Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability

Research output: Contribution to journalJournal articleResearchpeer-review

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Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability. / Jimenez, Samuel; Mordillo-Mateos, Laura; Dileone, Michele; Campolo, Michela; Carrasco-Lopez, Carmen; Moitinho-Ferreira, Fabricia; Gallego-Izquierdo, Tomas; Siebner, Hartwig R; Valls-Solé, Josep; Aguilar, Juan; Oliviero, Antonio.

In: PLoS ONE, Vol. 13, No. 2, e0192471, 2018.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jimenez, S, Mordillo-Mateos, L, Dileone, M, Campolo, M, Carrasco-Lopez, C, Moitinho-Ferreira, F, Gallego-Izquierdo, T, Siebner, HR, Valls-Solé, J, Aguilar, J & Oliviero, A 2018, 'Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability', PLoS ONE, vol. 13, no. 2, e0192471. https://doi.org/10.1371/journal.pone.0192471

APA

Jimenez, S., Mordillo-Mateos, L., Dileone, M., Campolo, M., Carrasco-Lopez, C., Moitinho-Ferreira, F., Gallego-Izquierdo, T., Siebner, H. R., Valls-Solé, J., Aguilar, J., & Oliviero, A. (2018). Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability. PLoS ONE, 13(2), [e0192471]. https://doi.org/10.1371/journal.pone.0192471

Vancouver

Jimenez S, Mordillo-Mateos L, Dileone M, Campolo M, Carrasco-Lopez C, Moitinho-Ferreira F et al. Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability. PLoS ONE. 2018;13(2). e0192471. https://doi.org/10.1371/journal.pone.0192471

Author

Jimenez, Samuel ; Mordillo-Mateos, Laura ; Dileone, Michele ; Campolo, Michela ; Carrasco-Lopez, Carmen ; Moitinho-Ferreira, Fabricia ; Gallego-Izquierdo, Tomas ; Siebner, Hartwig R ; Valls-Solé, Josep ; Aguilar, Juan ; Oliviero, Antonio. / Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability. In: PLoS ONE. 2018 ; Vol. 13, No. 2.

Bibtex

@article{3aff7f1b4d1948edbca1b7775096f480,
title = "Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability",
abstract = "Spinal plasticity is thought to contribute to sensorimotor recovery of limb function in several neurological disorders and can be experimentally induced in animals and humans using different stimulation protocols. In healthy individuals, electrical continuous Theta Burst Stimulation (TBS) of the median nerve has been shown to change spinal motoneuron excitability in the cervical spinal cord as indexed by a change in mean H-reflex amplitude in the flexor carpi radialis muscle. It is unknown whether continuous TBS of a peripheral nerve can also shift motoneuron excitability in the lower limb. In 26 healthy subjects, we examined the effects of electrical TBS given to the tibial nerve in the popliteal fossa on the excitability of lumbar spinal motoneurons as measured by H-reflex amplitude of the soleus muscle evoked by tibial nerve stimulation. Continuous TBS was given at 110% of H-reflex threshold intensity and compared to non-patterned regular electrical stimulation at 15 Hz. To disclose any pain-induced effects, we also tested the effects of TBS at individual sensory threshold. Moreover, in a subgroup of subjects we evaluated paired-pulse inhibition of H-reflex. Continuous TBS at 110% of H-reflex threshold intensity induced a short-term reduction of H-reflex amplitude. The other stimulation conditions produced no after effects. Paired-pulse H-reflex inhibition was not modulated by continuous TBS or non-patterned repetitive stimulation at 15 Hz. An effect of pain on the results obtained was discarded, since non-patterned 15 Hz stimulation at 110% HT led to pain scores similar to those induced by EcTBS at 110% HT, but was not able to induce any modulation of the H reflex amplitude. Together, the results provide first time evidence that peripheral continuous TBS induces a short-lasting change in the excitability of spinal motoneurons in lower limb circuitries. Future studies need to investigate how the TBS protocol can be optimized to produce a larger and longer effect on spinal cord physiology and whether this might be a useful intervention in patients with excessive excitability of the spinal motorneurons.",
keywords = "Adult, Female, H-Reflex, Humans, Male, Median Nerve/physiology, Middle Aged, Motor Neurons/physiology, Muscle, Skeletal/innervation, Spinal Cord/cytology, Tibial Nerve/physiology, Transcutaneous Electric Nerve Stimulation/methods, Young Adult",
author = "Samuel Jimenez and Laura Mordillo-Mateos and Michele Dileone and Michela Campolo and Carmen Carrasco-Lopez and Fabricia Moitinho-Ferreira and Tomas Gallego-Izquierdo and Siebner, {Hartwig R} and Josep Valls-Sol{\'e} and Juan Aguilar and Antonio Oliviero",
year = "2018",
doi = "10.1371/journal.pone.0192471",
language = "English",
volume = "13",
journal = "PLoS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "2",

