Evidence map›Paper›PMID 30555120›Full record

ArticleNeurologia medico-chirurgica2019

Real-time Imaging of an Experimental Intracranial Aneurysm in Rats.

Haruka Miyata, Kampei Shimizu, Hirokazu Koseki, Yu Abekura, Hiroharu Kataoka, Susumu Miyamoto, Kazuhiko Nozaki, Shuh Narumiya, Tomohiro Aoki

Open access · goldAbstract read
In one paragraph

Article in Neurologia medico-chirurgica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. A novel histological occlusion classification for coiled aneurysms based on multiphoton microscopy.Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2025
    Article
  3. Article
  4. 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

9 authors at 4 institutions in 1 country.

Haruka MiyataDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular Center.
Kampei ShimizuDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular Center.
Hirokazu KosekiDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular Center.
Yu AbekuraDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular Center.
Hiroharu KataokaDepartment of Neurosurgery, Kyoto University Graduate School of Medicine.
Susumu MiyamotoDepartment of Neurosurgery, Kyoto University Graduate School of Medicine.
Kazuhiko NozakiDepartment of Neurosurgery, Shiga University of Medical Science.
Shuh NarumiyaAlliance Laboratory for Advanced Medical Research, Medical Innovation Center, Kyoto University Graduate School of Medicine.
Tomohiro AokiDepartment of Molecular Pharmacology, Research Institute, National Cerebral and Cardiovascular Center.
Kyoto University · JPShiga University of Medical Science · JPJapan Agency for Medical Research and Development · JPTokyo Women's Medical University Adachi Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subarachnoid hemorrhage due to rupture of a pre-existing intracranial aneurysm has quite a poor outcome in spite of intensive medical care. Hemodynamic stress loaded on intracranial arterial walls is considered as a trigger and a regulator of formation and progression of the disease, but how intracranial arterial walls or intracranial aneurysm walls behave under hemodynamic stress loading remains unclear. The purpose of this study was to visualize and analyze the wall motion of intracranial aneurysms to detect a pathological flow condition. We subjected a transgenic rat line, in which endothelial cells are specifically visualized by expression of a green fluorescent protein, to an intracranial aneurysm model and observed a real-time motion of intracranial arterial walls or intracranial aneurysm walls by a multiphoton laser confocal microscopy. The anterior cerebral artery-olfactory artery bifurcation was surgically exposed for the monitoring. First, we observed the proper flow-dependent physiological dilatation of a contralateral intracranial artery in response to increase of blood flow by one side of carotid ligation. Next, we observed intracranial aneurysm lesions induced in a rat model and confirmed that a wall motion of the dome was static, whereas that of the neck was more dynamic in response to pulsation of blood flow. We successfully monitored a real-time motion of intracranial aneurysm walls. Findings obtained from such a real-time imaging will provide us many insights especially about the correlation of mechanical force and the pathogenesis of the disease and greatly promote our understanding of the disease.

Indexed as

AnimalsDisease Models, AnimalIntracranial AneurysmMicroscopy, ConfocalRatsRats, WistarVasodilationbio-imagingintracranial aneurysmratreal-time imagingwall motion

Identifiers

PMID30555120
PMCPMC6350001
OpenAlexW2904895505

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.