Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Reflex, Monosynaptic”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 937 records · Page 52Linked to original sources

[Study of postinhibitory "rebound" in individual motor units of human hand muscles].

Analysis of poststimulus histograms and interspike intervals of firing motor units showed that the burst following the silent period under evoked muscle contraction is the result of synchronous motoneuron escape from inhibition. Under strong evoked isotonic muscle contraction a true facilitation was revealed. The latency of this facilitation was too long for spinal monosynaptic reflex related to spindles elongation at the muscle relaxation stage.

Electric Stimulation↗

[Effect of ethanol on components of the nonspecific startle reaction in man].

The components of the startle reaction (SR) (reactions of nonspecific motor activation, the wink reflex and reflectory alleviation of motoneurones) were utilized as indices of the functional status of the midbrain system of cerebral nonspecific activation. Healthy subjects and chronic alcoholics in the abstinence period were examined. The patients exhibited significantly lower SR thresholds, a shortened latent period and a stronger reaction as compared with the healthy subjects which was suggestive of the irritation of the mesencephalic activating mechanisms in patients during the period of abstinence. Intake of the euphorizing doses of ethanol depressed the acoustic SR in both patients and controls. It is concluded that ethanol exerts an inhibitory action on the midbrain system of brain nonspecific activation.

Acoustic Stimulation↗

[State of mechanisms regulating muscle tone in amyotrophic lateral sclerosis (clinico-electromyographic study)].

For studying the mechanisms of spasticity electromyographic examinations were carried out in 54 patients suffering from lateral amyotrophic sclerosis at various stages of the disease. At the beginning of the spasticity formation disturbances of the functions of the checking spinal mechanisms and the gamma-system were revealed, while those of alpha-mononeurons (tested by the H-reflex) showed no statistically significant changes. In the late period (pronounced spasticity) disturbances of all the motor systems mentioned were noted. The role of various mechanisms in the development of muscular hypertonicity in lateral amyotrophic sclerosis is discussed.

Adolescent↗

[Pathophysiology of spinal shock in man according to the results of stimulation electromyography].

Electromyography was made in 5 patients with a clinical picture of spinal shock. Within the first 4 days of the disease the disappearance of T potential of the soleus muscle was accompanied by the decreased amplitude of its H reflex, the enhancement of the phenomenon of H reflex depression upon low-frequency stimulation and predominance of the reflex component in the central response of the medial muscles of the foot sole. During weeks 4 and 8 of the spinal shock, there disappeared not only T potential but also H reflex of the soleus muscle and the central response of the foot muscles. It is concluded that during acute total disconnection of the descending control there is a successive loss of the functions of gamma-motoneurons, interneurones that mediate the segmental (probably, presynaptic) inhibition, and of alpha-motoneurons.

Adult↗

Reflex facilitation by remote contraction: topographic aspects.

This study compares the facilitation of various lower limb reflex arcs brought about by a selective contraction of a well-defined upper limb muscle group in able-bodied healthy subjects. Quantitatively (results expressed as a percentage of maximal motor response), the quadriceps tendon reflex is facilitated more than the soleus and biceps femoris tendon reflexes. The time course of facilitation is similar for the 3 reflexes and exhibits 3 distinct phases. Electrically induced reflexes in the quadriceps are facilitated as much as the tendon jerk but only during the 2nd phase. Complementarily, the effects of contraction of different upper limb muscle groups on a single lower limb reflex (quadriceps tendon jerk) were also investigated. This reflex is facilitated more (especially in the 2nd phase) by contraction of thenar muscle than by that of deltoid muscles and more by wrist extensors than wrist flexors. Differences in facilitation are only apparent when the effects are quantified. They depend on the segmental level of the reflex under test (more marked proximally than distally) and on the conditioning muscle group; both facts must be taken into consideration in the interpretation of the functional role of remote contraction.

Female↗

[Nonspecific activation response upon exposure to unanticipated and voluntarily controlled acoustic stimuli].

Normal subjects revealed these components of startle-response to unexpected stimulation followed by no visible wincing: blink reflex, facilitation of spinal motoneurons (augmentation of the H-reflex), the EEG vertex potential, and skin galvanic response. With voluntary, control of the stimulation the components of the response are either absent or less obvious, excepting skin galvanic response. The weakening of the startle-response in this case seems to be associated with the mechanisms of the selective sensory attention and to be determined by cortico-fugal inhibition of reticular interneurons mediating in this response.

Acoustic Stimulation↗

Pharmacological characterization of dynorphin A (1-17)-induced effects on spinal cord-evoked potentials.

