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Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans
Cerebrospinal fluid (CSF) flow maintains healthy brain homeostasis, facilitating solute transport and the exchange of brain waste products. CSF flow is thus important for brain health, but the mechanisms that control its large-scale movement through the ventricles are not well understood. While it i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062585/ https://www.ncbi.nlm.nih.gov/pubmed/36996009 http://dx.doi.org/10.1371/journal.pbio.3002035 |
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author | Williams, Stephanie D. Setzer, Beverly Fultz, Nina E. Valdiviezo, Zenia Tacugue, Nicole Diamandis, Zachary Lewis, Laura D. |
author_facet | Williams, Stephanie D. Setzer, Beverly Fultz, Nina E. Valdiviezo, Zenia Tacugue, Nicole Diamandis, Zachary Lewis, Laura D. |
author_sort | Williams, Stephanie D. |
collection | PubMed |
description | Cerebrospinal fluid (CSF) flow maintains healthy brain homeostasis, facilitating solute transport and the exchange of brain waste products. CSF flow is thus important for brain health, but the mechanisms that control its large-scale movement through the ventricles are not well understood. While it is well established that CSF flow is modulated by respiratory and cardiovascular dynamics, recent work has also demonstrated that neural activity is coupled to large waves of CSF flow in the ventricles during sleep. To test whether the temporal coupling between neural activity and CSF flow is in part due to a causal relationship, we investigated whether CSF flow could be induced by driving neural activity with intense visual stimulation. We manipulated neural activity with a flickering checkerboard visual stimulus and found that we could drive macroscopic CSF flow in the human brain. The timing and amplitude of CSF flow was matched to the visually evoked hemodynamic responses, suggesting neural activity can modulate CSF flow via neurovascular coupling. These results demonstrate that neural activity can contribute to driving CSF flow in the human brain and that the temporal dynamics of neurovascular coupling can explain this effect. |
format | Online Article Text |
id | pubmed-10062585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100625852023-03-31 Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans Williams, Stephanie D. Setzer, Beverly Fultz, Nina E. Valdiviezo, Zenia Tacugue, Nicole Diamandis, Zachary Lewis, Laura D. PLoS Biol Short Reports Cerebrospinal fluid (CSF) flow maintains healthy brain homeostasis, facilitating solute transport and the exchange of brain waste products. CSF flow is thus important for brain health, but the mechanisms that control its large-scale movement through the ventricles are not well understood. While it is well established that CSF flow is modulated by respiratory and cardiovascular dynamics, recent work has also demonstrated that neural activity is coupled to large waves of CSF flow in the ventricles during sleep. To test whether the temporal coupling between neural activity and CSF flow is in part due to a causal relationship, we investigated whether CSF flow could be induced by driving neural activity with intense visual stimulation. We manipulated neural activity with a flickering checkerboard visual stimulus and found that we could drive macroscopic CSF flow in the human brain. The timing and amplitude of CSF flow was matched to the visually evoked hemodynamic responses, suggesting neural activity can modulate CSF flow via neurovascular coupling. These results demonstrate that neural activity can contribute to driving CSF flow in the human brain and that the temporal dynamics of neurovascular coupling can explain this effect. Public Library of Science 2023-03-30 /pmc/articles/PMC10062585/ /pubmed/36996009 http://dx.doi.org/10.1371/journal.pbio.3002035 Text en © 2023 Williams et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Short Reports Williams, Stephanie D. Setzer, Beverly Fultz, Nina E. Valdiviezo, Zenia Tacugue, Nicole Diamandis, Zachary Lewis, Laura D. Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
title | Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
title_full | Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
title_fullStr | Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
title_full_unstemmed | Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
title_short | Neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
title_sort | neural activity induced by sensory stimulation can drive large-scale cerebrospinal fluid flow during wakefulness in humans |
topic | Short Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10062585/ https://www.ncbi.nlm.nih.gov/pubmed/36996009 http://dx.doi.org/10.1371/journal.pbio.3002035 |
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