Abbott NJ, Bundgaard M, Cserr HF. (1985). Tightness of the blood-brain barrier and evidence for brain interstitial fluid flow in the cuttlefish, Sepia officinalis. The Journal of physiology. 368 [PubMed]
Aitken PG, Somjen GG. (1986). The sources of extracellular potassium accumulation in the CA1 region of hippocampal slices. Brain research. 369 [PubMed]
Albeck MJ, Børgesen SE, Gjerris F, Schmidt JF, Sørensen PS. (1991). Intracranial pressure and cerebrospinal fluid outflow conductance in healthy subjects. Journal of neurosurgery. 74 [PubMed]
Amiry-Moghaddam M, Frydenlund DS, Ottersen OP. (2004). Anchoring of aquaporin-4 in brain: molecular mechanisms and implications for the physiology and pathophysiology of water transport. Neuroscience. 129 [PubMed]
Arizono M, Inavalli VVGK, Bancelin S, Fernández-Monreal M, Nägerl UV. (2021). Super-resolution shadow imaging reveals local remodeling of astrocytic microstructures and brain extracellular space after osmotic challenge. Glia. 69 [PubMed]
Asgari M, de Zélicourt D, Kurtcuoglu V. (2015). How astrocyte networks may contribute to cerebral metabolite clearance. Scientific reports. 5 [PubMed]
Bakker EN et al. (2016). Lymphatic Clearance of the Brain: Perivascular, Paravascular and Significance for Neurodegenerative Diseases. Cellular and molecular neurobiology. 36 [PubMed]
Bell M, Bartol T, Sejnowski T, Rangamani P. (2019). Dendritic spine geometry and spine apparatus organization govern the spatiotemporal dynamics of calcium. The Journal of general physiology. 151 [PubMed]
Bohr T et al. (2022). The glymphatic system: Current understanding and modeling. iScience. 25 [PubMed]
Bojarskaite L et al. (2020). Astrocytic Ca2+ signaling is reduced during sleep and is involved in the regulation of slow wave sleep. Nature communications. 11 [PubMed]
Bojarskaite L et al. (2023). Sleep cycle-dependent vascular dynamics in male mice and the predicted effects on perivascular cerebrospinal fluid flow and solute transport. Nature communications. 14 [PubMed]
Bradbury MW, Cserr HF, Westrop RJ. (1981). Drainage of cerebral interstitial fluid into deep cervical lymph of the rabbit. The American journal of physiology. 240 [PubMed]
Chen KC, Nicholson C. (2000). Spatial buffering of potassium ions in brain extracellular space. Biophysical journal. 78 [PubMed]
Croci M, Vinje V, Rognes ME. (2019). Uncertainty quantification of parenchymal tracer distribution using random diffusion and convective velocity fields. Fluids and barriers of the CNS. 16 [PubMed]
Cserr HF, Cooper DN, Suri PK, Patlak CS. (1981). Efflux of radiolabeled polyethylene glycols and albumin from rat brain. The American journal of physiology. 240 [PubMed]
Daversin-Catty C, Vinje V, Mardal KA, Rognes ME. (2020). The mechanisms behind perivascular fluid flow. PloS one. 15 [PubMed]
Dietzel I, Heinemann U, Hofmeier G, Lux HD. (1982). Stimulus-induced changes in extracellular Na+ and Cl- concentration in relation to changes in the size of the extracellular space. Experimental brain research. 46 [PubMed]
Eide PK. (2008). Comparison of simultaneous continuous intracranial pressure (ICP) signals from ICP sensors placed within the brain parenchyma and the epidural space. Medical engineering & physics. 30 [PubMed]
Eide PK, Saehle T. (2010). Is ventriculomegaly in idiopathic normal pressure hydrocephalus associated with a transmantle gradient in pulsatile intracranial pressure? Acta neurochirurgica. 152 [PubMed]
Ellingsrud AJ, Boullé N, Farrell PE, Rognes ME. (2021). Accurate numerical simulation of electrodiffusion and water movement in brain tissue. Mathematical medicine and biology : a journal of the IMA. 38 [PubMed]
Fultz NE et al. (2019). Coupled electrophysiological, hemodynamic, and cerebrospinal fluid oscillations in human sleep. Science (New York, N.Y.). 366 [PubMed]