}

RIS

TY - JOUR

T1 - Effects of patterned peripheral nerve stimulation on soleus spinal motor neuron excitability

AU - Jimenez, Samuel

AU - Mordillo-Mateos, Laura

AU - Dileone, Michele

AU - Campolo, Michela

AU - Carrasco-Lopez, Carmen

AU - Moitinho-Ferreira, Fabricia

AU - Gallego-Izquierdo, Tomas

AU - Siebner, Hartwig R

AU - Valls-Solé, Josep

AU - Aguilar, Juan

AU - Oliviero, Antonio

PY - 2018

Y1 - 2018

N2 - Spinal plasticity is thought to contribute to sensorimotor recovery of limb function in several neurological disorders and can be experimentally induced in animals and humans using different stimulation protocols. In healthy individuals, electrical continuous Theta Burst Stimulation (TBS) of the median nerve has been shown to change spinal motoneuron excitability in the cervical spinal cord as indexed by a change in mean H-reflex amplitude in the flexor carpi radialis muscle. It is unknown whether continuous TBS of a peripheral nerve can also shift motoneuron excitability in the lower limb. In 26 healthy subjects, we examined the effects of electrical TBS given to the tibial nerve in the popliteal fossa on the excitability of lumbar spinal motoneurons as measured by H-reflex amplitude of the soleus muscle evoked by tibial nerve stimulation. Continuous TBS was given at 110% of H-reflex threshold intensity and compared to non-patterned regular electrical stimulation at 15 Hz. To disclose any pain-induced effects, we also tested the effects of TBS at individual sensory threshold. Moreover, in a subgroup of subjects we evaluated paired-pulse inhibition of H-reflex. Continuous TBS at 110% of H-reflex threshold intensity induced a short-term reduction of H-reflex amplitude. The other stimulation conditions produced no after effects. Paired-pulse H-reflex inhibition was not modulated by continuous TBS or non-patterned repetitive stimulation at 15 Hz. An effect of pain on the results obtained was discarded, since non-patterned 15 Hz stimulation at 110% HT led to pain scores similar to those induced by EcTBS at 110% HT, but was not able to induce any modulation of the H reflex amplitude. Together, the results provide first time evidence that peripheral continuous TBS induces a short-lasting change in the excitability of spinal motoneurons in lower limb circuitries. Future studies need to investigate how the TBS protocol can be optimized to produce a larger and longer effect on spinal cord physiology and whether this might be a useful intervention in patients with excessive excitability of the spinal motorneurons.

AB - Spinal plasticity is thought to contribute to sensorimotor recovery of limb function in several neurological disorders and can be experimentally induced in animals and humans using different stimulation protocols. In healthy individuals, electrical continuous Theta Burst Stimulation (TBS) of the median nerve has been shown to change spinal motoneuron excitability in the cervical spinal cord as indexed by a change in mean H-reflex amplitude in the flexor carpi radialis muscle. It is unknown whether continuous TBS of a peripheral nerve can also shift motoneuron excitability in the lower limb. In 26 healthy subjects, we examined the effects of electrical TBS given to the tibial nerve in the popliteal fossa on the excitability of lumbar spinal motoneurons as measured by H-reflex amplitude of the soleus muscle evoked by tibial nerve stimulation. Continuous TBS was given at 110% of H-reflex threshold intensity and compared to non-patterned regular electrical stimulation at 15 Hz. To disclose any pain-induced effects, we also tested the effects of TBS at individual sensory threshold. Moreover, in a subgroup of subjects we evaluated paired-pulse inhibition of H-reflex. Continuous TBS at 110% of H-reflex threshold intensity induced a short-term reduction of H-reflex amplitude. The other stimulation conditions produced no after effects. Paired-pulse H-reflex inhibition was not modulated by continuous TBS or non-patterned repetitive stimulation at 15 Hz. An effect of pain on the results obtained was discarded, since non-patterned 15 Hz stimulation at 110% HT led to pain scores similar to those induced by EcTBS at 110% HT, but was not able to induce any modulation of the H reflex amplitude. Together, the results provide first time evidence that peripheral continuous TBS induces a short-lasting change in the excitability of spinal motoneurons in lower limb circuitries. Future studies need to investigate how the TBS protocol can be optimized to produce a larger and longer effect on spinal cord physiology and whether this might be a useful intervention in patients with excessive excitability of the spinal motorneurons.

KW - Adult

KW - Female

KW - H-Reflex

KW - Humans

KW - Male

KW - Median Nerve/physiology

KW - Middle Aged

KW - Motor Neurons/physiology

KW - Muscle, Skeletal/innervation

KW - Spinal Cord/cytology

KW - Tibial Nerve/physiology

KW - Transcutaneous Electric Nerve Stimulation/methods

KW - Young Adult

U2 - 10.1371/journal.pone.0192471

DO - 10.1371/journal.pone.0192471

M3 - Journal article

C2 - 29451889

VL - 13

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 2

M1 - e0192471

ER -

ID: 213000434