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Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism

A “glymphatic system,” which involves convective fluid transport from para-arterial to paravenous cerebrospinal fluid through brain extracellular space (ECS), has been proposed to account for solute clearance in brain, and aquaporin-4 water channels in astrocyte endfeet may have a role in this proce...

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Autores principales: Jin, Byung-Ju, Smith, Alex J., Verkman, Alan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129742/
https://www.ncbi.nlm.nih.gov/pubmed/27836940
http://dx.doi.org/10.1085/jgp.201611684
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author Jin, Byung-Ju
Smith, Alex J.
Verkman, Alan S.
author_facet Jin, Byung-Ju
Smith, Alex J.
Verkman, Alan S.
author_sort Jin, Byung-Ju
collection PubMed
description A “glymphatic system,” which involves convective fluid transport from para-arterial to paravenous cerebrospinal fluid through brain extracellular space (ECS), has been proposed to account for solute clearance in brain, and aquaporin-4 water channels in astrocyte endfeet may have a role in this process. Here, we investigate the major predictions of the glymphatic mechanism by modeling diffusive and convective transport in brain ECS and by solving the Navier–Stokes and convection–diffusion equations, using realistic ECS geometry for short-range transport between para-arterial and paravenous spaces. Major model parameters include para-arterial and paravenous pressures, ECS volume fraction, solute diffusion coefficient, and astrocyte foot-process water permeability. The model predicts solute accumulation and clearance from the ECS after a step change in solute concentration in para-arterial fluid. The principal and robust conclusions of the model are as follows: (a) significant convective transport requires a sustained pressure difference of several mmHg between the para-arterial and paravenous fluid and is not affected by pulsatile pressure fluctuations; (b) astrocyte endfoot water permeability does not substantially alter the rate of convective transport in ECS as the resistance to flow across endfeet is far greater than in the gaps surrounding them; and (c) diffusion (without convection) in the ECS is adequate to account for experimental transport studies in brain parenchyma. Therefore, our modeling results do not support a physiologically important role for local parenchymal convective flow in solute transport through brain ECS.
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spelling pubmed-51297422017-06-01 Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism Jin, Byung-Ju Smith, Alex J. Verkman, Alan S. J Gen Physiol Research Articles A “glymphatic system,” which involves convective fluid transport from para-arterial to paravenous cerebrospinal fluid through brain extracellular space (ECS), has been proposed to account for solute clearance in brain, and aquaporin-4 water channels in astrocyte endfeet may have a role in this process. Here, we investigate the major predictions of the glymphatic mechanism by modeling diffusive and convective transport in brain ECS and by solving the Navier–Stokes and convection–diffusion equations, using realistic ECS geometry for short-range transport between para-arterial and paravenous spaces. Major model parameters include para-arterial and paravenous pressures, ECS volume fraction, solute diffusion coefficient, and astrocyte foot-process water permeability. The model predicts solute accumulation and clearance from the ECS after a step change in solute concentration in para-arterial fluid. The principal and robust conclusions of the model are as follows: (a) significant convective transport requires a sustained pressure difference of several mmHg between the para-arterial and paravenous fluid and is not affected by pulsatile pressure fluctuations; (b) astrocyte endfoot water permeability does not substantially alter the rate of convective transport in ECS as the resistance to flow across endfeet is far greater than in the gaps surrounding them; and (c) diffusion (without convection) in the ECS is adequate to account for experimental transport studies in brain parenchyma. Therefore, our modeling results do not support a physiologically important role for local parenchymal convective flow in solute transport through brain ECS. The Rockefeller University Press 2016-12 /pmc/articles/PMC5129742/ /pubmed/27836940 http://dx.doi.org/10.1085/jgp.201611684 Text en © 2016 Jin et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Jin, Byung-Ju
Smith, Alex J.
Verkman, Alan S.
Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
title Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
title_full Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
title_fullStr Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
title_full_unstemmed Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
title_short Spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
title_sort spatial model of convective solute transport in brain extracellular space does not support a “glymphatic” mechanism
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129742/
https://www.ncbi.nlm.nih.gov/pubmed/27836940
http://dx.doi.org/10.1085/jgp.201611684
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