The DOI matches its Crossref record; 204 of the 204 references it cites were found in a registry or an index.
The role of brain barriers in fluid movement in the CNS: is there a ‘glymphatic’ system?
Open accessAbstract
, and protein to optimise signalling and minimise neurotoxicity. At the same time, neuronal and astroglial waste must be promptly removed. The interstitial fluid (ISF) of the brain tissue and the cerebrospinal fluid (CSF) bathing the CNS are integral to this homeostasis and the idea of a glia-lymph or 'glymphatic' system for waste clearance from brain has developed over the last 5 years. This links bulk (convective) flow of CSF into brain along the outside of penetrating arteries, glia-mediated convective transport of fluid and solutes through the brain extracellular space (ECS) involving the aquaporin-4 (AQP4) water channel, and finally delivery of fluid to venules for clearance along peri-venous spaces. However, recent evidence favours important amendments to the 'glymphatic' hypothesis, particularly concerning the role of glia and transfer of solutes within the ECS. This review discusses studies which question the role of AQP4 in ISF flow and the lack of evidence for its ability to transport solutes; summarizes attributes of brain ECS that strongly favour the diffusion of small and large molecules without ISF flow; discusses work on hydraulic conductivity and the nature of the extracellular matrix which may impede fluid movement; and reconsiders the roles of the perivascular space (PVS) in CSF-ISF exchange and drainage. We also consider the extent to which CSF-ISF exchange is possible and desirable, the impact of neuropathology on fluid drainage, and why using CSF as a proxy measure of brain components or drug delivery is problematic. We propose that new work and key historical studies both support the concept of a perivascular fluid system, whereby CSF enters the brain via PVS convective flow or dispersion along larger caliber arteries/arterioles, diffusion predominantly regulates CSF/ISF exchange at the level of the neurovascular unit associated with CNS microvessels, and, finally, a mixture of CSF/ISF/waste products is normally cleared along the PVS of venules/veins as well as other pathways; such a system may or may not constitute a true 'circulation', but, at the least, suggests a comprehensive re-evaluation of the previously proposed 'glymphatic' concepts in favour of a new system better taking into account basic cerebrovascular physiology and fluid transport considerations.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Leveraging convective CSF flow along perivascular spaces could overcome diffusional limitations and provide a direct mechanism for transport to deep brain structures [13–15].”
From Elucidating brain transport pathways and cell type-dependent gene silencing of a durable lipid–siRNA conjugate administered into cerebrospinal fluid (2025) · cites this paper as [13]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Iliff, J. J., Wang, M., Liao, Y., Plogg, B. A., Peng, W., Gundersen, G. A., Benveniste, H., Vates, G. E., Deane, R., Goldman, S. A., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003748 · Cited by 5,824
Astrocyte-endothelial interactions at the blood-brain barrier
Abbott, N. J., Rönnbäck, L., & Hansson, E. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1824 · Cited by 5,595
Self-citationSleep Drives Metabolite Clearance from the Adult Brain
Xie, L., Kang, H., Xu, Q., Chen, M. J., Liao, Y., Thiyagarajan, M., O’Donnell, J., Christensen, D. J., Nicholson, C., Iliff, J. J., et al. (2013) · Science · doi:10.1126/science.1241224 · Cited by 5,411
Structural and functional features of central nervous system lymphatic vessels
Louveau, A., Smirnov, I., Keyes, T. J., Eccles, J. D., Rouhani, S. J., Peske, J. D., Derecki, N. C., Castle, D., Mandell, J. W., Lee, K. S., et al. (2015) · Nature · doi:10.1038/nature14432 · Cited by 4,413
