flupirtine in rats.

The present study examined in urethane-chloralose anaesthetized rats whether N-methyl-D-aspartate (NMDA) is involved in the depressant effect of flupirtine on the monosynaptic Hoffmann (H)-reflex recorded from plantar foot muscles and on polysynaptic flexor reflexes recorded from tibialis muscle. Intrathecal administration of both the specific NMDA antagonist (-)-2-amino-7-phosphonoheptanoate and of flupirtine depressed the polysynaptic flexor reflex without affecting the monosynaptic H-reflex. In contrast, the non-NMDA antagonist 6,7-dinitroquinoxaline-2,3-dione depressed the H-reflex without affecting the flexor reflex. The depressant effect of flupirtine on the flexor reflex was prevented by co-administration of NMDA, but not by co-administration of the non-NMDA agonist alpha-amino-3-hydroxy-5-tertbutyl-4-isoxazolepropionic acid. These observations suggest that NMDA might be involved in the action of flupirtine.

Aminopyridines↗
PubMed1987

Afferent and efferent control of stance and gait: developmental changes in children.

Comparisons were made between the cerebral potentials (CPs) and EMG responses of leg muscles evoked by perturbation impulses during stance and gait in normal children aged from 1 to 10 years. Changes in the efferent arm of the reflex systems during development were reflected in parallel changes with age of the afferent system, expressed in the CP: in the youngest children (1-2 years of age) monosynaptic stretch reflex potentials appeared following perturbations during both stance and gait, together with a reduced level of longer latency EMG responses. The CP, too, had a profile that did not, at this early stage, differ in either condition. In children from 6 to 10 years of age, the adult pattern was reached, with the suppression of monosynaptic stretch reflexes and the early part of the CP during gait perturbation. This is interpreted as an inhibition of group I afferents at both segmental and supraspinal levels, involving suppression of both segmental stretch reflexes and group I signals to supraspinal centres. This control of afferent information had yet to be established in early infancy. The age group from 2 to 6 years showed progressive changes, with an increase in both the level and phasic nature of polysynaptic EMG responses and a corresponding transformation of the latency and shape of the CP. It is suggested that maturation of compensatory EMG responses during gait is achieved by the establishment of descending inhibition of group I afferents and facilitation of polysynaptic spinal reflexes via group II afferents.

Afferent Pathways↗
PubMed1984

Definition of human reflex excitability by statistical analysis of quantal EMG responses.

A precise method has been devised to estimate soleus motoneurone pool excitability by probit analysis of quantal (all-or-none) reflex EMG responses to critical electrical stimulation. The technique is shown to be sensitive to changes induced by weak excitatory or inhibitory inputs and is likely to be useful in the study of monosynaptic proprioceptive reflexes.

Adolescent↗
PubMed1989

Encoding of nociceptive thermal stimuli by diffuse noxious inhibitory controls in humans.

1. It has previously been shown that, in normal humans, heterotopic painful thermal conditioning stimuli induce parallel increase in the thresholds of a spinal nociceptive flexion reflex (RIII reflex) and the concurrent sensation of pain elicited by electrical stimulation of the sural nerve. On the basis of analogous animal studies, we proposed that such phenomena could be related to diffuse noxious inhibitory controls (DNIC), which have been described in the rat. The present study, which was carried out on normal volunteer subjects, was particularly concerned with the extent and temporal characteristics of the depressive effects of DNIC triggered by painful thermal stimuli on RIII reflex activity. In addition, because it was possible that these depressive effects could have resulted from a direct postsynaptic inhibition of motoneurons, a second part of the study was aimed at determining whether or not the heterotopic noxious thermal stimuli also affected the excitability of alpha-motoneurons, as monitored by the monosynaptic Hoffmann reflex (H reflex) technique. 2. In the 11 subjects under study, application of moderate, nonnoxious temperatures (40-44 degree C) to the contralateral hand (via a thermoregulated and agitated waterbath) did not modify the RIII reflex nor the associated sensation of pain. By contrast noxious temperatures clearly depressed the RIII reflex and the concurrent sensation of pain, both during and after the conditioning procedure (CP), in a direct linear relationship to the temperature of the waterbath in the 45-47 degree C range; the maximal depressive effect was observed with the highest conditioning temperature. A significant relationship was also found between the extent of the RIII depression during the CP and that during a 10-min period of post-CP observation. 3. The depressive effects observed on both the RIII reflex and pain were not associated with clear change in autonomic functions. Respiration remained stable during the sessions, with no significant relationship between the temperatures of the waterbath and respiratory rate. Heart rate was slightly but significantly increased during the immersion of the hand in the 46 or 47 degree C waterbaths; this increase, however, ceased with the end of CP. 4. Application of thermal conditioning stimuli produced a slight but nonsignificant increase of the monosynaptic H reflex during the first minute of CP, no matter what was the temperature of the waterbath. However, there were no subsequent variations during the 6-min period of post-CP observation.(ABSTRACT TRUNCATED AT 400 WORDS)

Adult↗
PubMed2001

Soleus H-reflex gain in humans walking and running under simulated reduced gravity.