Dynorphin A (1-17) was applied directly onto the spinal cord of rats during electrophysiologic recording of the dorsal root potential (DRP) and the ventral root potentials (VRPs), i.e., monosynaptic reflex and polysynaptic reflexes. Dynorphin application resulted in a dose-dependent depression of the DRP (ED50, 4.5 nmol) which persisted for 30 to 50 min. This effect was not antagonized by nor-binaltorphimine, a kappa-opioid receptor antagonist. During this depression we observed a potentiation of the VRPs which persisted for 4 to 5 min and preceded depression of the VRPs (ED50, 4.0-4.9 nmol). The depression of the VRPs was antagonized competitively by nor-binaltorphimine, although the potentiation was not. beta-Funaltrexamine, a mu-opioid receptor antagonist, had no influence on dynorphin-induced changes of evoked potentials. These data indicate that dynorphin-induced depression of the VRPs is mediated by kappa-opioid receptor activity, whereas neither potentiation of the VRPs nor depression of the DRP appears to be mediated by an opioid receptor effect.

Animals↗

Glutamate receptor-mediated hyperexcitability after ethanol exposure in isolated neonatal rat spinal cord.

This study examined the mechanism for hyperexcitability after ethanol withdrawal from isolated neonatal rat spinal cord. Ethanol (65-130 mM, 30 min) significantly depressed the glutamate receptor-mediated population excitatory postsynaptic potential (pEPSP) underlying the monosynaptic reflex. On washing with drug-free solution the response recovered to levels significantly above control. Minimum ethanol exposure time required for induction of withdrawal hyperexcitability was approximately 15 min. A second application of ethanol after washout depressed the pEPSP to an extent similar to the first, and a second wash did not elevate response significantly more than the initial wash. Ethanol-induced hyperexcitability thus develops with a time course of minutes and plays a role in determining apparent initial ethanol potency. Both alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate and N-methyl-D-aspartate receptor-mediated components of the pEPSP were necessary for the expression of hyperexcitability on withdrawal but not for its induction. Butanol withdrawal also was associated with hyperexcitability, methanol was not. The case with octanol is uncertain because of slow recovery from this more lipophilic agent. Hyperexcitability on ethanol withdrawal was specific to the glutamate receptor-mediated pEPSP and not generalized to other evoked potentials. These results may be relevant to rapid and/or very rapid acute functional tolerance and to ethanol withdrawal.

Animals↗

Interstitial adenosine and serotonin in the feline lumbar spinal cord during short-term ischaemia.

During controlled ischaemia (aortal snare occlusion) of the lumbar spinal cord, microcirculatory (laser-Doppler flowmetry) and segmental neurophysiological parameters (monosynaptic reflexes, polysynaptic reflexes, cord dorsum potential=CDP) as well as interstitial concentrations of adenosine and serotonin (5-HT) were determined in the grey matter using the microdialysis/HPLC method. Ischaemic periods of 1-7 min with a residual blood flow in the lumbar spinal cord of 10-30 % of the preischaemic control blood flow caused a blockade of spinal pathways and an increase of concentrations of interstitial adenosine and 5-HT. This increase started immediately after the initiation of the ischaemic period and reached a maximum at the end or shortly after the end of the ischaemic period during postischaemic hyperaemia. A close correlation between the duration of ischaemia and the interstitial concentration of adenosine and 5-HT was not found. Repetition of ischaemic periods in an experiment did not lead to an extracellular accumulation or an exhaustion of the release of 5-HT, whereas some indication was found for an exhaustion of adenosine release. The course of the increase of interstitial adenosine and 5-HT was partly found to correlate to the loss and recovery of the CDP following ischaemia. The concentrations usually reached control levels before spinal reflexes reappeared. The highly dynamic changes in concentrations of adenosine and 5-HT in the extracellular space of the spinal cord during and after short-term ischaemia revealed some relation to the time course of recovery of segmental spinal functions by reflecting the course of spinal neuronal metabolism.

Adenosine↗

Compensation of translational and rotational perturbations in human posture: stabilization of the centre of gravity.

EMG responses in the leg muscles, head acceleration and joint movements induced by dorsiflexing rotation of the ankle have been analysed. Perturbations were induced while subjects were standing on a platform with the ankle joints co-linear with the axis of rotation or while standing above the axis (between 5 and 25 cm), which introduced an additional translational component to the displacement. The former condition was followed by a monosynaptic gastrocnemius reflex potential and a late tibialis anterior activation (latency about 100 ms); in the latter condition the monosynaptic reflex response became smaller and a longer latency gastrocnemius response (latency about 70 ms) appeared, the strength and duration of which increased in parallel with the translational component, while the amplitude of the tibialis anterior activity decreased. Neither vestibulospinal nor muscle proprioceptive mechanisms can solely account for this effect as the biomechanical parameters were little changed in the different conditions. It is suggested that the controlled variable in the investigated task is to hold the bodies' centre of gravity over the feet which makes the change in the pattern meaningful: pure dorsiflexion of the feet is followed by a backwards sway of the body, thus a tibialis anterior activation is functionally essential to hold the centre of gravity over the feet. A backwards translation of the feet withdraws the supporting surface, thus a gastrocnemius activation is needed to restore the centre of gravity over the feet. The inhibition of the monosynaptic reflex with increasing translation is suggested to arise from a reciprocal modulation of mono- and polysynaptic gastrocnemius reflex responses.