Neuropathological alterations in Alzheimer disease
Serrano-Pozo, A., Frosch, M. P., Masliah, E., & Hyman, B. T. (2011) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006189 · Cited by 3,345
JUNCTIONS BETWEEN INTIMATELY APPOSED CELL MEMBRANES IN THE VERTEBRATE BRAIN
Brightman, M., & Reese, T. S. (1969) · The Journal of Cell Biology · doi:10.1083/jcb.40.3.648 · Cited by 2,457
A dural lymphatic vascular system that drains brain interstitial fluid and macromolecules
Aspelund, A., Antila, S., Proulx, S. T., Karlsen, T. V., Karaman, S., Detmar, M., Wiig, H., & Alitalo, K. (2015) · Journal of Experimental Medicine · doi:10.1084/jem.20142290 · Cited by 2,198
The glymphatic system: a beginner's guide
Jessen, N. A., Munk, A. S. F., Lundgaard, I., & Nedergaard, M. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1581-6 · Cited by 2,075
The Pathobiology of Vascular Dementia
Iadecola, C. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.008 · Cited by 1,857
Signaling Mechanisms Regulating Endothelial Permeability
Mehta, D., & Malik, A. B. (2005) · Physiological Reviews · doi:10.1152/physrev.00012.2005 · Cited by 1,754
Research works printed but not linked: 4
- Bauer HJ (1993) The Quincke centennial lecture. In: Felgenhauer K, Holzgraefe M, Prange H (eds) CNS barriers mod diagnostics. VCH, Weinheim, pp 27–32
- Davson H, Segal MB (1995) Phyioslogy of the CSF and blood–brain barriers, 1st edn. CRC Press Inc, Boca Raton
- Iliff JJ, Wang M, Liao Y, Plogg BA, Peng W, Gundersen GA, Benveniste H, Vates GE, Deane R, Goldman SA, Nagelhus EA, Nedergaard M (2012) A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid β. Sci Transl Med. https://doi.org/10.1126/scitranslmed.3003748 · DOI · Paper page
- Shirai Y (1921) On the transplantation of the rat sarcoma in adult heterogeneous animals. Japan Med World 1:14–15
Cited by
Sorted by citations
Items 101–200 of 596
Basal lamina changes in neurodegenerative disorders
Nguyen, B., Bix, G., & Yao, Y. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00502-y · Cited by 75
Brain pharmacokinetics of two BBB penetrating bispecific antibodies of different size
Faresjö, R., Bonvicini, G., Fang, X. T., Aguilar, X., Sehlin, D., & Syvänen, S. (2021) · Fluids and Barriers of the CNS · doi:10.1186/s12987-021-00257-0 · Cited by 80
Cresto, N., Forner-Piquer, I., Baig, A. H., Chatterjee, M., Perroy, J., Goracci, J., & Marchi, N. (2023) · Chemosphere · doi:10.1016/j.chemosphere.2023.138251 · Cited by 77
Caruso, P., Signori, R., & Moretti, R. (2019) · Vascular Health and Risk Management · doi:10.2147/vhrm.s190470 · Cited by 78
Border-associated macrophages as gatekeepers of brain homeostasis and immunity
Vara‐Pérez, M., & Movahedi, K. (2025) · Immunity · doi:10.1016/j.immuni.2025.04.005 · Cited by 84
Breakdown of blood brain barrier as a mechanism of post-traumatic epilepsy
Dadas, A., & Janigro, D. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.06.022 · Cited by 78
Self-citationFluid Flow and Mass Transport in Brain Tissue
Ray, L., & Heys, J. J. (2019) · Fluids · doi:10.3390/fluids4040196 · Cited by 78
Pulsatile flow drivers in brain parenchyma and perivascular spaces: a resistance network model study
Rey, J. A., & Sarntinoranont, M. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0105-6 · Cited by 74
Sleep as a Therapeutic Target in the Aging Brain
Bah, T. M., Goodman, J. R., & Iliff, J. J. (2019) · Neurotherapeutics · doi:10.1007/s13311-019-00769-6 · Cited by 76
Stevens, K. A., Cai, S., Ladrón-de-Guevara, A., Sun, J., Zheng, X., Du, T., Thomas, J. H., Nedergaard, M., Karniadakis, G. E., & Kelley, D. H. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2217744120 · Cited by 75
Noninvasive Magnetic Resonance Imaging Measures of Glymphatic System Activity
Kamagata, K., Saito, Y., Andica, C., Uchida, W., Takabayashi, K., Yoshida, S., Hagiwara, A., Fujita, S., Nakaya, M., Akashi, T., et al. (2023) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.28977 · Cited by 76