The Hoffmann (H-) reflex is an electrical analogue of the monosynaptic stretch reflex, elicited by bypassing the muscle spindle and directly stimulating the afferent nerve. Studying H-reflex modulation provides insight into how the nervous system centrally modulates stretch reflex responses.A common measure of H-reflex gain is the slope of the relationship between H-reflex amplitude and EMG amplitude. To examine soleus H-reflex gain across a range of EMG levels during human locomotion, we used simulated reduced gravity to reduce muscle activity. We hypothesised that H-reflex gain would be independent of gravity level.We recorded EMG from eight subjects walking (1.25 m s-1) and running (3.0 m s-1) at four gravity levels (1.0, 0.75, 0.5 and 0.25 G (Earth gravity)). We normalised the stimulus M-wave and resulting H-reflex to the maximal M-wave amplitude (Mmax) elicited throughout the stride to correct for movement of stimulus and recording electrodes relative to nerve and muscle fibres. Peak soleus EMG amplitude decreased by ~30% for walking and for running over the fourfold change in gravity. As hypothesised, slopes of linear regressions fitted to H-reflex versus EMG data were independent of gravity for walking and running (ANOVA, P > 0.8). The slopes were also independent of gait (P > 0.6), contrary to previous studies. Walking had a greater y-intercept (19.9% Mmax) than running (-2.5% Mmax; P < 0.001). At all levels of EMG, walking H-reflex amplitudes were higher than running H-reflex amplitudes by a constant amount. We conclude that the nervous system adjusts H-reflex threshold but not H-reflex gain between walking and running. These findings provide insight into potential neural mechanisms responsible for spinal modulation of the stretch reflex during human locomotion.

Adult↗
PubMed1977

Responses in human pretibial muscles to sudden stretch and to nerve stimulation.

Electromyograms have been recorded from the human tibialis anterior muscle during voluntary contraction. The accessibility of the nerve to this muscle (common peroneal) has permitted a comparison of reflex responses to low threshold electrical stimulation of the nerve with those to stretch of the muscle itself. Nerve stimulation elicited a reflex at monosynaptic latency (V1 at 28-29 ms) and a second response (V2 at 50-52 ms). A tendon tap induced two responses (M1 at 29 ms and M2 at 50 ms). The responses to a 'ramp' stretch were similar. The homology of V1 with M1, and of V2 with M2 is discussed. V2 and M2 probably correspond to the 'transcortical' reflexes described from other muscles. Neither V1, V2, M1 nor M2 were influenced by anaesthesia of the foot. M1 and M2 were both reduced in amplitude by a selective gamma-efferent block produced by local anaesthetic in the common peroneal nerve. It is concluded, that muscle spindles are the receptors predominantly responsible for M2 ('transcortical') responses. The amplitudes of M1 and M2, but not V1 and V2 were augmented by prior instruction to 'resist' the stimulus. This is interpreted as evidence for voluntary modulation of gamma-efferent activity at a constant force of contraction.

Anesthesia↗
PubMed1987

Electrically evoked responses of the human external oblique abdominal muscle.

An electric shock delivered to a mixed intercostal nerve of a standing human subject evokes two responses in the external oblique abdominal EMG, namely an M-wave and an electrically elicited reflex. The reflex latency is very close to that of the mechanically elicited phasic stretch reflex of the external oblique, suggesting that it is a monosynaptic spinal reflex. However, several of its characteristics make it very different from the mechanically evoked reflex and the H-responses of calf or jaw muscles. Unlike the mechanically evoked reflex, the electrically elicited reflex is neither modulated by respiration nor attenuated when the subject assumes a supine posture. Unlike the H-response of calf or jaw muscles, the electrically elicited reflex is extremely reproducible from trial to trial, displays no antidromic occlusion in response to an increase in shock strength, and is neither suppressed nor potentiated by abdominal muscle vibration. A silent period, i.e., an indicator of alpha-motoneuron suppression, follows an electrically elicited reflex only when the subject rotates his trunk away from the recording site. Presumably, inputs from external oblique muscle receptors inhibit their homonymous motoneurons effectively when the muscle is functioning as the chief power generator, but not when it is functioning as an agonist. Using single motor unit analysis, the electrically elicited reflex was shown to be comprised of monosynaptic, oligosynaptic, and multisegmental components with the major component being monosynaptic. These unique characteristics of the EER are presumably a reflection of the external oblique's multisegmental innervation, multilayered anatomy, short neuronal pathways, and diverse functions.

