Evidence map›Paper›PMID 34691061›Full record

ReviewFrontiers in immunology2021

Neuroinflammatory Triangle Presenting Novel Pharmacological Targets for Ischemic Brain Injury.

Zaib A Shaheryar, Mahtab A Khan, Ch Sherjeel Adnan, Awais Ali Zaidi, Daniel Hänggi, Sajjad Muhammad

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

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  15. Macrophages in immunoregulation and therapeutics.Signal transduction and targeted therapy · 2023
    Review
  16. Association between fibrinogen-to-albumin ratio and hemorrhagic transformation after intravenous thrombolysis in ischemic stroke patients.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
    Article
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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

6 authors.

Zaib A ShaheryarInstitute for Experimental and Clinical Pharmacology and Toxicology, University of Lübeck, Lübeck, Germany.
Mahtab A KhanFaculty of Pharmacy, University of Central Punjab, Lahore, Pakistan.
Ch Sherjeel AdnanFaculty of Pharmacy, University of Lahore, Lahore, Pakistan.
Awais Ali ZaidiFaculty of Pharmacy, University of Lahore, Lahore, Pakistan.
Daniel HänggiDepartment of Neurosurgery, Faculty of Medicine and University Hospital Düsseldorf, Heinrich-Heine University Düsseldorf, Düsseldorf, Germany.
Sajjad MuhammadDepartment of Neurosurgery, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ischemic stroke is one of the leading causes of morbidity and mortality globally. Hundreds of clinical trials have proven ineffective in bringing forth a definitive and effective treatment for ischemic stroke, except a myopic class of thrombolytic drugs. That, too, has little to do with treating long-term post-stroke disabilities. These studies proposed diverse options to treat stroke, ranging from neurotropic interpolation to venting antioxidant activity, from blocking specific receptors to obstructing functional capacity of ion channels, and more recently the utilization of neuroprotective substances. However, state of the art knowledge suggests that more pragmatic focus in finding effective therapeutic remedy for stroke might be targeting intricate intracellular signaling pathways of the 'neuroinflammatory triangle': ROS burst, inflammatory cytokines, and BBB disruption. Experimental evidence reviewed here supports the notion that allowing neuroprotective mechanisms to advance, while limiting neuroinflammatory cascades, will help confine post-stroke damage and disabilities.

Indexed as

AldehydesBlood-Brain BarrierBrain IschemiaCytokinesDrug DiscoveryEndothelin-1Gene Expression RegulationHumansMalondialdehydeMicrogliaMolecular Targeted TherapyNeuroinflammatory DiseasesNeuroprotective AgentsNitric OxideOxidation-ReductionReactive Oxygen Species4-hydroxy-2-nonenalAldehydesCytokinesEndothelin-1MalondialdehydeNeuroprotective AgentsNitric OxideReactive Oxygen SpeciesReceptors, Cytokineblood brain barrierbrain microvascular endothelial cellcytokineneuroinflammationreactive oxidative species

Identifiers

PMID34691061
PMCPMC8529160

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.