Mehta, R. I., Carpenter, J. S., Mehta, R. I., Haut, M. W., Wang, P., Ranjan, M., Najib, U., D’Haese, P.-F., & Rezai, A. R. (2023) · Fluids and Barriers of the CNS · doi:10.1186/s12987-023-00447-y · Cited by 74
Functional hyperemia drives fluid exchange in the paravascular space
Kedarasetti, R. T., Turner, K. L., Echagarruga, C., Gluckman, B. J., Drew, P. J., & Costanzo, F. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00214-3 · Cited by 72
The molecular anatomy and functions of the choroid plexus in healthy and diseased brain
Kratzer, I., Ek, C. J., & Stolp, H. B. (2020) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2020.183430 · Cited by 74
Patharapankal, E. J., Ajiboye, A. L., Mattern, C., & Trivedi, V. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics16010066 · Cited by 75
McDonald, S. J., Shultz, S. R., & Agoston, D. V. (2021) · Journal of Neurotrauma · doi:10.1089/neu.2021.0011 · Cited by 70
Li, Q., Shao, X., Dai, X., Guo, Q., Yuan, B., Liu, Y., & Jiang, W. (2022) · NPG Asia Materials · doi:10.1038/s41427-022-00362-y · Cited by 69
Arterial vasodilation drives convective fluid flow in the brain: a poroelastic model
Kedarasetti, R. T., Drew, P. J., & Costanzo, F. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-022-00326-y · Cited by 71
Chowdhury, E. A., Noorani, B., Alqahtani, F., Bhalerao, A., Raut, S., Sivandzade, F., & Cucullo, L. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20985946 · Cited by 77
Peritumoral Edema in Gliomas: A Review of Mechanisms and Management
Ohmura, K., Tomita, H., & Hara, A. (2023) · Biomedicines · doi:10.3390/biomedicines11102731 · Cited by 71
Chi, L., Xiao, C., Lin, L., Yang, T., Sun, J., Feng, Y., Liang, F., Pei, Z., & Teng, W. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.755925 · Cited by 69
Giorgi, F. S., Galgani, A., Puglisi‐Allegra, S., Limanaqi, F., Busceti, C. L., & Fornai, F. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24718 · Cited by 69
Rasschaert, M., Weller, R. O., Schroeder, J. A., Brochhausen, C., & Idée, J. (2020) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.27124 · Cited by 65
Local diffusion in the extracellular space of the brain
Tønnesen, J., Hrabětová, S., & Soria, F. N. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105981 · Cited by 66
Spectral Diffusion Analysis of Intravoxel Incoherent Motion MRI in Cerebral Small Vessel Disease
Wong, S. M., Backes, W. H., Drenthen, G. S., Zhang, C. E., Voorter, P., Staals, J., van Oostenbrugge, R. J., & Jansen, J. F. A. (2019) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.26920 · Cited by 62
A real-time in vivo clearance assay for quantification of glymphatic efflux
Plá, V., Bork, P., Harnpramukkul, A., Olveda, G., Ladrón-de-Guevara, A., Giannetto, M. J., Hussain, R., Wang, W., Kelley, D. H., Hablitz, L. M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111320 · Cited by 64
Homocysteine in Neurology: A Possible Contributing Factor to Small Vessel Disease
Moretti, R., Giuffrè, M., Caruso, P., Gazzin, S., & Tiribelli, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042051 · Cited by 64
Kumar, N. N., Pizzo, M. E., Nehra, G., Wilken-Resman, B., Boroumand, S., & Thorne, R. G. (2018) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.8b00548 · Cited by 60
Self-citationThe novel role of lymphatic vessels in the pathogenesis of ocular diseases
Clahsen, T., Hadrian, K., Notara, M., Schlereth, S. L., Howaldt, A., Prokosch, V., Volatier, T. L. A., Hos, D., Schroedl, F., Kaser-Eichberger, A., et al. (2023) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2022.101157 · Cited by 59
Role of aquaporin-4 polarization in extracellular solute clearance
Bojarskaite, L., Nafari, S., Ravnanger, A. K., Frey, M. M., Skauli, N., Åbjørsbråten, K. S., Roth, L. C., Amiry-Moghaddam, M. R., Nagelhus, E. A., Ottersen, O. P., et al. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00527-7 · Cited by 65
Small Vessel Disease-Related Dementia: An Invalid Neurovascular Coupling?
