Immediate effects of tDCS on the µ-opioid system of a chronic pain patient

We developed a unique protocol where transcranial direct current stimulation (tDCS) of the motor cortex is performed during positron emission tomography (PET) scan using a µ-opioid receptor (µOR) selective radiotracer, [11C]carfentanil. This is one of the most important central neu...

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Main Authors: Marcos Fabio DosSantos, Tiffany M Love, Ilkka Kristian Martikainen, Thiago Dias Nascimento, Felipe eFregni, Chelsea eCummiford, Misty Dawn Deboer, Jon Kar Zubieta, Alexandre F DaSilva
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-11-01
Series:Frontiers in Psychiatry
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpsyt.2012.00093/full
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author Marcos Fabio DosSantos
Marcos Fabio DosSantos
Tiffany M Love
Ilkka Kristian Martikainen
Ilkka Kristian Martikainen
Thiago Dias Nascimento
Felipe eFregni
Chelsea eCummiford
Misty Dawn Deboer
Jon Kar Zubieta
Alexandre F DaSilva
author_facet Marcos Fabio DosSantos
Marcos Fabio DosSantos
Tiffany M Love
Ilkka Kristian Martikainen
Ilkka Kristian Martikainen
Thiago Dias Nascimento
Felipe eFregni
Chelsea eCummiford
Misty Dawn Deboer
Jon Kar Zubieta
Alexandre F DaSilva
author_sort Marcos Fabio DosSantos
collection DOAJ
description We developed a unique protocol where transcranial direct current stimulation (tDCS) of the motor cortex is performed during positron emission tomography (PET) scan using a µ-opioid receptor (µOR) selective radiotracer, [11C]carfentanil. This is one of the most important central neuromechanisms associated with pain perception and regulation. We measured µOR non-displaceable binding potential (µOR BPND) in a trigeminal neuropathic pain patient (TNP) without creating artifacts, or posing risks to the patient (e.g., monitoring of resistance). The active session directly improved in 36.2% the threshold for experimental cold pain in the trigeminal allodynic area, mandibular branch, but not the TNP patient’s clinical pain. Interestingly, the single active tDCS application considerably decreased µORBPND levels in (sub)cortical pain-matrix structures compared to sham tDCS, especially in the posterior thalamus. Suggesting that the µ-opioidergic effects of a single tDCS session are subclinical at immediate level, and repetitive sessions are necessary to revert ingrained neuroplastic changes related to the chronic pain. To our knowledge, we provide data for the first time in-vivo that there is possibly an instant increase of endogenous µ-opioid release during acute motor cortex neuromodulation with tDCS.
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spelling doaj.art-bf6616278b8541c397170a9e5d93eff62022-12-21T17:32:00ZengFrontiers Media S.A.Frontiers in Psychiatry1664-06402012-11-01310.3389/fpsyt.2012.0009331714Immediate effects of tDCS on the µ-opioid system of a chronic pain patientMarcos Fabio DosSantos0Marcos Fabio DosSantos1Tiffany M Love2Ilkka Kristian Martikainen3Ilkka Kristian Martikainen4Thiago Dias Nascimento5Felipe eFregni6Chelsea eCummiford7Misty Dawn Deboer8Jon Kar Zubieta9Alexandre F DaSilva10University of MichiganUniversidade Federal do Rio de JaneiroUniversity of MichiganUniversity of MichiganUniversity of MichiganUniversity of MichiganHarvard UniversityUniversity of MichiganUniversity of MichiganUniversity of MichiganUniversity of MichiganWe developed a unique protocol where transcranial direct current stimulation (tDCS) of the motor cortex is performed during positron emission tomography (PET) scan using a µ-opioid receptor (µOR) selective radiotracer, [11C]carfentanil. This is one of the most important central neuromechanisms associated with pain perception and regulation. We measured µOR non-displaceable binding potential (µOR BPND) in a trigeminal neuropathic pain patient (TNP) without creating artifacts, or posing risks to the patient (e.g., monitoring of resistance). The active session directly improved in 36.2% the threshold for experimental cold pain in the trigeminal allodynic area, mandibular branch, but not the TNP patient’s clinical pain. Interestingly, the single active tDCS application considerably decreased µORBPND levels in (sub)cortical pain-matrix structures compared to sham tDCS, especially in the posterior thalamus. Suggesting that the µ-opioidergic effects of a single tDCS session are subclinical at immediate level, and repetitive sessions are necessary to revert ingrained neuroplastic changes related to the chronic pain. To our knowledge, we provide data for the first time in-vivo that there is possibly an instant increase of endogenous µ-opioid release during acute motor cortex neuromodulation with tDCS.http://journal.frontiersin.org/Journal/10.3389/fpsyt.2012.00093/fullneuroplasticityPETtDCSopioid receptorsTrigeminal Neuropathic PainPost-herpetic Neuralgia
spellingShingle Marcos Fabio DosSantos
Marcos Fabio DosSantos
Tiffany M Love
Ilkka Kristian Martikainen
Ilkka Kristian Martikainen
Thiago Dias Nascimento
Felipe eFregni
Chelsea eCummiford
Misty Dawn Deboer
Jon Kar Zubieta
Alexandre F DaSilva
Immediate effects of tDCS on the µ-opioid system of a chronic pain patient
Frontiers in Psychiatry
neuroplasticity
PET
tDCS
opioid receptors
Trigeminal Neuropathic Pain
Post-herpetic Neuralgia
title Immediate effects of tDCS on the µ-opioid system of a chronic pain patient
title_full Immediate effects of tDCS on the µ-opioid system of a chronic pain patient
title_fullStr Immediate effects of tDCS on the µ-opioid system of a chronic pain patient
title_full_unstemmed Immediate effects of tDCS on the µ-opioid system of a chronic pain patient
title_short Immediate effects of tDCS on the µ-opioid system of a chronic pain patient
title_sort immediate effects of tdcs on the 181 opioid system of a chronic pain patient
topic neuroplasticity
PET
tDCS
opioid receptors
Trigeminal Neuropathic Pain
Post-herpetic Neuralgia
url http://journal.frontiersin.org/Journal/10.3389/fpsyt.2012.00093/full
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