Evidence map›Paper›PMID 28429734›Full record

ArticleScientific reports2017

Neuroprotective pentapeptide CN-105 is associated with reduced sterile inflammation and improved functional outcomes in a traumatic brain injury murine model.

Daniel T Laskowitz, Haichen Wang, Tony Chen, David T Lubkin, Viviana Cantillana, Tian Ming Tu, Dawn Kernagis, Guanen Zhou, Gary Macy, Bradley J Kolls and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03711903 (A Phase 2, Randomized, Double Blind, Placebo , Controlled Study To Evaluate The Administration of CN-105 In Participants With Acute Supratentorial Intracerebral Hemorrhage), which is not on this map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–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.

NCT03711903 phase2completednot on this mapstarted 2019, after this paper: background citation

A Phase 2, Randomized, Double Blind, Placebo , Controlled Study To Evaluate The Administration of CN-105 In Participants With Acute Supratentorial Intracerebral Hemorrhage

TypeinterventionalSponsorNational Neuroscience InstituteRan2019 to 2022Enrolled60ConditionsIntracerebral HemorrhageArmsAcetyl-Valine-Serine-Arginine-Arginine-Arginine-NH2 (Ac-VSRRR- NH2)., 0.9% Sodium-chloride
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  9. ApoE Mimetic Peptides as Therapy for Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
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  11. 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

11 authors.

Daniel T LaskowitzDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Haichen WangDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Tony ChenDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
David T LubkinDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Viviana CantillanaDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Tian Ming TuDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Dawn KernagisDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Guanen ZhouDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Gary MacyDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Bradley J KollsDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.
Hana N DawsonDepartment of Neurology, Duke University School of Medicine, Durham, NC 27710, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At present, there are no proven pharmacological treatments demonstrated to improve long term functional outcomes following traumatic brain injury(TBI). In the setting of non-penetrating TBI, sterile brain inflammatory responses are associated with the development of cerebral edema, intracranial hypertension, and secondary neuronal injury. There is increasing evidence that endogenous apolipoprotein E(apoE) modifies the neuroinflammatory response through its role in downregulating glial activation, however, the intact apoE holoprotein does not cross the blood-brain barrier due to its size. To address this limitation, we developed a small 5 amino acid apoE mimetic peptide(CN-105) that mimics the polar face of the apoE helical domain involved in receptor interactions. The goal of this study was to investigate the therapeutic potential of CN-105 in a murine model of closed head injury. Treatment with CN-105 was associated with a durable improvement in functional outcomes as assessed by Rotarod and Morris Water Maze and a reduction in positive Fluoro-Jade B stained injured neurons and microglial activation. Administration of CN-105 was also associated with reduction in mRNA expression of a subset of inflammatory and immune-related genes.

Indexed as

AnimalsApolipoproteins EBrain Injuries, TraumaticHippocampusInflammationMiceModels, AnimalNeuronsNeuroprotective AgentsPeptide FragmentsRecovery of FunctionApolipoproteins ENeuroprotective AgentsPeptide Fragments

Identifiers

PMID28429734
PMCPMC5399447

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Registered trials

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.