Moretti, R., & Caruso, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031095 · Cited by 62
Transferrin receptor-targeted anti-amyloid antibody enhances brain delivery and mitigates ARIA.
Pizzo, M. E., Plowey, E. D., Khoury, N., Kwan, W., Abettan, J., DeVos, S. L., Discenza, C. B., Earr, T., Joy, D., Lye-Barthel, M., et al. (2025) · Science · doi:10.1126/science.ads3204 · Cited by 63
Self-citationCerebrospinal fluid drainage kinetics across the cribriform plate are reduced with aging
Brady, M., Rahman, A., Combs, A. L., Venkatraman, C., Kasper, R. T., McQuaid, C., Kwok, W. E., Wood, R. W., & Deane, R. (2020) · Fluids and Barriers of the CNS · doi:10.1186/s12987-020-00233-0 · Cited by 56
Current Techniques for Investigating the Brain Extracellular Space
Soria, F. N., Miguélez, C., Peñagarikano, O., & Tønnesen, J. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.570750 · Cited by 53
Advances in designing of polymeric micelles for biomedical application in brain related diseases
Kaur, J., Gulati, M., Kapoor, B., Jha, N. K., Gupta, P. K., Gupta, G., Chellappan, D. K., Devkota, H. P., Prasher, P., Ansari, M. S., et al. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.109960 · Cited by 55
Verghese, J. P., Terry, A., de Natale, E. R., & Politis, M. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11236964 · Cited by 61
Aquaporin‐4‐independent volume dynamics of astroglial endfeet during cortical spreading depression
Rosic, A. B., Dukefoss, D. B., Åbjørsbråten, K. S., Tang, W., Jensen, V., Ottersen, O. P., Enger, R., & Nagelhus, E. A. (2019) · Glia · doi:10.1002/glia.23604 · Cited by 51
The glymphatic system and its role in cerebral homeostasis
Benveniste, H., Elkin, R., Heerdt, P. M., Koundal, S., Xue, Y., Lee, H., Wardlaw, J. M., & Tannenbaum, A. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00852.2019 · Cited by 57
Upright versus supine MRI: effects of body position on craniocervical CSF flow
Muccio, M., Chu, D., Minkoff, L. A., Kulkarni, N., Damadian, B. E., Damadian, R. V., & Ge, Y. (2021) · Fluids and Barriers of the CNS · doi:10.1186/s12987-021-00296-7 · Cited by 57
Matsumae, M., Kuroda, K., Yatsushiro, S., Hirayama, A., Hayashi, N., TAKIZAWA, K., Atsumi, H., & Sorimachi, T. (2019) · Neurologia medico-chirurgica · doi:10.2176/nmc.ra.2018-0272 · Cited by 52
Dwellers and Trespassers: Mononuclear Phagocytes at the Borders of the Central Nervous System
Ivan, D. C., Walthert, S., Berve, K., Steudler, J., & Locatelli, G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.609921 · Cited by 55
Glymphatic pathways in the gyrencephalic brain
Bèchet, N. B., Shanbhag, N. C., & Lundgaard, I. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x21996175 · Cited by 58
Liu, C., Habib, T., Salimeen, M., Pradhan, A., Singh, M., Wang, M., Wu, F., Zhang, Y., Gao, L., Yang, G., et al. (2020) · Seizure · doi:10.1016/j.seizure.2020.02.015 · Cited by 53
Cherkaoui, M. B., Vacca, O., Izabelle, C., Boulay, A., Boulogne, C., Gillet, C., Barnier, J., Rendón, Á., Cohen‐Salmon, M., & Vaillend, C. (2020) · Glia · doi:10.1002/glia.23941 · Cited by 52
Fang, Y., Huang, L., Wang, X., Si, X., Lenahan, C., Shi, H., Shao, A., Tang, J., Chen, S., Zhang, J., et al. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x211045748 · Cited by 52