Abdominal Muscles↗
PubMed1976

Actions of methoxamine and tryptamine and their interactions with cyproheptadine and phenoxybenzamine on cat spinal cord segmental reflexes.

The effects of norepinephrine, methoxamine and tryptamine were assessed on the monosynaptic and polysynaptic segmental reflexes in the unanesthetized, decerebrated acute spinal cat. Their selectivity of action was determined by studying the interactions of methoxamine and tryptamine with two antagonists, cyproheptadine and phenoxybenzamine. Potentials were evoked by stimulating either the L7 or S1 dorsal root and were recorded from the corresponding ipsilateral ventral root. Norepinephrine did not affect reflex activity, whereas methoxamine facilitated both the monosynaptic and polysynaptic potentials in a dose-related manner when infused over 20 minutes. Tryptamine facilitated both the monosynaptic and polysynaptic reflex potentials. This increase was dose related for the monosynaptic reflex but not for the polysynaptic reflex. Phenoxybenzamine blocked the facilitatory effects of methoxamine and did not antagonize the effects of tryptamine on the segmental reflex. The facilitatory effects of tryptamine were effectively blocked by cyproheptadine. Cyproheptadine failed to reduce the polysynaptic response to methoxamine, although it partially antagonized the monosynaptic facilitation. These findings demonstrate that methoxamine and tryptamine facilitate the segmental reflex by different modes of action and provide additional evidence for noradrenergic and tryptaminergic systems in the spinal cord.

Animals↗
PubMed1994

Effects of chronic spinalization on ankle extensor motoneurons. II. Motoneuron electrical properties.

1. Intracellular recording and stimulation techniques were used in a comparison of electrical properties of triceps surae and plantaris motoneurons between unlesioned and 6-wk chronic spinal (L1-L2) cats. The primary analysis was restricted to 195 motoneurons with action potential heights > or = 80 mV. 2. Voltage transients resulting from short-duration current pulses (0.5 ms) were used to estimate membrane time constant (tau m) and equivalent cylinder electrotonic length (L). Although L was unchanged, tau m and the equalization phase time constant were significantly lower (17%) in motoneurons from chronic spinal preparations. Estimated total cell surface area was also reduced by 11%. The incidence of sag conductances, as judged from observations of the decay of voltage transients, increased from 3% to 29% after chronic spinalization. 3. Input resistance, as measured from either the amplitude of voltage responses to long-duration (50 ms) hyperpolarizing pulses (RinL) or from the area of the short-duration current pulse-induced voltage transients, was unchanged in the chronic spinal preparation. 4. Rheobase current was unchanged but threshold voltage (V Th) was increased in chronic spinal motoneurons. Increased V Th was not a result of membrane hyperpolarization because both mean action potential height (88 mV) and resting membrane potential (70 mV) were identical in both preparations. 5. The threshold current for action potential activation by short-duration (0.5 ms) current pulses increased 28% in chronic spinal preparations. This is consistent with the increase in V Th in the same motoneurons. 6. Measured V Th was identical to that calculated from the product of RinL and rheobase in the unlesioned preparation but was significantly larger than calculated V Th in chronic spinal preparations. This may indicate an increased incidence or magnitude of subthreshold rectification processes in motoneurons from chronic spinal preparations. These results in barbiturate-anesthetized preparations suggest that ankle extensor motoneurons are less excitable in the chronic spinal state. 7. Mean afterhyperpolarization duration was 10% shorter in motoneurons from chronic spinal preparations, whereas amplitude was unchanged. 8. Electrical properties were also compared in chronic spinal and unlesioned preparations using motoneurons with action potential heights of 60-79 mV. In these motoneurons with presumably poorer impalements there were no significant differences between unlesioned and chronic spinal preparations. 9. Ia monosynaptic excitatory postsynaptic potentials (EPSPs) recorded in the same motoneurons have decreased half-widths and rise times and increased amplitudes.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1978

Hemiplegic spasticity: neurophysiologic studies.

The excitability of segmental reflex pathways in normal subjects and in patients with hemiplegia has been examined by conditioning the monosynaptic H reflex with a 200 msec burst of vibration applied to the tendo Achilles. In 6 normal subjects, the burst of vibration produced a short-latency facilitation of soleus motoneurons (attributed to monosynaptic excitation) which was followed by a longer-latency inhibition. A similar response was observed in 8 patients with hemiplegia, but the late inhibition was significantly less. The loss of an inhibitory mechanism may contribute to the exaggerated reflexes observed in patients with hemiplegia.

