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Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation
Whether you are reading, running or sleeping, your brain and its fluid environment continuously interacts to distribute nutrients and clear metabolic waste. Yet, the precise mechanisms for solute transport within the human brain have remained hard to quantify using imaging techniques alone. From mul...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439559/ https://www.ncbi.nlm.nih.gov/pubmed/37596635 http://dx.doi.org/10.1186/s12987-023-00459-8 |
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author | Vinje, Vegard Zapf, Bastian Ringstad, Geir Eide, Per Kristian Rognes, Marie E. Mardal, Kent-Andre |
author_facet | Vinje, Vegard Zapf, Bastian Ringstad, Geir Eide, Per Kristian Rognes, Marie E. Mardal, Kent-Andre |
author_sort | Vinje, Vegard |
collection | PubMed |
description | Whether you are reading, running or sleeping, your brain and its fluid environment continuously interacts to distribute nutrients and clear metabolic waste. Yet, the precise mechanisms for solute transport within the human brain have remained hard to quantify using imaging techniques alone. From multi-modal human brain MRI data sets in sleeping and sleep-deprived subjects, we identify and quantify CSF tracer transport parameters using forward and inverse subject-specific computational modelling. Our findings support the notion that extracellular diffusion alone is not sufficient as a brain-wide tracer transport mechanism. Instead, we show that human MRI observations align well with transport by either by an effective diffusion coefficent 3.5[Formula: see text] that of extracellular diffusion in combination with local clearance rates corresponding to a tracer half-life of up to 5 h, or by extracellular diffusion augmented by advection with brain-wide average flow speeds on the order of 1–9 [Formula: see text] m/min. Reduced advection fully explains reduced tracer clearance after sleep-deprivation, supporting the role of sleep and sleep deprivation on human brain clearance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00459-8. |
format | Online Article Text |
id | pubmed-10439559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104395592023-08-20 Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation Vinje, Vegard Zapf, Bastian Ringstad, Geir Eide, Per Kristian Rognes, Marie E. Mardal, Kent-Andre Fluids Barriers CNS Research Whether you are reading, running or sleeping, your brain and its fluid environment continuously interacts to distribute nutrients and clear metabolic waste. Yet, the precise mechanisms for solute transport within the human brain have remained hard to quantify using imaging techniques alone. From multi-modal human brain MRI data sets in sleeping and sleep-deprived subjects, we identify and quantify CSF tracer transport parameters using forward and inverse subject-specific computational modelling. Our findings support the notion that extracellular diffusion alone is not sufficient as a brain-wide tracer transport mechanism. Instead, we show that human MRI observations align well with transport by either by an effective diffusion coefficent 3.5[Formula: see text] that of extracellular diffusion in combination with local clearance rates corresponding to a tracer half-life of up to 5 h, or by extracellular diffusion augmented by advection with brain-wide average flow speeds on the order of 1–9 [Formula: see text] m/min. Reduced advection fully explains reduced tracer clearance after sleep-deprivation, supporting the role of sleep and sleep deprivation on human brain clearance. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00459-8. BioMed Central 2023-08-18 /pmc/articles/PMC10439559/ /pubmed/37596635 http://dx.doi.org/10.1186/s12987-023-00459-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Vinje, Vegard Zapf, Bastian Ringstad, Geir Eide, Per Kristian Rognes, Marie E. Mardal, Kent-Andre Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation |
title | Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation |
title_full | Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation |
title_fullStr | Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation |
title_full_unstemmed | Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation |
title_short | Human brain solute transport quantified by glymphatic MRI-informed biophysics during sleep and sleep deprivation |
title_sort | human brain solute transport quantified by glymphatic mri-informed biophysics during sleep and sleep deprivation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439559/ https://www.ncbi.nlm.nih.gov/pubmed/37596635 http://dx.doi.org/10.1186/s12987-023-00459-8 |
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