The Role of Basement Membranes in Cerebral Amyloid Angiopathy
Howe, M. D., McCullough, L. D., & Urayama, A. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.601320 · Cited by 50
Mehta, N. H., Suss, R. A., Dyke, J. P., Theise, N. D., Chiang, G. C.-Y., Strauß, S., Saint-Louis, L. A., Li, Y., Pahlajani, S. S., Babaria, V., et al. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105776 · Cited by 51
Noninvasive ultrasonic induction of cerebrospinal fluid flow enhances intrathecal drug delivery
Aryal, M., Azadian, M. M., Hart, A. R., Macedo, N., Zhou, Q., Rosenthal, E. L., & Airan, R. D. (2022) · Journal of Controlled Release · doi:10.1016/j.jconrel.2022.06.067 · Cited by 54
The impact of ATP-binding cassette transporters in the diseased brain: Context matters
Baltira, C., Aronica, E., Elmquist, W. F., Langer, O., Löscher, W., Sarkaria, J. N., Wesseling, P., de Gooijer, M. C., & van Tellingen, O. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101609 · Cited by 54
Fluid outflow in the rat spinal cord: the role of perivascular and paravascular pathways
Liu, S., Lam, M. A., Sial, A. W., Hemley, S. J., Bilston, L. E., & Stoodley, M. A. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0098-1 · Cited by 52
Paravascular spaces: entry to or exit from the brain?
Bakker, E. N. T. P., Naessens, D. M. P., & VanBavel, E. (2018) · Experimental Physiology · doi:10.1113/ep087424 · Cited by 50
Direct nose to the brain nanomedicine delivery presents a formidable challenge
Yokel, R. A. (2021) · Wiley Interdisciplinary Reviews Nanomedicine and Nanobiotechnology · doi:10.1002/wnan.1767 · Cited by 53
Croci, M., Vinje, V., & Rognes, M. E. (2019) · Fluids and Barriers of the CNS · doi:10.1186/s12987-019-0152-7 · Cited by 50
Surface periarterial spaces of the mouse brain are open, not porous
Rivas, F. M., Liu, J., Martell, B. C., Du, T., Mestre, H., Nedergaard, M., Tithof, J., Thomas, J. H., & Kelley, D. H. (2020) · Journal of The Royal Society Interface · doi:10.1098/rsif.2020.0593 · Cited by 49
Computational modelling of fluid and solute transport in the brain
Martinac, A. D., & Bilston, L. E. (2019) · Biomechanics and Modeling in Mechanobiology · doi:10.1007/s10237-019-01253-y · Cited by 49
Quantitative analysis of macroscopic solute transport in the murine brain
Ray, L., Pike, M. M., Simon, M. J., Iliff, J. J., & Heys, J. J. (2021) · Fluids and Barriers of the CNS · doi:10.1186/s12987-021-00290-z · Cited by 50
DAT and TH expression marks human Parkinson’s disease in peripheral immune cells
Gopinath, A., Mackie, P. M., Hashimi, B., Buchanan, A. M., Smith, A. R., Bouchard, R. S., Shaw, G., Badov, M., Saadatpour, L., Gittis, A. H., et al. (2022) · npj Parkinson s Disease · doi:10.1038/s41531-022-00333-8 · Cited by 47
Correa, D., Scheuber, M. I., Shan, H., Weinmann, O., Baumgartner, Y. A., Harten, A., Wahl, A.-S., Skaar, K., & Schwab, M. E. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2200057120 · Cited by 51
Resolving the mysteries of brain clearance and immune surveillance
Kipnis, J., Benveniste, H., Eichmann, A., Thomas, J., Reich, D. S., Lewis, L. D., Tsai, L., Drieu, A., Bakker, E. N. T. P., Kelley, D. H., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.10.036 · Cited by 56
