Evidence map›Paper›PMID 25690472›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2015

A mouse model of small-vessel disease that produces brain-wide-identified microocclusions and regionally selective neuronal injury.

Gergely Silasi, Jennifer She, Jamie D Boyd, Songchao Xue, Timothy H Murphy

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 62 citations in OpenAlex.

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  11. Non-classical monocytes promote neurovascular repair in cerebral small vessel disease associated with microinfarctions via CX3CR1.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
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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

5 authors at 1 institution in 1 country.

Gergely Silasi1] Department of Psychiatry, Kinsmen Laboratory of Neurological Research, Vancouver, British Columbia, Canada [2] Brain Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.
Jennifer SheDepartment of Psychiatry, Kinsmen Laboratory of Neurological Research, Vancouver, British Columbia, Canada.
Jamie D Boyd1] Department of Psychiatry, Kinsmen Laboratory of Neurological Research, Vancouver, British Columbia, Canada [2] Brain Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.
Songchao XueDepartment of Psychiatry, Kinsmen Laboratory of Neurological Research, Vancouver, British Columbia, Canada.
Timothy H Murphy1] Department of Psychiatry, Kinsmen Laboratory of Neurological Research, Vancouver, British Columbia, Canada [2] Brain Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.
University of British Columbia · CA

Funding

Canadian Institutes of Health Research MOP-111009
6 · The paper itself

Abstract

We developed a mouse model of small-vessel disease where occlusions are produced through endovascular injection of fluorescent microspheres that target ~12 μm diameter penetrating arterioles and can be localized in histology. Using Thy1-GFP transgenic mice, we visualized the impact of microocclusions on neuronal structure. Microocclusions in the hippocampus produce cell loss or neuronal atrophy (~7% of lodged microspheres led to microinfarcts), while axons within white matter tracts, as well as the striatum and thalamus became blebbed or disrupted. Although the neocortex contained more occlusions than other structures, labeled layer 5 neurons were relatively resistant to structural damage, with <2% of the lodged microspheres producing obvious neuronal damage.

Indexed as

Arterial Occlusive DiseasesAxonsCerebrovascular DisordersHippocampusWhite MatterAnimalsArteriolesFemaleHumansMaleMiceMice, TransgenicMicrospheres

Identifiers

PMID25690472
PMCPMC4420872
OpenAlexW2005059170

What OpenQuestion holds

Textmetadata
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.