Evidence map›Paper›PMID 29569041›Full record

ArticleTranslational stroke research2019

Non-Invasive Multimodality Imaging Directly Shows TRPM4 Inhibition Ameliorates Stroke Reperfusion Injury.

Bo Chen, Gandi Ng, Yahui Gao, See Wee Low, Edwin Sandanaraj, Boominathan Ramasamy, Sakthivel Sekar, Kishore Bhakoo, Tuck Wah Soong, Bernd Nilius and 4 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Translational stroke research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  4. TRP Channels in Stroke.Neuroscience bulletin · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

Bo ChenDepartment of Research, National Neuroscience Institute, Singapore, Singapore.
Gandi NgDepartment of Research, National Neuroscience Institute, Singapore, Singapore.
Yahui GaoDepartment of Research, National Neuroscience Institute, Singapore, Singapore.
See Wee LowDepartment of Research, National Neuroscience Institute, Singapore, Singapore.
Edwin SandanarajDepartment of Research, National Neuroscience Institute, Singapore, Singapore.
Boominathan RamasamySingapore Bioimaging Consortium, Agency for Science, Technology and Research (A*STAR), 07-10 HELIOS, 11 Biopolis Way, Singapore, 138667, Singapore.
Sakthivel SekarSingapore Bioimaging Consortium, Agency for Science, Technology and Research (A*STAR), 07-10 HELIOS, 11 Biopolis Way, Singapore, 138667, Singapore.
Kishore BhakooSingapore Bioimaging Consortium, Agency for Science, Technology and Research (A*STAR), 07-10 HELIOS, 11 Biopolis Way, Singapore, 138667, Singapore.
Tuck Wah SoongDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Bernd NiliusDepartment of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Carol TangDepartment of Research, National Neuroscience Institute, Singapore, Singapore.
Edward G RobinsSingapore Bioimaging Consortium, Agency for Science, Technology and Research (A*STAR), 07-10 HELIOS, 11 Biopolis Way, Singapore, 138667, Singapore.
Julian GoggiSingapore Bioimaging Consortium, Agency for Science, Technology and Research (A*STAR), 07-10 HELIOS, 11 Biopolis Way, Singapore, 138667, Singapore. julian_goggi@sbic.a-star.edu.sg.
Ping LiaoDepartment of Research, National Neuroscience Institute, Singapore, Singapore. ping_liao@nni.com.sg.
National Neuroscience Institute · SGAgency for Science, Technology and Research · SGSingapore Bioimaging Consortium · SGDuke-NUS Medical School · SGKU Leuven · BELaboratoire d'Excellence Canaux Ioniques d'Intérêt Thérapeutique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transient receptor potential melastatin 4 (TRPM4) channel has been suggested to play a key role in the treatment of ischemic stroke. However, in vivo evaluation of TRPM4 channel, in particular by direct channel suppression, is lacking. In this study, we used multimodal imaging to assess edema formation and quantify the amount of metabolically functional brain salvaged after a rat model of stroke reperfusion. TRPM4 upregulation in endothelium emerges as early as 2 h post-stroke induction. Expression of TRPM4 channel was suppressed directly in vivo by treatment with siRNA; scrambled siRNA was used as a control. T2-weighted MRI suggests that TRPM4 inhibition successfully reduces edema by 30% and concomitantly salvages functionally active brain, measured by

Indexed as

AnimalsBlood-Brain BarrierBrain EdemaDisease Models, AnimalFluorodeoxyglucose F18Functional LateralityGene Expression RegulationImage Processing, Computer-AssistedInfarction, Middle Cerebral ArteryMaleMicroarray AnalysisMultimodal ImagingPhosphopyruvate HydrataseRatsRats, WistarReperfusion InjuryFluorodeoxyglucose F18Phosphopyruvate HydrataseRNA, MessengerRNA, Small InterferingTRPM4 protein, ratTRPM Cation Channelsvon Willebrand FactorEndotheliumMRIPETReperfusionStroke

Identifiers

PMID29569041
PMCPMC6327008
OpenAlexW2791600949

What OpenQuestion holds

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LicenceCC BY
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.