Acceleration↗

The spinal interneurons and properties of glutamatergic synapses in a primitive vertebrate cutaneous flexion reflex.

Unlike the monosynaptic "stretch" reflex, the exact neuronal pathway for a simple cutaneous reflex has not yet been defined in any vertebrate. In young frog tadpoles, we made whole-cell recordings from pairs of spinal neurons. We found direct, excitatory, glutamatergic synapses from touch-sensitive skin-sensory neurons to sensory pathway interneurons, and then from these sensory interneurons to motoneurons and premotor interneurons on the other side of the body. We conclude that the minimal pathway for this primitive reflex, in which stroking the skin on one side leads to flexion on the other side, is disynaptic. This detailed circuit information has allowed us to ask whether the properties of glutamatergic synapses during the first day of CNS development are tuned to their function in the tadpole's responses. Stroking the skin excites a few sensory neurons. These activate primarily AMPA receptors producing short, strong excitation that activates many sensory pathway interneurons but only allows temporal summation of closely synchronous inputs. In contrast, the excitation produced in contralateral neurons by the sensory pathway interneurons is weak and primarily mediated by NMDA receptors. As a result, considerable summation is required for this excitation to lead to postsynaptic neuron firing and a contralateral flexion. We conclude that from their early functioning, synapses from sensory neurons are strong and those from sensory pathway interneurons are weak. The distribution of glutamate receptors at synapses in this developing circuit is tuned so that synapses have properties suited to their roles in the whole animal's reflex responses.

Afferent Pathways↗

An electrophysiological investigation into the monosynaptic H-reflex in the rat.

In order to set up a non-invasive, reliable and reproducible model for investigating alpha-motoneuronal activity, we studied the electrophysiological features of a monosynaptic H-reflex in anaesthetised intact rats, anaesthetised and non-anaesthetised rats transected at the level of the obex. Electrical stimulation of the tibial nerve at the ankle elicited an H-reflex, an F-wave and a direct motor (M) response in the plantaris muscles of all preparations. The H-reflex and F-wave exhibited very similar latencies. The H-reflex had a low threshold and a constant latency. Its amplitude increased as a function of stimulus intensity to reach a maximum value but then decreased when the stimulus intensity was further increased. It could follow high rates of stimulation without any change in shape or latency. The F-wave had a lower amplitude which together with its latency varied from one stimulus to the next. It appeared with intensities of stimulation that elicited an almost maximal M-response and did not decrease when the stimulation was increased. It did not appear systematically from one stimulus to the next. The H-reflex, but neither the F-wave nor the direct motor M-response, was depressed both by vibratory stimuli applied on the Achilles' tendon and following nociceptive stimulation of the flexor reflex afferents. This model could be used for assessing any potential direct effect on motoneurones of a physiological or pharmacological conditioning procedure.

Achilles Tendon↗

Absence of linear correlation between fluctuations in area of simultaneous recorded monosynaptic responses and Hoffmann's reflexes in the rat.

In this study we analyze the possible relationship between fluctuations in area of monosynaptic reflex responses (MSR) and Hoffmann's reflex (H reflexes) in the plantar closed loop pathway of the anesthetized rat. These reflexes were evoked by low-frequency stimuli applied to the sciatic nerve or lateral plantar nerve and then concurrently recorded on the distal tibial nerve or lateral plantar nerve, respectively as well as the lateral plantar muscles in the foot of the anesthetized rat. From trial to trial, H reflexes showed higher variability in area than MSR, whether the latter was recorded in the distal tibial nerve (n=8 experiments) or in the lateral plantar nerve (n=5 experiments). No linear correlation was found between changes in area of concurrently evoked MSR and H reflexes (r(MSR-H,n=8)=0.11+/-0.03 and r(MSR-H,n=5)=0.08+/-0.09, respectively). These findings suggest that trial-to-trial fluctuations in area of H reflexes may involve interaction of several sources of variation, among others to MSR variability (due to pre-, and post-synaptic factors influencing the excitability of spinal motoneurons) in combination with those related to peripheral mechanisms, such as trial to trial activation of a different number of muscle fibers, either by the probabilistic transmitter release from neuromuscular junctions, by activation of motor units of variable size or to fluctuations in excitability of muscle fibers.

Action Potentials↗