Ren, X., Liu, S., Lian, C., Li, H., Li, K., Li, L., & Zhao, G. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.659457 · Cited by 47
Immediate impact of yogic breathing on pulsatile cerebrospinal fluid dynamics
Yildiz, S., Grinstead, J. W., Hildebrand, A. D., Oshinski, J. N., Rooney, W. D., Lim, M. M., & Oken, B. (2022) · Scientific Reports · doi:10.1038/s41598-022-15034-8 · Cited by 44
Smith, A. J., & Verkman, A. S. (2019) · The Journal of Physiology · doi:10.1113/jp277636 · Cited by 52
Meningeal Lymphatics: A Review and Future Directions From a Clinical Perspective
Hershenhouse, K. S., Shauly, O., Gould, D. J., & Patel, K. M. (2019) · Neuroscience Insights · doi:10.1177/1179069519889027 · Cited by 47
Si, X., Gu, L., Song, Z., Zhou, C., Fang, Y., Jin, C., Wu, J., Gao, T., Guo, T., Guan, X., et al. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.580853 · Cited by 48
Sangalli, L., & Boggero, I. A. (2022) · Sleep Medicine · doi:10.1016/j.sleep.2022.11.012 · Cited by 50
Laaker, C. J., Baenen, C. M., Kovacs, K. G., Sándor, M., & Fábry, Z. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1233908 · Cited by 55
Correale, J. D., Halfón, M. J., Jack, D. L., Rubstein, A., & Villa, A. M. (2021) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2021.103264 · Cited by 48
The complex role of inflammation and gliotransmitters in Parkinson's disease
Gopinath, A., Mackie, P. M., Phan, L. T., Tansey, M. G., & Khoshbouei, H. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105940 · Cited by 48
Rodrigues, R. O., Shin, S.-R., & Bañobre-López, M. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02720-0 · Cited by 44
Association between Sleep, Alzheimer’s, and Parkinson’s Disease
Matsumoto, S., & Tsunematsu, T. (2021) · Biology · doi:10.3390/biology10111127 · Cited by 45
The blood–CSF–brain route of neurological disease: The indirect pathway into the brain
Cousins, O., Hodges, A., Schubert, J. J., Veronese, M., Turkheimer, F., Miyan, J. A., Engelhardt, B., & Roncaroli, F. (2021) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12789 · Cited by 49
Huttunen, K. M., Terasaki, T., Urtti, A. O., Montaser, A. B., & Uchida, Y. (2022) · Pharmaceutical Research · doi:10.1007/s11095-022-03193-2 · Cited by 45
Longitudinally persistent cerebrospinal fluid B cells can resist treatment in multiple sclerosis
Greenfield, A. L., Dandekar, R., Ramesh, A., Eggers, E. L., Wu, H., Laurent, S. A., Harkin, W. E., Pierson, N. S., Weber, M. S., Henry, R. G., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.126599 · Cited by 46
Naganawa, S., Ito, R., Kawai, H., Taoka, T., Yoshida, T., & Sone, M. (2020) · Magnetic Resonance in Medical Sciences · doi:10.2463/mrms.mp.2019-0182 · Cited by 41
Potential Role of Venular Amyloid in Alzheimer’s Disease Pathogenesis
Morrone, C. D., Bishay, J., & McLaurin, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061985 · Cited by 43
Modeling of Astrocyte Networks: Toward Realistic Topology and Dynamics
Вячеславовна, В. Д., Verisokin, A. Y., Postnov, D. E., & Brazhe, A. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.645068 · Cited by 44
The stress of losing sleep: Sex-specific neurobiological outcomes
