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Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS
Glutamate is involved in excitatory neurotransmission and metabolic processes related to brain function. Previous studies using proton functional magnetic resonance spectroscopy ((1)H fMRS) have demonstrated elevated cortical glutamate levels by 2–4% during visual and motor stimulation, relative to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845718/ https://www.ncbi.nlm.nih.gov/pubmed/29559930 http://dx.doi.org/10.3389/fpsyt.2018.00066 |
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author | Woodcock, Eric A. Anand, Chaitali Khatib, Dalal Diwadkar, Vaibhav A. Stanley, Jeffrey A. |
author_facet | Woodcock, Eric A. Anand, Chaitali Khatib, Dalal Diwadkar, Vaibhav A. Stanley, Jeffrey A. |
author_sort | Woodcock, Eric A. |
collection | PubMed |
description | Glutamate is involved in excitatory neurotransmission and metabolic processes related to brain function. Previous studies using proton functional magnetic resonance spectroscopy ((1)H fMRS) have demonstrated elevated cortical glutamate levels by 2–4% during visual and motor stimulation, relative to periods of no stimulation. Here, we extended this approach to working memory cognitive task performance, which has been consistently associated with dorsolateral prefrontal cortex (dlPFC) activation. Sixteen healthy adult volunteers completed a continuous visual fixation “rest” task followed by a letter 2-back working memory task during (1)H fMRS acquisition of the left dlPFC, which encompassed Brodmann areas 45 and 46 over a 4.5-cm(3) volume. Using a 100% automated fitting procedure integrated with LCModel, raw spectra were eddy current-, phase-, and shift-corrected prior to quantification resulting in a 32s temporal resolution or 8 averages per spectra. Task compliance was high (95 ± 11% correct) and the mean Cramer-Rao Lower Bound of glutamate was 6.9 ± 0.9%. Relative to continuous passive visual fixation, left dlPFC glutamate levels were significantly higher by 2.7% (0.32 mmol/kg wet weight) during letter 2-back performance. Elevated dlPFC glutamate levels reflect increased metabolic activity and excitatory neurotransmission driven by working memory-related cognitive demands. These results provide the first in vivo demonstration of elevated dlPFC glutamate levels during working memory. |
format | Online Article Text |
id | pubmed-5845718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58457182018-03-20 Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS Woodcock, Eric A. Anand, Chaitali Khatib, Dalal Diwadkar, Vaibhav A. Stanley, Jeffrey A. Front Psychiatry Psychiatry Glutamate is involved in excitatory neurotransmission and metabolic processes related to brain function. Previous studies using proton functional magnetic resonance spectroscopy ((1)H fMRS) have demonstrated elevated cortical glutamate levels by 2–4% during visual and motor stimulation, relative to periods of no stimulation. Here, we extended this approach to working memory cognitive task performance, which has been consistently associated with dorsolateral prefrontal cortex (dlPFC) activation. Sixteen healthy adult volunteers completed a continuous visual fixation “rest” task followed by a letter 2-back working memory task during (1)H fMRS acquisition of the left dlPFC, which encompassed Brodmann areas 45 and 46 over a 4.5-cm(3) volume. Using a 100% automated fitting procedure integrated with LCModel, raw spectra were eddy current-, phase-, and shift-corrected prior to quantification resulting in a 32s temporal resolution or 8 averages per spectra. Task compliance was high (95 ± 11% correct) and the mean Cramer-Rao Lower Bound of glutamate was 6.9 ± 0.9%. Relative to continuous passive visual fixation, left dlPFC glutamate levels were significantly higher by 2.7% (0.32 mmol/kg wet weight) during letter 2-back performance. Elevated dlPFC glutamate levels reflect increased metabolic activity and excitatory neurotransmission driven by working memory-related cognitive demands. These results provide the first in vivo demonstration of elevated dlPFC glutamate levels during working memory. Frontiers Media S.A. 2018-03-06 /pmc/articles/PMC5845718/ /pubmed/29559930 http://dx.doi.org/10.3389/fpsyt.2018.00066 Text en Copyright © 2018 Woodcock, Anand, Khatib, Diwadkar and Stanley. 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 | Psychiatry Woodcock, Eric A. Anand, Chaitali Khatib, Dalal Diwadkar, Vaibhav A. Stanley, Jeffrey A. Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS |
title | Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS |
title_full | Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS |
title_fullStr | Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS |
title_full_unstemmed | Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS |
title_short | Working Memory Modulates Glutamate Levels in the Dorsolateral Prefrontal Cortex during (1)H fMRS |
title_sort | working memory modulates glutamate levels in the dorsolateral prefrontal cortex during (1)h fmrs |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845718/ https://www.ncbi.nlm.nih.gov/pubmed/29559930 http://dx.doi.org/10.3389/fpsyt.2018.00066 |
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