Evidence map›Paper›PMID 26660233›Full record

ArticleJournal of neuroscience research2016

An optimized dosing regimen of cimaglermin (neuregulin 1β3, glial growth factor 2) enhances molecular markers of neuroplasticity and functional recovery after permanent ischemic stroke in rats.

Jennifer F Iaci, Tom J Parry, Zhihong Huang, Elias Pavlopoulos, Seth P Finklestein, Jingmei Ren, Anthony Caggiano

Abstract read
In one paragraph

Article in Journal of neuroscience research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. The case for neuregulin-1 as a clinical treatment for stroke.Frontiers in cellular neuroscience · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Neuregulin in Health and Disease.International journal of brain disorders and treatment · 2018
    Article
  10. A Growth Tonic for Heart Failure?JACC. Basic to translational science · 2016
    Article
  11. Article
  12. Article
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.

Jennifer F IaciAcorda Therapeutics, Inc., Ardsley, New York.
Tom J ParryAcorda Therapeutics, Inc., Ardsley, New York.
Zhihong HuangAcorda Therapeutics, Inc., Ardsley, New York.
Elias PavlopoulosAcorda Therapeutics, Inc., Ardsley, New York.
Seth P FinklesteinBiotrofix, Inc., Waltham, Massachusetts.
Jingmei RenBiotrofix, Inc., Waltham, Massachusetts.
Anthony CaggianoAcorda Therapeutics, Inc., Ardsley, New York.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cimaglermin (neuregulin 1β3, glial growth factor 2) is a neuregulin growth factor family member in clinical development for chronic heart failure. Previously, in a permanent middle cerebral artery occlusion (pMCAO) rat stroke model, systemic cimaglermin treatment initiated up to 7 days after ischemia onset promoted recovery without reduced lesion volume. Presented here to extend the evidence are two studies that use a rat stroke model to evaluate the effects of cimaglermin dose level and dose frequency initiated 24 hr after pMCAO. Forelimb- and hindlimb-placing scores (proprioceptive behavioral tests), body-swing symmetry, and infarct volume were compared between treatment groups (n = 12/group). Possible mechanisms underlying cimaglermin-mediated neurologic recovery were examined through axonal growth and synapse formation histological markers. Cimaglermin was evaluated over a wider dose range (0.02, 0.1, or 1.0 mg/kg) than doses previously shown to be effective but used the same dosing regimen (2 weeks of daily intravenous administration, then 1 week without treatment). The dose-frequency study used the dose-ranging study's most effective dose (1.0 mg/kg) to compare daily, once per week, and twice per week dosing for 3 weeks (then 1 week without treatment). Dose- and frequency-dependent functional improvements were observed with cimaglermin without reduced lesion volume. Cimaglermin treatment significantly increased growth-associated protein 43 expression in both hemispheres (particularly somatosensory and motor cortices) and also increased synaptophysin expression. These data indicate that cimaglermin enhances recovery after stroke. Immunohistochemical changes were consistent with axonal sprouting and synapse formation but not acute neuroprotection. Cimaglermin represents a potential clinical development candidate for ischemic stroke treatment.

Indexed as

Gene Expression RegulationInfarction, Middle Cerebral ArteryNerve Tissue ProteinsNeuregulin-1Recovery of FunctionAnalysis of VarianceAnimalsBrain InfarctionDisease Models, AnimalDose-Response Relationship, DrugDrug Administration ScheduleMaleRatsRats, Sprague-DawleyTime FactorsNerve Tissue ProteinsNeuregulin-1growth factorischemiaplasticityRRID:AB_10374876RRID:AB_10562420RRID:AB_10562715RRID:AB_2107282RRID:AB_2138153RRID:AB_2298772RRID:AB_2313609RRID:AB_778203RRID:RGD_734476

Identifiers

PMID26660233
PMCPMC4737294

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.