Evidence map›Paper›PMID 19372455›Full record

ArticleStroke2009

Acute vascular disruption and aquaporin 4 loss after stroke.

Beth Friedman, Christian Schachtrup, Philbert S Tsai, Andy Y Shih, Katerina Akassoglou, David Kleinfeld, Patrick D Lyden

Open access · hybridAbstract read
In one paragraph

Article in Stroke, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 69 citations in OpenAlex.

  1. Influence of an AQP4 haplotype and sleep duration on early Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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  19. Improved long-term outcome after transient cerebral ischemia in aquaporin-4 knockout mice.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2017
    Article
  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

7 authors at 1 institution in 1 country.

Beth FriedmanDepartment of Neurosciences, UCSD School of Medicine, San Diego, CA, USA.
Christian Schachtrup
Philbert S Tsai
Andy Y Shih
Katerina Akassoglou
David Kleinfeld
Patrick D Lyden
United States Department of Veterans Affairs · US

Funding

UltrasoundP50NS044148 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MEYER, BRETT C · 2003 to 2012
$15.1M
U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
Mechanisms of Fibrin Action in Multiple SclerosisR01NS052189 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI AKASSOGLOU, KATERINA · 2005 to 2016
$5.1M
Sensorimotor Loops in Vibrissa SomatosensationR01NS058668 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KLEINFELD, DAVID · 2007 to 2016
$2.4M
Role of Angiogenesis Following StrokeR01NS043300 · NINDS · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI LYDEN, PATRICK D · 2003 to 2006
$1.1M
Quantitation of Early Vascular Leakage after StrokeR21NS052565 · NINDS · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI LYDEN, PATRICK D · 2005 to 2006
$363k
NINDS NIH HHS NS047101NINDS NIH HHS NS052189NINDS NIH HHS NS052565NINDS NIH HHS NS058668NINDS NIH HHS NS43300NINDS NIH HHS P30 NS047101NINDS NIH HHS P50 NS044148NINDS NIH HHS R01 NS043300NINDS NIH HHS R01 NS052189NINDS NIH HHS R01 NS058668NINDS NIH HHS R21 NS052565PHS HHS EBOO383201
6 · The paper itself

Abstract

background and purposeIschemic protection has been demonstrated by a decrease in stroke-infarct size in transgenic mice with deficient Aquaporin 4 (AQP4) expression. However, it is not known whether AQP4 is rapidly reduced during acute stroke in animals with normal AQP4 phenotype, which may provide a potential self-protective mechanism.

methodsAdult male rats underwent transient occlusion of the middle cerebral artery (tMCAo) for 1 to 8 hours followed by reperfusion for 30 minutes. Protein and mRNA expression of AQP4 and glial fibrillary acidic protein (GFAP) were determined by Western blot and rtPCR. Fluorescence quantitation was obtained with laser scanning cytometry (LSC) for Cy5-tagged immunoreactivity along with fluorescein signals from pathological uptake of plasma-borne high-molecular-weight fluorescein-dextran. Cell death was assessed with in vivo Propidium Iodide (PI) nucleus labeling.

resultsIn the ischemic hemisphere in tissue sections, patches of fluorescein-dextran uptake were overlapped with sites of focal loss of AQP4 immunoreactivity after tMCAo of 1 to 8 hours duration. However, the average levels of AQP4 protein and mRNA, determined in homogenates of whole striatum, were not significantly reduced after 8 hours of tMCAo. Tissue section cytometry (LSC) of immunoreactivity in scan areas with high densities of fluorescein-dextran uptake demonstrated reductions in AQP4, but not in IgG or GFAP, after tMCAo of 2 hours or longer. Scan areas with low densities of fluorescein-dextran did not lose AQP4. There was sparse astrocyte cell death as only 1.7+/-0.85% (mean, SD) of DAPI labeled cells were PI- and GFAP-labeled after 8 hours of tMCAo.

conclusionsDuring acute tMCAo, a rapid loss of AQP4 immunoreactivity from viable astrocytes can occur. However, AQP4 loss is spatially selective and occurs primarily in regions of vascular damage.

Indexed as

Acute DiseaseAnimalsAquaporin 4AstrocytesBlood VesselsBlotting, WesternBrain EdemaCapillariesColoring AgentsGlial Fibrillary Acidic ProteinImage Processing, Computer-AssistedImmunohistochemistryMaleMicroscopy, Fluorescence, MultiphotonMiddle Cerebral ArteryPropidiumAquaporin 4Coloring AgentsGlial Fibrillary Acidic ProteinPropidiumRNA

Identifiers

PMID19372455
PMCPMC2753985
OpenAlexW2098732711

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.