Evidence map›Paper›PMID 28260801›Full record

ReviewActa pharmacologica Sinica2017

Regulation of microglial activation in stroke.

Shou-Cai Zhao, Ling-Song Ma, Zhao-Hu Chu, Heng Xu, Wen-Qian Wu, Fudong Liu

Open access · bronzeAbstract readReview
In one paragraph

Review in Acta pharmacologica Sinica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 219 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
219citing papers in PubMed, 2 pooled it
12.2field-weighted citation impact, top 1% 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

219 citing papers in PubMed, 2 syntheses or guidelines pooled it, 416 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. A combined extract ofJournal of ginseng research · 2026
    Article
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  6. Lipid metabolism, microglia, and stroke.Neural regeneration research · 2026
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159 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 2 countries.

Shou-Cai ZhaoDepartment of Neurology, Wannan Medical College Yijishan Hospital, Wuhu 241001, China.
Ling-Song MaDepartment of Neurology, Wannan Medical College Yijishan Hospital, Wuhu 241001, China.
Zhao-Hu ChuDepartment of Neurology, Wannan Medical College Yijishan Hospital, Wuhu 241001, China.
Heng XuDepartment of Neurology, Wannan Medical College Yijishan Hospital, Wuhu 241001, China.
Wen-Qian WuDepartment of Neurology, Wannan Medical College Yijishan Hospital, Wuhu 241001, China.
Fudong LiuDepartment of Neurology, University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX 77030, USA.
Wannan Medical College · CNFirst Affiliated Hospital of Wannan Medical College · CNThe University of Texas Health Science Center at Houston · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When ischemic stroke occurs, oxygen and energy depletion triggers a cascade of events, including inflammatory responses, glutamate excitotoxicity, oxidative stress, and apoptosis that result in a profound brain injury. The inflammatory response contributes to secondary neuronal damage, which exerts a substantial impact on both acute ischemic injury and the chronic recovery of the brain function. Microglia are the resident immune cells in the brain that constantly monitor brain microenvironment under normal conditions. Once ischemia occurs, microglia are activated to produce both detrimental and neuroprotective mediators, and the balance of the two counteracting mediators determines the fate of injured neurons. The activation of microglia is defined as either classic (M1) or alternative (M2): M1 microglia secrete pro-inflammatory cytokines (TNFα, IL-23, IL-1β, IL-12, etc) and exacerbate neuronal injury, whereas the M2 phenotype promotes anti-inflammatory responses that are reparative. It has important translational value to regulate M1/M2 microglial activation to minimize the detrimental effects and/or maximize the protective role. Here, we discuss various regulators of microglia/macrophage activation and the interaction between microglia and neurons in the context of ischemic stroke.

Indexed as

AnimalsAntigens, CDAstrocytesBrain IschemiaHumansInflammationInflammation MediatorsInterferon Regulatory FactorsMacrophage ActivationMicrogliaMicroRNAsNeuronsOligodendrogliaReceptor Cross-TalkReceptors, ImmunologicSignal TransductionAntigens, CDInflammation MediatorsInterferon Regulatory FactorsMicroRNAsReceptors, Immunologic

Identifiers

PMID28260801
PMCPMC5386316
OpenAlexW2592378998

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.