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Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation

Few preclinical or clinical studies have evaluated the effect of anesthetics on motor evoked potentials (MEPs), either alone or in the presence of conditioning stimuli such as deep brain stimulation (DBS). In this study we evaluated the effects of two commonly used anesthetic agents, propofol and ke...

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Autores principales: Furmaga, Havan, Park, Hyun-Joo, Cooperrider, Jessica, Baker, Kenneth B., Johnson, Matthew, Gale, John T., Machado, Andre G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033249/
https://www.ncbi.nlm.nih.gov/pubmed/24904312
http://dx.doi.org/10.3389/fnsys.2014.00089
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author Furmaga, Havan
Park, Hyun-Joo
Cooperrider, Jessica
Baker, Kenneth B.
Johnson, Matthew
Gale, John T.
Machado, Andre G.
author_facet Furmaga, Havan
Park, Hyun-Joo
Cooperrider, Jessica
Baker, Kenneth B.
Johnson, Matthew
Gale, John T.
Machado, Andre G.
author_sort Furmaga, Havan
collection PubMed
description Few preclinical or clinical studies have evaluated the effect of anesthetics on motor evoked potentials (MEPs), either alone or in the presence of conditioning stimuli such as deep brain stimulation (DBS). In this study we evaluated the effects of two commonly used anesthetic agents, propofol and ketamine (KET), on MEPs elicited by intra-cortical microstimulation of the motor cortex in a rodent model with and without DBS of the dentatothalamocortical (DTC) pathway. The effects of propofol anesthesia on MEP amplitudes during DTC DBS were found to be highly dose dependent. Standard, but not high, dose propofol potentiated the facilitatory effects of 30 Hz DTC DBS on MEPs. This facilitation was sustained and phase-dependent indicating that, compared to high dose propofol, standard dose propofol has a beta-band excitatory effect on cortical networks. In contrast, KET anesthetic demonstrated a monotonic relationship with increasing frequencies of stimulation, such that the highest frequency of stimulation resulted in the greatest MEP amplitude. KET also showed phase dependency but less pronounced than standard dose propofol. The results underscore the importance of better understanding the complex effects of anesthetics on cortical networks and exogenous stimuli. Choice of anesthetic agents and dosing may significantly confound or even skew research outcomes, including experimentation in novel DBS indications and paradigms.
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spelling pubmed-40332492014-06-05 Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation Furmaga, Havan Park, Hyun-Joo Cooperrider, Jessica Baker, Kenneth B. Johnson, Matthew Gale, John T. Machado, Andre G. Front Syst Neurosci Neuroscience Few preclinical or clinical studies have evaluated the effect of anesthetics on motor evoked potentials (MEPs), either alone or in the presence of conditioning stimuli such as deep brain stimulation (DBS). In this study we evaluated the effects of two commonly used anesthetic agents, propofol and ketamine (KET), on MEPs elicited by intra-cortical microstimulation of the motor cortex in a rodent model with and without DBS of the dentatothalamocortical (DTC) pathway. The effects of propofol anesthesia on MEP amplitudes during DTC DBS were found to be highly dose dependent. Standard, but not high, dose propofol potentiated the facilitatory effects of 30 Hz DTC DBS on MEPs. This facilitation was sustained and phase-dependent indicating that, compared to high dose propofol, standard dose propofol has a beta-band excitatory effect on cortical networks. In contrast, KET anesthetic demonstrated a monotonic relationship with increasing frequencies of stimulation, such that the highest frequency of stimulation resulted in the greatest MEP amplitude. KET also showed phase dependency but less pronounced than standard dose propofol. The results underscore the importance of better understanding the complex effects of anesthetics on cortical networks and exogenous stimuli. Choice of anesthetic agents and dosing may significantly confound or even skew research outcomes, including experimentation in novel DBS indications and paradigms. Frontiers Media S.A. 2014-05-23 /pmc/articles/PMC4033249/ /pubmed/24904312 http://dx.doi.org/10.3389/fnsys.2014.00089 Text en Copyright © 2014 Furmaga, Park, Cooperrider, Baker, Johnson, Gale and Machado. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Neuroscience
Furmaga, Havan
Park, Hyun-Joo
Cooperrider, Jessica
Baker, Kenneth B.
Johnson, Matthew
Gale, John T.
Machado, Andre G.
Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
title Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
title_full Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
title_fullStr Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
title_full_unstemmed Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
title_short Effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
title_sort effects of ketamine and propofol on motor evoked potentials elicited by intracranial microstimulation during deep brain stimulation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033249/
https://www.ncbi.nlm.nih.gov/pubmed/24904312
http://dx.doi.org/10.3389/fnsys.2014.00089
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