Gardner-Medwin AR. (1983). Analysis of potassium dynamics in mammalian brain tissue. The Journal of physiology. 335 [PubMed]
Geva-Sagiv M, Nir Y. (2019). Local Sleep Oscillations: Implications for Memory Consolidation. Frontiers in neuroscience. 13 [PubMed]
Gleiser C et al. (2016). Aquaporin-4 in Astroglial Cells in the CNS and Supporting Cells of Sensory Organs-A Comparative Perspective. International journal of molecular sciences. 17 [PubMed]
Grisar T. (1984). Glial and neuronal Na+-K+ pump in epilepsy. Annals of neurology. 16 Suppl [PubMed]
Halnes G et al. (2016). Effect of Ionic Diffusion on Extracellular Potentials in Neural Tissue. PLoS computational biology. 12 [PubMed]
Halnes G, Ostby I, Pettersen KH, Omholt SW, Einevoll GT. (2013). Electrodiffusive model for astrocytic and neuronal ion concentration dynamics. PLoS computational biology. 9 [PubMed]
Holter KE et al. (2017). Interstitial solute transport in 3D reconstructed neuropil occurs by diffusion rather than bulk flow. Proceedings of the National Academy of Sciences of the United States of America. 114 [PubMed]
Iliff JJ et al. (2012). A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid ß. Science translational medicine. 4 [PubMed]
Jin BJ, Smith AJ, Verkman AS. (2016). Spatial model of convective solute transport in brain extracellular space does not support a "glymphatic" mechanism. The Journal of general physiology. 148 [PubMed]
Jin BJ, Zhang H, Binder DK, Verkman AS. (2013). Aquaporin-4-dependent K(+) and water transport modeled in brain extracellular space following neuroexcitation. The Journal of general physiology. 141 [PubMed]
Kedarasetti RT, Drew PJ, Costanzo F. (2020). Arterial pulsations drive oscillatory flow of CSF but not directional pumping. Scientific reports. 10 [PubMed]
Kedarasetti RT, Drew PJ, Costanzo F. (2022). Arterial vasodilation drives convective fluid flow in the brain: a poroelastic model. Fluids and barriers of the CNS. 19 [PubMed]
LaMontagne E, Muotri AR, Engler AJ. (2022). Recent advancements and future requirements in vascularization of cortical organoids. Frontiers in bioengineering and biotechnology. 10 [PubMed]
Larsen BR, MacAulay N. (2017). Activity-dependent astrocyte swelling is mediated by pH-regulating mechanisms. Glia. 65 [PubMed]
Li Y, Konstantopoulos K, Zhao R, Mori Y, Sun SX. (2020). The importance of water and hydraulic pressure in cell dynamics. Journal of cell science. 133 [PubMed]
Liu S et al. (2019). Regulation of Cell Behavior by Hydrostatic Pressure. Applied mechanics reviews. 71 [PubMed]
Lu YB et al. (2006). Viscoelastic properties of individual glial cells and neurons in the CNS. Proceedings of the National Academy of Sciences of the United States of America. 103 [PubMed]
MacAulay N. (2021). Molecular mechanisms of brain water transport. Nature reviews. Neuroscience. 22 [PubMed]
Mestre H et al. (2020). Cerebrospinal fluid influx drives acute ischemic tissue swelling. Science (New York, N.Y.). 367 [PubMed]
Mestre H et al. (2018). Aquaporin-4-dependent glymphatic solute transport in the rodent brain. eLife. 7 [PubMed]
Nagelhus EA, Mathiisen TM, Ottersen OP. (2004). Aquaporin-4 in the central nervous system: cellular and subcellular distribution and coexpression with KIR4.1. Neuroscience. 129 [PubMed]
Nedergaard M, Goldman SA. (2020). Glymphatic failure as a final common pathway to dementia. Science (New York, N.Y.). 370 [PubMed]
Newman EA. (1993). Inward-rectifying potassium channels in retinal glial (Müller) cells. The Journal of neuroscience : the official journal of the Society for Neuroscience. 13 [PubMed]
Newton AJH, McDougal RA, Hines ML, Lytton WW. (2018). Using NEURON for Reaction-Diffusion Modeling of Extracellular Dynamics. Frontiers in neuroinformatics. 12 [PubMed]
