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Imaging localized neuronal activity at fast time scales through biomechanics

Mapping neuronal activity noninvasively is a key requirement for in vivo human neuroscience. Traditional functional magnetic resonance (MR) imaging, with a temporal response of seconds, cannot measure high-level cognitive processes evolving in tens of milliseconds. To advance neuroscience, imaging o...

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Autores principales: Patz, Samuel, Fovargue, Daniel, Schregel, Katharina, Nazari, Navid, Palotai, Miklos, Barbone, Paul E., Fabry, Ben, Hammers, Alexander, Holm, Sverre, Kozerke, Sebastian, Nordsletten, David, Sinkus, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469937/
https://www.ncbi.nlm.nih.gov/pubmed/31001585
http://dx.doi.org/10.1126/sciadv.aav3816
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author Patz, Samuel
Fovargue, Daniel
Schregel, Katharina
Nazari, Navid
Palotai, Miklos
Barbone, Paul E.
Fabry, Ben
Hammers, Alexander
Holm, Sverre
Kozerke, Sebastian
Nordsletten, David
Sinkus, Ralph
author_facet Patz, Samuel
Fovargue, Daniel
Schregel, Katharina
Nazari, Navid
Palotai, Miklos
Barbone, Paul E.
Fabry, Ben
Hammers, Alexander
Holm, Sverre
Kozerke, Sebastian
Nordsletten, David
Sinkus, Ralph
author_sort Patz, Samuel
collection PubMed
description Mapping neuronal activity noninvasively is a key requirement for in vivo human neuroscience. Traditional functional magnetic resonance (MR) imaging, with a temporal response of seconds, cannot measure high-level cognitive processes evolving in tens of milliseconds. To advance neuroscience, imaging of fast neuronal processes is required. Here, we show in vivo imaging of fast neuronal processes at 100-ms time scales by quantifying brain biomechanics noninvasively with MR elastography. We show brain stiffness changes of ~10% in response to repetitive electric stimulation of a mouse hind paw over two orders of frequency from 0.1 to 10 Hz. We demonstrate in mice that regional patterns of stiffness modulation are synchronous with stimulus switching and evolve with frequency. For very fast stimuli (100 ms), mechanical changes are mainly located in the thalamus, the relay location for afferent cortical input. Our results demonstrate a new methodology for noninvasively tracking brain functional activity at high speed.
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spelling pubmed-64699372019-04-18 Imaging localized neuronal activity at fast time scales through biomechanics Patz, Samuel Fovargue, Daniel Schregel, Katharina Nazari, Navid Palotai, Miklos Barbone, Paul E. Fabry, Ben Hammers, Alexander Holm, Sverre Kozerke, Sebastian Nordsletten, David Sinkus, Ralph Sci Adv Research Articles Mapping neuronal activity noninvasively is a key requirement for in vivo human neuroscience. Traditional functional magnetic resonance (MR) imaging, with a temporal response of seconds, cannot measure high-level cognitive processes evolving in tens of milliseconds. To advance neuroscience, imaging of fast neuronal processes is required. Here, we show in vivo imaging of fast neuronal processes at 100-ms time scales by quantifying brain biomechanics noninvasively with MR elastography. We show brain stiffness changes of ~10% in response to repetitive electric stimulation of a mouse hind paw over two orders of frequency from 0.1 to 10 Hz. We demonstrate in mice that regional patterns of stiffness modulation are synchronous with stimulus switching and evolve with frequency. For very fast stimuli (100 ms), mechanical changes are mainly located in the thalamus, the relay location for afferent cortical input. Our results demonstrate a new methodology for noninvasively tracking brain functional activity at high speed. American Association for the Advancement of Science 2019-04-17 /pmc/articles/PMC6469937/ /pubmed/31001585 http://dx.doi.org/10.1126/sciadv.aav3816 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Patz, Samuel
Fovargue, Daniel
Schregel, Katharina
Nazari, Navid
Palotai, Miklos
Barbone, Paul E.
Fabry, Ben
Hammers, Alexander
Holm, Sverre
Kozerke, Sebastian
Nordsletten, David
Sinkus, Ralph
Imaging localized neuronal activity at fast time scales through biomechanics
title Imaging localized neuronal activity at fast time scales through biomechanics
title_full Imaging localized neuronal activity at fast time scales through biomechanics
title_fullStr Imaging localized neuronal activity at fast time scales through biomechanics
title_full_unstemmed Imaging localized neuronal activity at fast time scales through biomechanics
title_short Imaging localized neuronal activity at fast time scales through biomechanics
title_sort imaging localized neuronal activity at fast time scales through biomechanics
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469937/
https://www.ncbi.nlm.nih.gov/pubmed/31001585
http://dx.doi.org/10.1126/sciadv.aav3816
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