Evidence map›Paper›PMID 31833045›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2020

Poly-Arginine Peptide-18 (R18) Reduces Brain Injury and Improves Functional Outcomes in a Nonhuman Primate Stroke Model.

Bruno P Meloni, Yining Chen, Kathleen A Harrison, Joseph Y Nashed, David J Blacker, Samantha M South, Ryan S Anderton, Frank L Mastaglia, Andrew Winterborn, Neville W Knuckey and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.6field-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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  12. Reperfusion plus Selective Intra-arterial Cooling (SI-AC) Improve Recovery in a Nonhuman Primate Model of Stroke.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Article
  13. Review
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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

11 authors at 3 institutions in 2 countries.

Bruno P MeloniPerron Institute for Neurological and Translational Science, Nedlands, Western Australia, 6009, Australia.
Yining ChenCentre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
Kathleen A HarrisonCentre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
Joseph Y NashedCentre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
David J BlackerPerron Institute for Neurological and Translational Science, Nedlands, Western Australia, 6009, Australia.
Samantha M SouthOffice of Research Enterprise, The University of Western Australia, Perth, Western Australia, Australia.
Ryan S AndertonPerron Institute for Neurological and Translational Science, Nedlands, Western Australia, 6009, Australia.
Frank L MastagliaPerron Institute for Neurological and Translational Science, Nedlands, Western Australia, 6009, Australia.
Andrew WinterbornCentre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
Neville W KnuckeyPerron Institute for Neurological and Translational Science, Nedlands, Western Australia, 6009, Australia.
Douglas J CookCentre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada. dj.cook@queensu.ca.
Queen's University · CAUniversity of Western Australia · AUPerron Institute for Neurological and Translational Science · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poly-arginine peptide-18 (R18) is neuroprotective in different rodent middle cerebral artery occlusion (MCAO) stroke models. In this study, we examined whether R18 treatment could reduce ischemic brain injury and improve functional outcome in a nonhuman primate (NHP) stroke model. A stroke was induced in male cynomolgus macaques by MCAO distal to the orbitofrontal branch of the MCA through a right pterional craniotomy, using a 5-mm titanium aneurysm clip for 90 min. R18 (1000 nmol/kg) or saline vehicle was administered intravenously 60 min after the onset of MCAO. Magnetic resonance imaging (MRI; perfusion-weighted imaging, diffusion-weighted imaging, or T2-weighted imaging) of the brain was performed 15 min, 24 h, and 28 days post-MCAO, and neurological outcome was assessed using the NHP stroke scale (NHPSS). Experimental endpoint was 28 days post-MCAO, treatments were randomized, and all procedures were performed blinded to treatment status. R18 treatment reduced infarct lesion volume by up to 65.2% and 69.7% at 24 h and 28 days poststroke, respectively. Based on NHPSS scores, R18-treated animals displayed reduced functional deficits. This study confirms the effectiveness of R18 in reducing the severity of ischemic brain injury and improving functional outcomes after stroke in a NHP model, and provides further support for its clinical development as a stroke neuroprotective therapeutic.

Indexed as

AnimalsBrainDisease Models, AnimalIntracellular Signaling Peptides and ProteinsMacaca fascicularisMaleNeuroprotective AgentsRecovery of FunctionStrokeIntracellular Signaling Peptides and ProteinsNeuroprotective AgentsR18 peptidemiddle cerebral artery occlusionneuroprotectionnonhuman primate (macaque)poly-arginine peptide-18R18Stroke

Identifiers

PMID31833045
PMCPMC7283416
OpenAlexW2996258182

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.