Nicholson C, ten Bruggencate G, Stöckle H, Steinberg R. (1978). Calcium and potassium changes in extracellular microenvironment of cat cerebellar cortex. Journal of neurophysiology. 41 [PubMed]
Nielsen S et al. (1997). Specialized membrane domains for water transport in glial cells: high-resolution immunogold cytochemistry of aquaporin-4 in rat brain. The Journal of neuroscience : the official journal of the Society for Neuroscience. 17 [PubMed]
Odette LL, Newman EA. (1988). Model of potassium dynamics in the central nervous system. Glia. 1 [PubMed]
Ransom BR, Yamate CL, Connors BW. (1985). Activity-dependent shrinkage of extracellular space in rat optic nerve: a developmental study. The Journal of neuroscience : the official journal of the Society for Neuroscience. 5 [PubMed]
Rasmussen R, O'Donnell J, Ding F, Nedergaard M. (2020). Interstitial ions: A key regulator of state-dependent neural activity? Progress in neurobiology. 193 [PubMed]
Ray L, Iliff JJ, Heys JJ. (2019). Analysis of convective and diffusive transport in the brain interstitium. Fluids and barriers of the CNS. 16 [PubMed]
Ray LA, Pike M, Simon M, Iliff JJ, Heys JJ. (2021). Quantitative analysis of macroscopic solute transport in the murine brain. Fluids and barriers of the CNS. 18 [PubMed]
Rosenberg GA, Kyner WT, Estrada E. (1980). Bulk flow of brain interstitial fluid under normal and hyperosmolar conditions. The American journal of physiology. 238 [PubMed]
Salman MM, Kitchen P, Iliff JJ, Bill RM. (2021). Aquaporin 4 and glymphatic flow have central roles in brain fluid homeostasis. Nature reviews. Neuroscience. 22 [PubMed]
Stokum JA et al. (2018). SUR1-TRPM4 and AQP4 form a heteromultimeric complex that amplifies ion/water osmotic coupling and drives astrocyte swelling. Glia. 66 [PubMed]
Szczygielski J, Kopańska M, Wysocka A, Oertel J. (2021). Cerebral Microcirculation, Perivascular Unit, and Glymphatic System: Role of Aquaporin-4 as the Gatekeeper for Water Homeostasis. Frontiers in neurology. 12 [PubMed]
Szentistványi I, Patlak CS, Ellis RA, Cserr HF. (1984). Drainage of interstitial fluid from different regions of rat brain. The American journal of physiology. 246 [PubMed]
Tait MJ, Saadoun S, Bell BA, Papadopoulos MC. (2008). Water movements in the brain: role of aquaporins. Trends in neurosciences. 31 [PubMed]
Utzschneider D, Kocsis J, Devor M. (1992). Mutual excitation among dorsal root ganglion neurons in the rat. Neuroscience letters. 146 [PubMed]
Vinje V et al. (2019). Respiratory influence on cerebrospinal fluid flow - a computational study based on long-term intracranial pressure measurements. Scientific reports. 9 [PubMed]
Wagshul ME, Eide PK, Madsen JR. (2011). The pulsating brain: A review of experimental and clinical studies of intracranial pulsatility. Fluids and barriers of the CNS. 8 [PubMed]
Walz W, Hertz L. (1983). Intracellular ion changes of astrocytes in response to extracellular potassium. Journal of neuroscience research. 10 [PubMed]
Walz W, Hinks EC. (1985). Carrier-mediated KCl accumulation accompanied by water movements is involved in the control of physiological K+ levels by astrocytes. Brain research. 343 [PubMed]
Wang T, Kleiven S, Li X. (2021). Electroosmosis Based Novel Treatment Approach for Cerebral Edema. IEEE transactions on bio-medical engineering. 68 [PubMed]
Xie L et al. (2013). Sleep drives metabolite clearance from the adult brain. Science (New York, N.Y.). 342 [PubMed]
Xu ZY et al. (2009). Responses of astrocyte to simultaneous glutamate and arachidonic acid treatment. Neurochemistry international. 55 [PubMed]
Østby I et al. (2009). Astrocytic mechanisms explaining neural-activity-induced shrinkage of extraneuronal space. PLoS computational biology. 5 [PubMed]