Evidence map›Paper›PMID 27514013›Full record

ArticleBrain pathology (Zurich, Switzerland)2017

Long-term survival and regeneration of neuronal and vasculature cells inside the core region after ischemic stroke in adult mice.

Michael Qize Jiang, Ying-Ying Zhao, Wenyuan Cao, Zheng Zachory Wei, Xiaohuan Gu, Ling Wei, Shan Ping Yu

Abstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 66 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

7 authors at 3 institutions in 2 countries.

Michael Qize JiangDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Ying-Ying ZhaoDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Wenyuan CaoDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Zheng Zachory WeiDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Xiaohuan GuDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Ling WeiDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Shan Ping YuDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA.
Emory University · USAtlanta VA Health Care System · USCapital Medical University · CN

Funding

Stroke Treatment by Chemically-induced HypothermiaR44NS073378 · NINDS · JT PHARMACEUTICALS, INC. · PI DIX, THOMAS A., YU, SHAN P. · 2017 to 2019
$2.9M
Application of optogenetics in iPS cell transplantation therapy for ischemic stroR01NS085568 · NINDS · EMORY UNIVERSITY · PI GROSS, ROBERT E, WEI, LING · 2014 to 2018
$1.7M
Stem cell transplantation therapy via intranasal delivery after strokeR01NS091585 · NINDS · EMORY UNIVERSITY · PI WEI, LING · 2016 to 2020
$1.7M
Transplantation of Pre-conditioned Bone Marrow Mesenchymal Stem Cells after IscheR01NS062097 · NINDS · EMORY UNIVERSITY · PI WEI, LING · 2010 to 2014
$1.7M
Stroke Treatment by Chemically-induced HypothermiaR42NS073378 · NINDS · JT PHARMACEUTICALS, INC. · PI DIX, THOMAS A., YU, SHAN P. · 2015 to 2016
$1.5M
Stroke Treatment by Chemically-Induced HypothermiaR41NS073378 · NINDS · HALIMED PHARMACEUTICALS, INC. · PI DIX, THOMAS A., YU, SHAN P. · 2011 to 2012
$884k
FEI Transmission Electron Microscope with Tomography CapabilityS10RR025679 · NCRR · EMORY UNIVERSITY · PI SPEARMAN, PAUL W. · 2009 to 2009
$500k
Promoting axonal growth and tissue repair in stem cell therapy after strokeR21NS075338 · NINDS · EMORY UNIVERSITY · PI WEI, LING · 2011 to 2012
$426k
Protection of the Brain by Chemical HypothermiaI01RX000666 · VA · VETERANS HEALTH ADMINISTRATION · PI YU, SHAN P. · 2015 to 2016
–
NCRR NIH HHS S10 RR025679NINDS NIH HHS R01 NS062097NINDS NIH HHS R01 NS085568NINDS NIH HHS R01 NS091585NINDS NIH HHS R21 NS075338NINDS NIH HHS R41 NS073378NINDS NIH HHS R42 NS073378NINDS NIH HHS R44 NS073378RRD VA I01 RX000666
6 · The paper itself

Abstract

Focal cerebral ischemia results in an ischemic core surrounded by the peri-infarct region (penumbra). Most research attention has been focused on penumbra while the pattern of cell fates inside the ischemic core is poorly defined. In the present investigation, we tested the hypothesis that, inside the ischemic core, some neuronal and vascular cells could survive the initial ischemic insult while regenerative niches might exist many days after stroke in the adult brain. Adult mice were subjected to focal cerebral ischemia induced by permanent occlusion of distal branches of the middle cerebral artery (MCA) plus transient ligations of bilateral common carotid artery (CCA). The ischemic insult uniformly reduced the local cerebral blood flow (LCBF) by 90%. Massive cell death occurred due to multiple mechanisms and a significant infarction was cultivated in the ischemic cortex 24 h later. Nevertheless, normal or even higher levels of brain-derived neurotrophic factor (BDNF) and vascular endothelial growth factor (VEGF) persistently remained in the core tissue, some NeuN-positive and Glut-1/College IV-positive cells with intact ultrastructural features resided in the core 7-14 days post stroke. BrdU-positive but TUNEL-negative neuronal and endothelial cells were detected in the core where extensive extracellular matrix infrastructure developed. Meanwhile, GFAP-positive astrocytes accumulated in the penumbra and Iba-1-positive microglial/macrophages invaded the core several days after stroke. The long term survival of neuronal and vascular cells inside the ischemic core was also seen after a severe ischemic stroke induced by permanent embolic occlusion of the MCA. We demonstrate that a therapeutic intervention of pharmacological hypothermia could save neurons/endothelial cells inside the core. These data suggest that the ischemic core is an actively regulated brain region with residual and newly formed viable neuronal and vascular cells acutely and chronically after at least some types of ischemic strokes.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalBrain InfarctionCarotid StenosisCells, CulturedCerebrovascular CirculationDisease Models, AnimalEndothelial CellsGene Expression RegulationGlucose Transporter Type 1Infarction, Middle Cerebral ArteryMembrane ProteinsMiceMice, Inbred C57BLMice, TransgenicMicrogliaABS-201Anti-Inflammatory Agents, Non-Steroidalbeta3 tubulin, mouseGlucose Transporter Type 1Membrane ProteinsNeuroprotective AgentsOligopeptidespenumbra protein, mousePhosphopyruvate HydrataseSlc2a1 protein, mouseTubulincell survivalischemic coreneurotrophic factorsneurovasculatureregeneration

Identifiers

PMID27514013
PMCPMC5303567
OpenAlexW2510802850

What OpenQuestion holds

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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.