Evidence map›Paper›PMID 30909935›Full record

ArticleFluids and barriers of the CNS2019

Effect of extradural constriction on CSF flow in rat spinal cord.

Joel A Berliner, Thomas Woodcock, Elmira Najafi, Sarah J Hemley, Magdalena Lam, Shaokoon Cheng, Lynne E Bilston, Marcus A Stoodley

Open access · goldAbstract read
In one paragraph

Article in Fluids and barriers of the CNS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Subarachnoid-subarachnoid bypass versus extradural decompression for adhesive syringomyelia: experimental and early clinical evaluation.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
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  11. Ependymal Cilia: Physiology and Role in Hydrocephalus.Frontiers in molecular neuroscience · 2022
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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

8 authors at 3 institutions in 2 countries.

Joel A BerlinerFaculty of Medicine and Health Sciences, Macquarie University, Technology Place, Sydney, NSW, 2109, Australia. joel.berliner@hdr.mq.edu.au.
Thomas WoodcockFaculty of Medicine and Health Sciences, Macquarie University, Technology Place, Sydney, NSW, 2109, Australia.
Elmira NajafiFaculty of Medicine and Health Sciences, Macquarie University, Technology Place, Sydney, NSW, 2109, Australia.
Sarah J HemleyFaculty of Medicine and Health Sciences, Macquarie University, Technology Place, Sydney, NSW, 2109, Australia.
Magdalena LamFaculty of Medicine and Health Sciences, Macquarie University, Technology Place, Sydney, NSW, 2109, Australia.
Shaokoon ChengDepartment of Engineering, Faculty of Science and Engineering, Macquarie University, Sydney, NSW, 2109, Australia.
Lynne E BilstonNeuroscience Research Australia, Margarete Ainsworth Building, Barker Street, Sydney, NSW, 2031, Australia.
Marcus A StoodleyFaculty of Medicine and Health Sciences, Macquarie University, Technology Place, Sydney, NSW, 2109, Australia.
Macquarie University · AUJohn F. Kennedy University · USUNSW Sydney · AU

Funding

Brain Foundation of Australia -Column of Hope Research Grant -National Health and Medical Research Council 604008
6 · The paper itself

Abstract

backgroundFluid homeostasis in the central nervous system (CNS) is essential for normal neurological function. Cerebrospinal fluid (CSF) in the subarachnoid space and interstitial fluid circulation in the CNS parenchyma clears metabolites and neurotransmitters and removes pathogens and excess proteins. A thorough understanding of the normal physiology is required in order to understand CNS fluid disorders, including post-traumatic syringomyelia. The aim of this project was to compare fluid transport, using quantitative imaging of tracers, in the spinal cord from animals with normal and obstructed spinal subarachnoid spaces.

methodsA modified extradural constriction model was used to obstruct CSF flow in the subarachnoid space at the cervicothoracic junction (C7-T1) in Sprague-Dawley rats. Alexa-Fluor 647 Ovalbumin conjugate was injected into the cisterna magna at either 1 or 6 weeks post-surgery. Macroscopic and microscopic fluorescent imaging were performed in animals sacrificed at 10 or 20 min post-injection. Tracer fluorescence intensity was compared at cervical and thoracic spinal cord levels between control and constriction animals at each post-surgery and post-injection time point. The distribution of tracer around arterioles, venules and capillaries was also compared.

resultsMacroscopically, the fluorescence intensity of CSF tracer was significantly greater in spinal cords from animals with a constricted subarachnoid space compared to controls, except at 1 week post-surgery and 10 min post-injection. CSF tracer fluorescence intensity from microscopic images was significantly higher in the white matter of constriction animals 1 week post surgery and 10 min post-injection. At 6 weeks post-constriction surgery, fluorescence intensity in both gray and white matter was significantly increased in animals sacrificed 10 min post-injection. At 20 min post-injection this difference was significant only in the white matter and was less prominent. CSF tracer was found predominantly in the perivascular spaces of arterioles and venules, as well as the basement membrane of capillaries, highlighting the importance of perivascular pathways in the transport of fluid and solutes in the spinal cord.

conclusionsThe presence of a subarachnoid space obstruction may lead to an increase in fluid flow within the spinal cord tissue, presenting as increased flow in the perivascular spaces of arterioles and venules, and the basement membranes of capillaries. Increased fluid retention in the spinal cord in the presence of an obstructed subarachnoid space may be a critical step in the development of post-traumatic syringomyelia.

Indexed as

Cerebrospinal FluidHydrodynamicsAnimalsConstriction, PathologicDisease Models, AnimalFluorescent DyesMaleMicroscopy, FluorescenceOptical ImagingRats, Sprague-DawleySpinal CordSubarachnoid SpaceSyringomyeliaFluorescent DyesCerebrospinal fluidPerivascularSpinal cordSyringomyelia

Identifiers

PMID30909935
PMCPMC6434898
OpenAlexW2936756030

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.