# Brain Extracellular Space: From an Overlooked Dimension to Catalyst of a Novel Neuroscience Paradigm

**Authors:** Hongbin Han, Hui Dai, Leonor Serrano Lopes, Ruiqing Ni, Benjamin F. Combes, Yangjing Song, Hanbo Tan, Meng Xu, Hongfeng Li, Shuhong Lv, Zhaohe Yang, Tianzi Gao, Mengyu Zhang, Yang Shi, Jingjing Shao, Yanni Zhang, Wanyi Fu

PMC · DOI: 10.34133/cbsystems.0529 · Cyborg and Bionic Systems · 2026-03-04

## TL;DR

This paper argues that ignoring the brain's extracellular space has hindered progress in treating brain disorders and proposes a new approach that includes it.

## Contribution

The paper introduces a novel neuroscience paradigm by emphasizing the importance of the brain extracellular space in drug development and clinical practice.

## Key findings

- Ignoring the brain extracellular space is linked to low translational success of CNS therapies.
- Recent imaging and measurement advances make it feasible to integrate the ECS into neuroscience research.
- Incorporating the ECS could reshape therapeutic strategies for brain disorders.

## Abstract

Despite huge investment, therapies for brain disorders remain largely ineffective in clinical practice. Accumulating evidence indicates that this low translational success is closely linked to the long-standing overlook of the brain extracellular space (ECS) in preclinical research, clinical practice, and regulatory frameworks. After over 4 decades of scientific exploration, particularly with recent breakthroughs in imaging and quantitative measurement methods, it is timely to integrate the ECS into the current neuroscience framework. This paper investigates underlying determinants of low translational success of central nervous system drugs and therapeutic devices, reviews the historical and technical bottlenecks that lead to the neglect of ECS research, and emphasizes its transformative potential in reshaping therapeutic strategies. We propose incorporating the ECS into neuroscience research, clinical regulatory assessment, and medical education, thereby establishing a comprehensive paradigm that omits no physical space for precision therapeutics targeting brain disorders.

## Full-text entities

- **Genes:** Vegfc (vascular endothelial growth factor C) [NCBI Gene 114111], Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, Tnc (tenascin C) [NCBI Gene 116640], Snca (synuclein alpha) [NCBI Gene 29219], ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, CHAT (choline O-acetyltransferase) [NCBI Gene 1103] {aka CHOACTASE, CMS1A, CMS1A2, CMS6}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Mir146a (microRNA 146a) [NCBI Gene 100314241] {aka rno-mir-146a}, Aqp4 (aquaporin 4) [NCBI Gene 11829] {aka WCH4}, Fn1 (fibronectin 1) [NCBI Gene 25661] {aka FIBNEC, fn-1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, Ntrk2 (neurotrophic receptor tyrosine kinase 2) [NCBI Gene 25054] {aka RATTRKB1, TRKB1, Tkrb, trk-B, trkB}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}, Psen1 (presenilin 1) [NCBI Gene 19164] {aka Ad3h, PS-1, PS1, S182}, AQP4 (aquaporin 4) [NCBI Gene 361] {aka MIWC, MLC4, WCH4, hAQP4}, Slc1a2 (solute carrier family 1 member 2) [NCBI Gene 29482] {aka Eaat2, Glt, Glt-1}, ADH5 (alcohol dehydrogenase 5 (class III), chi polypeptide) [NCBI Gene 128] {aka ADH-3, ADHX, AMEDS, BMFS7, FALDH, FDH}, Aqp4 (aquaporin 4) [NCBI Gene 25293] {aka AQP-4, Miwc, WCH4}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** phototoxicity (MESH:D017484), infarct (MESH:D007238), somatic symptom disorder (MESH:D000071896), neurological diseases (MESH:D020271), cerebral edema (MESH:D001929), postoperative delirium (MESH:D000071257), Neuronal damage (MESH:D009410), Stroke (MESH:D020521), dementia (MESH:D003704), amyloid (MESH:C000718787), moyamoya ischemic disease (MESH:D009072), MDI (MESH:C564543), neurological deficits (MESH:D009461), MDD (MESH:D003865), ischemia (MESH:D007511), seizure (MESH:D012640), metabolic abnormalities (MESH:D008659), MS (MESH:D009103), brain tumors (MESH:D001932), memory deficits (MESH:D008569), ALS (MESH:D008113), neurofibrillary (MESH:D055956), glioblastoma (MESH:D005909), status epilepticus (MESH:D013226), cognitive and memory impairment (MESH:D003072), axonal injury (MESH:D001480), fibrosis (MESH:D005355), Glioma (MESH:D005910), Epilepsy (MESH:D004827), reperfusion injury (MESH:D015427), amyotrophic lateral sclerosis (MESH:D000690), neurodegeneration (MESH:D019636), PVS (MESH:D018458), neural injury (MESH:D014947), inflammation (MESH:D007249), ISS (MESH:D007984), PD (MESH:D010300), bradykinesia (MESH:D018476), tremor (MESH:D014202), MCAO (MESH:D020244), mitochondrial dysfunction (MESH:D028361), pain (MESH:D010146), Demyelination (MESH:D003711), hypertensive (MESH:D006973), brain disease (MESH:D001927), cerebral ischemia (MESH:D002545), cerebral ischemic injury (MESH:D017202), malignant (MESH:D009369), Ischemic stroke (MESH:D002544), temporal lobe epilepsy (MESH:D004833), ALPS (MESH:D056735), AD (MESH:D000544), neurotoxic (MESH:D020258), edema (MESH:D004487), CNS diseases (MESH:D002493), ECS (MESH:C535509), SCZ (MESH:D012559), neuroinflammation (MESH:D000090862), traumatic brain injury (MESH:D000070642), cerebrovascular dysregulation (MESH:D002561)
- **Chemicals:** mannitol (MESH:D008353), IP3 (MESH:D015544), galantamine (MESH:D005702), ATP (MESH:D000255), water (MESH:D014867), Ach (MESH:D000109), TB (MESH:D013725), TMA (MESH:C071868), isoflurane (MESH:D007530), hydrogen (MESH:D006859), glutamate (MESH:D018698), tacrine (MESH:D013619), bumetanide (MESH:D002034), norepinephrine (MESH:D009638), GABA (MESH:D005680), Dopaminergic (MESH:D004298), HA (MESH:D006820), ROS (MESH:D017382), formaldehyde (MESH:D005557), NO (MESH:D009569), donepezil (MESH:D000077265), dextrans (MESH:D003911), levodopa (MESH:D007980), tetramethylammonium (MESH:C027917), Ca2+ (-), rivastigmine (MESH:D000068836), sodium (MESH:D012964), citicoline (MESH:D003566), Gd-DTPA (MESH:D019786), K+ (MESH:D011188), polyethylene glycol (MESH:D011092), furosemide (MESH:D005665), dexmedetomidine (MESH:D020927), aducanumab (MESH:C000600266), pentobarbital (MESH:D010424), coenzyme Q10 (MESH:C024989), ADP (MESH:D000244), agar (MESH:D000362)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12957555/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12957555/full.md

## References

225 references — full list in the complete paper: https://tomesphere.com/paper/PMC12957555/full.md

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Source: https://tomesphere.com/paper/PMC12957555