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Measuring glymphatic function: assessing the toolkit

  • University of Oxford
  • Department of Physiology, Anatomy and Genetics, Kavli Institute for NanoScience Discovery, University of Oxford, Parks Road, OX1 3PT Oxford, UK.; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK.

Research output: Contribution to journalArticlepeer-review

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Abstract

Glymphatic flow has been proposed to clear brain waste while we sleep. Cerebrospinal fluid moves from periarterial to perivenous spaces through the parenchyma, with subsequent cerebrospinal fluid drainage to dural lymphatics. Glymphatic disruption is associated with neurological conditions such as Alzheimer’s disease and traumatic brain injury. Therefore, investigating its structure and function may improve understanding of pathophysiology. The recent controversy on whether glymphatic flow increases or decreases during sleep demonstrates that the glymphatic hypothesis remains contentious. However, discrepancies between different studies could be due to limitations of the specific techniques used and confounding factors. Here, we review the methods used to study glymphatic function and provide a toolkit from which researchers can choose. We conclude that tracer analysis has been useful, ex vivo techniques are unreliable, and in vivo imaging is still limited. Finally, we explore the potential for future methods and highlight the need for in vitro models, such as microfluidic devices, which may address technique limitations and enable progression of the field.
Original languageEnglish
Pages (from-to)534-541
Number of pages8
JournalNeural Regeneration Research
Volume21
Issue number2
Early online date25 Mar 2025
DOIs
Publication statusPublished - 1 Feb 2026

Bibliographical note

Copyright © 2025 Neural Regeneration Research. This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License (http://creativecommons.org/licenses/by-nc-sa/4.0/), which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

Funding

Funding: LU was supported by the European Union Horizon 2020 Research and Innovation Programme (Marie Sk\u0142odowska-Curie grant agreement No 847419). PK was supported by the Biotechnology and Biological Sciences Research Council via a Discovery Fellowship (BB/W00934X/1), and the Aston University RKE Pump Priming Programme. The Aston Institute for Membrane Excellence (AIME) is funded by UKRI\u2019s Research England as part of their Expanding Excellence in England (E3) fund. RMB was supported by a UKRI Frontier Research Grant EP/Y023684/1 (following assessment as an ERC Advanced grant, FORTIFY, ERC-2022-ADG-101096882 under the UK Government Guarantee scheme) and acknowledged a Biotechnology and Biological Sciences Research Council Pioneer Award (BB/Y512874/1). MMS was supported by a Medical Research Council Career Development Award (MR/W027119/1) and acknowledged support from the BHF Centre of Research Excellence, University of Oxford (grant code: RE/24/130024) and a Biotechnology and Biological Sciences Research Council Pioneer Award (BB/Y512874/1).

Keywords

  • aquaporin-4
  • cerebrospinal fluid
  • efflux
  • glymphatics
  • imaging
  • influx
  • methods
  • microfluidics
  • parenchyma
  • periarterial
  • perivenous
  • tracer

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