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FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity
Positive blood oxygenation level-dependent (BOLD) responses (PBR), as measured by functional Magnetic Resonance Imaging (fMRI), are the most utilized measurements to non-invasively map activity in the brain. Recent studies have consistently shown that BOLD responses are not exclusively positive. Neg...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046332/ https://www.ncbi.nlm.nih.gov/pubmed/34363092 http://dx.doi.org/10.1007/s00429-021-02342-4 |
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author | Fracasso, Alessio Gaglianese, Anna Vansteensel, Mariska J. Aarnoutse, Erik J. Ramsey, Nick F. Dumoulin, Serge O. Petridou, Natalia |
author_facet | Fracasso, Alessio Gaglianese, Anna Vansteensel, Mariska J. Aarnoutse, Erik J. Ramsey, Nick F. Dumoulin, Serge O. Petridou, Natalia |
author_sort | Fracasso, Alessio |
collection | PubMed |
description | Positive blood oxygenation level-dependent (BOLD) responses (PBR), as measured by functional Magnetic Resonance Imaging (fMRI), are the most utilized measurements to non-invasively map activity in the brain. Recent studies have consistently shown that BOLD responses are not exclusively positive. Negative BOLD responses (NBR) have been reported in response to specific sensory stimulations and tasks. However, the exact relationship between NBR and the underlying metabolic and neuronal demand is still under debate. In this study, we investigated the neurophysiological basis of negative BOLD using fMRI and intra-cranial electrophysiology (electrocorticography, ECoG) measurements from the same human participants. We show that, for those electrodes that responded to visual stimulation, PBR are correlated with high-frequency band (HFB) responses. Crucially, NBR were associated with an absence of HFB power responses and an unpredicted decrease in the alpha power responses. |
format | Online Article Text |
id | pubmed-9046332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-90463322022-05-07 FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity Fracasso, Alessio Gaglianese, Anna Vansteensel, Mariska J. Aarnoutse, Erik J. Ramsey, Nick F. Dumoulin, Serge O. Petridou, Natalia Brain Struct Funct Original Article Positive blood oxygenation level-dependent (BOLD) responses (PBR), as measured by functional Magnetic Resonance Imaging (fMRI), are the most utilized measurements to non-invasively map activity in the brain. Recent studies have consistently shown that BOLD responses are not exclusively positive. Negative BOLD responses (NBR) have been reported in response to specific sensory stimulations and tasks. However, the exact relationship between NBR and the underlying metabolic and neuronal demand is still under debate. In this study, we investigated the neurophysiological basis of negative BOLD using fMRI and intra-cranial electrophysiology (electrocorticography, ECoG) measurements from the same human participants. We show that, for those electrodes that responded to visual stimulation, PBR are correlated with high-frequency band (HFB) responses. Crucially, NBR were associated with an absence of HFB power responses and an unpredicted decrease in the alpha power responses. Springer Berlin Heidelberg 2021-08-07 2022 /pmc/articles/PMC9046332/ /pubmed/34363092 http://dx.doi.org/10.1007/s00429-021-02342-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Fracasso, Alessio Gaglianese, Anna Vansteensel, Mariska J. Aarnoutse, Erik J. Ramsey, Nick F. Dumoulin, Serge O. Petridou, Natalia FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity |
title | FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity |
title_full | FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity |
title_fullStr | FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity |
title_full_unstemmed | FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity |
title_short | FMRI and intra-cranial electrocorticography recordings in the same human subjects reveals negative BOLD signal coupled with silenced neuronal activity |
title_sort | fmri and intra-cranial electrocorticography recordings in the same human subjects reveals negative bold signal coupled with silenced neuronal activity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9046332/ https://www.ncbi.nlm.nih.gov/pubmed/34363092 http://dx.doi.org/10.1007/s00429-021-02342-4 |
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