Evidence map›Paper›PMID 28779572›Full record

ReviewReviews in the neurosciences2017

Brain extracellular space, hyaluronan, and the prevention of epileptic seizures.

Katherine L Perkins, Amaia M Arranz, Yu Yamaguchi, Sabina Hrabetova

Open access · greenAbstract readReview
In one paragraph

Review in Reviews in the neurosciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Ephaptic conduction in tonic-clonic seizures.Frontiers in neurology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Biomaterial-basedCancer pathogenesis and therapy · 2023
    Review
  11. Extracellular Matrix Regulation in Physiology and in Brain Disease.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Fluid transport in the brain.Physiological reviews · 2022
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Katherine L PerkinsDepartment of Physiology and Pharmacology and The Robert F. Furchgott Center for Neural and Behavioral Science, State University of New York Downstate Medical Center, 450 Clarkson Avenue, MSC 29, Brooklyn, NY 11203, USA
Amaia M ArranzVIB Center for Brain and Disease Research, 3000 Leuven, Belgium; and KU Leuven Department for Neurosciences, Leuven Institute for Neurodegenerative Disorders (LIND) and Universitaire Ziekenhuizen Leuven, University of Leuven, 3000 Leuven, Belgium
Yu YamaguchiHuman Genetics Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA
Sabina HrabetovaDepartment of Cell Biology and The Robert F. Furchgott Center for Neural and Behavioral Science, State University of New York Downstate Medical Center, Brooklyn, NY 11203, USA
SUNY Downstate Health Sciences University · USSanford Burnham Prebys Medical Discovery Institute · USVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

Dynamic Microdomains in Brain Extracellular SpaceR01NS047557 · NINDS · SUNY DOWNSTATE MEDICAL CENTER · PI HRABETOVA, SABINA · 2004 to 2014
$2.6M
NINDS NIH HHS R01 NS047557
6 · The paper itself

Abstract

Mutant mice deficient in hyaluronan (HA) have an epileptic phenotype. HA is one of the major constituents of the brain extracellular matrix. HA has a remarkable hydration capacity, and a lack of HA causes reduced extracellular space (ECS) volume in the brain. Reducing ECS volume can initiate or exacerbate epileptiform activity in many in vitro models of epilepsy. There is both in vitro and in vivo evidence of a positive feedback loop between reduced ECS volume and synchronous neuronal activity. Reduced ECS volume promotes epileptiform activity primarily via enhanced ephaptic interactions and increased extracellular potassium concentration; however, the epileptiform activity in many models, including the brain slices from HA synthase-3 knockout mice, may still require glutamate-mediated synaptic activity. In brain slice epilepsy models, hyperosmotic solution can effectively shrink cells and thus increase ECS volume and block epileptiform activity. However, in vivo, the intravenous administration of hyperosmotic solution shrinks both brain cells and brain ECS volume. Instead, manipulations that increase the synthesis of high-molecular-weight HA or decrease its breakdown may be used in the future to increase brain ECS volume and prevent seizures in patients with epilepsy. The prevention of epileptogenesis is also a future target of HA manipulation. Head trauma, ischemic stroke, and other brain insults that initiate epileptogenesis are known to be associated with an early decrease in high-molecular-weight HA, and preventing that decrease in HA may prevent the epileptogenesis.

Indexed as

AnimalsBrainEpilepsyExtracellular SpaceHyaluronan SynthasesHyaluronic AcidMiceHyaluronan SynthasesHyaluronic Acidanticonvulsantephapticepilepsyextracellular matrixhyaluronic acidpotassium

Identifiers

PMID28779572
PMCPMC5705429
OpenAlexW2744076086

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.