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Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans

Background: Dorsolateral prefrontal cortex (DLPFC) low frequency repetitive transcranial magnetic stimulation (LF-rTMS) has shown promise as a treatment and investigative tool in the medical and research communities. Researchers have made significant progress elucidating DLPFC LF-rTMS effects—primar...

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Autores principales: Bridges, Nathaniel R., McKinley, Richard A., Boeke, Danielle, Sherwood, Matthew S., Parker, Jason G., McIntire, Lindsey K., Nelson, Justin M., Fletchall, Catherine, Alexander, Natasha, McConnell, Amanda, Goodyear, Chuck, Nelson, Jeremy T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879132/
https://www.ncbi.nlm.nih.gov/pubmed/29632477
http://dx.doi.org/10.3389/fnhum.2018.00077
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author Bridges, Nathaniel R.
McKinley, Richard A.
Boeke, Danielle
Sherwood, Matthew S.
Parker, Jason G.
McIntire, Lindsey K.
Nelson, Justin M.
Fletchall, Catherine
Alexander, Natasha
McConnell, Amanda
Goodyear, Chuck
Nelson, Jeremy T.
author_facet Bridges, Nathaniel R.
McKinley, Richard A.
Boeke, Danielle
Sherwood, Matthew S.
Parker, Jason G.
McIntire, Lindsey K.
Nelson, Justin M.
Fletchall, Catherine
Alexander, Natasha
McConnell, Amanda
Goodyear, Chuck
Nelson, Jeremy T.
author_sort Bridges, Nathaniel R.
collection PubMed
description Background: Dorsolateral prefrontal cortex (DLPFC) low frequency repetitive transcranial magnetic stimulation (LF-rTMS) has shown promise as a treatment and investigative tool in the medical and research communities. Researchers have made significant progress elucidating DLPFC LF-rTMS effects—primarily in individuals with psychiatric disorders. However, more efforts investigating underlying molecular changes and establishing links to functional and behavioral outcomes in healthy humans are needed. Objective: We aimed to quantify neuromolecular changes and relate these to functional changes following a single session of DLPFC LF-rTMS in healthy participants. Methods: Eleven participants received sham-controlled neuronavigated 1 Hz rTMS to the region most activated by a 7-letter Sternberg working memory task (SWMT) within the left DLPFC. We quantified SWMT performance, functional magnetic resonance activation and proton Magnetic resonance spectroscopy (MRS) neurometabolite measure changes before and after stimulation. Results: A single LF-rTMS session was not sufficient to change DLPFC neurometabolite levels and these changes did not correlate with DLPFC activation changes. Real rTMS, however, significantly altered neurometabolite correlations (compared to sham rTMS), both with baseline levels and between the metabolites themselves. Additionally, real rTMS was associated with diminished reaction time (RT) performance improvements and increased activation within the motor, somatosensory and lateral occipital cortices. Conclusion: These results show that a single session of LF-rTMS is sufficient to influence metabolite relationships and causes widespread activation in healthy humans. Investigating correlational relationships may provide insight into mechanisms underlying LF-rTMS.
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spelling pubmed-58791322018-04-09 Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans Bridges, Nathaniel R. McKinley, Richard A. Boeke, Danielle Sherwood, Matthew S. Parker, Jason G. McIntire, Lindsey K. Nelson, Justin M. Fletchall, Catherine Alexander, Natasha McConnell, Amanda Goodyear, Chuck Nelson, Jeremy T. Front Hum Neurosci Neuroscience Background: Dorsolateral prefrontal cortex (DLPFC) low frequency repetitive transcranial magnetic stimulation (LF-rTMS) has shown promise as a treatment and investigative tool in the medical and research communities. Researchers have made significant progress elucidating DLPFC LF-rTMS effects—primarily in individuals with psychiatric disorders. However, more efforts investigating underlying molecular changes and establishing links to functional and behavioral outcomes in healthy humans are needed. Objective: We aimed to quantify neuromolecular changes and relate these to functional changes following a single session of DLPFC LF-rTMS in healthy participants. Methods: Eleven participants received sham-controlled neuronavigated 1 Hz rTMS to the region most activated by a 7-letter Sternberg working memory task (SWMT) within the left DLPFC. We quantified SWMT performance, functional magnetic resonance activation and proton Magnetic resonance spectroscopy (MRS) neurometabolite measure changes before and after stimulation. Results: A single LF-rTMS session was not sufficient to change DLPFC neurometabolite levels and these changes did not correlate with DLPFC activation changes. Real rTMS, however, significantly altered neurometabolite correlations (compared to sham rTMS), both with baseline levels and between the metabolites themselves. Additionally, real rTMS was associated with diminished reaction time (RT) performance improvements and increased activation within the motor, somatosensory and lateral occipital cortices. Conclusion: These results show that a single session of LF-rTMS is sufficient to influence metabolite relationships and causes widespread activation in healthy humans. Investigating correlational relationships may provide insight into mechanisms underlying LF-rTMS. Frontiers Media S.A. 2018-03-26 /pmc/articles/PMC5879132/ /pubmed/29632477 http://dx.doi.org/10.3389/fnhum.2018.00077 Text en Copyright © 2018 Bridges, McKinley, Boeke, Sherwood, Parker, McIntire, Nelson, Fletchall, Alexander, McConnell, Goodyear and Nelson. 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 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
Bridges, Nathaniel R.
McKinley, Richard A.
Boeke, Danielle
Sherwood, Matthew S.
Parker, Jason G.
McIntire, Lindsey K.
Nelson, Justin M.
Fletchall, Catherine
Alexander, Natasha
McConnell, Amanda
Goodyear, Chuck
Nelson, Jeremy T.
Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans
title Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans
title_full Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans
title_fullStr Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans
title_full_unstemmed Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans
title_short Single Session Low Frequency Left Dorsolateral Prefrontal Transcranial Magnetic Stimulation Changes Neurometabolite Relationships in Healthy Humans
title_sort single session low frequency left dorsolateral prefrontal transcranial magnetic stimulation changes neurometabolite relationships in healthy humans
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879132/
https://www.ncbi.nlm.nih.gov/pubmed/29632477
http://dx.doi.org/10.3389/fnhum.2018.00077
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