Wright, C. J., Milosavljevic, S., & Pocivavsek, A. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100543 · Cited by 47
Gu, Z., Zhao, H., Song, Y., Kou, Y., Yang, W., Li, Y., Li, X., Ding, L., Sun, Z., Lin, J. Y., et al. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.01.019 · Cited by 46
Blood–Brain Barrier, Lymphatic Clearance, and Recovery: Ariadne’s Thread in Labyrinths of Hypotheses
SEMYACHKINA-GLUSHKOVSKAYA, O. V., Postnov, D. E., & Kurths, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123818 · Cited by 42
Gilbert, A., Elorza‐Vidal, X., Rancillac, A., Chagnot, A., Yetim, M., Hingot, V., Deffieux, T., Boulay, A.-C., Alvear‐Perez, R., Cisternino, S., et al. (2021) · eLife · doi:10.7554/elife.71379 · Cited by 43
Zhou, R., Li, J., Chen, Z., Wang, R., Shen, Y., Zhang, R., Zhou, F., & Zhang, Y. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02787-w · Cited by 41
Congdon, E. E., Jiang, Y., & Sigurdsson, E. M. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.12.002 · Cited by 38
Clearance Systems in the Brain, From Structure to Function
Liu, J., Guo, Y., Zhang, C., Zeng, Y., Luo, Y., & Wang, G. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.729706 · Cited by 46
Yoo, S., Kim, H., Kim, J., Kim, E., Kowsari, K., Reet, J. V., & Yoon, K. (2022) · Scientific Reports · doi:10.1038/s41598-022-17314-9 · Cited by 42
Integrated understanding of hydrocephalus — a practical approach for a complex disease
Thomale, U. (2021) · Child s Nervous System · doi:10.1007/s00381-021-05243-3 · Cited by 40
Impediment of Cerebrospinal Fluid Drainage Through Glymphatic System in Glioma
Xu, D., Zhou, J., Mei, H., Li, H., Sun, W., & Xu, H. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2021.790821 · Cited by 42
Magnetic Resonance Imaging and Modeling of the Glymphatic System
Kaur, J., Davoodi‐Bojd, E., Fahmy, L. M., Zhang, L., Ding, G., Hu, J., Zhang, Z., Chopp, M., & Jiang, Q. (2020) · Diagnostics · doi:10.3390/diagnostics10060344 · Cited by 40
CSF circulation and dispersion yield rapid clearance from intracranial compartments
Hornkjøl, M., Valnes, L. M., Ringstad, G. A., Rognes, M. E., Eide, P. K., Mardal, K., & Vinje, V. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.932469 · Cited by 41
Sensitivity analysis on a network model of glymphatic flow
Stevens, K. A., Tithof, J., Cook, D. D., Thomas, J. H., & Kelley, D. H. (2022) · Journal of The Royal Society Interface · doi:10.1098/rsif.2022.0257 · Cited by 39
Multimodal assessment of brain fluid clearance is associated with amyloid-beta deposition in humans
Zhou, L., Butler, T., Wang, X. H., Xi, K., Tanzi, E. B., Glodzik, L., Chiang, G. C.-Y., de Leon, M. J., & Li, Y. (2023) · Journal of Neuroradiology · doi:10.1016/j.neurad.2023.10.009 · Cited by 39
Sun, M., Zhang, M., Di, F., Bai, W., Sun, J., Zhang, M., Sun, J., Li, M., & Liang, X. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116874 · Cited by 41
Kamei, N., Suwabe, S., Arime, K., Bando, H., Murata, K., Yamaguchi, M., Yokoyama, N., Tanaka, E., Hashimoto, A., Kanazawa, T., et al. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13111745 · Cited by 38
Mechanisms of cerebrospinal fluid and brain interstitial fluid production