Adult↗
PubMed1987

A reflex behavior mediated by monosynaptic connections between hair afferents and motoneurons in the larval tobacco hornworm, Manduca sexta.

In the tobacco hornworm caterpillar, tactile stimulation of sensory hairs located on the tip of a proleg (the planta) evokes ipsilateral or bilateral retraction of the prolegs in that segment. We have used electrophysiological and anatomical methods to investigate the excitatory neural pathways linking the planta hair afferents and the proleg retractor motoneurons (MNs). An important technical innovation was the development of an isolated proleg and desheathed ganglion preparation that permits rapid and reversible ionic manipulations and drug applications. Action potentials (spikes) in individual planta hair afferents produce time-locked excitatory postsynaptic potentials (EPSPs) in ipsilateral proleg MNs which appear to be chemically-mediated and monosynaptic: the EPSPs have a short and constant latency, they follow afferent spikes without failure, they are reversibly abolished in elevated Mg++ saline, and they persist in saline with elevated Mg++ and Ca++ levels. Planta hair afferents also excite ipsilateral MNs by polysynaptic pathways, and their excitation of contralateral proleg MNs is exclusively polysynaptic. Cobalt-staining of the proleg MNs and planta hair afferents shows that the afferents terminate in ventral neuropil, and the proleg MNs have an unusual ventral projection into this region. The ventral projection is on the ipsilateral side, which is consistent with the electrophysiological finding that time-locked EPSPs are found only from ipsilateral hairs. Two factors that contribute to the strong monosynaptic excitation of proleg MNs by ipsilateral planta hairs are the convergence of many hair afferents onto each MN, and the facilitation shown at each afferent-MN synapse. At least 6 afferents converge on each MN, and at short interspike intervals the afferent-evoked EPSPs are enhanced by as much as 400% by homosynaptic facilitation. The EPSP is abolished reversibly by the cholinergic antagonists curare and atropine, suggesting that the neurotransmitter at the synapse is acetylcholine (ACh). This is of particular interest because the ACh receptors of tobacco-feeding Manduca larvae are reported to be less nicotine-sensitive than those of other insects.

Acetylcholine↗
PubMed1994

Responses during eye movements of brain stem neurons that receive monosynaptic inhibition from the flocculus and ventral paraflocculus in monkeys.

1. We have identified a group of brain stem cells called "flocculus target neurons" (or FTNs) because they are inhibited at monosynaptic latencies by stimulation of the flocculus and the ventral paraflocculus with single electrical pulses. We report the responses of FTNs, as well as those of other brain stem cells, during horizontal eye movements with the head stationary and during natural vestibular stimulation in monkeys. 2. FTNs discharged primarily in relation to eye movements. The majority (71%) showed increased firing for eye movement away from the side of the recording ("contraversive"), which is consistent with their inhibition by Purkinje cells that show increased firing for eye movement toward the side of recording. However, a significant and surprisingly large percentage (29%) of FTNs showed increased firing for eye movement toward the side of recording ("ipsiversive"). 3. The firing rate of FTNs showed strong modulation during pursuit of sinusoidal target motion with the head stationary and during the compensatory eye movements evoked by fixation of an earth-stationary target with sinusoidal head rotation. In addition, firing rate was related to eye position during steady fixation at different positions. Of the FTNs that showed increased firing for contraversive eye motion during pursuit with the head stationary, most had an infection in the relationship between firing rate and eye position so that the sensitivity to eye position was low for eye positions ipsilateral to straight-ahead gaze and high for eye positions contralateral to straight-ahead gaze. 4. When the monkey canceled the vestibuloocular reflex (VOR) by tracking a target that moved exactly with him during sinusoidal head rotation, the firing rate of FTNs was modulated much less strongly than during pursuit with the head stationary. In the FTNs that showed increased firing for contraversive eye motion during pursuit, firing rate during cancellation of the VOR increased for contraversive head motion during sinusoidal vestibular rotation at 0.4 Hz but was only weakly modulated during rotation at 0.2 Hz. 5. The position-vestibular-pause cells (PVP-cells), previously identified as interneurons in the disynaptic VOR pathways, were not inhibited by stimulation of the flocculus and ventral paraflocculus and had response properties that were different from FTNs. The majority (69%) showed increased firing for contraversive eye motion during pursuit and for ipsiversive head motion during cancellation of the VOR, whereas some (31%) showed the opposite direction preferences under both conditions.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