Evidence map›Paper›PMID 30286110›Full record

ArticlePloS one2018

Non-invasive evaluation of neurovascular coupling in the murine retina by dynamic retinal vessel analysis.

Walid Albanna, Konstantin Kotliar, Jan Niklas Lüke, Serdar Alpdogan, Catharina Conzen, Ute Lindauer, Hans Clusmann, Jürgen Hescheler, Walthard Vilser, Toni Schneider and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Walid AlbannaInstitute for Neurophysiology, University of Cologne, Cologne, Germany.ORCID 0000-0001-9986-8739
Konstantin KotliarDepartment of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Aachen, Germany.
Jan Niklas LükeInstitute for Neurophysiology, University of Cologne, Cologne, Germany.
Serdar AlpdoganInstitute for Neurophysiology, University of Cologne, Cologne, Germany.
Catharina ConzenDepartment of Neurosurgery, RWTH Aachen University, Aachen, Germany.
Ute LindauerDepartment of Neurosurgery, RWTH Aachen University, Aachen, Germany.
Hans ClusmannDepartment of Neurosurgery, RWTH Aachen University, Aachen, Germany.
Jürgen HeschelerInstitute for Neurophysiology, University of Cologne, Cologne, Germany.
Walthard VilserIMEDOS Systems UG, Jena, Germany.
Toni SchneiderInstitute for Neurophysiology, University of Cologne, Cologne, Germany.
Gerrit Alexander SchubertDepartment of Neurosurgery, RWTH Aachen University, Aachen, Germany.
University of Cologne · DERWTH Aachen University · DEFH Aachen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImpairment of neurovascular coupling (NVC) was recently reported in the context of subarachnoid hemorrhage and may correlate with disease severity and outcome. However, previous techniques to evaluate NVC required invasive procedures. Retinal vessels may represent an alternative option for non-invasive assessment of NVC.

methodsA prototype of an adapted retinal vessel analyzer was used to assess retinal vessel diameter in mice. Dynamic vessel analysis (DVA) included an application of monochromatic flicker light impulses in predefined frequencies for evaluating NVC. All retinae were harvested after DVA and electroretinograms were performed.

resultsA total of 104 retinal scans were conducted in 21 male mice (90 scans). Quantitative arterial recordings were feasible only in a minority of animals, showing an emphasized reaction to flicker light impulses (8 mice; 14 scans). A characteristic venous response to flicker light, however, could observed in the majority of animals. Repeated measurements resulted in a significant decrease of baseline venous diameter (7 mice; 7 scans, p < 0.05). Ex-vivo electroretinograms, performed after in-vivo DVA, demonstrated a significant reduction of transretinal signaling in animals with repeated DVA (n = 6, p < 0.001).

conclusionsTo the best of our knowledge, this is the first non-invasive study assessing murine retinal vessel response to flicker light with characteristic changes in NVC. The imaging system can be used for basic research and enables the investigation of retinal vessel dimension and function in control mice and genetically modified animals.

Indexed as

AnimalsElectroretinographyLightMaleMiceMice, Inbred C57BLNeurovascular CouplingPhotic StimulationRetinaRetinal Vessels

Identifiers

PMID30286110
PMCPMC6171857
OpenAlexW2895619215

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Registered trials

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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.