Evidence map›Paper›PMID 29177102›Full record

ArticleTranslational neuroscience2017

Assessment of R18, COG1410, and APP96-110 in Excitotoxicity and Traumatic Brain Injury.

Li Shan Chiu, Ryan S Anderton, Jane L Cross, Vince W Clark, Adam B Edwards, Neville W Knuckey, Bruno P Meloni

Open access · goldAbstract read
In one paragraph

Article in Translational neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Bidentatide, a Novel Plant Peptide Derived fromInternational journal of molecular sciences · 2021
    Article
  10. Article
  11. Advances in D-Amino Acids in Neurological Research.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Effect of Polyarginine Peptide R18D Following a Traumatic Brain Injury in Sprague-Dawley Rats.Current therapeutic research, clinical and experimental · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

7 authors at 3 institutions in 1 country.

Li Shan ChiuPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
Ryan S AndertonPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
Jane L CrossPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
Vince W ClarkPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
Adam B EdwardsPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
Neville W KnuckeyPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
Bruno P MeloniPerron Institute for Neurological and Translational Sciences, Nedlands, Western Australia, 6009, Australia.
University of Western Australia · AUPerron Institute for Neurological and Translational Science · AUSir Charles Gairdner Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cationic arginine-rich and poly-arginine peptides (referred to as CARPs) have potent neuroprotective properties in in vitro excitotoxicity and in vivo models of stroke. Traumatic brain injury (TBI) shares many pathophysiological processes as stroke, including excitotoxicity. Therefore, we evaluated our lead peptide, poly-arginine R18, with the COG1410 and APP96-110 peptides, which have neuroprotective actions following TBI. In an in vitro cortical neuronal glutamic acid excitotoxicity injury model, R18 was highly neuroprotective and reduced neuronal calcium influx, while COG1410 and APP96-110 displayed modest neuroprotection and were less effective at reducing calcium influx. In an impact-acceleration closed-head injury model (Marmarou model), R18, COG1410, and APP96-110 were administered intravenously (300 nmol/kg) at 30 minutes after injury in male Sprague-Dawley rats. When compared to vehicle, no peptide significantly improved functional outcomes, however the R18 and COG1410 treatment groups displayed positive trends in the adhesive tape test and rotarod assessments. Similarly, no peptide had a significant effect on hippocampal neuronal loss, however a significant reduction in axonal injury was observed for R18 and COG1410. In conclusion, this study has demonstrated that R18 is significantly more effective than COG1410 and APP96-110 at reducing neuronal injury and calcium influx following excitotoxicity, and that both R18 and COG1410 reduce axonal injury following TBI. Additional dose response and treatment time course studies are required to further assess the efficacy of R18 in TBI.

Indexed as

APP96-110axonal injurycationic arginine-rich peptides (CARPs)COG1410neuroprotectionR18TBI

Identifiers

PMID29177102
PMCPMC5700203
OpenAlexW2769348921

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.