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Functional hyperemia drives fluid exchange in the paravascular space

The brain lacks a conventional lymphatic system to remove metabolic waste. It has been proposed that directional fluid movement through the arteriolar paravascular space (PVS) promotes metabolite clearance. We performed simulations to examine if arteriolar pulsations and dilations can drive directio...

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Autores principales: Kedarasetti, Ravi Teja, Turner, Kevin L., Echagarruga, Christina, Gluckman, Bruce J., Drew, Patrick J., Costanzo, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441569/
https://www.ncbi.nlm.nih.gov/pubmed/32819402
http://dx.doi.org/10.1186/s12987-020-00214-3
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author Kedarasetti, Ravi Teja
Turner, Kevin L.
Echagarruga, Christina
Gluckman, Bruce J.
Drew, Patrick J.
Costanzo, Francesco
author_facet Kedarasetti, Ravi Teja
Turner, Kevin L.
Echagarruga, Christina
Gluckman, Bruce J.
Drew, Patrick J.
Costanzo, Francesco
author_sort Kedarasetti, Ravi Teja
collection PubMed
description The brain lacks a conventional lymphatic system to remove metabolic waste. It has been proposed that directional fluid movement through the arteriolar paravascular space (PVS) promotes metabolite clearance. We performed simulations to examine if arteriolar pulsations and dilations can drive directional CSF flow in the PVS and found that arteriolar wall movements do not drive directional CSF flow. We propose an alternative method of metabolite clearance from the PVS, namely fluid exchange between the PVS and the subarachnoid space (SAS). In simulations with compliant brain tissue, arteriolar pulsations did not drive appreciable fluid exchange between the PVS and the SAS. However, when the arteriole dilated, as seen during functional hyperemia, there was a marked exchange of fluid. Simulations suggest that functional hyperemia may serve to increase metabolite clearance from the PVS. We measured blood vessels and brain tissue displacement simultaneously in awake, head-fixed mice using two-photon microscopy. These measurements showed that brain deforms in response to pressure changes in PVS, consistent with our simulations. Our results show that the deformability of the brain tissue needs to be accounted for when studying fluid flow and metabolite transport.
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spelling pubmed-74415692020-08-24 Functional hyperemia drives fluid exchange in the paravascular space Kedarasetti, Ravi Teja Turner, Kevin L. Echagarruga, Christina Gluckman, Bruce J. Drew, Patrick J. Costanzo, Francesco Fluids Barriers CNS Research The brain lacks a conventional lymphatic system to remove metabolic waste. It has been proposed that directional fluid movement through the arteriolar paravascular space (PVS) promotes metabolite clearance. We performed simulations to examine if arteriolar pulsations and dilations can drive directional CSF flow in the PVS and found that arteriolar wall movements do not drive directional CSF flow. We propose an alternative method of metabolite clearance from the PVS, namely fluid exchange between the PVS and the subarachnoid space (SAS). In simulations with compliant brain tissue, arteriolar pulsations did not drive appreciable fluid exchange between the PVS and the SAS. However, when the arteriole dilated, as seen during functional hyperemia, there was a marked exchange of fluid. Simulations suggest that functional hyperemia may serve to increase metabolite clearance from the PVS. We measured blood vessels and brain tissue displacement simultaneously in awake, head-fixed mice using two-photon microscopy. These measurements showed that brain deforms in response to pressure changes in PVS, consistent with our simulations. Our results show that the deformability of the brain tissue needs to be accounted for when studying fluid flow and metabolite transport. BioMed Central 2020-08-20 /pmc/articles/PMC7441569/ /pubmed/32819402 http://dx.doi.org/10.1186/s12987-020-00214-3 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Kedarasetti, Ravi Teja
Turner, Kevin L.
Echagarruga, Christina
Gluckman, Bruce J.
Drew, Patrick J.
Costanzo, Francesco
Functional hyperemia drives fluid exchange in the paravascular space
title Functional hyperemia drives fluid exchange in the paravascular space
title_full Functional hyperemia drives fluid exchange in the paravascular space
title_fullStr Functional hyperemia drives fluid exchange in the paravascular space
title_full_unstemmed Functional hyperemia drives fluid exchange in the paravascular space
title_short Functional hyperemia drives fluid exchange in the paravascular space
title_sort functional hyperemia drives fluid exchange in the paravascular space
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441569/
https://www.ncbi.nlm.nih.gov/pubmed/32819402
http://dx.doi.org/10.1186/s12987-020-00214-3
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