Cargando…

Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior

Neuronal control of stepping movement in healthy human is based on integration between brain, spinal neuronal networks, and sensory signals. It is generally recognized that there are continuously occurring adjustments in the physiological states of supraspinal centers during all routines movements....

Descripción completa

Detalles Bibliográficos
Autores principales: Gerasimenko, Yury, Sayenko, Dimitry, Gad, Parag, Kozesnik, Justin, Moshonkina, Tatiana, Grishin, Aleksandr, Pukhov, Aleksandr, Moiseev, Sergey, Gorodnichev, Ruslan, Selionov, Victor, Kozlovskaya, Inessa, Edgerton, V. Reggie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157483/
https://www.ncbi.nlm.nih.gov/pubmed/30283341
http://dx.doi.org/10.3389/fphys.2018.01196
_version_ 1783358277683249152
author Gerasimenko, Yury
Sayenko, Dimitry
Gad, Parag
Kozesnik, Justin
Moshonkina, Tatiana
Grishin, Aleksandr
Pukhov, Aleksandr
Moiseev, Sergey
Gorodnichev, Ruslan
Selionov, Victor
Kozlovskaya, Inessa
Edgerton, V. Reggie
author_facet Gerasimenko, Yury
Sayenko, Dimitry
Gad, Parag
Kozesnik, Justin
Moshonkina, Tatiana
Grishin, Aleksandr
Pukhov, Aleksandr
Moiseev, Sergey
Gorodnichev, Ruslan
Selionov, Victor
Kozlovskaya, Inessa
Edgerton, V. Reggie
author_sort Gerasimenko, Yury
collection PubMed
description Neuronal control of stepping movement in healthy human is based on integration between brain, spinal neuronal networks, and sensory signals. It is generally recognized that there are continuously occurring adjustments in the physiological states of supraspinal centers during all routines movements. For example, visual as well as all other sources of information regarding the subject's environment. These multimodal inputs to the brain normally play an important role in providing a feedforward source of control. We propose that the brain routinely uses these continuously updated assessments of the environment to provide additional feedforward messages to the spinal networks, which provides a synergistic feedforwardness for the brain and spinal cord. We tested this hypothesis in 8 non-injured individuals placed in gravity neutral position with the lower limbs extended beyond the edge of the table, but supported vertically, to facilitate rhythmic stepping. The experiment was performed while visualizing on the monitor a stick figure mimicking bilateral stepping or being motionless. Non-invasive electrical stimulation was used to neuromodulate a wide range of excitabilities of the lumbosacral spinal segments that would trigger rhythmic stepping movements. We observed that at the same intensity level of transcutaneous electrical spinal cord stimulation (tSCS), the presence or absence of visualizing a stepping-like movement of a stick figure immediately initiated or terminated the tSCS-induced rhythmic stepping motion, respectively. We also demonstrated that during both voluntary and imagined stepping, the motor potentials in leg muscles were facilitated when evoked cortically, using transcranial magnetic stimulation (TMS), and inhibited when evoked spinally, using tSCS. These data suggest that the ongoing assessment of the environment within the supraspinal centers that play a role in planning a movement can routinely modulate the physiological state of spinal networks that further facilitates a synergistic neuromodulation of the brain and spinal cord in preparing for movements.
format Online
Article
Text
id pubmed-6157483
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-61574832018-10-03 Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior Gerasimenko, Yury Sayenko, Dimitry Gad, Parag Kozesnik, Justin Moshonkina, Tatiana Grishin, Aleksandr Pukhov, Aleksandr Moiseev, Sergey Gorodnichev, Ruslan Selionov, Victor Kozlovskaya, Inessa Edgerton, V. Reggie Front Physiol Physiology Neuronal control of stepping movement in healthy human is based on integration between brain, spinal neuronal networks, and sensory signals. It is generally recognized that there are continuously occurring adjustments in the physiological states of supraspinal centers during all routines movements. For example, visual as well as all other sources of information regarding the subject's environment. These multimodal inputs to the brain normally play an important role in providing a feedforward source of control. We propose that the brain routinely uses these continuously updated assessments of the environment to provide additional feedforward messages to the spinal networks, which provides a synergistic feedforwardness for the brain and spinal cord. We tested this hypothesis in 8 non-injured individuals placed in gravity neutral position with the lower limbs extended beyond the edge of the table, but supported vertically, to facilitate rhythmic stepping. The experiment was performed while visualizing on the monitor a stick figure mimicking bilateral stepping or being motionless. Non-invasive electrical stimulation was used to neuromodulate a wide range of excitabilities of the lumbosacral spinal segments that would trigger rhythmic stepping movements. We observed that at the same intensity level of transcutaneous electrical spinal cord stimulation (tSCS), the presence or absence of visualizing a stepping-like movement of a stick figure immediately initiated or terminated the tSCS-induced rhythmic stepping motion, respectively. We also demonstrated that during both voluntary and imagined stepping, the motor potentials in leg muscles were facilitated when evoked cortically, using transcranial magnetic stimulation (TMS), and inhibited when evoked spinally, using tSCS. These data suggest that the ongoing assessment of the environment within the supraspinal centers that play a role in planning a movement can routinely modulate the physiological state of spinal networks that further facilitates a synergistic neuromodulation of the brain and spinal cord in preparing for movements. Frontiers Media S.A. 2018-09-19 /pmc/articles/PMC6157483/ /pubmed/30283341 http://dx.doi.org/10.3389/fphys.2018.01196 Text en Copyright © 2018 Gerasimenko, Sayenko, Gad, Kozesnik, Moshonkina, Grishin, Pukhov, Moiseev, Gorodnichev, Selionov, Kozlovskaya and Edgerton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Gerasimenko, Yury
Sayenko, Dimitry
Gad, Parag
Kozesnik, Justin
Moshonkina, Tatiana
Grishin, Aleksandr
Pukhov, Aleksandr
Moiseev, Sergey
Gorodnichev, Ruslan
Selionov, Victor
Kozlovskaya, Inessa
Edgerton, V. Reggie
Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior
title Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior
title_full Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior
title_fullStr Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior
title_full_unstemmed Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior
title_short Electrical Spinal Stimulation, and Imagining of Lower Limb Movements to Modulate Brain-Spinal Connectomes That Control Locomotor-Like Behavior
title_sort electrical spinal stimulation, and imagining of lower limb movements to modulate brain-spinal connectomes that control locomotor-like behavior
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157483/
https://www.ncbi.nlm.nih.gov/pubmed/30283341
http://dx.doi.org/10.3389/fphys.2018.01196
work_keys_str_mv AT gerasimenkoyury electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT sayenkodimitry electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT gadparag electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT kozesnikjustin electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT moshonkinatatiana electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT grishinaleksandr electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT pukhovaleksandr electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT moiseevsergey electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT gorodnichevruslan electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT selionovvictor electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT kozlovskayainessa electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior
AT edgertonvreggie electricalspinalstimulationandimaginingoflowerlimbmovementstomodulatebrainspinalconnectomesthatcontrollocomotorlikebehavior