Xiang, J., Hua, Y., Xi, G., & Keep, R. F. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106159 · Cited by 37
Akins, P. T., & Guppy, K. H. (2019) · World Neurosurgery · doi:10.1016/j.wneu.2019.07.041 · Cited by 38
Deep sleep drives brain fluid oscillations
Grubb, S., & Lauritzen, M. (2019) · Science · doi:10.1126/science.aaz5191 · Cited by 36
How the Chemical Properties of GBCAs Influence Their Safety Profiles In Vivo
Do, Q. N., Lenkinski, R. E., Tircsó, G., & Kovács, Z. Z. (2021) · Molecules · doi:10.3390/molecules27010058 · Cited by 35
Mechanisms Underlying Aquaporin-4 Subcellular Mislocalization in Epilepsy
Szu, J. I., & Binder, D. K. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.900588 · Cited by 38
Involvement of trigeminal axons in nose-to-brain delivery of glucagon-like peptide-2 derivative
Akita, T., Oda, Y., Kimura, R., Nagai, M., Tezuka, A., Shimamura, M., Washizu, K., Oka, J., & Yamashita, C. (2022) · Journal of Controlled Release · doi:10.1016/j.jconrel.2022.09.047 · Cited by 35
Glymphatic system: a self-purification circulation in brain
Chen, S., Wang, H., Zhang, L., Xi, Y., Lu, Y., Yu, K., Zhu, Y., Regina, I., Bi, Y., & Tong, F. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1528995 · Cited by 40
Porro, G., Basile, M., Xie, Z., Tuveri, G. M., Battaglia, G., & Lopes, C. D. F. (2025) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2025.115637 · Cited by 39
Metadata
- Authors
- Abbott, N. J., Pizzo, M. E., Preston, J. E., Janigro, D., & Thorne, R. G.
- Affiliations
- King's College London (GB)
- University of Wisconsin–Madison (US)
- Case Western Reserve University (US)
- Corresponding author
- Abbott, N. Joan
- Thorne, Robert G.
- Venue
- Acta Neuropathologica
- Published
- 2018-02-10
- Volume
- 135
- Issue
- 3
- Pages
- 387-407
- ISSN
- 0001-6322 (ISSN-L)
- 1432-0533
- OpenAlex
- W2789376055
- Cited by
- 593
- References
- 202
- Citations by year
- 2026: 38 · 2025: 55 · 2024: 72 · 2023: 64 · 2022: 102 · 2021: 84 · 2020: 79 · 2019: 63 · 2018: 35
- FWCI
- 8.45
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Acta Neuropathologica (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Research Portal (King's College London) (submittedVersion, other-oa)
- Funders
- Michael J. Fox Foundation for Parkinson's Research (Therapeutic Pipeline Grant Award)
- NIH National Center for Advancing Translational Sciences (UL1TR000427, KL2TR00428)
- National Science Foundation Graduate Research Fellowship Program (DGE-1256259)
- Medical Research Council
- NIH Predoctoral Training Fellowship-Univ Wisconsin-Madison Clinical Engineering Program (NRSA T32 EBO11434)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Cerebrospinal fluid and hydrocephalus
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Keywords
- glymphatic system, cerebrospinal fluid, interstitial fluid, brain extracellular space, aquaporin-4, perivascular spaces, brain waste clearance, astrocytes, hydraulic conductivity, extracellular matrix, neurovascular unit, cerebrospinal fluid drainage, brain drug delivery, neuropathology
- MeSH terms
- Animals, Blood-Brain Barrier, Cerebrospinal Fluid, Humans, Extracellular Fluid, Hydrodynamics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review